Hidehiro Mizusawa
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Computer Science
Hidehiro Mizusawa's Degrees
- PhD Computer Science University of Tokyo
- Masters Computer Science University of Tokyo
- Bachelors Computer Science University of Tokyo
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(Suggest an Edit or Addition)Hidehiro Mizusawa's Published Works
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Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author
Published Works
- Visualization of Aβ42(43) and Aβ40 in senile plaques with end-specific Aβ monoclonals: Evidence that an initially deposited species is Aβ42(43) (1994) (1560)
- Visualization of A beta 42(43) and A beta 40 in senile plaques with end-specific A beta monoclonals: evidence that an initially deposited species is A beta 42(43). (1994) (567)
- Ultrasensitive human prion detection in cerebrospinal fluid by real-time quaking-induced conversion (2011) (486)
- Down regulation of DJ-1 enhances cell death by oxidative stress, ER stress, and proteasome inhibition. (2003) (367)
- Quantifying prion disease penetrance using large population control cohorts (2016) (352)
- Inhibition of intracellular hepatitis C virus replication by synthetic and vector‐derived small interfering RNAs (2003) (312)
- 123I-metaiodobenzylguanidine myocardial scintigraphy in Parkinson’s disease (1999) (274)
- Delayed-onset ataxia in mice lacking α-tocopherol transfer protein: Model for neuronal degeneration caused by chronic oxidative stress (2001) (250)
- Spinocerebellar ataxia type 31 is associated with "inserted" penta-nucleotide repeats containing (TGGAA)n. (2009) (249)
- Mutations in COQ2 in familial and sporadic multiple-system atrophy. (2013) (246)
- Efficient In Vivo Delivery of siRNA to the Liver by Conjugation of α-Tocopherol. (2008) (226)
- Biochemical Characterization of the Core Structure of α-Synuclein Filaments* (2002) (214)
- 123I-MIBG myocardial scintigraphy for differentiating Parkinson's disease from other neurodegenerative parkinsonism: a systematic review and meta-analysis. (2012) (208)
- The neurology of COVID-19 revisited: A proposal from the Environmental Neurology Specialty Group of the World Federation of Neurology to implement international neurological registries (2020) (200)
- NKT cell-dependent amelioration of a mouse model of multiple sclerosis by altering gut flora. (2008) (193)
- NKT cell-dependent amelioration of a mouse model of multiple sclerosis by altering gut flora. (2008) (193)
- Midkine Inhibits Caspase‐Dependent Apoptosis via the Activation of Mitogen‐Activated Protein Kinase and Phosphatidylinositol 3‐Kinase in Cultured Neurons (1999) (190)
- Abundant expression and cytoplasmic aggregations of [alpha]1A voltage-dependent calcium channel protein associated with neurodegeneration in spinocerebellar ataxia type 6. (1999) (188)
- Cognitive status correlates with white matter alteration in Parkinson's disease (2012) (185)
- Genetic association of the very low density lipoprotein (VLDL) receptor gene with sporadic Alzheimer's disease (1995) (180)
- Profound Cardiac Sympathetic Denervation Occurs in Parkinson Disease (2005) (180)
- Prospective 10-year surveillance of human prion diseases in Japan. (2010) (168)
- Efficacy and safety of leuprorelin in patients with spinal and bulbar muscular atrophy (JASMITT study): a multicentre, randomised, double-blind, placebo-controlled trial (2010) (159)
- Lithium Therapy Improves Neurological Function and Hippocampal Dendritic Arborization in a Spinocerebellar Ataxia Type 1 Mouse Model (2007) (159)
- A carbohydrate-binding protein, Galectin-1, promotes proliferation of adult neural stem cells. (2006) (153)
- APP717 missense mutation affects the ratio of amyloid beta protein species (A beta 1-42/43 and a beta 1-40) in familial Alzheimer's disease brain. (1994) (150)
- Efficient in vivo delivery of siRNA to the liver by conjugation of alpha-tocopherol. (2008) (148)
- Human neural stem/progenitor cells, expanded in long‐term neurosphere culture, promote functional recovery after focal ischemia in Mongolian gerbils (2004) (147)
- R-spondin, a novel gene with thrombospondin type 1 domain, was expressed in the dorsal neural tube and affected in Wnts mutants. (2004) (147)
- Critical Contribution of Tumor Necrosis Factor–Related Apoptosis-Inducing Ligand (Trail) to Apoptosis of Human Cd4+T Cells in HIV-1–Infected Hu-Pbl-Nod-Scid Mice (2001) (144)
- Spinocerebellar ataxia type 6 knockin mice develop a progressive neuronal dysfunction with age-dependent accumulation of mutant CaV2.1 channels (2008) (141)
- ApoE–ε4 and early–onset Alzheimer's (1994) (137)
- Japanese families with autosomal dominant pure cerebellar ataxia map to chromosome 19p13.1-p13.2 and are strongly associated with mild CAG expansions in the spinocerebellar ataxia type 6 gene in chromosome 19p13.1. (1997) (135)
- Glycaemic control boosts glucosylated nanocarrier crossing the BBB into the brain (2017) (132)
- Consensus Paper: Neuroimmune Mechanisms of Cerebellar Ataxias (2015) (132)
- Early Detection of Abnormal Prion Protein in Genetic Human Prion Diseases Now Possible Using Real-Time QUIC Assay (2013) (131)
- An autosomal dominant cerebellar ataxia linked to chromosome 16q22.1 is associated with a single-nucleotide substitution in the 5' untranslated region of the gene encoding a protein with spectrin repeat and Rho guanine-nucleotide exchange-factor domains. (2005) (124)
- Friedreich‐like ataxia with retinitis pigmentosa caused by the His101Gln mutation of the α‐Tocopherol transfer protein gene (1997) (122)
- Spinocerebellar Ataxia Type 6 Mutation Alters P-type Calcium Channel Function* (2000) (122)
- Analysis of the Adrenal Gland Is Useful for Evaluating Pathology of the Peripheral Autonomic Nervous System in Lewy Body Disease (2007) (116)
- Clinical diagnosis of MM2-type sporadic Creutzfeldt-Jakob disease (2005) (112)
- Selective suppression of cerebellar GABAergic transmission by an autoantibody to glutamic acid decarboxylase (1999) (104)
- Clinical, neuropathological, and molecular study in two families with spinocerebellar ataxia type 6 (SCA6) (1999) (103)
- Biochemical characterization of the core structure of alpha-synuclein filaments. (2002) (101)
- Non-human primate model of amyotrophic lateral sclerosis with cytoplasmic mislocalization of TDP-43 (2012) (97)
- Depletion of Vitamin E Increases Amyloid β Accumulation by Decreasing Its Clearances from Brain and Blood in a Mouse Model of Alzheimer Disease* (2009) (97)
- Variants associated with Gaucher disease in multiple system atrophy (2015) (97)
- Regulatory Role of RNA Chaperone TDP-43 for RNA Misfolding and Repeat-Associated Translation in SCA31 (2017) (94)
- Ataxin-3 Is Translocated into the Nucleus for the Formation of Intranuclear Inclusions in Normal and Machado–Joseph Disease Brains (2000) (93)
- 123 I-metaiodobenzylguanidine myocardial scintigraphy in Parkinson’s disease (1999) (93)
- Galectin-1 regulates neurogenesis in the subventricular zone and promotes functional recovery after stroke (2007) (91)
- Bax-inhibiting peptide protects cells from polyglutamine toxicity caused by Ku70 acetylation (2007) (90)
- Regional analysis of age‐related decline in dopamine transporters and dopamine D2‐like receptors in human striatum (2009) (89)
- Deletion of vitamin E enhances phenotype of Alzheimer disease model mouse. (2006) (86)
- DNA/RNA heteroduplex oligonucleotide for highly efficient gene silencing (2015) (84)
- Aβ1–40 but not Aβ1–42 levels in cortex correlate with apolipoprotein E ϵ4 allele dosage in sporadic Alzheimer's disease (1997) (84)
- Morphological Purkinje cell changes in spinocerebellar ataxia type 6 (2000) (83)
- Intensity of chronic cerebral hypoperfusion determines white/gray matter injury and cognitive/motor dysfunction in mice (2009) (81)
- A gene on SCA4 locus causes dominantly inherited pure cerebellar ataxia (2000) (81)
- Comprehensive systematic review summary: Treatment of cerebellar motor dysfunction and ataxia (2018) (81)
- Suppression of Experimental Autoimmune Encephalomyelitis by Ghrelin1 (2009) (80)
- Dose‐dependent association of apolipoprotein e allele ε4 with late‐onset, sporadic Alzheimer's disease (1994) (78)
- Chronic inflammatory demyelinating polyneuropathy: decreased claudin-5 and relocated ZO-1 (2004) (77)
- Tumor necrosis factor-related apoptosis-inducing ligand induces neuronal death in a murine model of HIV central nervous system infection (2003) (76)
- Cytoplasmic and nuclear polyglutamine aggregates in SCA6 Purkinje cells (2001) (75)
- Altered Microstructure in Corticospinal Tract in Idiopathic Normal Pressure Hydrocephalus: Comparison with Alzheimer Disease and Parkinson Disease with Dementia (2011) (74)
- Postmortem study of ataxia with retinitis pigmentosa by mutation of the α-tocopherol transfer protein gene (2000) (74)
- Selective loss of Purkinje cells in a patient with anti-glutamic acid decarboxylase antibody-associated cerebellar ataxia (2006) (71)
- Distal myopathy with rimmed vacuoles: Novel mutations in the GNE gene (2002) (70)
- A clinical and genetic study in a large cohort of patients with spinocerebellar ataxia type 6 (2004) (70)
- Amyloid β protein 1–42/43 (Aβ 1–42/43) in cerebellar diffuse plaques: enzyme-linked immunosorbent assay and immunocytochemical study (1995) (70)
- White Matter Alteration in Idiopathic Normal Pressure Hydrocephalus: Tract-Based Spatial Statistics Study (2012) (70)
- A clinical, genetic, and neuropathologic study in a family with 16q-linked ADCA type III (2005) (68)
- Skein-like inclusions in the anterior horn cells in motor neuron disease (1991) (68)
- Close association of water channel AQP1 with amyloid-β deposition in Alzheimer disease brains (2008) (63)
- High-density lipoprotein facilitates in vivo delivery of α-tocopherol-conjugated short-interfering RNA to the brain. (2011) (61)
- A Novel Mutation in ELOVL4 Leading to Spinocerebellar Ataxia (SCA) With the Hot Cross Bun Sign but Lacking Erythrokeratodermia: A Broadened Spectrum of SCA34. (2015) (61)
