Toru Iwaki

Q: What Schools Are Affiliated With Toru Iwaki

Toru Iwaki is affiliated with the following schools: Kyushu University, University of Tokyo, Institute of Science Tokyo, Kyoto University

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Toru Iwaki

Computer Science

#9047

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#9506

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Computational Linguistics

#2124

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#2146

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Machine Learning

#3868

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#3914

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Artificial Intelligence

#4194

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#4252

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computer-science Degrees

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Computer Science

Toru Iwaki's Degrees

PhD Computer Science University of Tokyo
Masters Computer Science University of Tokyo
Bachelors Computer Science University of Tokyo

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Toru Iwaki'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

αB-crystallin is expressed in non-lenticular tissues and accumulates in Alexander's disease brain (1989) (485)
Pivotal role of cerebral interleukin-17–producing γδT cells in the delayed phase of ischemic brain injury (2009) (472)
Hydrated autoclave pretreatment enhances tau immunoreactivity in formalin-fixed normal and Alzheimer's disease brain tissues. (1991) (332)
Lysosomotropic Agents and Cysteine Protease Inhibitors Inhibit Scrapie-Associated Prion Protein Accumulation (2000) (297)
Cellular distribution of alpha B-crystallin in non-lenticular tissues. (1990) (294)
Macrophage infiltration and heme oxygenase-1 expression correlate with angiogenesis in human gliomas. (1999) (293)
Amide proton transfer imaging of adult diffuse gliomas: correlation with histopathological grades. (2014) (282)
Reduction of KCC2 Expression and GABAAReceptor-Mediated Excitation after In Vivo Axonal Injury (2002) (267)
Accumulation of alpha B-crystallin in central nervous system glia and neurons in pathologic conditions. (1992) (262)
Altered Expression of Diabetes-Related Genes in Alzheimer's Disease Brains: The Hisayama Study (2013) (245)
Insulin resistance is associated with the pathology of Alzheimer disease (2010) (243)
Intracellular Aβ42 activates p53 promoter: a pathway to neurodegeneration in Alzheimer's disease (2005) (237)
Glucose tolerance status and risk of dementia in the community (2011) (226)
Midlife and Late-Life Blood Pressure and Dementia in Japanese Elderly: The Hisayama Study (2011) (211)
Perfusion Imaging of Brain Tumors Using Arterial Spin-Labeling: Correlation with Histopathologic Vascular Density (2008) (207)
Treatment of Transmissible Spongiform Encephalopathy by Intraventricular Drug Infusion in Animal Models (2004) (207)
Histopathological aspects of dural arteriovenous fistulas in the transverse-sigmoid sinus region in nine patients. (1997) (146)
Trends in dementia prevalence, incidence, and survival rate in a Japanese community (2017) (137)
Trends in prevalence of Alzheimer’s disease and vascular dementia in a Japanese community: the Hisayama Study (2010) (131)
Hakata Antigen, a New Member of the Ficolin/Opsonin p35 Family, Is a Novel Human Lectin Secreted into Bronchus/Alveolus and Bile (1999) (126)
Alpha B-crystallin is expressed in non-lenticular tissues and accumulates in Alexander's disease brain. (1989) (122)
Rosenthal fibers share epitopes with alpha B-crystallin, glial fibrillary acidic protein, and ubiquitin, but not with vimentin. Immunoelectron microscopy with colloidal gold. (1991) (122)
Incidence and survival of dementia in a general population of Japanese elderly: the Hisayama study (2008) (113)
Inhibitory effects of aripiprazole on interferon‐γ‐induced microglial activation via intracellular Ca2+ regulation in vitro (2008) (113)
Intracellular Abeta42 activates p53 promoter: a pathway to neurodegeneration in Alzheimer's disease. (2005) (111)
Differentiation of high-grade and low-grade diffuse gliomas by intravoxel incoherent motion MR imaging. (2016) (106)
Differentiating primary CNS lymphoma from glioblastoma multiforme: assessment using arterial spin labeling, diffusion-weighted imaging, and 18F-fluorodeoxyglucose positron emission tomography (2013) (105)
Accumulation of 8-oxo-2'-deoxyguanosine and increased expression of hMTH1 protein in brain tumors. (2001) (103)
Sense and antisense modification of glial alpha B-crystallin production results in alterations of stress fiber formation and thermoresistance (1994) (101)
Detection of human T lymphotrophic virus type I (HTLV-I) proviral DNA and analysis of T cell receptor V beta CDR3 sequences in spinal cord lesions of HTLV-I-associated myelopathy/tropical spastic paraparesis (1994) (101)
Comparative profiling of cortical gene expression in Alzheimer’s disease patients and mouse models demonstrates a link between amyloidosis and neuroinflammation (2017) (100)
Molecular pathophysiology of impaired glucose metabolism, mitochondrial dysfunction, and oxidative DNA damage in Alzheimer's disease brain (2017) (92)
Impairment of mitochondrial DNA repair enzymes against accumulation of 8-oxo-guanine in the spinal motor neurons of amyotrophic lateral sclerosis (2002) (91)
Identification and Characterization of the Gene Encoding a New Member of the α-Crystallin/Small hsp Family, Closely Linked to the αB-Crystallin Gene in a Head-to-Head Manner (1997) (90)
Enhanced expression of NADPH oxidase Nox4 in human gliomas and its roles in cell proliferation and survival (2008) (89)
Age-associated prevalence and risk factors of Lewy body pathology in a general population: the Hisayama study (2003) (86)
Clusterin/apolipoprotein J is associated with cortical Lewy bodies: immunohistochemical study in cases with α-synucleinopathies (2002) (84)
Connexin 43 Astrocytopathy Linked to Rapidly Progressive Multiple Sclerosis and Neuromyelitis Optica (2013) (83)
Multiple system degeneration with basophilic inclusions in Japanese ALS patients with FUS mutation (2010) (81)
Vascular endothelial growth factor in chronic subdural haematomas (2001) (80)
A comparative immunohistochemical study of Kuru and senile plaques with a special reference to glial reactions at various stages of amyloid plaque formation. (1991) (76)
Altered expressions of glutamate transporter subtypes in rat model of neonatal cerebral hypoxia-ischemia. (2001) (76)
Quinoline Derivatives Are Therapeutic Candidates for Transmissible Spongiform Encephalopathies (2004) (75)
Grading diffuse gliomas without intense contrast enhancement by amide proton transfer MR imaging: comparisons with diffusion- and perfusion-weighted imaging (2017) (74)
Expression of 8-oxoguanine DNA glycosylase is reduced and associated with neurofibrillary tangles in Alzheimer's disease brain (2002) (74)
Clinicopathological features of solitary fibrous tumor of the meninges: An immunohistochemical reappraisal of cases previously diagnosed to be fibrous meningioma or hemangiopericytoma (2000) (72)
Distinctive immunohistochemical profiles of small heat shock proteins (Heat shock protein 27 and αB‐crystallin) in human brain tumors (1996) (71)
Clinicopathological Outline of Dementia with Lewy Bodies Applying the Revised Criteria: The Hisayama Study (2008) (70)
De novo apparently balanced complex chromosome rearrangement (CCR) involving chromosomes 4, 18, and 21 in a girl with mental retardation: report and review. (1998) (70)
Immunohistochemical study of intracranial cysts. (1988) (69)
Involvement of cathepsin B in the motor neuron degeneration of amyotrophic lateral sclerosis (2003) (69)
Intracellular accumulation of toxic turn amyloid-β is associated with endoplasmic reticulum stress in Alzheimer's disease. (2013) (69)
Photofabricated Gelatin-Based Nerve Conduits: Nerve Tissue Regeneration Potentials (2004) (66)
Association of HSPB2, a member of the small heat shock protein family, with mitochondria. (2001) (63)