- Cerebrovascular lesions in acquired immune deficiency syndrome (AIDS) (2004) (60)
- Brain regional differences in the expansion of a CAG repeat in the spinocerebellar ataxias: Dentatorubral‐pallidoluysian atrophy, machado‐joseph disease, and spinocerebellar ataxia type 1 (1997) (60)
- Upper limits from the LIGO and TAMA detectors on the rate of gravitational-wave bursts (2005) (60)
- Spreading of amyotrophic lateral sclerosis lesions—multifocal hits and local propagation? (2013) (59)
- Novel Cav2.1 Splice Variants Isolated from Purkinje Cells Do Not Generate P-type Ca2+ Current* (2002) (59)
- Pale Neurites, Premature α‐Synuclein Aggregates with Centripetal Extension from Axon Collaterals (2012) (59)
- Proteolytic cleavage and cellular toxicity of the human α1A calcium channel in spinocerebellar ataxia type 6 (2003) (58)
- The influence of PRNP polymorphisms on human prion disease susceptibility: an update (2015) (57)
- Significant association of cadaveric dura mater grafting with subpial Aβ deposition and meningeal amyloid angiopathy (2016) (56)
- Clinical features and diagnosis of dura mater graft–associated Creutzfeldt–Jakob disease (2007) (56)
- Efficient in vivo delivery of siRNA into brain capillary endothelial cells along with endogenous lipoprotein. (2011) (56)
- Rate of Complications Among the Recipients of Intrathecal Baclofen Pump in Japan: A Multicenter Study (2013) (56)
- Disease-specific monoclonal antibodies targeting glutamate decarboxylase impair GABAergic neurotransmission and affect motor learning and behavioral functions (2015) (53)
- An inherited prion disease with a PrP P105L mutation (1999) (51)
- Impaired striatal dopamine release in homozygous Vps35 D620N knock-in mice. (2016) (51)
- Chimeric Antisense Oligonucleotide Conjugated to α-Tocopherol (2015) (51)
- Peroxiredoxin I (macrophage 23 kDa stress protein) is highly and widely expressed in the rat nervous system (2000) (50)
- siRNA-based inhibition specific for mutant SOD1 with single nucleotide alternation in familial ALS, compared with ribozyme and DNA enzyme. (2004) (48)
- A novel mutation in the GNE gene and a linkage disequilibrium in Japanese pedigrees (2002) (47)
- Motor weakness and cerebellar ataxia in Sjögren syndrome—identification of antineuronal antibody: a case report (2002) (47)
- Abnormal RNA structures (RNA foci) containing a penta‐nucleotide repeat (UGGAA)n in the Purkinje cell nucleus is associated with spinocerebellar ataxia type 31 pathogenesis (2013) (47)
- Distinct effects of caudalizing factors on regional specification of embryonic stem cell-derived neural precursors. (2005) (47)
- Focal accumulation of phosphorylated neurofilaments within anterior horn cell in familial amyotrophic lateral sclerosis (2004) (46)
- The carboxy-terminal fragment of α1A calcium channel preferentially aggregates in the cytoplasm of human spinocerebellar ataxia type 6 Purkinje cells (2009) (45)
- Pentanucleotide repeats at the spinocerebellar ataxia type 31 (SCA31) locus in Caucasians (2011) (45)
- Intrathecal AAV serotype 9-mediated delivery of shRNA against TRPV1 attenuates thermal hyperalgesia in a mouse model of peripheral nerve injury. (2014) (45)
- Transgenic Small Interfering RNA Halts Amyotrophic Lateral Sclerosis in a Mouse Model* (2005) (44)
- Clinical evaluation of plasma exchange and high dose intravenous immunoglobulin in a patient with Isaacs' syndrome. (1994) (44)
- Spinocerebellar ataxia type 36 exists in diverse populations and can be caused by a short hexanucleotide GGCCTG repeat expansion (2014) (44)
- Increased CSF tau protein in corticobasal degeneration (1997) (44)
- Studies on neurotransmitter markers and neuronal cell density in the cerebellar system in olivopontocerebellar atrophy and cortical cerebellar atrophy (1985) (44)
- Anti-GM1 antibody facilitates leakage in an in vitro blood–nerve barrier model (2000) (44)
- Heterogeneity of Nigral and Cortical Lewy Bodies Differentiated by Amplified Triple-Labeling for Alpha-Synuclein, Ubiquitin, and Thiazin Red (2002) (43)
- Cerebral cortical pathology of sporadic olivopontocerebellar atrophy (1993) (43)
- Three‐Layered Structure Shared Between Lewy Bodies and Lewy Neurites—Three‐Dimensional Reconstruction of Triple‐Labeled Sections (2008) (43)
- Chronic levodopa therapy enhances dopa absorption: Contribution to wearing-off (2005) (43)
- Analyses of copy number and mRNA expression level of the alpha-synuclein gene in multiple system atrophy. (2008) (43)
- The risk of iatrogenic Creutzfeldt‐Jakob disease through medical and surgical procedures (2009) (43)
- Familial mitochondrial myopathy associated with peripheral neuropathy: Partial deficiencies of complex I and complex IV (1988) (42)
- Dual impairment of GABAA- and GABAB-receptor-mediated synaptic responses by autoantibodies to glutamic acid decarboxylase (2003) (42)
- Two different clinical phenotypes of Creutzfeldt-Jakob disease with a M232R substitution (2007) (41)
- Calbindin-D 28k immunoreactivity in the cerebellum of spinocerebellar degeneration (1995) (41)
- Joint LIGO and TAMA300 search for gravitational waves from inspiralling neutron star binaries (2006) (41)
- Association of presenilin-1 polymorphism with cerebral amyloid angiopathy in the elderly. (1997) (41)
- Distal myopathy with rimmed vacuoles (DMRV) (2004) (41)
- Dura mater graft‐associated Creutzfeldt‐Jakob disease in Japan: Clinicopathological and molecular characterization of the two distinct subtypes (2009) (41)
- Absence of association between codon 129/219 polymorphisms of the prion protein gene and Alzheimer's disease in Japan (2003) (40)
- Progressive supranuclear palsy presenting with pure akinesia. (1993) (40)
- Peripheral neuropathy of mitochondrial myopathies. (1991) (40)
- Association of α1‐antichymotrypsin polymorphism with cerebral amyloid angiopathy (1998) (40)
- Age at onset in genetic prion disease and the design of preventive clinical trials (2019) (39)
- Differentiating between progressive supranuclear palsy and corticobasal degeneration by brain perfusion SPET (2001) (39)
- Coexistence of CJD and Alzheimer's disease: An autopsy case showing typical clinical features of CJD (2004) (39)
- Self-secretion of fibroblast growth factor-9 supports basal forebrain cholinergic neurons in an autocrine/paracrine manner (2000) (39)
- Association of neprilysin polymorphism with cerebral amyloid angiopathy (2003) (39)
- Glycosphingolipid antibodies and blood–nerve barrier in autoimmune demyelinative neuropathy (2000) (38)
- Tandem internal models execute motor learning in the cerebellum (2018) (38)
- Content of mutant mitochondrial DNA and organ dysfunction in a patient with a MELAS subgroup of mitochondrial encephalomyopathies (1993) (38)
- Development of Purkinje cell degeneration in a knockin mouse model reveals lysosomal involvement in the pathogenesis of SCA6 (2012) (38)
- Sequence‐dependent and independent inhibition specific for mutant ataxin‐3 by small interfering RNA (2004) (38)
- A Score for Predicting Paroxysmal Atrial Fibrillation in Acute Stroke Patients: iPAB Score. (2015) (38)
- Blood–brain barrier destruction determines Fisher/Bickerstaff clinical phenotypes: an in vitro study (2013) (37)
- Efficacy of intravenous methylprednisolone pulse therapy in patients with multiple sclerosis and neuromyelitis optica (2016) (37)
- Sera from Guillain-Barré patients enhance leakage in blood–nerve barrier model (2003) (37)
- Electrophysiological evaluation of conduction in the most proximal motor root segment (2002) (37)
- Association of a polymorphism of the transforming growth factor-β1 gene with cerebral amyloid angiopathy (2005) (37)
- A Japanese family with spinocerebellar ataxia type 6 which includes three individuals homozygous for an expanded CAG repeat in the SCA6/CACNL1A4 gene (1998) (37)
- Duration of Prion Disease is Longer in Japan Than in Other Countries (2011) (36)
- Decreased expression of myotonic dystrophy protein kinase and disorganization of sarcoplasmic reticulum in skeletal muscle of myotonic dystrophy (1999) (36)
- Validation of cardiac 123I-MIBG scintigraphy in patients with Parkinson’s disease who were diagnosed with dopamine PET (2009) (36)
- 18F-FDG PET successfully detects spinal cord sarcoidosis (2009) (36)
- Clinical features of genetic Creutzfeldt-Jakob disease with V180I mutation in the prion protein gene (2014) (36)
- Efficient regulation of viral replication by siRNA in a non-human primate surrogate model for hepatitis C. (2007) (35)
- Neurological Dysfunctions Versus Regional Infarction Volume After Focal Ischemia in Mongolian Gerbils (2003) (35)
- High incidence of HAM/TSP-like symptoms in WKA rats after administration of human T-cell leukemia virus type 1-producing cells (1994) (34)
- Insight into the frequent occurrence of dura mater graft-associated Creutzfeldt-Jakob disease in Japan (2013) (34)
- Intractable hiccup caused by medulla oblongata lesions: A study of an autopsy patient with possible neuromyelitis optica (2009) (34)
- Cerebral networks for spontaneous and synchronized singing and speaking (2006) (34)
- Relationships between Clinicopathological Features and Cerebrospinal Fluid Biomarkers in Japanese Patients with Genetic Prion Diseases (2013) (33)
- Lack of association of neprilysin polymorphism with Alzheimer's disease and Alzheimer's disease-type neuropathological changes (2001) (33)
- New RNAi strategy for selective suppression of a mutant allele in polyglutamine disease. (2005) (33)
- Brain perfusion SPECT in patients with corticobasal degeneration: Analysis using statistical parametric mapping (2003) (32)
- Clinical, biochemical and molecular investigation of adult-onset glutaric acidemia type II: Characteristics in comparison with pediatric cases (2016) (32)
- The effect of 3,4-diaminopyridine on the patients with hereditary pure cerebellar ataxia (2010) (32)
- Reversible acute axonal polyneuropathy associated with Wernicke-Korsakoff syndrome: impaired physiological nerve conduction due to thiamine deficiency? (2003) (32)
- Clinicopathological characteristics of FTLD-TDP showing corticospinal tract degeneration but lacking lower motor neuron loss (2010) (32)
- A case of cluster headache associated with mitochondrial DNA deletions (1997) (32)
- No association of paraoxonase gene polymorphism with atherosclerosis or Alzheimer’s disease (1999) (31)
- Developmental regulation of Ubc9 in the rat nervous system. (2008) (31)
- Low-Titer Anti-GAD-Antibody-Positive Cerebellar Ataxia (2013) (31)
- Senile Dementia of the Neurofibrillary Tangle Type: A Comparison with Alzheimer’s Disease (2001) (31)
- Involvement of the spinal posterior horn in Gerstmann–Sträussler–Scheinker disease (PrP P102L) (1999) (31)
- Screening of the mis-sense mutation producing the 717Val → Ile substitution in the amyloid precursor protein in Japanese familial and sporadic Alzheimer's disease (1993) (31)
- Efficient generation of mature cerebellar Purkinje cells from mouse embryonic stem cells (2010) (31)
- Reversibility of cerebellar GABAergic synapse impairment induced by anti-glutamic acid decarboxylase autoantibodies (2008) (31)
- A −16C>T substitution in the 5′ UTR of the puratrophin-1 gene is prevalent in autosomal dominant cerebellar ataxia in Nagano (2006) (30)
- Very early onset Alzheimer's disease with spastic paraparesis associated with a novel presenilin 1 mutation (Phe237Ile) (2001) (30)
- Relocation of p25α/tubulin polymerization promoting protein from the nucleus to the perinuclear cytoplasm in the oligodendroglia of sporadic and COQ2 mutant multiple system atrophy (2014) (30)
- Characteristic changes in T2-value, apparent diffusion coefficient, and ultrastructure of substantia nigra evolving exofocal postischemic neuronal death in rats (2001) (30)
- Constant and severe involvement of Betz cells in corticobasal degeneration is not consistent with pyramidal signs: a clinicopathological study of ten autopsy cases (2005) (30)
- Enteral siRNA delivery technique for therapeutic gene silencing in the liver via the lymphatic route (2015) (29)
- Ultrastructural and MRI study of the substantia nigra evolving exofocal post‐ischemic neuronal death in the rat (2002) (29)
- Medical Procedures and Risk for Sporadic Creutzfeldt-Jakob Disease, Japan, 1999–2008 (2009) (29)
- Neuronal expression of the fukutin gene. (2000) (28)
- Ubiquitinated αB-crystallin in glial cytoplasmic inclusions from the brain of a patient with multiple system atrophy (1995) (28)
- Update: Dura Mater Graft–Associated Creutzfeldt-Jakob Disease — Japan, 1975–2017 (2018) (28)
- Different Patterns of Fornix Damage in Idiopathic Normal Pressure Hydrocephalus and Alzheimer Disease (2012) (28)
- Acute autonomic and sensory neuropathy after interferon α-2b therapy for chronic hepatitis C (2001) (28)
- Autonomic dysfunction and orthostatic hypotention caused by vitamin B12 deficiency (1999) (28)
- Age of onset in genetic prion disease and the design of preventive clinical trials (2018) (27)
- Glycosphingolipid composition of primary cultured human brain microvascular endothelial cells (2004) (27)
- ORANGE's challenge: developing wide-ranging dementia research in Japan (2016) (27)
- Sural nerve biopsy in vasculitic neuropathies: morphometric analysis of the caliber of involved vessels. (1996) (27)
- Structural connectivity in spatial attention network: reconstruction from left hemispatial neglect (2018) (26)
- Serum level of soluble CX3CL1/fractalkine is elevated in patients with polymyositis and dermatomyositis, which is correlated with disease activity (2012) (26)
- Physical map and haplotype analysis of 16q-linked autosomal dominant cerebellar ataxia (ADCA) type III in Japan (2003) (26)
- Utility of F-18 FDG PET/CT in Screening for Paraneoplastic Neurological Syndromes (2012) (26)
- Thyrotropin-Releasing Hormone-Induced Myoclonus and Tremor in a Patient With Hashimoto’s Encephalopathy (1995) (26)
- A case of cortical tremor as a variant of cortical reflex myoclonus. (1995) (26)
- A 3-year cohort study of the natural history of spinocerebellar ataxia type 6 in Japan (2014) (26)
- Triad proteins and intracellular Ca2+ transients during development of human skeletal muscle cells in aneural and innervated cultures (2004) (26)
- Skeletal muscle MRI in complex regional pain syndrome. (2009) (26)
- α2-Macroglobulin polymorphism is not associated with AD or AD-type neuropathology in the Japanese (2000) (26)
- Primary position upbeat nystagmus increased on downward gaze (1998) (25)
- Presenilin 1 intronic polymorphism is not associated with Alzheimer type neuropathological changes or sporadic Alzheimer’s disease (1998) (25)
- Quantitative Evaluation of Human Cerebellum-Dependent Motor Learning through Prism Adaptation of Hand-Reaching Movement (2015) (25)
- FGF-9 is an autocrine/paracrine neurotrophic substance for spinal motoneurons (1999) (25)
- In vivo delivery of small interfering RNA targeting brain capillary endothelial cells. (2006) (24)
- Transplantation of neuronal cells induced from human mesenchymal stem cells improves neurological functions after stroke without cell fusion (2010) (24)
- Distal hyperintense vessels on FLAIR images predict large-artery stenosis in patients with transient ischemic attack (2013) (24)
- Loss of MyD88 alters neuroinflammatory response and attenuates early Purkinje cell loss in a spinocerebellar ataxia type 6 mouse model (2015) (24)
- Long-term cognitive and neuropsychological symptoms after global cerebral ischemia in Mongolian gerbils. (2006) (24)
- HTLV‐1‐associated Myelopathy/Tropical Spastic Paraparesis‐like Rats by Intravenous Injection of HTLV‐1‐producing Rabbit or Human T‐Cell Line into Adult WKA Rats (1993) (24)
- Multicentre multiobserver study of diffusion-weighted and fluid-attenuated inversion recovery MRI for the diagnosis of sporadic Creutzfeldt–Jakob disease: a reliability and agreement study (2012) (23)
- Autosomal dominant pure cerebellar ataxia. A clinical and genetic analysis of eight Japanese families. (1996) (23)
- Two region‐dependent pathways of eosinophilic neuronal death after transient cerebral ischemia (2009) (23)
- Cerebrospinal fluid endothelin-1 in Alzheimer's disease and senile dementia of Alzheimer type (1992) (23)
- Malignant hyperthermia in a patient with Becker muscular dystrophy: Dystrophin analysis and caffeine contracture study (1995) (22)
- Proliferating Immature Schwann Cells Contribute to Nerve Regeneration After Ischemic Peripheral Nerve Injury (2012) (22)
- Cell-type-specific alternative splicing in spinocerebellar ataxia type 6 (2008) (22)
- Occurrence of basophilic inclusions and FUS-immunoreactive neuronal and glial inclusions in a case of familial amyotrophic lateral sclerosis (2010) (22)
- Binding of Pramipexole to Extrastriatal Dopamine D2/D3 Receptors in the Human Brain: A Positron Emission Tomography Study Using 11C-FLB 457 (2011) (22)
- Reduced brain‐derived neurotrophic factor (BDNF) mRNA expression and presence of BDNF‐immunoreactive granules in the spinocerebellar ataxia type 6 (SCA6) cerebellum (2012) (21)
- Abeta1-40 but not Abeta1-42 levels in cortex correlate with apolipoprotein E epsilon4 allele dosage in sporadic Alzheimer's disease. (1997) (21)
- Myocardial nerve fibers are preserved in MPTP-treated mice, despite cardiac sympathetic dysfunction (2008) (21)
- Redefining the disease locus of 16q22.1-linked autosomal dominant cerebellar ataxia (2007) (21)
- Elevated platelet microparticle levels after acute ischemic stroke with concurrent idiopathic thrombocytopenic purpura. (2014) (21)
- Coexistence of fast and slow types of myosin light chains in a single fiber of rat soleus muscle. (1982) (21)
- Pathology of the dentate nucleus in progressive supranuclear palsy: a histological, immunohistochemical and ultrastructural study (2004) (21)
- An autopsy case of chronic active Epstein–Barr virus infection (CAEBV): Distribution of central nervous system (CNS) lesions (2008) (21)
- [Distal myopathy with rimmed vacuoles]. (2001) (21)
- Degeneration of the thalamus and inferior olives associated with spongiform encephalopathy of the cerebral cortex. (1988) (21)
- Sequential changes in the non-coding control region sequences of JC polyomaviruses from the cerebrospinal fluid of patients with progressive multifocal leukoencephalopathy (2012) (21)
- Characteristics of progressive multifocal leukoencephalopathy clarified through internet-assisted laboratory surveillance in Japan (2012) (21)
- Progressive accumulation of ubiquitin and disappearance of α-synuclein epitope in multiple system atrophy-associated glial cytoplasmic inclusions: triple fluorescence study combined with Gallyas-Braak method (2005) (20)
- [Anti-VGKC antibody-associated limbic encephalitis/Morvan syndrome]. (2010) (20)
- Significance of Development and Reversion of Collaterals on MRI in Early Neurologic Improvement and Long-Term Functional Outcome after Intravenous Thrombolysis for Ischemic Stroke (2015) (20)
- Mutation of the EYA1 Gene in Patients with Branchio-oto Syndrome (2003) (20)
- Intrathecal shRNA-AAV9 inhibits target protein expression in the spinal cord and dorsal root ganglia of adult mice. (2012) (20)
- Mounding phenomenon (1983) (20)
- Failure of mefloquine therapy in progressive multifocal leukoencephalopathy: Report of two Japanese patients without human immunodeficiency virus infection (2013) (19)
- Spinal cord ring enhancement in patients with neuromyelitis optica (2015) (19)
- Unmyelinated nerve fibers in sural nerve in pure autonomic failure (1998) (19)
- A novel neurotrophic pyrimidine compound MS‐818 enhances neurotrophic effects of basic fibroblast growth factor (1998) (19)
- Spinal cord ring enhancement in patients with neuromyelitis optica (2015) (19)
- Tacrolimus Monotherapy: A Promising Option for Ocular Myasthenia Gravis (2013) (19)
- Extrapyramidal motor symptoms versus striatal infarction volume after focal ischemia in mongolian gerbils (2004) (19)
- Reversible central neurogenic hyperventilation in an awake patient with multiple sclerosis (2007) (19)
- A linkage disequilibrium at the candidate gene locus for 16q-linked autosomal dominant cerebellar ataxia type III in Japan (2001) (18)