Expression of neurofibromatosis 2 protein in human brain tumors: an immunohistochemical study (1997) (63)
Amyloid imaging probes are useful for detection of prion plaques and treatment of transmissible spongiform encephalopathies. (2004) (63)
α-Synuclein is expressed in a variety of brain tumors showing neuronal differentiation (2000) (61)
Multiple mRNAs of rat brain alpha-crystallin B chain result from alternative transcriptional initiation. (1990) (60)
Results of a long-term follow-up after neuroendoscopic biopsy procedure and third ventriculostomy in patients with intracranial germinomas. (2007) (60)
Immunohistochemical distribution of amyloid precursor protein during normal rat development. (1993) (59)
Brain-Derived Neurotrophic Factor Induces Sustained Elevation of Intracellular Ca2+ in Rodent Microglia1 (2009) (58)
Chordoma in early childhood: a clinicopathological study. (1991) (56)
Prevalence and clinicopathological features of H3.3 G34-mutant high-grade gliomas: a retrospective study of 411 consecutive glioma cases in a single institution (2017) (54)
Molecular cloning of a novel apoptosis-related gene, human Nap1 (NCKAP1), and its possible relation to Alzheimer disease. (2000) (53)
Aquaporin-4 astrocytopathy in Baló’s disease (2010) (53)
Extensive loss of connexins in Baló’s disease: evidence for an auto-antibody-independent astrocytopathy via impaired astrocyte–oligodendrocyte/myelin interaction (2012) (53)
Expression of αB-crystallin in the developing rat kidney (1991) (52)
Expression of hMTH1 in the hippocampi of control and Alzheimer's disease (2001) (51)
Distinctions between pituicytoma and ordinary pilocytic astrocytoma. Case report. (2003) (51)
Amplification and Overexpression of mdm2 Gene in Ependymomas (2000) (49)
Association of Alzheimer disease pathology with abnormal lipid metabolism (2011) (49)
Midlife and Late‐Life Smoking and Risk of Dementia in the Community: The Hisayama Study (2015) (48)
Astrocytoma of the pituitary gland (pituicytoma): case report (2002) (48)
Impaired Cytoplasmic–Nuclear Transport of Hypoxia‐Inducible Factor‐1α in Amyotrophic Lateral Sclerosis (2013) (48)
Epithelial properties of pleomorphic xanthoastrocytomas determined in ultrastructural and immunohistochemical studies (1987) (48)
Reappraisal of Aquaporin‐4 Astrocytopathy in Asian Neuromyelitis Optica and Multiple Sclerosis Patients (2011) (48)
Glial progenitors in the brainstem give rise to malignant gliomas by platelet‐derived growth factor stimulation (2010) (48)
Loss of hnRNPA1 in ALS spinal cord motor neurons with TDP‐43‐positive inclusions (2015) (48)
Hemangiopericytoma of the meninges: a clinicopathologic and immunohistochemical study. (1988) (47)
Surface plasmon resonance analysis for the screening of anti-prion compounds. (2006) (47)
Increased clusterin (apolipoprotein J) expression in human and mouse brains infected with transmissible spongiform encephalopathies (2002) (46)
Expression patterns of LIS1, dynein and their interaction partners dynactin, NudE, NudEL and NudC in human gliomas suggest roles in invasion and proliferation (2007) (43)
A case of hereditary diffuse leukoencephalopathy with axonal spheroids caused by a de novo mutation in CSF1R masquerading as primary progressive multiple sclerosis (2013) (42)
Identification and characterization of the gene encoding a new member of the alpha-crystallin/small hsp family, closely linked to the alphaB-crystallin gene in a head-to-head manner. (1997) (42)
Colocalization of prion protein and β protein in the same amyloid plaques in patients with Gerstmann-Sträussler Syndrome (2004) (41)
Differential Expression of Metallothioneins in Human Prion Diseases (2000) (41)
Altered Expression of COX-2 in Subdivisions of the Hippocampus during Aging and in Alzheimer’s Disease: The Hisayama Study (2007) (40)
Skein-like inclusions in the neostriatum from a case of amyotrophic lateral sclerosis with dementia (1998) (40)
Quantitative analysis of neurofibrillary pathology in a general population to reappraise neuropathological criteria for senile dementia of the neurofibrillary tangle type (tangle‐only dementia): The Hisayama study (2006) (39)
Spinal cord lesions of myelitis with hyperIgEemia and mite antigen specific IgE (atopic myelitis) manifest eosinophilic inflammation (2001) (39)
AlphaB-crystallin protects glial cells from hypertonic stress. (1996) (39)
Expression of VEGF and its receptor genes in intracranial schwannomas (2007) (38)
Choroid plexus papillomas: an immunohistochemical study with particular reference to the coexpression of prealbumin. (1988) (38)
Intraneuronal amyloid β42 enhanced by heating but counteracted by formic acid (2007) (38)
Cognitive dysfunction in patients with amyotrophic lateral sclerosis is associated with spherical or crescent-shaped ubiquitinated intraneuronal inclusions in the parahippocampal gyrus and amygdala, but not in the neostriatum (2001) (37)
Immunohistochemical demonstration of alphaB-crystallin in hamartomas of tuberous sclerosis. (1991) (37)
Eosinophilic myelitis associated with atopic diathesis: a combined neuroimaging and histopathological study (2003) (37)
Accumulation of αB-crystallin in brains of patients with Alexander's disease is not due to an abnormality of the 5′-flanking and coding sequence of the genomic DNA (1992) (36)
Cellular Distribution of NDRG1 Protein in the Rat Kidney and Brain During Normal Postnatal Development (2003) (36)
[Alexander's disease]. (2000) (35)
Acute Megakaryoblastic Leukemia After Transient Myeloproliferative Disorder With Clonal Karyotype Evolution in a Phenotypically Normal Neonate (2002) (35)
Diagnosis of new variant Creutzfeldt-Jakob disease by tonsil biopsy (1997) (35)
Electron microscopic investigations of synaptonemal complexes in an infertile human male carrier of a pericentric inversion inv(1)(p32q42) (1987) (34)
αB-Crystallin in C6 glioma cells supports their survival in elevated extracellular K+: the implication of a protective role of αB-crystallin accumulation in reactive glia (1995) (34)
Genomic organization and localization of gene for human carbonic anhydrase IV to chromosome 17q. (1993) (34)
Diagnostic utility of intravoxel incoherent motion mr imaging in differentiating primary central nervous system lymphoma from glioblastoma multiforme (2016) (33)
Massive accumulation of modified tau and severe depletion of normal tau characterize the cerebral cortex and white matter of Alzheimer's disease. Demonstration using the hydrated autoclaving method. (1992) (33)
Creutzfeldt-Jakob disease with codon 129 polymorphism (Valine): a comparative study of patients with codon 102 point mutation or without mutations (1992) (33)
An atypical case of sporadic Creutzfeldt–Jakob disease with Parkinson's disease (2001) (32)
Allelic losses of chromosome 10 in glioma tissues detected by quantitative single-strand conformation polymorphism analysis. (2006) (31)
Expression of glutamate transporter subtypes during normal human corticogenesis and type II lissencephaly. (2005) (31)
An autopsy case of spinocerebellar ataxia type 6 with mental symptoms of schizophrenia and dementia. (1999) (31)
Increased STAG2 dosage defines a novel cohesinopathy with intellectual disability and behavioral problems. (2015) (31)
Clinical features and neuropathological findings of familial amyotrophic lateral sclerosis with a His46Arg mutation in Cu/Zn superoxide dismutase (2002) (30)
Molecular characteristics of glioblastoma with 1p/19q co-deletion (2012) (30)
Characterization of the biological functions of a transcription factor, c-myc intron binding protein 1 (MIBP1). (2002) (29)
Styrylbenzoazole derivatives for imaging of prion plaques and treatment of transmissible spongiform encephalopathies (2006) (29)
Discrepancy in Programmed Cell Death-Ligand 1 Between Primary and Metastatic Non-small Cell Lung Cancer. (2017) (29)
Clinicopathological review of solitary fibrous tumors: dedifferentiation is a major cause of patient death (2019) (29)
Association of adipocyte enhancer‐binding protein 1 with Alzheimer's disease pathology in human hippocampi (2018) (29)