- Pattern of epitopic reactivity of the anti-Hu antibody on HuD with and without paraneoplastic syndrome (1999) (18)
- Midkine inhibits apoptosis via extracellular signal regulated kinase (ERK) activation in PC12 cells. (1999) (18)
- Rimmed vacuolar distal myopathy: a clinical, electrophysiological, histopathological and computed tomographic study of seven cases (1987) (18)
- Anhidrosis associated with hypothalamic lesions related to anti-aquaporin 4 autoantibody (2011) (17)
- Sphingosine-1-Phosphate Receptor-1 Selective Agonist Enhances Collateral Growth and Protects against Subsequent Stroke (2015) (17)
- Discrepancy between tau immunoreactivity and argyrophilia by the Bodian method in neocortical neurons of corticobasal degeneration (1998) (17)
- Posterior Cerebral Artery Laterality on Magnetic Resonance Angiography Predicts Long-Term Functional Outcome in Middle Cerebral Artery Occlusion (2013) (17)
- TNF-related apoptosis-inducing ligand (TRAIL) induces neuronal apoptosis in HIV-encephalopathy. (2003) (17)
- COVID-19 international neurological registries (2020) (17)
- Down-regulation of an ankyrin repeat-containing protein, V-1, during skeletal muscle differentiation and its re-expression in the regenerative process of muscular dystrophy (2003) (17)
- Prevalence of inositol 1, 4, 5-triphosphate receptor type 1 gene deletion, the mutation for spinocerebellar ataxia type 15, in Japan screened by gene dosage (2012) (17)
- Transition of areas of eosinophilic neurons and reactive astrocytes to delayed cortical infarcts after transient unilateral forebrain ischemia in Mongolian gerbils (2005) (17)
- Prevalence and clinicoradiological features of spinocerebellar ataxia type 34 in a Japanese ataxia cohort. (2019) (17)
- Proximal motor conduction evaluated by transcranial magnetic stimulation in acquired inflammatory demyelinating neuropathies (2001) (17)
- Re-evaluation of soluble APP-α and APP-β in cerebrospinal fluid as potential biomarkers for early diagnosis of dementia disorders (2017) (17)
- Enhanced Phospholipase A2 Group 3 Expression by Oxidative Stress Decreases the Insulin-Degrading Enzyme (2015) (17)
- Competition between 11C-raclopride and endogenous dopamine in Parkinson's disease (2010) (16)
- Intraperitoneal AAV9-shRNA inhibits target expression in neonatal skeletal and cardiac muscles. (2011) (16)
- Prevalence of Autoantibodies and the Efficacy of Immunotherapy for Autoimmune Cerebellar Ataxia. (2016) (16)
- In vivo application of an RNAi strategy for the selective suppression of a mutant allele. (2011) (16)
- Intraperitoneal administration of AAV9-shRNA inhibits target gene expression in the dorsal root ganglia of neonatal mice (2013) (16)
- Slowly progressive Foix–Chavany–Marie syndrome associated with chronic herpes simplex encephalitis (2002) (16)
- Neural Substrates for Semantic Memory of Familiar Songs: Is There an Interface between Lyrics and Melodies? (2012) (16)
- A Case of Creutzfeldt-Jakob Disease Presenting with Auditory Agnosia as an Initial Manifestation (2000) (16)
- Cytoplasmic Location of α1A Voltage-Gated Calcium Channel C-Terminal Fragment (Cav2.1-CTF) Aggregate Is Sufficient to Cause Cell Death (2013) (16)
- Dynamic imbalance in gait ataxia. Characteristics of plantar pressure measurements (2006) (16)
- Introduction of short interfering RNA to silence endogenous E-selectin in vascular endothelium leads to successful inhibition of leukocyte adhesion. (2003) (16)
- No Association of Paraoxonase Genotype or Atherosclerosis With Cerebral Amyloid Angiopathy (2002) (16)
- Presenilin-1 holoprotein is an interacting partner of sarco endoplasmic reticulum calcium-ATPase and confers resistance to endoplasmic reticulum stress. (2010) (16)
- An experimental study for analyzing nerve conduction velocity. (1986) (15)
- Hydrocephalus in the Otx2+/−Mutant Mouse (1997) (15)
- Argentophilic intracytoplasmic inclusions in multiple system atrophy (1992) (15)
- ANovel Mutation in ELOVL 4 Leading to Spinocerebellar Ataxia ( SCA ) With the Hot Cross Bun Sign but Lacking Erythrokeratodermia A Broadened Spectrum of SCA 34 (2015) (15)
- Recurrent aseptic meningitis: a new CSF complication of Sjogren’s syndrome (2007) (15)
- Vocal cord abductor paralysis in spinocerebellar ataxia type 1 (1999) (15)
- Creutzfeldt–Jakob disease with a novel insertion and codon 219 Lys/Lys polymorphism in PRNP (2004) (15)
- Ataxic phenotype with altered CaV3.1 channel property in a mouse model for spinocerebellar ataxia 42 (2019) (15)
- The professional practice and training of neurology in the Asian and Oceanian Region: A cross-sectional survey by the Asian and Oceanian Association of Neurology (AOAN) (2017) (15)
- Case Report: Thyrotropin‐Releasing Hormone‐Induced Myoclonus and Tremor in a Patient With Hashimoto's Encephalopathy (1995) (15)
- Transplantation of human neural stem/progenitor cells overexpressing galectin-1 improves functional recovery from focal brain ischemia in the mongolian gerbil (2011) (14)
- The evaluation of polyglutamine repeats in autosomal dominant Parkinson's disease (2014) (14)
- Motor nerve conduction study in cauda equina with high‐voltage electrical stimulation in multifocal motor neuropathy and amyotrophic lateral sclerosis (2011) (14)
- Glial expression of presenilin epitopes in human brain with cerebral infarction and in astrocytoma (1999) (14)
- [A case of Hashimoto's encephalopathy with a relapsing course related to menstrual cycle]. (1993) (14)
- 5-FU-induced acute leukoencephalopathy. (2004) (14)
- Tyrosol Reduces Amyloid-β Oligomer Neurotoxicity and Alleviates Synaptic, Oxidative, and Cognitive Disturbances in Alzheimer's Disease Model Mice. (2019) (14)
- Cerebrospinal fluid metabolite and nigrostriatal dopaminergic function in Parkinson’s disease (2009) (14)
- Butyrylcholinesterase K variant and cerebral amyloid angiopathy. (1998) (14)
- [A case of HLA-DR2, DQw1 negative post-traumatic narcolepsy]. (1995) (14)
- Randomized phase 2 study of perampanel for sporadic amyotrophic lateral sclerosis (2021) (13)
- Ubiquitinated alpha B-crystallin in glial cytoplasmic inclusions from the brain of a patient with multiple system atrophy. (1995) (13)
- FALS with Gly72Ser mutation in SOD1 gene: Report of a family including the first autopsy case (2011) (13)
- Gluten Ataxia in Japan (2014) (13)
- Visual Reproduction on the Wechsler Memory Scale-Revised as a Predictor of Alzheimer’s Disease in Japanese Patients with Mild Cognitive Impairments (2013) (13)
- The chromosome 16q‐linked autosomal dominant cerebellar ataxia (16q‐ADCA): A newly identified degenerative ataxia in Japan showing peculiar morphological changes of the Purkinje cell (2010) (13)
- Specific clinical signs and symptoms are predictive of clinical course in sporadic Creutzfeldt−Jakob disease (2016) (13)
- Three-repeat Tau 69 is a major tau isoform in laser-microdissected Pick bodies (2006) (13)
- Effects of pericytes and various cytokines on integrity of endothelial monolayer originated from blood-nerve barrier: an in vitro study. (1999) (13)
- Lewy body-like inclusions in Onuf's nucleus from two cases of sporadic amyotrophic lateral sclerosis (1993) (13)
- Spinocerebellar ataxia type 6 (SCA 6) (1998) (13)
- Hypertrophic cranial pachymeningitis with spinal epidural granulomatous lesion. (1995) (13)
- On autosomal dominant cerebellar ataxia (ADCA) other than polyglutamine diseases, with special reference to chromosome 16q22.1‐linked ADCA (2006) (13)
- Progressive Multifocal Leukoencephalopathy with Balanced CD4/CD8 T-Cell Infiltration and Good Response to Mefloquine Treatment. (2016) (13)
- Assessment and Rating of Motor Cerebellar Ataxias With the Kinect v2 Depth Sensor: Extending Our Appraisal (2020) (12)
- Serum amyloid A level is increased in neuromyelitis optica and atypical multiple sclerosis with smaller T2 lesion volume in brain MRI (2013) (12)
- When should we test patients with familial ataxias for SCA31? A misdiagnosed condition outside Japan? (2015) (12)
- Ophthalmic Surgery in Prion Diseases (2007) (12)
- Lack of Genetic Associations of Alpha-1-Antichymotrypsin Polymorphism with Alzheimer-Type Neuropathological Changes or Sporadic Alzheimer’s Disease (1999) (12)
- Pseudopolyneuritic form of ALS revisited: Clinical and pathological heterogeneity (2009) (12)
- Chiasmal optic neuritis following mumps parotitis (2008) (12)
- Serum amyloid A level is increased in neuromyelitis optica and atypical multiple sclerosis with smaller T2 lesion volume in brain MRI (2013) (12)
- A clinical, genetic, neuropathological study in a Japanese family with SCA 6 and a review of Japanese autopsy cases of autosomal dominant cortical cerebellar atrophy (1998) (12)
- Creutzfeldt-Jakob disease after Jannetta’s operation with cadaveric dura mater graft: initial manifestations related to the grafted site (2002) (12)
- Spinocerebellar ataxia type 6 with motor neuron loss: A follow-up autopsy report (2002) (12)
- The identified clinical features of Parkinson's disease in homo-, heterozygous and digenic variants of PINK1 (2020) (11)
- Glucose hypometabolism in medial frontal cortex of patients with apraxia of lid opening (2003) (11)
- Sequence configuration of spinocerebellar ataxia type 8 repeat expansions in a Japanese cohort of 797 ataxia subjects (2017) (11)
- MM2-type sporadic Creutzfeldt-Jakob disease: new diagnostic criteria for MM2-cortical type (2020) (11)
- Presenilin-1 holoprotein is an interacting partner of sarco endoplasmic reticulum calcium-ATPase and confers resistance to endoplasmic reticulum stress (2010) (11)
- Association between Delirium and Prehospitalization Medication in Poststroke Patients. (2018) (11)
- Presynaptic dysfunction caused by cerebrospinal fluid from a patient with the ataxic form of Hashimoto's encephalopathy (2014) (11)
- Gene dosage effect in spinocerebellar ataxia type 6 homozygotes: A clinical and neuropathological study (2017) (11)
- A diagnostic decision tree for adult cerebellar ataxia based on pontine magnetic resonance imaging (2018) (11)
- Classification of cerebellar atrophy using voxel-based morphometry and SPECT with an easy Z-score imaging system. (2010) (11)
- A case of Listeria meningitis associated with increased adenosine deaminase in cerebrospinal fluid. (2007) (11)
- Histological determination of nitric oxide synthase (NOS) and NADPH-diaphorase in ragged-red fibers from patients with mitochondrial encephalomyopathies (1997) (10)
- Multiple sclerosis and neuromyelitis optica spectrum disorders: some similarities in two distinct diseases (2016) (10)
- Chronic inflammatory demyelinating polyradiculoneuropathy in a patient with Crohn's disease. (2013) (10)
- Association between butyrylcholinesterase K variant and the Alzheimer type neuropathological changes in apolipoprotein E ε4 carriers older than 75 years (1999) (10)
- Association of alpha1-antichymotrypsin polymorphism with cerebral amyloid angiopathy. (1998) (10)
- Graft-related disease progression in dura mater graft-associated Creutzfeldt-Jakob disease: a cross-sectional study (2013) (10)
- Survey of Subacute Sclerosing Panencephalitis in Japan (2012) (10)
- Amyloid beta protein 1-42/43 (A beta 1-42/43) in cerebellar diffuse plaques: enzyme-linked immunosorbent assay and immunocytochemical study. (1995) (10)
- Frontotemporal lobar degeneration with motor neuron disease showing severe and circumscribed atrophy of anterior temporal lobes (2010) (10)
- Depressive disorder may be associated with raphe nuclei lesions in patients with brainstem infarction. (2017) (10)
- Basement membrane-like matrix sponge for the three-dimensional proliferation culture of differentiated retinal horizontal interneurons. (2011) (10)
- Relationship and factor structure in multisystem neurodegeneration in Parkinson's disease (2014) (10)
- Multiple sclerosis and neuromyelitis optica spectrum disorders: some similarities in two distinct diseases (2016) (10)
- [A case of Garcin's syndrome caused by pachymeningitis secondary to otitis media, responsive to antibiotic therapy]. (1991) (10)
- Two distinct prions in fatal familial insomnia and its sporadic form (2019) (10)
- Aortic dissection as a possible cause of pure transient global amnesia: a case report and literature review (2009) (10)
- Pure cerebellar ataxia phenotype in Machado-Joseph disease (1996) (9)
- Brain volume loss is present in Japanese multiple sclerosis patients with no evidence of disease activity (2017) (9)
- [Mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS) associated with hypothalamo-pituitary hypofunction--a case report]. (1991) (9)
- Bilateral facial nerve palsy caused by a metastatic malignant lymphoma. (2011) (9)
- More than a 100-fold increase in immunoblot signals of laser-microdissected inclusion bodies with an excessive aggregation property by oligomeric actin interacting protein 2/D-lactate dehydrogenase protein 2. (2005) (9)
- Highly diffusion-sensitized tensor imaging of unilateral cerebral arterial occlusive disease. (2005) (9)
- Delayed leukoencephalopathy after carbon monoxide poisoning presenting as subacute dementia. (2014) (9)
- A Deletion Polymorphism of α2-Macroglobulin Gene and Cerebral Amyloid Angiopathy (1999) (9)
- Ischemic stroke in a young adult with Turner syndrome (2011) (9)
- Acute multiple brain infarction in large‐artery atherosclerosis is associated with hyperhomocyst(e)inemia (2007) (9)
- [An autopsy case of HTLV-I associated myelopathy (HAM) with adult T-cell leukemia (ATL)]. (1990) (9)
- Involvement of hippocampus in Creutzfeldt-Jakob disease (1987) (9)
- Efficacy of methylprednisolone pulse therapy for acute relapse in Japanese patients with multiple sclerosis and neuromyelitis optica: A multicenter retrospective analysis – 1. Whole group analysis (2013) (8)
- AJM300 (Carotegrast Methyl), an Oral Antagonist of α4-Integrin, as Induction Therapy for Patients with Moderately Active Ulcerative Colitis: A Multicentre, Randomised, Double-Blind, Placebo-Controlled Phase 3 Study (2021) (8)
- The human brain and its disorders (2007) (8)
- A possible novel isoform of peripheral myelin P0 protein: a target antigen recognized by an autoantibody in a patient with malignant lymphoma and peripheral neuropathy (2001) (8)
- Hereditary neuropathy with liability to pressure palsy combined with suspected schwannomas of the peroneal and radial nerves (2012) (8)
- A neuropathological study of paraparetic rats injected with HTLV-I-producing T cells (1994) (8)
- Initiative on Rare and Undiagnosed Disease in Japan (2021) (8)
- Direct and accurate measurement of CAG repeat configuration in the ataxin-1 (ATXN-1) gene by “dual-fluorescence labeled PCR-restriction fragment length analysis” (2008) (8)
- Serum retinol levels are associated with brain volume loss in patients with multiple sclerosis (2017) (8)
- Impaired Adaptive Motor Learning Is Correlated With Cerebellar Hemispheric Gray Matter Atrophy in Spinocerebellar Ataxia Patients: A Voxel-Based Morphometry Study (2019) (8)
- Nonsystemic vasculitic neuropathy presenting with truncal segmental sensory disturbance and hyperhidrosis (1999) (8)
- Early and persistent sensory-psychiatric symptoms in an inherited prion disease with a PrP P105L mutation (2002) (8)
- Marked hypertrophy of the cauda equina in a patient with chronic inflammatory demyelinating polyradiculoneuropathy presenting as lumbar stenosis (2005) (8)
- Progressive Encephalomyelitis with Rigidity and Myoclonus Resolving after Thymectomy with Subsequent Anasarca: An Autopsy Case (2018) (8)
- Pathological features of FTLD-FUS in a Japanese population: Analyses of nine cases (2013) (8)
- Six years’ accomplishment of the Initiative on Rare and Undiagnosed Diseases: nationwide project in Japan to discover causes, mechanisms, and cures (2022) (7)
- Suppression of Experimental Autoimmune Encephalomyelitis by Ghrelin (2009) (7)
- [Malignant lymphoma presented as left trigeminal neuralgia]. (2009) (7)
- Secondary cardiac involvement in anti-SRP-antibody-positive myopathy: an 87-year-old woman with heart failure symptoms as the first clinical presentation (2020) (7)
- A case of dermatomyositis with rhabdomyolysis, rescued by intravenous immunoglobulin (2015) (7)
- [A case of unilateral gustatory disturbance produced by the contralateral midbrain lesion]. (1994) (7)
- [Reflex sympathetic dystrophy secondary to lumbar disk herniation]. (1994) (7)
- Short interfering RNA and the central nervous system: development of nonviral delivery systems (2013) (7)
- Relocation of p25α/tubulin polymerization promoting protein from the nucleus to the perinuclear cytoplasm in the oligodendroglia of sporadic and COQ2 mutant multiple system atrophy (2014) (7)
- Thalamic involvement determined using VSRAD advance on MRI and easy Z-score analysis of 99mTc-ECD-SPECT in Gerstmann-Sträussler-Scheinker syndrome with P102L mutation (2017) (7)
- [Case of an 81-year-old woman with theophylline-associated seizures followed by partial seizures due to vitamin B6 deficiency]. (2008) (7)
- Metronidazole-induced encephalopathy. (2013) (7)
- Silencing efficiency differs among tissues and endogenous microRNA pathway is preserved in short hairpin RNA transgenic mice (2009) (7)
- Hemichorea improved by extracranial–intracranial bypass surgery for middle cerebral artery occlusion (2010) (7)
- Muscular abnormalities in experimental hypothyroidism of rats with special reference to the mounding phenomenon (1984) (7)
- Clinical features of the behavioural variant of frontotemporal dementia that are useful for predicting underlying pathological subtypes of frontotemporal lobar degeneration (2018) (6)
- [Prion disease--the characteristics and diagnostic points in Japan]. (2010) (6)
- [Pseudoradicular sensory impairment caused by parietal lesions: report of two cases]. (1996) (6)
- Idiopathic cerebellar ataxia (IDCA): Diagnostic criteria and clinical analyses of 63 Japanese patients (2018) (6)
- A comparison of long-term neurological symptoms after two different focal ischemic models in Mongolian gerbils. (2003) (6)
- Cortical auditory disorder caused by bilateral temporal infarctions. (1995) (6)
- Hyaline and Skein‐like Inclusions in Amyotrophic Lateral Sclerosis (1993) (6)
- Atherosclerosis is not implicated in association of APOE epsilon4 with AD. (1999) (6)
- Metastatic CNS lymphoma presenting with periventricular dissemination — MRI and neuropathological findings in an autopsy case (2009) (6)
- Analysis of risk factors for mild cognitive impairment based on word list memory test results and questionnaire responses in healthy Japanese individuals registered in an online database (2018) (6)
- Somatosensory‐evoked cortical potential during attacks of paroxysmal dysesthesia in multiple sclerosis (2005) (6)
- Unexpected clinicopathological phenotype linked to small elongation of CAG repeat in SCA1 gene (2006) (6)
- [Clinical features and MRI findings in spinocerebellar ataxia type 31 (SCA31) comparing with spinocerebellar ataxia type 6 (SCA6)]. (2014) (6)
- Iatrogenic Creutzfeldt-Jakob disease. (2018) (5)
- Autoimmune polyendocrine syndrome-3 in a patient with late-onset multiple sclerosis. (2012) (5)
- [Two distinct types of neuropathy associated with Sjögren's syndrome developed in one patient. The importance of the selection of an appropriate therapeutic regimen]. (2003) (5)
- Cryptococcal meningitis accompanying lymphocytic inflammation predominantly in cerebral deep white matter: A possible manifestation of immune reconstitution inflammatory syndrome (2014) (5)
- l-threo-3,4-dihydroxyphenylserine enhances the orthostatic responses of plasma renin activity and angiotensin II in multiple system atrophy (1999) (5)
- Methionine homozygosity for PRNP polymorphism and susceptibility to human prion diseases (2022) (5)
- [Bilateral medial medullary infarction presented with monoplegia of the lower limb, followed by paraplegia and finally by tetraplegia]. (2003) (5)
- Progression of bilateral internal carotid artery dissection during antiplatelet therapy. (2013) (5)
- Dropped head in polymyositis (2012) (5)
- Nuclear bridges in multinucleated giant cells associated with primary lymphoma of the brain in acquired immune deficiency syndrome (AIDS) (2004) (5)