TAR DNA-binding protein 43 pathology in a case clinically diagnosed with facial-onset sensory and motor neuronopathy syndrome: An autopsied case report and a review of the literature (2013) (29)
DELETION MAPPING OF CRITICAL REGION FOR HYPOSPADIAS, PENOSCROTAL TRANSPOSITION AND IMPERFORATE ANUS ON HUMAN CHROMOSOME 13. (2006) (29)
Expression of the α2-macroglobulin-encoding gene in rat brain and cultured astrocytes (1994) (29)
A simple VNTR-PCR method for detecting maternal cell contamination in prenatal diagnosis. (1998) (29)
Immunohistochemical analysis of spinal cord lesions in amyotrophic lateral sclerosis using microtubule-associated protein 2 (MAP2) antibodies (1999) (28)
Intradural, extramedullary spinal Ewing’s sarcoma in childhood (2003) (28)
A comprehensive analysis identifies BRAF hotspot mutations associated with gliomas with peculiar epithelial morphology (2017) (28)
Arterial spin labeling of hemangioblastoma: differentiation from metastatic brain tumors based on quantitative blood flow measurement (2012) (28)
Expression of the lysosome-associated membrane proteins in myopathies with rimmed vacuoles (2001) (27)
Early and extensive spinal white matter involvement in neuromyelitis optica (2017) (27)
Translocation of glutamate transporter subtype excitatory amino acid carrier 1 protein in kainic acid-induced rat epilepsy. (2003) (27)
Protease‐resistant PrP and PrP oligomers in the brain in human prion diseases after intraventricular pentosan polysulfate infusion (2012) (27)
Apolipoprotein Genotype for Prediction of Alzheimer's Disease in Older Japanese: The Hisayama Study (2011) (26)
Familial Creutzfeldt-Jakob disease with D178N-129M mutation ofPRNP presenting as cerebellar ataxia without insomnia (2000) (26)
An immunohistochemical study of tissue transglutaminase in gliomas with reference to their cell dying processes. (1994) (25)
An autopsied case of sporadic adult‐onset amyotrophic lateral sclerosis with FUS‐positive basophilic inclusions (2011) (25)
Neurodegeneration in the limbic and paralimbic system in progressive supranuclear palsy (1995) (25)
Anti-Ri-associated paraneoplastic cerebellar degeneration without opsoclonus in a patient with a neuroendocrine carcinoma of the stomach. (2000) (25)
CD9 Expression in Solid Non-neuroepithelial Tumors and Infiltrative Astrocytic Tumors (2002) (24)
Clinical Significance of PD-L1 Expression in Brain Metastases from Non-small Cell Lung Cancer. (2018) (24)
Focal cortical dysplasia type IIa underlying epileptogenesis in patients with epilepsy associated with Sturge‐Weber syndrome (2012) (24)
Accumulation of Neurofilaments in a Sporadic Case of Amyotrophic Lateral Sclerosis (1986) (24)
Elevated expression of fatty acid synthase and nuclear localization of carnitine palmitoyltransferase 1C are common among human gliomas (2014) (24)
A unique case of a cutaneous lesion resembling mammary analog secretory carcinoma: a case report and review of the literature. (2015) (24)
Correlation between arterial spin-labeling perfusion and histopathological vascular density of pediatric intracranial tumors (2017) (24)
A comparative study of localization of heat shock protein 27 and heat shock protein 72 in the developmental and degenerative intervertebral discs. (2002) (24)
A comparative immunohistochemistry of O6‐methylguanine–DNA methyltransferase and p53 in diffusely infiltrating astrocytomas (2003) (24)
Defense mechanism to oxidative DNA damage in glial cells (2004) (24)
Autopsy case of autosomal recessive hereditary spastic paraplegia with reference to the muscular pathology (2001) (24)
Prostaglandin D Synthase (β-Trace) in Meningeal Hemangiopericytoma (2001) (23)
Genomic organization of the human gene (CA5) and pseudogene for mitochondrial carbonic anhydrase V and their localization to chromosomes 16q and 16p. (1995) (23)
Development of oligomeric prion‐protein aggregates in a mouse model of prion disease (2009) (23)
Measurement of the perfusion fraction in brain tumors with intravoxel incoherent motion MR imaging: validation with histopathological vascular density in meningiomas. (2018) (23)
A comparative study of embedded nerve tissue in six NF2-associated schwannomas and 17 nonassociated NF2 schwannomas. (1997) (22)
Down‐regulation of MET in hippocampal neurons of Alzheimer's disease brains (2014) (22)
Increased cerebrospinal fluid levels of substance P in patients with amyotrophic lateral sclerosis (1999) (22)
Abnormal cytoarchitecture of cortical dysplasia verified by immunohistochemistry. (1998) (22)
Immunohistochemical study of ependymal neoplasms: histological subtypes and glial and epithelial characteristics (2005) (21)
HIGHLY SELECTIVE LEPTOMENINGEAL AMYLOIDOSIS WITH TRANSTHYRETIN VARIANT ALA25THR (2009) (21)
Immunohistochemistry of Chondromodulin-I in the Human Intervertebral Discs with Special Reference to the Degenerative Changes (2000) (21)
Enhanced CD9 Expression in the Mouse and Human Brains Infected with Transmissible Spongiform Encephalopathies (2000) (21)
Possible Roles of Transglutaminases in Alzheimer’s Disease (1998) (21)
Ganglioglioma in the third ventricle: report on two cases (2007) (21)
Anti-dorsal root ganglion neuron antibody in a case of dorsal root ganglionitis associated with Sjögren's syndrome (1995) (20)
Extensive distribution of glial cytoplasmic inclusions in an autopsied case of multiple system atrophy with a prolonged 18‐year clinical course (2012) (20)
Familial complex chromosome rearrangement giving rise to balanced and unbalanced recombination products. (1998) (20)
Evaluation of sensitivity and specificity of doublecortin immunostatining for the detection of infiltrating glioma cells (2008) (19)
Rapid diagnosis of Miller-Dieker syndrome and isolated lissencephaly sequence by the polymerase chain reaction (1990) (19)
A comparative study of abnormal prion protein isoforms between Gerstmann-Sträussler-Scheinker syndrome and Creutzfeldt-Jakob disease (1998) (19)
Quantitative digital assessment of MGMT immunohistochemical expression in glioblastoma tissue (2011) (19)
Trends in autopsy‐verified dementia prevalence over 29 years of the Hisayama study (2016) (19)
Multiplexed Analysis of Post‐PCR Fluorescence‐labeled Microsatellite Alleles and Statistical Evaluation of Their Imbalance in Brain Tumors (2002) (19)
Molecular diagnosis of diffuse glioma using a chip-based digital PCR system to analyze IDH, TERT, and H3 mutations in the cerebrospinal fluid (2021) (19)
Widespread distribution of tau in the astrocytic elements of glial tumors (1993) (19)
Adrenoleukodystrophy gene encodes an 80 kDa membrane protein. (1994) (19)
Narrowing down the common deleted region of 5q to 6.0 Mb in blastic plasmacytoid dendritic cell neoplasms. (2013) (19)
Purely cystic form of choroid plexus papilloma with acute hydrocephalus in an infant. Case report. (2006) (19)
Proliferative activity of meningiomas as evaluated by bromodeoxyuridine uptake examination (1986) (18)
Novel TLE4‐NTRK2 fusion in a ganglioglioma identified by array‐CGH and confirmed by NGS: Potential for a gene targeted therapy (2018) (18)
αB-crystallin in oxidative muscle fibers and its accumulation in ragged-red fibers: a comparative immunohistochemical and histochemical study in human skeletal muscle (1993) (18)
Preferential neurodegeneration in the cervical spinal cord of progressive supranuclear palsy (1999) (18)
Reclassification of 400 consecutive glioma cases based on the revised 2016WHO classification (2018) (18)
Donor-derived adult T-cell leukaemia (2011) (18)
Is t(6;14) a non-random translocation in childhood acute mixed lineage leukemia? (1996) (18)
Predicting TERT promoter mutation using MR images in patients with wild-type IDH1 glioblastoma. (2019) (18)
Two autopsy cases with Pelizaeus-Merzbacher disease phenotype of adult onset, without mutation of proteolipid protein gene (2000) (17)
Preferential involvement of the short arm in chromosome 8-derived supernumerary markers and ring as identified by chromosome arm painting. (2000) (17)
[An autopsy case of amyotrophic lateral sclerosis with ampulla cardiomyopathy]. (2008) (17)
Clusterin expression in follicular dendritic cells associated with prion protein accumulation (2006) (17)