- Familial ataxia with isolated vitamin E deficiency not due to mutation of α-TTP (1999) (5)
- AJM300 (carotegrast methyl), an oral antagonist of α4-integrin, as induction therapy for patients with moderately active ulcerative colitis: a multicentre, randomised, double-blind, placebo-controlled, phase 3 study. (2022) (5)
- [Bilateral medial medullary infarction presented with monoplegia of the lower limb, followed by paraplegia and finally by tetraplegia]. (2003) (5)
- Teaching NeuroImages: Reversible cognitive impairment with bithalamic lesions caused by a dural arteriovenous fistula (2013) (5)
- Pure sensory infarct in the territories of anterior cerebral artery (2010) (5)
- Taste impairment in Miller Fisher syndrome (2015) (5)
- Biochemical features of genetic Creutzfeldt-Jakob disease with valine-to-isoleucine substitution at codon 180 on the prion protein gene. (2018) (5)
- Opsoclonus caused by diphenhydramine self-poisoning. (2009) (5)
- Developmental regulation of rat Ubc13 and Uev1B genes in the nervous system. (2007) (5)
- Pure pandysautonomia associated with interferon-alpha therapy (2007) (4)
- Rimmed vacuolar distal myopathy (1987) (4)
- Dissection of the polygenic architecture of neuronal Aβ production using a large sample of individual iPSC lines derived from Alzheimer’s disease patients (2022) (4)
- Pure pandysautonomia associated with interferon-alpha therapy (2007) (4)
- [Optic nerve swelling and gadolinium contrast enhancement on magnetic resonance imaging in the subacute stage of Leber's hereditary optic neuropathy: a case report]. (2012) (4)
- The familial occurrence may give a clue to the pathogenesis of inclusion body myositis. (2003) (4)
- Increase of disease duration of amyotrophic lateral sclerosis in a mouse model by transgenic small interfering RNA. (2007) (4)
- [Tibial muscular dystrophy]. (2001) (4)
- Application of Laser Capture Microdissection to Periodontal Tissue (2007) (4)
- Can Anti-AQP4 Antibody Damage the Blood-Brain Barrier? (2014) (4)
- [Pneumatosis intestinalis in a patient of myasthenia gravis treated with high-dose corticosteroid]. (2003) (4)
- Intramedullary spinal cord metastasis with a longitudinally extensive spinal cord lesion. (2011) (4)
- Atypical FTLD‐FUS associated with ALS‐TDP: A case report (2013) (4)
- A sporadic case of late-onset familial amyloid polyneuropathy with Bence-Jones proteinuria (1999) (4)
- Significant increase in the expression of matrix metalloproteinase 7 in primary CNS lymphoma (2008) (4)
- Amino acid conditions near the GPI anchor attachment site of prion protein for the conversion and the GPI anchoring. (2010) (4)
- [Spinocerebellar ataxia type 6 (SCA6)]. (1999) (4)
- Aging of the human limbic system: Observations of centenarian brains and analyses of genetic risk factors for senile changes (1998) (4)
- Environmental challenges for the nervous system and the brain in Japan. (2019) (3)
- Japanese encephalitis - serial CT findings and neuropathology in an autopsy case. (2009) (3)
- Cervical dystonia in an Alzheimer’s disease patient treated with donepezil (2013) (3)
- A case of anti-AQP4 antibody-positive neuromyelitis optica spectrum disorder with MRI-proven lesions in lumbar nerve roots. (2020) (3)
- False-negative and False-positive Diffusion-weighted MR Findings in Acute Ischemic Stroke and Stroke-like Episodes (2005) (3)
- Elevation of 8‐hydroxy‐2′‐deoxyguanosine in the cerebrospinal fluid of three patients with superficial siderosis (2015) (3)
- Brainstem congestion due to carotid-cavernous fistula via a shunt from the external carotid artery (2011) (3)
- [Brain ischemia--regenerative therapy using human neural stem cells]. (2003) (3)
- Time profile of eosinophilic neurons in the cortical layers and cortical atrophy. (2006) (3)
- Serum amyloid A level correlates with T2 lesion volume and cortical volume in patients with multiple sclerosis (2020) (3)
- Geographic Difference of Mortality of Creutzfeldt-Jakob Disease in Japan (2006) (3)
- Potential value of soluble APPα and APPβ in CSF as biomarkers of dementia disorders: Unresolved issues and perspectives (2018) (3)
- Primary ocular and central nervous system malignant lymphoma first manifested as uveitis: possible role of single photon emission computed tomography with N-isopropyl-123I-p-iodoamphetamine in the diagnostic procedure. (1994) (3)
- Specific amyloid-β42 deposition in the brain of a Gerstmann-Sträussler-Scheinker disease patient with a P105L mutation on the prion protein gene (2018) (3)
- Fatal encephalitis in a case of hypereosinophilic syndrome: MRI and autopsy findings. (2011) (3)
- Antihistamine‐associated myoclonus: A case report (2008) (3)
- Efficient in vivo delivery of antisense oligonucleotide to choroid plexus. (2013) (3)
- Current Evidence for the Association between Air Pollution and Parkinson's Disease (2022) (3)
- Subacute Supranuclear Palsy in anti-Hu Paraneoplastic Encephalitis (2017) (3)
- A case of Creutzfeldt-Jakob disease with a novel insertion mutation and codon 219 Lysine/Lysine polymorphism in the prion protein gene (2005) (3)
- Morel's laminar sclerosis showing apraxia of speech: Distribution of cortical lesions in an autopsy case (2010) (3)
- Is Anti-Gliadin Antibody Pathogenic in Gluten Ataxia? Analysis using Rat Cerebellar Slices and Patch-Clamp Recording (2013) (3)
- [Mononeuropathy multiplex in a patient receiving interferon alpha therapy for chronic hepatitis C]. (1995) (3)
- [Autosomal recessive distal muscular dystrophy(Miyoshi)]. (2001) (2)
- Recurrent breast cancer with metastatic brachial plexopathy. (2010) (2)
- [Rapid progressive HTLV-1-associated myelopathy with bronchoalveolar lesions and a long spinal cord lesion extending to almost the entire spinal cord]. (2011) (2)
- Theory of mind and its neuroanatomical correlates in people with multiple sclerosis. (2021) (2)
- Immune-mediated neuropathy with Epstein-Barr virus-positive T-cell lymphoproliferative disease. (2015) (2)
- Mexiletine is effective on segmental hyperhidrosis: report of two cases (2002) (2)
- Overexpression of wild type TDP-43 in motoneuron of non-human primate (2010) (2)
- A deletion polymorphism of alpha(2)-macroglobulin gene and cerebral amyloid angiopathy. (1999) (2)
- Acute Disseminated Myelitis Associated with 5-Fluorouracil and l-Leucovorin Treatment (2006) (2)
- Spinal Epidural Abscess Caused by Bacteroides Fragilis Group after Dilation and Curettage for Incomplete Abortion (2012) (2)
- An Early Change of Neurofibrillary Tangle Formation (1990) (2)
- [A case of antisynthetase syndrome with anti-EJ antibody complicated by pericarditis]. (2019) (2)
- Efficacy of Oral Rifampicin in Multiple System Atrophy (P04.159) (2013) (2)
- Soluble APP-α and APP-β in cerebrospinal fluid as potential biomarkers for differential diagnosis of mild cognitive impairment (2021) (2)
- Serial magnetic resonance imaging changes in sporadic Creutzfeldt-Jakob disease with valine homozygosity at codon 129 of the prion protein gene. (2014) (2)
- [Glial fibrillary tangle]. (2011) (2)
- [Prion disease surveillance in Japan: analysis of 1,241 patients]. (2009) (2)
- Epidemiologic Features of Human Prion Diseases in Japan: A Prospective 14-year Surveillance. (2014) (2)
- Leftward movement in severe neglect (2000) (2)
- Clinical characteristics of combined cases of spinocerebellar ataxia types 6 and 31 (2015) (2)
- Localization and trafficking of endogenous anterior pharynx-defective 1, a component of Alzheimer's disease related γ-secretase (2010) (2)
- [Detection of the primary tumor site in tumor-induced osteomalacia by indium-111 octreotide scintigraphy: a case report]. (2008) (2)
- Vagus nerve palsy caused by varicella zoster virus infection without rash (2007) (2)
- Predominant motor symptoms in a 74‐year‐old man with a small elongation in the spinocerebellar atrophy type 1 gene (2006) (2)
- [Progressive multifocal leukoencephalopathy (PML)]. (2011) (2)
- [Pathology of motor neuron diseases]. (1999) (2)
- CADASIL with a novel NOTCH3 mutation (Cys478Tyr). (2015) (2)
- [Multiple cerebral embolism caused by a patent foramen ovale and a uterine myoma]. (2003) (2)
- ONLINE REGISTRY FOR THE PREVENTION OF DEMENTIA IN JAPAN (2016) (2)
- [Regeneration therapy for ischemic stroke using neural stem cell transplantation]. (2006) (2)
- [Programs for continuing medical education: A session; 3. Pathogenesis and treatment of cerebellar ataxia-recent progresses]. (2012) (2)
- Longitudinal analysis of risk factors for dementia based on Mild Cognitive Impairment Screen results and questionnaire responses from healthy Japanese individuals registered in an online database (2019) (2)
- [Spinocerebellar ataxia type 6]. (2001) (1)
- Long-term Effects of Intravenous Cyclophosphamide in Combination with Mesna Provided Intravenously and via Bladder Perfusion in a Patient with Severe Multifocal Motor Neuropathy (2017) (1)
- [SCA6: From gene identification to recent progress on pathogenesis]. (2010) (1)
- Visual reproduction on the Wechsler Memory Scale-Revised as a predictor of Alzheimer's disease in Japanese people with mild cognitive impairment (2013) (1)
- High-Dose Ubiquinol Supplementation in Multiple-System Atrophy: A Multicentre, Randomised, Double-Blinded, Placebo-Controlled Phase 2 Trial (2023) (1)
- Book review – Announcements (2001) (1)
- [A case of post-poliomyelitis muscular atrophy with cranial nerve signs and widespread muscular atrophy of the extremities]. (1997) (1)
- Descriptive Epidemiology of Prion Disease in Japan: 1999–2012 (2015) (1)
- Corrigendum to “Depth perception from moving cast shadow in macaque monkey” [Behavioural Brain Research (2015) Jul 15; 288: 63–70 (BBR9527)] (2015) (1)
- EXPRESSION OF ALPHA IA-VOLTAGE-DEPENDENT CALCIUM CHANNEL MESSENGER RNA/PROTEIN IN BRAINS OF SPINOCEREBELLAR ATAXIA TYPE 6 (SCA6) (1999) (1)
- Nuclear bridges within multinucleated giant cells in subacute encephalitis of acquired immune deficiency syndrome (AIDS) (2004) (1)
- [The utility of voxel-based morphometry in the diagnosis of spinocerebellar degeneration]. (2014) (1)
- High voltage electrical stimulation of the proximal hypoglossal nerve in normal subjects (2002) (1)
- Erratum: siRNA-based inhibition specific for mutant SOD1 with single nucleotide alternation in familial ALS, compared with ribozyme and DNA enzyme (Biochemical and Biophysical Research Communications (2004) 314 (283-291) DOI: 10.1016/j.bbrc.2003.12.098) (2004) (1)
- UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase in nuclei and rimmed vacuoles of muscle fibers in DMRV (distal myopathy with rimmed vacuoles). (2008) (1)
- Familial ataxia with isolated vitamin E deficiency not due to mutation of alpha-TTP. (1999) (1)
- [Dissecting molecular mechanism of spinocerebellar ataxia type 31]. (2011) (1)
- Usefulness of logical memory II of WMS-R in memory clinic outpatients (2010) (1)
- [A case of potassium-sensitive periodic paralysis with cardiac dysrhythmia]. (1997) (1)
- Subject Index Vol. 44, 2000 (2000) (1)
- NUCLEAR BRIDGES IN MULTINUCLEATED GIANT CELLS ASSOCIATED WITH PRIMARY LYMPHOMA OF THE BRAIN IN AN AIDS PATIENT.: 50 (1987) (1)
- [Overcoming neurological diseases-breakthrough for new era]. (2013) (1)
- Safety and Efficacy of Perampanel for Sporadic Amyotrophic Lateral Sclerosis: A Multicentre, Double-Blind, Randomised Phase 2 Trial (2020) (1)
- Immunocytochemical Studies of Substance P and Met-Enkephalin in the Globus Pallidus of Progressive Supranuclear Palsy (1990) (1)
- Notes on the Launch of Neurology and Clinical Neuroscience (2013) (1)
- A Novel Form of Reversible Subacute Spongiform Leukoencephalopathy (2001) (1)
- Expression of triad proteins (dihydropyridine receptor, ryanodine receptor, and triadin) and intracellular Ca2+ transient during development of human skeletal muscle (1998) (1)
- Hemorrhagic bulla in Churg-Strauss syndrome. (2011) (1)
- Lacunar thalamic infarction with isolated dysesthesia in contralateral fingers (2013) (1)
- Transient Charles Bonnet syndrome in a patient with reversible cerebral vasoconstriction syndrome (2013) (1)
- [Spinocerebellar ataxia type 31]. (2010) (1)
- Subject Index Vol. 54, 2005 (2006) (1)
- Characterization of Sporadic Creutzfeldt-Jakob Disease and History of Neurosurgery to Identify Potential Iatrogenic Cases (2020) (1)
- A reply to Treglia et al. (2012) (1)
- [Autoantibodies to GAD and autoimmune-mediated neurological diseases]. (2013) (1)
- [Role of lyrics and melody in song recognition: why is song recognition faster?]. (2009) (1)
- Pseudoradicular sensory loss caused by a cerebral demyelinative lesion. (2008) (0)
- Nominees for the Best Presentation Award for Japanese Young Neurologist. (2015) (0)
- Human prion diseases in Japan: analysis of 1,552 patients in a prospective 11-year surveillance (2011) (0)
- A nationwide survey of episodic ataxia in Japan (2021) (0)
- Author's response in reply to “Question about data: Importance of serum amyloid A level in patients with multiple sclerosis” (2021) (0)
- Gluten Ataxia in Japan (2014) (0)
- Parkinson’s disease and other movement disorders (2008) (0)
- O1-04-03 Creutzfeldt-Jakob Disease (CJD) surveillance in Japan: Two distinct subtypes of CJD associated with cadaveric dura mater graft and the first Japanese case of variant CJD (2006) (0)
- Prism Adaptation Test (PAT): A Practical and Quantitative Method to Evaluate Cerebellar Function (2021) (0)
- Title Clinical features of genetic Creutzfeldt-Jakob disease with V 180 I mutationin the prion protein gene (2017) (0)
- Sequential changes in the non-coding control region sequences of JC polyomaviruses from the cerebrospinal fluid of patients with progressive multifocal leukoencephalopathy (2012) (0)
- Nationwide Laboratory Surveillance of Progressive Multifocal Leukoencephalopathy in Japan: Fiscal Years 2011–2020 (2023) (0)
- P4.61 Prominent respiratory muscle involvement in adPEO with POLG1 mutation (2010) (0)
- Non-human primate model of ALS with cytoplasmic mislocalization of wild-type TDP-43 (2011) (0)
- Alternative BSE risk assessment methodology for beef and beef offal imported into Japan. (2012) (0)
- Nicotine receptor and amyloid burden for frontal activation in Alzheimer disease (0)
- [Postgraduate training program of neurology in Tokyo Medical and Dental University]. (2006) (0)
- Subject Index Vol. 46, 2001 (2001) (0)
- Educational lecture 9. Prion disease. (2003) (0)
- Japan Consortium of Ataxias (J-Cat): A Cloud -Based national registry for degenerative ataxias providing framework for genetic diagnosis and Prospective Natural History Researches (2017) (0)
- [A case of familial mitochondrial myopathy associated with peripheral neuropathy and optic atrophy]. (1987) (0)
- [Prion disease]. (2003) (0)
- An Autosomal Dominant Cerebellar Ataxia Linked to Chromosome 16q22.1 Is Associated with a Single-Nucleotide Substitution in the 5 (cid:1) Untranslated Region of the Gene Encoding a Protein with Spectrin Repeat and Rho Guanine-Nucleotide Exchange-Factor Domains Autosomal dominant cerebellar ataxia (2005) (0)
- Stroke presenting with monoparesis in the lower limb. (2012) (0)
- Contents Vol. 46, 2001 (2001) (0)
- MATTERS ARISING (1995) (0)
- Epidemiological study of Gerstmann-Sträussler-Scheinker disease with codon 102 mutation in Japan (2019) (0)
- A Novel de novo KIF1A Mutation in a Patient with Ataxia, Intellectual Disability and Mild Foot Deformity. (2022) (0)
- [Molecular targeted therapy towards neurological disorders]. (2012) (0)
- Genetic Creutzfeldt‒Jakob disease with 5-octapeptide repeats presented as frontotemporal dementia (2023) (0)
- 2. Compound nerve action potential (CNAP) study is a useful examination for evaluating muscle afferent Ia fibers (2011) (0)
- Periodic encephalographic study in nation-wide Creutzfeldt Jakob disease surveillance in Japan (2017) (0)
- When Should We Test Patients With Familial Ataxias For SCA31? (P2.035) (2014) (0)
- Diffusion-weighted magnetic resonance imaging in dura mater graft-associated Creutzfeldt-Jakob disease (2020) (0)
- Evaluation of Rehabilitation for Upper Limb Ataxia (2019) (0)
- FUS regulates RAN translation through modulating the G-quadruplex structure of GGGGCC repeat RNA in C9orf72-linked ALS/FTD (2022) (0)
- Evaluation of Intensity Signal in Dentate Nucleus on T2-Weighted Imaging To Diagnose Patients with Cerebellar Ataxia (P05.026) (2012) (0)
- Parkinson's Disease: The Dirty Truth About the Air – Authors' Reply (2022) (0)
- Paraventricular Infarct in the Corona Radiata (1994) (0)
- Supplement Note (2016) (0)
- [Advances in neuroscience and therapeutic research on neurological diseases--the present status and future prospects (discussion)]. (2007) (0)
- 52. Study of albumin leakage and peripheral nerve-conduction study in Guillain–Barré syndrome (2008) (0)
- Effect of Sera from Bickerstaff Brainstem Encephalitis and Miller Fisher Syndrome Patients Against Human Blood-Brain Barrier and Blood-Nerve Barrier In Vitro Models (P06.141) (2012) (0)
- F.26. Alteration of Gut Flora Ameliorates Experimental Autoimmune Encephalomyelitis in Association with Contraction of Inflammatory Th17 Cells (2008) (0)
- [Tailored therapy for multiple sclerosis]. (2008) (0)
- Human prion diseases in Japan: a prospective surveillance from 1999 (2013) (0)
- A new autosomal dominant cerebellar ataxia linked to chromosome 16q22.1 (16q-ADCA) (2007) (0)
- Spinocerebellar Ataxia Type 4 (SCA4) (2003) (0)
- [Recommendations (Proposal) for promoting research for overcoming neurological diseases 2020]. (2021) (0)
- Temporal Relationship between Impairment of Cerebellar Motor Learning and Deterioration of Ataxia in Patients with Cerebellar Degeneration. (2023) (0)
- Encephalomyelitis by Ghrelin Suppression of Experimental Autoimmune (0)
- [Clinical diagnosis of acute stroke]. (2006) (0)
- [Prion disease]. (2010) (0)
- MM2 type sporadic Creutzfeldt-Jakob disease: clinicoradiologic features and clinical diagnosis (2005) (0)
- Multifocal motor neuropathy with conduction block which demonstrated by the flexor digitorum profundus muscle innervated from the ulnar nerve (2023) (0)
- Preventive or promotive effects of PRNP polymorphic heterozygosity on the onset of prion disease (2023) (0)
- [Progress in diagnosis of and therapy for diabetic neuropathies]. (2004) (0)
- 1-1-05. Electroencephalographic diagnosis of prion disease in Japanese CJD surveillance (2017) (0)
- [Recommendations (Proposal) for promoting research for overcoming neurological diseases 2020]. (2022) (0)
- ANALYSIS OF RISK FACTORS FOR DEMENTIA BASED ON 10-WORD MEMORY TEST RESULTS AND QUESTIONNAIRE RESPONSES IN HEALTHY JAPANESE INDIVIDUALS REGISTERED IN AN ONLINE REGISTRY (2018) (0)
- Pattern of beta-amyloid production by mouse embryonic fibroblasts overexpressing psen1 with I143T mutation (2012) (0)
- Molecular mechanism of a newly identified hereditary cerebellar ataxia, 16q-ADCA (2009) (0)
- [Prion disease]. (2006) (0)
- [Establishment of the concept of prion diseases]. (2007) (0)
- Impaired DNA Damage Response in the Pathogenesis of Multiple System Atrophy: A Histopathological Study (P3.016) (2015) (0)
- P2-157: Serine422 phosphorylation of tau protein by oxidative stress via c-Jun N-terminal kinase (JNK) activation (2008) (0)
- Pentanucleotide-repeat-associated unconventional translation is observed in spinocerebellar ataxia type 31 (2017) (0)
- Skeletal anomaly and opisthotonus in early-onset epileptic encephalopathy with KCNQ2 abnormality (2023) (0)
- [New tests that are necessary and those that are important to clinical practitioners. 8. Neuromuscular diseases]. (2008) (0)
- Forefront of medical science and medical care.Pathology of motor neuron disease. (1999) (0)
- P2.04 DMRV and GNE mutations: genotype–phenotype correlation in 100 Japanese patients (2010) (0)
- Parkinsonism and Related Disorders (2012) (0)
- [Conquering intractable neurological diseases using an approach with single gene defects]. (2010) (0)
- Patients of Parkinson's disease may have dysfunction in vection (self-motion perception) (2017) (0)
- [Towards the establishment of a postgraduate training program of neurology--in the case of Tokyo Medical and Dental University]. (2004) (0)
- [Medical treatment of dyskinesia]. (2004) (0)