Malignant transformation of a desmoplastic infantile ganglioglioma in an infant carrier of a nonsynonymous TP53 mutation. (2014) (17)
Enhanced expression of DNA topoisomerase II genes in human medulloblastoma and its possible association with etoposide sensitivity (2007) (17)
[Extracranial metastasis of glioblastoma to the lung and heart with a histological resemblance to small cell carcinoma of the lung: an autopsy case]. (2001) (16)
An exon 8-spliced out transcript of neurofibromatosis 2 gene is constitutively expressed in various human tissues. (1994) (16)
High‐resolution melting and immunohistochemical analysis efficiently detects mutually exclusive genetic alterations of adamantinomatous and papillary craniopharyngiomas (2018) (16)
EWS/FLI-1 fusion signal inserted into chromosome 11 in one patient with morphologic features of Ewing sarcoma, but lacking t(11;22). (2002) (16)
A lateral ventricular gliosarcoma arising in an ependymoma. (2001) (16)
Proliferating potential of folliculo-stellate cells in human pituitary adenomas (2004) (15)
DCTN1 F52L mutation case of Perry syndrome with progressive supranuclear palsy-like tauopathy. (2018) (15)
Myeloradiculitis caused by Cryptococcus neoformans infection in a patient with ulcerative colitis: A neuropathological study (2006) (15)
Prion protein oligomers in Creutzfeldt‐Jakob disease detected by gel‐filtration centrifuge columns (2009) (15)
Effects of l-NMMA and l-NNA on the Selective ATP-Induced Enhancement of Intratumoral Blood Flow (1992) (15)
Detection of SV40 T antigen genome in human gliomas (2006) (15)
Trisomy 15 is frequently observed as a minor clone in patients with Anemia/MDS/NHL and as a major clone in patients with AML. (2000) (15)
Dorsal root rupture injury induces extension of astrocytic processes into the peripheral nervous system and expression of GDNF in astrocytes (2002) (15)
Dynamic analysis of glioma cells: Looking into “movement phenotypes” (2005) (15)
Oculo‐auriculo‐vertebral spectrum, cat eye, and distal 22q11 microdeletion syndromes: A unique double rearrangement (2013) (15)
Prostaglandin D synthase (beta-trace) in meningeal hemangiopericytoma. (2001) (14)
MUTYH Actively Contributes to Microglial Activation and Impaired Neurogenesis in the Pathogenesis of Alzheimer's Disease (2021) (14)
An astroblastoma case associated with loss of heterozygosity on chromosome 9p (2006) (14)
Lymphoblastic Leukemia With Mature B-Cell Phenotype in Infancy. (2004) (14)
Diagnostic accuracy for the epileptogenic zone detection in focal epilepsy could be higher in FDG-PET/MRI than in FDG-PET/CT (2020) (14)
An autopsy case of adult-onset hereditary spastic paraplegia type 2 with a novel mutation in exon 7 of the proteolipid protein 1 gene (2011) (14)
Deletion of MYC and presence of double minutes with MYC amplification in a morphologic acute promyelocytic leukemia-like case lacking RARA rearrangement: could early exclusion of double-minute chromosomes be a prognostic factor? (2006) (14)
Case of lipoblastoma with two derivative chromosomes 8 containing homogeneously staining-like regions and a review of the literature: lipoblastoma and chromosome 8. (2001) (14)
A case of intracranial solitary fibrous tumor/hemangiopericytoma with dedifferentiated component (2015) (14)
Ubiquitin-immunoreactive skein-like inclusions in the neostriatum are not restricted to amyotrophic lateral sclerosis, but are rather aging-related structures (2000) (14)
Intravoxel Incoherent Motion MR Imaging of Pediatric Intracranial Tumors: Correlation with Histology and Diagnostic Utility (2019) (13)
Hypertrophic Pachymeningitis as a Result of a Retropharyngeal Inflammatory Pseudotumor: Case Report (2002) (13)
Fatal familial insomnia with an unusual prion protein deposition pattern: an autopsy report with an experimental transmission study (2005) (13)
Ectopic pituitary adenoma in the cavernous sinus causing oculomotor nerve paresis--case report. (2003) (13)
Narrowing of the regions of allelic losses of chromosome 1p36 in meningioma tissues by an improved SSCP analysis (2007) (13)
Increased asymmetric pulvinar magnetic resonance imaging signals in Creutzfeldt–Jakob disease with florid plaques following a cadaveric dura mater graft (2006) (13)
Non-isotopic in situ hybridization of CD44 transcript in formalin-fixed paraffin-embedded sections. (1999) (13)
Clinical significance of CDKN2A homozygous deletion in combination with methylated MGMT status for IDH‐wildtype glioblastoma (2021) (13)
Tauopathy in basal ganglia involvement is exacerbated in a subset of patients with Alzheimer's disease: The Hisayama study (2019) (13)
Cytoplasmic inclusions of astrocytic elements of glial tumors: special reference to round granulated body and eosinophilic hyaline droplets (2004) (13)
Argyrophilic grains in late‐onset Creutzfeldt–Jakob diseased brain (1999) (13)
Sporadic Creutzfeldt–Jakob Disease MM1+2C and MM1 are Identical in Transmission Properties (2016) (13)
Pituitary tumours in adolescence: clinical behaviour and neuroimaging features of seven cases (2001) (13)
Autosomal dominant tauopathy with parkinsonism and central hypoventilation (2012) (12)
Expression of alpha B-crystallin in the developing rat kidney. (1991) (12)
Dynactin is involved in Lewy body pathology (2018) (12)
Radiological Features of Brain Metastases from Non-small Cell Lung Cancer Harboring EGFR Mutation (2018) (12)
MOG antibody disease manifesting as progressive cognitive deterioration and behavioral changes with primary central nervous system vasculitis. (2019) (12)
Acute promyelocytic leukemia and HIV‐1 infection: Case report and review of the literature (2004) (12)
Dorsal horn lesion resulting from spinal root avulsion leads to the accumulation of stress-responsive proteins (2001) (12)
IgH Intronic Enhancer Element HE2 (μB) Functions as a cis‐Activator in Choroid Plexus Cells at the Cellular Level as well as in Transgenic Mice (1995) (12)
Insular primary glioblastomas with IDH mutations: Clinical and biological specificities (2017) (12)
Traumatic neuroma of the anterior cervical nerve root with no subjective episode of trauma. Report of four cases. (2002) (11)
Establishment and Characterization of Choroid Plexus Carcinoma Cell Lines: Connection between Choroid Plexus and Immune Systems (1996) (11)
Patient survival and microsatellite instability in gliomas by high-resolution fluorescent analysis. (1999) (11)
Alpha B-crystallin in oxidative muscle fibers and its accumulation in ragged-red fibers: a comparative immunohistochemical and histochemical study in human skeletal muscle. (1993) (11)
Immunohistochemical analysis in a case of idiopathic Lennox-Gastaut syndrome. (1999) (11)
Expression of the alpha 2-macroglobulin-encoding gene in rat brain and cultured astrocytes. (1994) (11)
Radiation-induced meningiomas and their proliferative activity. Cytokinetic study using bromodeoxyuridine. (1990) (11)
[Astrocytopathy in neuromyelitis optica, multiple sclerosis and Baló's disease]. (2011) (11)
Arterial spin-labeling is useful for the diagnosis of residual or recurrent meningiomas (2018) (10)
Deferred radiotherapy and upfront procarbazine–ACNU–vincristine administration for 1p19q codeleted oligodendroglial tumors are associated with favorable outcome without compromising patient performance, regardless of WHO grade (2016) (10)
Pediatric ganglioglioma with an H3 K27M mutation arising from the cervical spinal cord (2018) (10)
Jumping translocations of 3q in acute promyelocytic leukemia. (1999) (10)
Radiation-induced spinal cord glioblastoma with cerebrospinal fluid dissemination subsequent to treatment of lymphoblastic lymphoma (2013) (10)
Limbic encephalitis associated with recurrent thymoma: A postmortem study (2001) (10)
Neuron-specific γ-enolase derived from human glioma (1986) (10)
Differential expression of CD44 variants among meningioma subtypes (1996) (10)
Recent Increases in Hippocampal Tau Pathology in the Aging Japanese Population: The Hisayama Study. (2016) (10)
Trisomy 15 in a case of pediatric hemangiopericytoma and review of the literature. (2002) (10)
Modified Array-based Comparative Genomic Hybridization Detects Cryptic and Variant PML-RARA Rearrangements in Acute Promyelocytic Leukemia Lacking Classic Translocations (2013) (10)
Cell kinetics of the malignant evolution of meningothelial meningioma (2004) (10)
C-Terminal-Deleted Prion Protein Fragment Is a Major Accumulated Component of Systemic PrP Deposits in Hereditary Prion Disease With a 2-Bp (CT) Deletion in PRNP Codon 178 (2016) (10)
Leser-Trélat sign with anaplastic ependymoma – an autopsy case (1996) (10)
Active clearance of human amyloid β 1–42 peptide aggregates from the rat ventricular system (2004) (10)
Synchronous quadruple primary neoplasms: glioblastoma, neuroendocrine tumor, schwannoma and sessile serrated adenoma in a patient with history of prostate cancer. (2015) (9)
Magnetic resonance appearance of multiple intracranial epidermoid cysts: intrathecal seeding of the cysts? Case report. (2000) (9)
Forced retraction of spinal root injury enhances activation of p38 MAPK cascade in infiltrating macrophages (2005) (9)
Deletion of 3'-CBFB gene in association with an inversion (16)(p13q22) and a loss of the Y chromosome in a 2-year-Old child with acute myelogenous leukemia-M4. (2000) (9)
Expanded polyglutamine impairs normal nuclear distribution of fused in sarcoma and poly (rC)‐binding protein 1 in Huntington's disease (2019) (9)
Second reported patient with del(1)(p32.1p32.3) and similar clinical features suggesting a recognizable chromosomal syndrome (2003) (9)
Distinct microglial and macrophage distribution patterns in the concentric and lamellar lesions in Baló's disease and neuromyelitis optica spectrum disorders (2020) (9)
Dura mater graft‐associated Creutzfeldt‐Jakob disease with 30‐year incubation period (2017) (9)
Distal Sox binding elements of the alphaB-crystallin gene show lens enhancer activity in transgenic mouse embryos. (2004) (8)
Multiple palisading granulomas in the scalp of an infant: a case report. (2001) (8)
[A case of subacute necrotizing lymphadenitis complicated with brachial plexus neuritis]. (1998) (8)
Subacute autonomic and sensory ganglionopathy: a postmortem case (1998) (8)
Meiotic chromosome pairing in the human male: experience from surface spread synaptonemal complexes (1987) (8)
A simple and high‐yield method for preparation of rat microglial cultures utilizing Aclar plastic film (2011) (8)
Small heat-shock protein is expressed in meningiomas and in granulofilamentous inclusion bodies (2004) (8)
‘PrP systemic deposition disease’: clinical and pathological characteristics of novel familial prion disease with 2‐bp deletion in codon 178 (2016) (8)
Simultaneous presence of t(2;8)(p12;q24) and t(14;18)(q32;q21) in a B-cell lymphoproliferative disorder with features suggestive of an aggressive variant of splenic marginal-zone lymphoma. (2000) (8)
Distinct pattern of PCR-SSCP analysis of p53 mutations in human astrocytomas. (1999) (8)
Proliferative activity and apoptosis of Langerhans histiocytes in eosinophilic granulomas as evaluated by MIB-1 and TUNEL methods (1995) (8)
[A case of Gerstmann-Sträussler-Scheinker syndrome (GSS) with late onset--a haplotype analysis of Glu219Lys polymorphism in PrP gene]. (2001) (8)
Biphenotypic hematological malignancy with T-lymphoid and myeloid differentiation: association with t(3;12)(p25;q24.3). Case report and review of the literature. (1999) (8)
Prolidase Deficiency in a Mexican-American Patient Identified by Array CGH Reveals a Novel and the Largest PEPD Gene Deletion (2016) (8)
Differentiation of high-grade from low-grade diffuse gliomas using diffusion-weighted imaging: a comparative study of mono-, bi-, and stretched-exponential diffusion models (2020) (8)
Microsphere formation in a subtype of Creutzfeldt–Jakob disease with a V180I mutation and codon 129 MM polymorphism (2013) (7)
Intraorbital lobular capillary hemangioma (pyogenic granuloma) (2008) (7)
Co-existence of alternative forms of 8q gain in cytogenetic clones of three patients with acute myeloid leukemia, pointing to 8q22∼8qter as a region of biologic significance (2001) (7)
Pediatric glioblastoma with oligodendroglioma component: Aggressive clinical phenotype with distinct molecular characteristics (2013) (7)
[An autopsy case of rhino-orbito-cerebral mucormycosis associated with multiple cranial nerve palsy and subsequent subarachnoid hemorrhage]. (1998) (7)
Spinal endodermal cyst resembling an arachnoid cyst in appearance: Pitfalls in intraoperative diagnosis of cystic lesions (2012) (7)
Sporadic hereditary diffuse leukoencephalopathy with axonal spheroids showing numerous lesions with restricted diffusivity caused by a novel splice site mutation in the CSF1R gene (2013) (7)
Radiation-induced meningiomas and their proliferative activity (1990) (7)
Accumulation of MDM2 in pleomorphic xanthoastrocytomas (2004) (7)
Transactivation response DNA‐binding protein of 43 kDa proteinopathy and lysosomal abnormalities in spastic paraplegia type 11 (2021) (6)
Accumulation of prion protein in muscle fibers of experimental chloroquine myopathy: in vivo model for deposition of prion protein in non-neuronal tissues (2004) (6)
Lectin histochemistry of human fetal notochord, ecchordosis physaliphora, and chordomas. (1992) (6)
SUBCELLULAR LOCALIZATION OF α-CRYSTALLIN B CHAIN IN CNS GLIA: 251 (1990) (6)
Neuropathological features of a case with schizophrenia and prion protein gene P102L mutation before onset of Gerstmann-Sträussler-Scheinker disease (2003) (6)
Different responses of benign and atypical meningiomas to gamma-knife radiosurgery: report of two cases with immunohistochemical analysis (2006) (6)
Expression of CRYM in different rat organs during development and its decreased expression in degenerating pyramidal tracts in amyotrophic lateral sclerosis (2018) (6)
Three Novel Aberrations Involving PLAG1 Leading to Lipoblastoma in Three Different Patients: High Amplification, Partial Deletion, and a Unique Complex Rearrangement (2019) (6)
[A patient with vitamin E deficient, myopathy presenting with amyotrophy]. (2001) (6)
Loss of heterozygosity analysis in an anaplastic oligodendroglioma arising after radiation therapy (2007) (6)
ABL1 gene involvement within a complex three-way translocation (2;9;4) in perineurioma characterized by molecular cytogenetic methods. (2014) (6)
[Temporal lobe epilepsy associated with old intracerebral hemorrhage due to capillary telangiectasis in the temporal lobe: case report]. (1999) (6)
Toxic myopathy with multiple deletions in mitochondrial DNA associated with long‐term use of oral anti‐viral drugs for hepatitis B: A case study (2019) (6)
Upregulation of Annexin A1 in Reactive Astrocytes and Its Subtle Induction in Microglia at the Boundaries of Human Brain Infarcts. (2019) (6)
Increased expression of manganese superoxide dismutase is associated with that of nitrotyrosine in myopathies with rimmed vacuoles (2014) (6)
Combined immunodeficiency in a 3‐year‐old boy with 16p11.2 and 20p12.2‐11.2 chromosomal duplications (2014) (5)
Case report of a 3-year-old girl with pleuropulmonary blastoma and family history of a tumor predisposition syndrome with c. 2830 gene mutation in DICER1 (2015) (5)
Co-existence of alternative forms of 8q gain in cytogenetic clones of three patients with acute myeloid leukemia, pointing to 8q22 approximately 8qter as a region of biologic significance. (2001) (5)
Rescue of the HNF4 --> HNF1alpha pathway in hepatoma variant cells containing human chromosome 12. (1998) (5)
Spontaneous resolution of myelodysplastic cytogenetic abnormality developed during the treatment of leukemia. (1998) (5)
PCBP2 Is Downregulated in Degenerating Neurons and Rarely Observed in TDP-43-Positive Inclusions in Sporadic Amyotrophic Lateral Sclerosis. (2020) (5)
Relevance of calcification and contrast enhancement pattern for molecular diagnosis and survival prediction of gliomas based on the 2016 World Health Organization Classification (2019) (5)
Ossification of the posterior atlantoaxial membrane. Case report. (2003) (5)
A Novel Combination of Prion Strain Co-Occurrence in Patients with Sporadic Creutzfeldt-Jakob Disease. (2019) (5)
Character changes from idiopathic cranial pachymeningoencephalitis (2006) (5)
Recurrent Trigeminal Neuralgia due to Granulomatous Change in a Prosthesis for Microvascular Decompression: A Case Report (1997) (5)
Concurrent cardiac transthyretin and brain β amyloid accumulation among the older adults: The Hisayama study (2021) (5)
Brain injury does not modify transmissible spongiform encephalopathy caused by intraperitoneal inoculation with Fukuoka-1 strain. (1999) (5)
[A case of progressive multifocal leukoencephalopathy with methionine uptake demonstrated by PET]. (1996) (5)
EXPRESSION OF THE B-CHAIN OF α-CRYSTALLIN IN CNS GLIA: 250 (1990) (5)
Papillary Thyroid Cancer in Struma Testis with Malignant Transformation in the Lung Associated with Trisomy 17 Successfully Treated with Total Thyroidectomy and Radioiodine Ablation (2014) (4)
[Exacerbation of radiation induced meningioma due to hemorrhage after cerebral angiography: a case report]. (2011) (4)
Four‐repeat tau dominant pathology in a congenital myotonic dystrophy type 1 patient with mental retardation (2018) (4)
[An autopsy case of malignant schwannoma in the brachial plexus extending into the spinal canal]. (1986) (4)
Accumulation of Astrocytic Aquaporin 4 and Aquaporin 1 in Prion Protein Plaques. (2020) (4)
A 6‐YEAR‐OLD GIRL WITH AN EXTRA‐AXIAL MASS IN THE MIDDLE CRANIAL FOSSA (2010) (4)
Immunophenotype Expression Change From CD52+ to CD52- on Erythrodermic Peripheral T-cell Lymphoma, Not Otherwise Specified After Treatment With Alemtuzumab. (2017) (4)
Brain-Derived Neurotrophic Factor (BDNF) Induces Sustained Elevation of Intracellular Ca in Rodent Microglia (2009) (4)
Deceptively benign low-grade fibromyxoid sarcoma: array-comparative genomic hybridization decodes the diagnosis. (2013) (4)
Symmetrical glial hyperplasia in the brainstem of fibrodysplasia ossificans progressiva (2021) (4)
A comparative immunohistochemical study of tissue transglutaminase and factor XIIIa in hemangioblastoma (1998) (4)
Comprehensive lectin histochemistry of normal and neoplastic human choroid plexus cells: alternation of lectin-binding patterns through neoplastic transformation (2004) (4)
Coexistence of neocentromeric marker 3q and trisomy 3 in two different tissues in a 3-year-old boy with peripheral T-cell lymphoma: support for a gene dosage effect hypothesis. (2006) (4)
Degenerative and protective reactions of the rat trigeminal motor nucleus after removal of the masseter and temporal muscles. (2009) (4)
A clinically aggressive, polymorphic, polyclonal posttransplantation lymphoproliferative disorder. (1998) (4)
Mosaic isodicentric chromosome 9 with triplication (9p22-pter) and no deletion in an abnormal infant presenting with clinical features of trisomy 9; a new type of isodicentric chromosome formation (1994) (4)
Vascular permeability and cell kinetics of ethylnitrosourea (ENU)-induced rat brain tumours (2005) (4)
Unusual aberration involving the short arm of chromosome 11 in an 8-month-old patient with a supratentorial primitive neuroectodermal tumor. (2003) (4)
Abnormal prion protein deposits with high seeding activities in the skeletal muscle, femoral nerve, and scalp of an autopsied case of sporadic Creutzfeldt–Jakob disease (2021) (4)
Anaplastic large cell ki-1 lymphoma in the central nervous system: Report of an autopsy case (2004) (4)
Opposite Effects of Cyclic AMP and Cell Density on Expression of αB-Crystallin and Glial Fibrillary Acidic Protein in C-6 Glioma Cells (1991) (4)
Alectinib‐responsive infantile anaplastic ganglioglioma with a novel VCL–ALK gene fusion (2021) (3)
Apoptotic bodies in the cerebellum of Japanese patients with Creutzfeldt–Jakob disease (2001) (3)
Focal cortical dysplasia coexisting with diffuse astrocytoma in childhood: A case report and reappraisal of the glial component in archival FCD cases (2011) (3)
CD206 Expression in Induced Microglia-Like Cells From Peripheral Blood as a Surrogate Biomarker for the Specific Immune Microenvironment of Neurosurgical Diseases Including Glioma (2021) (3)
Toxic myocardial damage due to intravenous phenytoin administration (1995) (3)
Frequent Detection of Pituitary-Derived PrPres in Human Prion Diseases. (2019) (3)
Evaluation of sensitivity and specifi city of doublecortin immunostaining for the detection of infi ltrating glioma cells (2008) (3)
Persistent roles of signal transduction of platelet-derived growth factor B in genesis, growth, and anaplastic transformation of gliomas in an in-vivo serial transplantation model (2011) (3)
Cerebral B-cell lymphoma following treatment for Tolosa-Hunt syndrome. (1999) (3)
Pleomorphic xanthoastrocytoma with predominantly exophytic growth: case report. (2001) (3)
Accumulation of class I mutant p53 and apoptosis induced by carboplatin in a human glioma cell line (2006) (3)
Multiphasic acute disseminated encephalomyelitis associated with atypical rubella virus infection (2015) (3)
Different Complicated Brain Pathologies in Monozygotic Twins With Gerstmann–Sträussler–Scheinker Disease (2017) (3)
Clinical implications of molecular analysis in diffuse glioma stratification (2021) (3)
First-dose idarubicin cardiomyopathy: a case of new heart failure after induction chemotherapy for acute myeloid leukaemia (2019) (3)
Detection of Human T Lymphotrophic Virus Type I ( HTLV-I ) Proviral DNA and Analysis of T Cell Receptor V / 3 CDR 3 Sequences in Spinal Cord Lesions of HTLV-I-associated Myelopathy / Tropical Spastic (3)
An intragenic deletion of the gene MNAT1 in a family with pectus deformities (2014) (3)
A juvenile case of epilepsy‐associated, isocitrate dehydrogenase wild‐type/histone 3 wild‐type diffuse glioma with a rare BRAF A598T mutation (2020) (3)
A case of ganglioglioma grade 3 with H3 K27M mutation arising in the medial temporal lobe in an elderly patient (2022) (3)
Aluminum chloride does not facilitate deposition of human synthetic amyloid β1–42 peptide in the rat ventricular system of a short‐term infusion model (2005) (3)
Large hypothalamic hamartoma with calcification and cystic components in an adult--case report. (2010) (3)
Cryptic deletion of EGR1 in association with a novel balanced t(5;22)(q31;q11.2) in a patient with myelodysplastic syndrome. (2009) (3)
Autopsy Case of Later-Onset Pontocerebellar Hypoplasia Type 1: Pontine Atrophy and Pyramidal Tract Involvement (2010) (3)
Spindle cell/sclerosing rhabdomyosarcoma with intracranial invasion without destroying the bone of the skull base: a case report and literature review (2017) (3)
Instability of Isochromosome 4p in a Child with Pure Trisomy 4p Syndrome Features and Entire 4q-Arm Translocation (2015) (3)
Author Correction: Comparative profiling of cortical gene expression in Alzheimer’s disease patients and mouse models demonstrates a link between amyloidosis and neuroinflammation (2017) (3)
Primary pineal yolk sac tumor: ultrastructural and immunohistochemical features--case report. (1986) (3)
[Increased intracranial pressure caused by obstruction of torcular herophili with hemangiopericytoma: a case report]. (2001) (3)
Mitochondrial dysfunction and altered ribostasis in hippocampal neurons with cytoplasmic inclusions of multiple system atrophy (2018) (3)
Intracytoplasmic inclusion of Hirano type in Purkinje cells. (1986) (3)
An elderly case of malignant small cell glioma with hemorrhage coexistent with a calcified pilocytic astrocytoma component in the cerebellar hemisphere (2018) (2)
Lymphoblastic leukemia with mature B-cell phenotype in infancy. (2004) (2)
Atlas of Cytogenomics in Oncology and Hematology: a Platform-Neutral Clinical Cancer Genomics Database (2012) (2)
[Solitary neurofibroma presenting as a tender soft-to-firm tumor at the temporal head region masquerading as temporal arteritis]. (2009) (2)
Convexity meningioma with galactorrhea and hyperprolactinemia. A case report. (1989) (2)
Subcutaneous melanocytoma mimicking a lipoma: a rare presentation of a rare neoplasm with histological, immunohistochemical, cytogenetic and molecular characterization (2016) (2)
Immunotherapy‐refractory vacuolar myopathy with mucin deposition in scleromyxedema: A possible role of fibroblast growth factor 2 (2020) (2)
Differences between primary central nervous system lymphoma and glioblastoma: topographic analysis using voxel-based morphometry. (2019) (2)
[An autopsy case of dementia with motor neuron disease accompanying Alzheimer's disease lesion]. (2001) (2)
Narrowing down the Common Cytogenetic Deletion 14q to a 5.6-Mb Critical Region in 1p/19q Codeletion Oligodendroglioma-Relapsed Patients Points to Two Potential Relapse-Related Genes: SEL1L and STON2 (2020) (2)
CBIO-01COEXPRESSION OF FATTY ACID SYNTHASE (FASN) AND CARNITINE PALMITOYLTRANSFERASE 1C (CPT1C) IN HUMAN GLIOMAS (2015) (1)
A Rare Recurrent 4q25 Proximal Deletion Not Involving the PITX2 Gene: A Genomic Disorder Distinct from Axenfeld-Rieger Syndrome (2016) (1)
Differential activation of proapoptotic molecules between mouse and rat models of distal motor trigeminal denervation. (2012) (1)
Predictors of recurrence and postoperative outcomes in patients with non-skull base meningiomas based on modern neurosurgical standards (2019) (1)
[An autopsy case with lower motor neuron disease showing a transient-appearance of anti-GM1 antibody and an improvement of conduction block after gamma-globulin administration]. (1999) (1)
αB-CRYSTALLIN IS A MAJOR COMPONENT OF ROSENTHAL FIBERS: 228 (1989) (1)
Prion Gene PRNP Y162X Truncation Mutation Can Induce a Refractory Esophageal Achalasia. (2020) (1)
Balanced chromosomal rearrangements offer insights into coding and noncoding genomic features associated with developmental disorders (2022) (1)
The 92nd Neuropathological Meeting of Kyushu District 22 July 2006 (2006) (1)
Alzheimer病の病理学と耐糖能異常との関連性(Association of Alzheimer disease pathology with impaired glucose tolerance) (2008) (1)
Mystery solved: The evolution of diagnostic abilities in genetic testing. (2011) (1)
Roberts-SC phocomelia syndrome in a baboon (Papio anubis). (1992) (1)
Familial translocation t(10;14) (q26.1;q32.3): report of three offspring with 10q deletion and 14q duplication (1994) (1)
Lymphoplasmacytic lymphoma/Waldenström macroglobulinemia with inv(16)(p13q22) as a sole genetic abnormality. (2007) (1)
The Combined Use of Composite Ceramic Granules and Fibrin Glue for Cranioplasties : Results of a Rat Model Study and Clinical Findings with Regard to Biocompatibility (1995) (1)
Quantitative relaxometry using synthetic MRI could be better than T2-FLAIR mismatch sign for differentiation of IDH-mutant gliomas: a pilot study (2022) (1)
A fibrotic nodule arising from the cerebellopontine angle (2013) (1)
Cerebral Tuberculoma with Mild Posterior Cervical Pain as the Main Symptom Despite Extensive Brain Lesions (2022) (1)
TISSUE DISTRIBUTION OF αB-CRYSTALLIN IN RAT ORGANS: 188 (1989) (1)
Neuropathology of classic myotonic dystrophy type 1 is characterized by both early initiation of primary age-related tauopathy of the hippocampus and unique 3-repeat tauopathy of the brainstem. (2022) (1)
Intraventricular mucin‐producing glioblastoma arising in the septum pellucidum at the frontal horn of the lateral ventricle: A case report (2021) (1)
Neuron-specific gamma-enolase derived from human glioma. (1986) (1)
Masked hypodiploidy in anaplastic meningiomas by duplication of the original clone found in atypical meningiomas: Illustration of the evolution of genetic alterations (2014) (1)
HGG-24. HIGH-GRADE GLIOMA WITH A NOVEL FUSION GENE OF VCL-ALK (2020) (1)
[An autopsied case of severe varicella zoster virus-associated encephalomyelitis under immunosuppressant therapy]. (2020) (1)
Author Correction: Comparative profiling of cortical gene expression in Alzheimer’s disease patients and mouse models demonstrates a link between amyloidosis and neuroinflammation (2021) (1)
Optic nerve atrophy and visual disturbance following PRNP Y162X truncation mutation (2021) (1)
A case of overlapping adult‐onset linear scleroderma and Parry‐Romberg syndrome presenting with widespread ipsilateral neurogenic involvement (2019) (1)
Histological background of dedifferentiated solitary fibrous tumour (2021) (1)
[An autopsy case of Alzheimer's disease presenting with corticobasal syndrome]. (2013) (1)
A Unique Case of Epstein-Barr Virus Related Hemophagocytic Lymphohistiocytosis with Very Complex Cytogenetics in an Adult Male (2016) (0)
3 Cases of Intraspinal Cysts Causing Bony Erosion. (2002) (0)
The 88th Neuropathological Meeting of Kyushu District 26 June 2004 (2004) (0)
Holt-Oram syndrome and diaphragmatic hernia associate with paracentric inversion of chromosome 8 (1994) (0)
Neonatal Pancytopenia Associated With De Novo 1q43-44 Deletion and 10p15 Duplication (2013) (0)
非定型的致死性家族性不眠症 PRNP D178N-129M突然変異を伴った家族性Creutzfelt-Jakob病の1剖検例(Atypical fatal familial insomnia: an autopsy case of familial Creutzfeldt-Jakob disease with PRNP D178N-129M mutation) (2001) (0)
The 78th Neuropathological Meeting of Kyushu District 11 April 1998 (1998) (0)
Contents Vol. 144, 2014 (2015) (0)
[Idiopathic Intracranial Hypotension]. (2017) (0)
Acute-phase electroencephalography for an infantile atypical teratoid/rhabdoid tumor (2021) (0)
The 89th Neuropathological Meeting of Kyushu District 18 December 2004 (2005) (0)
髄膜メラノサイトの反応性過形成を合併した非定型髄膜腫の1症例(A case of atypical meningioma associated with reactive hyperplasia of meningeal melanocytes) (2007) (0)
[Pathological study on abducent paralysis of the vocal cord in a patient having multiple system atrophy with nasogastric intubation]. (2007) (0)
Neuropathology of spinocerebellar ataxia type 8: Common features and unique tauopathy. (2023) (0)
Multiple mtDNA deletions due to mitochondrion toxicity of anti‐hepadnaviral drugs: Comments to the letter from J. Finsterer (2019) (0)
Aggresomal property of glial cytoplasmic inclusions (2009) (0)
Intronic variant in IQGAP3 associated with hereditary neuropathy with proximal lower dominancy, urinary disturbance, and paroxysmal dry cough (2020) (0)
Subject Index Vol. 23, 2007 (2007) (0)
61-year-old woman presenting with deep coma during treatment for adrenal insufficiency. (2002) (0)
Acute aortic dissection associated with wild‐type transthyretin amyloid (2021) (0)
Symposium : How to calibrate clinical diagnosis by feedback through neuropathology Trends in autopsy-veri fi ed dementia prevalence over 29 years of the Hisayama study (2016) (0)
Hypothalamic mass in a 28-year-old man with diabetes insipidus ataxia, nystagmus and dysarthria. (2001) (0)
Cell kinetics of intracerebrally implanted RG-C6 tumors in rats--effects of intracarotid hyperosmolar mannitol measured by 3H-thymidine autoradiography and bromodeoxyuridine uptake. (1988) (0)
The 99th Neuropathological Meeting of Kyushu District 4 December 2010 (2011) (0)
プリオン感染培養細胞株プリオン蛋白重合度の解析(Analysis of polymerization degree of prion protein in the prion-infected culture cell lines) (2009) (0)
プリオン蛋白質オリゴマーの簡単な検出法(The simplified detection method for the prion protein oligomers) (2008) (0)
伝達性海綿状脳症(TSE)の診断的及び治療的化合物としての(trans,trans),-1-bromo-2,5-bis-(3-hydroxycarbonyl-4-hydroxy) styrylbenzene(BSB)(BSB as a diagnostic and therapeutic chemical for TSEs) (2003) (0)
The 94th Neuropathological Meeting of Kyushu District 30 June 2007 (2007) (0)
New pretreatment method for immunohistochemistry for abnormal prion protein (2005) (0)
Ki67 index: An independent prognostic factor in meningiomas and supratentorial astrocytomas (1996) (0)
新規のTyr262Cysプロテオリピド蛋白遺伝子変異を伴う成人発症痙性対麻痺2型の1剖検例(An autopsy case of adult-onset spastic paraplegia type 2 with a novel Tyr262Cys proteolipid protein gene mutation) (2008) (0)
postmortem case Subacute autonomic and sensory ganglionopathy: a (2007) (0)
Corrigendum to “Clinical features and neuropathological findings of familial amyotrophic lateral sclerosis with a His46Arg mutation in Cu/Zn superoxide dismutase” [J. Neurol. Sci. 197 (2002) 73–78] (2002) (0)
Erratum to: Dorsal horn lesion resulting from spinal root avulsion leads to the accumulation of stress-responsive proteins [Brain Research 893 (2001) 84–94] (2001) (0)
Changes in the Relapse Pattern and Prognosis of Glioblastoma After Approval of First-Line Bevacizumab: A Single-Center Retrospective Study (2021) (0)
情動障害を伴うALSにおけるtauopathyおよびTDP-43 proteinopathyの免疫組織化学的評価(Immunohistochemical evaluation of tauopathy and TDP-43 proteinopathy in ALS with emotional disorders) (2010) (0)
ヒトのプリオン病におけるペントサン-ポリ硫酸脳室内注入治療後のプリオン蛋白重合度の解析(Analysis of the polymerization degree of prion protein after intraventricular pentosan-polysulfate infusion in human prion diseases) (2009) (0)
The 102nd Neuropathological Meeting of Kyushu District 3 November 2012 (2013) (0)
A Comparative Study of Site-Specific Distribution of Aging-Related Tau Astrogliopathy and Its Risk Factors Between Alzheimer Disease and Cognitive Healthy Brains: The Hisayama Study. (2021) (0)
多彩なプリオン蛋白質沈着パターンを呈したMM1+2孤発性Creutzfeldt-Jakob病の1例(An autopsy case of MM1+2 sporadic Creutzfeldt-Jakob disease with various prion-protein deposition patterns) (2009) (0)
Combined neuroendoscopic cyst wall fenestration and cyst-peritoneal shunt in an infant with glioependymal cyst (2022) (0)
The 97th Neuropathological Meeting of Kyushu District 6 December 2008 (2009) (0)
A Novel Variant Rearrangement of the Rare Aberration dic(17;20)(p11.2;q11.2) Characterized by Array-CGH as an Insertion in a Patient with Myelodysplastic Syndrome of Multilineage Dysplasia (MDS-MLD) (2020) (0)
The 100th Neuropathological Meeting of Kyushu District 9 July 2011 (2011) (0)
マウスのプリオン病モデルにおけるPrP凝集の経時的進展(Time-course development of PrP aggregates in a mouse model of prion disease) (2008) (0)
The 82nd Neuropathological Meeting of Kyushu District 16 December 2000 (2001) (0)
好塩基性ニューロン内封入体を有する孤発性成人発症筋萎縮性側索硬化症の1剖検例(An autopsy case of sporadic adult-onset amyotrophic lateral sclerosis with basophilic intraneuronal inclusion bodies) (2008) (0)
大脳皮質基底核変性症を臨床的に模倣したAlzheimer病の剖検例(An autopsy case of Alzheimer's disease clinically mimicking corticobasal degeneration) (2012) (0)
025 Possible implication of CD9 in the progression of subacute sclerosing panencephalitis (1999) (0)
伝染性海綿状脳症におけるシナプス関連タンパク質の経時的解析(Time-course analysis of synapse-related proteins in the transmissible spongiform encephalopathies) (2007) (0)
Corrigendum to “MUTYH Actively Contributes to Microglial Activation and Impaired Neurogenesis in the Pathogenesis of Alzheimer's Disease” (2023) (0)
[A case of congenital non-progressive cerebellar ataxia with pigmentary retinal degeneration, fiber type disproportion and hypercreatine kinasemia]. (1999) (0)
The 91st Neuropathological Meeting of Kyushu District 17 December 2005 (2006) (0)
metabolism : The Hisayama Study Association of Alzheimer disease pathology with abnormal lipid (2012) (0)
Contents Vol. 23, 2007 (2007) (0)
Detection of cutaneous prion protein deposits could help diagnose GPI‐anchorless prion disease with neuropathy (2021) (0)
Le hazard ou la nécessité? Comorbid pathologies of neurodegenerative diseases (2018) (0)
The 85th Neuropathological Meeting of Kyushu District 30 November 2002 (2003) (0)
Differential expression of CD 44 variants among meningioma subtypes S 0 (0)
Papillary craniopharyngioma coexisting with an intratumoral abscess in a pediatric patient: A case report and review of the literature (2021) (0)
The Hisayama Study Glucose tolerance status and risk of dementia in the community : September 20 , 2011 (2011) (0)
The 96th Neuropathological Meeting of Kyushu District 5 July 2008 (2008) (0)
Reply by Authors. (2018) (0)
Palisading Granulomas in the Scalp of an Infant: A Case Report (2001) (0)
Detection of prion protein oligomers by single molecule fluorescence imaging (2010) (0)
[CNS infection and prion diseases, no. 5 in series of articles: basic knowledge of neuropathology for neurosurgeons]. (2002) (0)
Critical Commentary to: Chordoid meningioma: A Case Report (2001) (0)
[Autopsy of a suspected venous circulatory disturbance localized in the medulla oblongata and upper cervical cord accompanied by an aneurysm]. (2008) (0)
The 95th Neuropathological Meeting of Kyushu District 15 December 2007 (2008) (0)
Developmental profiles of CRYM in rat newborn brains and its decreased expression in pyramidal tract degeneration of amyotrophic lateral sclerosis (2017) (0)
Hypothalamic mass in a 28‐year‐old man with diabetes insipidus ataxia, nystagmus and dysarthria (2001) (0)
Endonasal endoscopic surgery for temporal lobe epilepsy associated with sphenoidal encephalocele (2021) (0)
Reply by Authors. (2018) (0)
Quantitative Relaxometry using Synthetic MRI Could be Better than Qualitative T2-FLAIR Mismatch Sign: A Pilot Study (2021) (0)
Reply by Authors. (2016) (0)
Creutzfeldt-Jakob病症例に対する病理学的マッピングの標準化(Standardization of pathological mapping for the cases with Creutzfeldt-Jakob disease) (2005) (0)
Development Cellular Distribution of NDRG1 Protein in the Rat Kidney and Brain During Normal Postnatal (2013) (0)
PrP沈着の特異パターンを伴うV180I Creutzfeldt-Jakob病の剖検例(An autopsy case of V180I Creutzfeldt-Jakob disease with a peculiar pattern of PrP deposition) (2012) (0)
The 93rd Neuropathological Meeting of Kyushu District 2 December 2006 (2007) (0)
The 81st Neuropathological Meeting of Kyushu District 27 November 1999 (2000) (0)
Ruptured anterior communicating artery aneurysms associated with left common carotid artery occlusion due to Takayasu arteritis: an autopsy case report (2021) (0)
プリオン病の病理学的及び生化学的特徴の定量的評価(Quantitative evaluation of pathological and biochemical features in prion diseases) (2008) (0)
Gerstomann-Straussler-Scheinker病発症前に精神分裂病とプリオン蛋白遺伝子P102L変異を伴った症例の神経病理学的特徴(Neuropathologic features of a case with schizophrenia and prion protein gene P102L mutation before onset of Gerstmann-Straussler-Scheinker disease) (2003) (0)
プリオン感染細胞株におけるPrP重合に対する治療薬の影響(Effect of therapeutic drugs on PrP polymerization in the prion-infected cell line) (2010) (0)
Rosenthal fibers and glial filaments associated with hemidesmosome‐like structures in perivascular astrocytes in a juvenile form of Alexander's disease (1997) (0)
The 86th Neuropathological Meeting of Kyushu District 7 June 2003 (2003) (0)
Report on an 11-year analysis of neurology autopsy cases: Focusing on neurodegenerative diseases (2017) (0)
A case of leptomeningeal amyloidosis associated with TTR Ala25Thr without somatic or autonomic peripheral neuropathy (2007) (0)
Sixty‐one‐year‐old woman presenting with deep coma during treatment for adrenal insufficiency (2002) (0)
NGS mapped breakpoints in balanced chromosomal rearrangements including the first large cohort of healthy carriers (2017) (0)
Resources of genetic education for non-geneticists. (2004) (0)
The 84th Neuropathological Meeting of Kyushu District 1 June 2002 (2002) (0)
A novel aberration of COL1A1‐PDGFB fusion as an insertion in chromosome 15 in one case of dermatofibrosarcoma protuberans involving a rare location (2020) (0)
Recombinant chromosome 10 presenting as a prenatal central nervous system abnormality (2009) (0)
A Novel t(10;22) Translocation Harboring an IGL Gene Deletion in a CLL Patient Transforming to B-PLL with 1q Gain. (2020) (0)
The 90th Neuropathological Meeting of Kyushu District 25 June 2005 (2005) (0)
A case of suprasellar ganglioglioma arising from the genu‒rostrum of the corpus callosum composed of tumor cells in various stages of neuronal differentiation (2017) (0)
Multiphasic acute disseminated encephalomyelitis associated with atypical rubella virus infection – response to the letter from Wu et al (2015) (0)
Early and extensive alterations of glial connexins, distal oligodendrogliopathy type demyelination, and nodal/paranodal pathology are characteristic of multiple system atrophy (2022) (0)
Short communication Unusual aberration involving the short arm of chromosome 11 in an 8-month-old patient with a supratentorial primitive neuroectodermal tumor (2003) (0)
Cryptic insertion of 3'FOXO1 into inverted chromosome arm 2q in the presence of two normal chromosome 13s and 13 small interstitial duplications in a patient with alveolar rhabdomyosarcoma. (2015) (0)
Epithelial properties of pleomorphie xanthoastrocytomas determined in ultrastructural and immunohistochemical studies * (0)
A novel translocation t(10;17)(p13;q11.2) harboring two cryptic deletions identified by array‐CGH and characterized by SUZ12 overexpression in a patient with chronic thrombocytosis (2020) (0)
Hemorrhagic stroke due to leukostasis in pediatric mixed-phenotype acute leukemia (2021) (0)

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