- [Prion disease: recent progress]. (2004) (0)
- Motor unit number estimation in spinal and bulbar muscular atrophy (2007) (0)
- Contents Vol. 69, 2013 (2013) (0)
- Regional Cytoplasmic TDP-43 Mislocalization Is Recapitulated in Non-Human Primate Mimicking ALS (P03.178) (2012) (0)
- Gene mutations causing autosomal dominant cerebellar ataxia in Japan (2010) (0)
- [Diagnosis and therapy for patients with multiple system atrophy]. (2003) (0)
- [A case of distal myopathy with rimmed vacuole formation, progresses into proximal-dominant muscle involvement]. (1992) (0)
- [Roundtable discussion: advances in neuroscience and therapeutic research on neurological diseases--the present status and future prospects]. (2007) (0)
- [Professionalism and the Japanese Society of Neurology - for the next 100 years]. (2012) (0)
- [Glial cytoskeletal abnormality in neurodegenerative diseases: multiple system atrophy]. (1996) (0)
- Contents Vol. 72, 2014 (2014) (0)
- P2-540 Epidemiologic features of prion diseases in Japanese elderly: results from the surveillance (2011) (0)
- Cervical dystonia in an Alzheimer’s disease patient treated with donepezil (2012) (0)
- [Autosomal dominant hereditary distal myopathy linked to chromosome 14]. (2001) (0)
- Deletion of vitamin E increases Aβ accumulation by decreasing its clearances from brain and blood in a mouse model of Alzheimer's disease (2010) (0)
- Motor‐dominant chronic inflammatory demyelinating polyradiculoneuropathy with uhthoff‐like phenomenon is a distinct clinical entity? (2012) (0)
- ’ ichi Shoji L-threo-3 , 4-dihydroxyphenylserine enhances the orthostatic responses of plasma renin activity and angiotensin II in multiple system atrophy (0)
- [Non-Scandinavian late-onset distal myopathy]. (2001) (0)
- [Molecular genetic approach to spinocerebellar ataxias]. (2009) (0)
- 362 Significance of leuko-araiosis on computed tomography in patients with Alzheimer's disease (1996) (0)
- [Intrathecal baclofen therapy to spasticity]. (2007) (0)
- A method for promoting screening procedure proliferation of a neural stem cell and the promotion of neurite extension, promotor for neural stem cell pharmaceutical composition containing the test method, and survival, and / or (2004) (0)
- Central nervous system involvement in CD20-positive primary peripheral T-cell lymphoma, not otherwise specified (2017) (0)
- [Autosomal dominant spinocerebellar degeneration--new forms and pathomechanisms]. (2004) (0)
- [Welander's distal myopathy]. (2001) (0)
- P2-233 ASSESSMENT OF CEREBRALVASOREACTIVITY USING ULTRASOUND TECHNIQUES IN ALZHEIMER’S DISEASE (2013) (0)
- Profiling of miRNAs in Cerebrospinal Fluid From Patients With Amyotrophic Lateral Sclerosis (S26.005) (2014) (0)
- High-efficacy therapy reduces subcortical grey matter volume loss in Japanese patients with relapse-onset multiple sclerosis: A 2-year cohort study. (2022) (0)
- Meeting details (2005) (0)
- Bilateral Optic Nerve Edema in Central-variant Posterior Reversible Encephalopathy Syndrome (2020) (0)
- Title Ultrasensitive human prion detection in cerebrospinal fluid by real-timequaking-induced conversion (2017) (0)
- Structural connectivity in spatial attention network: reconstruction from left hemispatial neglect (2017) (0)
- Functional Connectivity and Small-World Networks in Prion Disease (2023) (0)
- POSSIBLE HUMAN-TO-HUMAN TRANSMISSION OF CEREBRAL β-AMYLOIDOSIS VIA CADAVERIC DURA MATER GRAFTING (2017) (0)
- 3-03-06 Radiological study on sympathetic denervation of myocardium in pure progressive autonomic failure (1997) (0)
- 5-33-03 The myotonin protein kinase decreases during somatic cell proliferation in vitro (1997) (0)
- Low-Titer Anti-GAD-Antibody-Positive Cerebellar Ataxia (2012) (0)
- Myotonic Dystrophy Protein Kinase Is a Sarcoplasmic Reticulum Protein Specifically Localized in Type I Muscle Fibers without Colocalization of SERCAII ATPase (2007) (0)
- [Prion disease--the present status and recent progress in Japan]. (2008) (0)
- Neurological insights on two siblings with GM3 synthase deficiency due to novel compound heterozygous ST3GAL5 variants (2023) (0)
- Case of relapsing remitting neuro‐Sweet disease mimicking immunoglobulin G4‐related disease (2018) (0)
- Changes in expression level of V-1, a novel protein containing ankyrin repeats during muscle cell differentiation in culture (1998) (0)
- Duration between initial manifestation of CJD and detection of PSD, specific findings on MRI, CSF 14-3-3 protein, or CSF high NSE (2005) (0)
- Post‐COVID ‐19 vaccination Guillain‐Barr é syndrome with sensory ataxia, gaze‐evoked nystagmus, mental‐status change, and positive pathological reflex (2023) (0)
- P4.61 Prominent respiratory muscle involvement in adPEO with POLG1 mutation (2010) (0)
- Memorial note - Professor Asao Hirano. (2020) (0)
- Contents Vol. 54, 2005 (2006) (0)
- Orthostatic Hypotension in a Case with Advanced Esophageal Cancer (2009) (0)
- [Cerebello-olivary atrophy (COA)]. (1999) (0)
- The truncation and phosphorylation of TDP-43 is not prerequisite for motoneuronal degeneration in non-human primate model of amyotrophic lateral sclerosis (2011) (0)
- Genome-wide identification of tandem repeats associated with splicing variation across 49 tissues in humans (2023) (0)
- Contents Vol. 44, 2000 (2000) (0)
- Neuroscience Committee (2008) (0)
- [Recommendations (Proposal) for promoting research for overcoming neurological diseases 2020]. (2022) (0)
- Abstract T P244: Risk Factors of Delirium During Acute Phase After a Stroke Screened by the Intensive Care Delirium Screening Checklist (2014) (0)
- Correction: A Novel de novo KIF1A Mutation in a Patient with Ataxia, Intellectual Disability and Mild Foot Deformity. (2022) (0)
- [Whether or not ALS lesions spread contiguously?]. (2012) (0)
- Lacunar thalamic infarction with isolated dysesthesia in contralateral fingers (2012) (0)
- RELATIONSHIP BETWEEN GAIT AND COGNITIVE FUNCTION IN PATIENTS WITH ALZHEIMER'S DISEASE (2014) (0)
- Re-evaluation of soluble APP-α and APP-β in cerebrospinal fluid as potential biomarkers for early diagnosis of dementia disorders (2017) (0)
- [112th Scientific Meeting of the Japanese Society of Internal Medicine: Presidential Lecture: Invited Lecture: Prion Diseases: The Present Status and Prospect of Overcoming]. (2015) (0)
- Differential diagnosis of CNS lymphomatoid granulomatosis (2010) (0)
- [Variant Creutzfeldt-Jakob disease]. (2004) (0)
- F.26. Alteration of Gut Flora Ameliorates Experimental Autoimmune Encephalomyelitis in Association with Contraction of Inflammatory Th17 Cells (2008) (0)
- [Case report; a case of chronic progressive neuro-Behcet's disease with extensive brain atrophy]. (2011) (0)
- PRION 2016 Tokyo Declaration (2016) (0)
- Anti-neutral glycolipids antibody-positive three men of combined central and peripheral demyelination mimicking Encephaloradiculoneuropathy phenotype (2017) (0)
- A Future Perspective of Researches on Neurodegenerative Diseases (2011) (0)
- ORIGINAL RESEARCH Different Patterns of Fornix Damage in Idiopathic Normal Pressure Hydrocephalus and Alzheimer Disease (2012) (0)
- Spinocerebellar Ataxia Type 31 Exacerbated by Anti-amino Terminal of Alpha-enolase Autoantibodies (2022) (0)
- Symposium 4: Chairman's remark (2003) (0)
- A BAC Transgenic Mouse Model of Spinocerebellar Ataxia Type 31 (SCA31) Manifests Late-Onset Motor Dysfunction and RNA Foci in Purkinje Cells (S43.007) (2013) (0)
- [Central nervous system infection presenting with cognitive impairment]. (2014) (0)
- Short communication Characteristic changes in T -value, apparent diffusion coefficient, and (2001) (0)
- GLYCOSPHINGOLIPID ANTIBODIES AND BLOOD‐NERVE BARRIER IN AUTOIMMUNE DEMYELINATIVE NEUROPATHY (2000) (0)
- 137. New feature of nerve conduction in anti-MAG antibody associated neuropathy (2009) (0)
- [A new murine model of HIV-associated encephalopathy]. (2004) (0)
- An Effect of I143T PSEN1 Mutation on The Generation of Amyloid B in Culture Cells (2011) (0)
- LETTERS TO THE EDITOR RITUXIMAB THERAPY FOR MORVAN SYNDROME ASSOCIATED WITH MYASTHENIA GRAVIS (2012) (0)
- Secreted appα and appβ in cerebrospinal fluid correlate with phosphorylated tau and are potentially useful biomarkers for early diagnosis of dementia disorders (2017) (0)
- Quantitative analysis of gait disorders in people with Alzheimer's disease by using a portable gait rhythmograph (2013) (0)
- [Holmes type cortical cerebellar atrophy (CCA)]. (1999) (0)
- COLOCALIZATION OF Aβ42 WITH PRPSC-PLAQUES IN THE BRAIN OF GERSTMANN-STRÄUSSLER-SCHEINKER DISEASE WITH THE P105L MUTATION (2016) (0)
- ENHANCED PLA2G3 EXPRESSION BY OXIDATIVE STRESS DECREASES THE IDE AND EXACERBATES AD (2016) (0)
- [Spinocerebellar degeneration and Ca channel abnormality]. (2001) (0)
- Questionnaire survey on the process of specialty training in neurology in Japan. (2017) (0)
- P2-9 Metabolic syndrome is a risk factor for exaggerating neuropathy in diabetic patients (2010) (0)
- [Neuromuscular side effects]. (2012) (0)
- [Clinical, neuropathological and genetic characteristics of spinocerebellar ataxia type 6 (SCA6)]. (1999) (0)
- 5. Prion Diseases: The Present Status and Prospect of Overcoming (2015) (0)
- [Research progress in slow virus infections in Japan and the diagnostic points]. (2007) (0)
- 1111 Neural influence on developmental expression of myotonin protein kinase in cultured human muscle cells (1997) (0)
- Protective effect of endogenous PS1 holoprotein under ER stress condition (2009) (0)
- [Corticobasal degeneration]. (2019) (0)
- Diverse and Unstable Pentanucleotide Repeats at the Spinocerebellar Ataxia Type 31 (SCA31) Locus in Caucasians (P05.017) (2012) (0)
- 18F-THK5351 positron emission tomography imaging for Gerstmann-Sträussler-Scheinker disease (2022) (0)
- Consensus Paper: Neuroimmune Mechanisms of Cerebellar Ataxias (2015) (0)
- Spinocerebellar ataxia type 31（SCA31）の臨床像，画像所見―Spinocerebellar ataxia type 6（SCA6）との小脳外症候の比較検討― (2014) (0)
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What Schools Are Affiliated With Hidehiro Mizusawa?
Hidehiro Mizusawa is affiliated with the following schools:
