Shu‐ichi Ikeda

Q: What Schools Are Affiliated With Shu‐ichi Ikeda

Shu‐ichi Ikeda is affiliated with the following schools: University of California, San Diego, Kumamoto University, Nihon University, Shinshu University

Shu‐ichi Ikeda's AcademicInfluence.com Rankings

Shu‐ichi Ikeda

Philosophy

#8395

World Rank

#11771

Historical Rank

Logic

#5434

World Rank

#6835

Historical Rank

philosophy Degrees

Shu‐ichi Ikeda

Biology

#11368

World Rank

#14759

Historical Rank

Neuroscience

#1840

World Rank

#1896

Historical Rank

Biochemistry

#1868

World Rank

#2009

Historical Rank

biology Degrees

Download Badge

Philosophy
Biology

Shu‐ichi Ikeda's Degrees

PhD Biochemistry Kyoto University
Doctorate Medicine Kyoto University

Why Is Shu‐ichi Ikeda Influential?

(Suggest an Edit or Addition)

(See a Problem?)

Shu‐ichi Ikeda's Published Works

Number of citations in a given year to any of this author's works

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

α‐Synuclein implicated in Parkinson's disease is present in extracellular biological fluids, including human plasma (2003) (563)
Guideline of transthyretin-related hereditary amyloidosis for clinicians (2013) (532)
Repurposing diflunisal for familial amyloid polyneuropathy: a randomized clinical trial. (2013) (527)
Amyloid fibril proteins and amyloidosis: chemical identification and clinical classification International Society of Amyloidosis 2016 Nomenclature Guidelines (2016) (468)
Nomenclature 2014: Amyloid fibril proteins and clinical classification of the amyloidosis (2014) (437)
A mutation in the ceruloplasmin gene is associated with systemic hemosiderosis in humans (1995) (436)
A primer of amyloid nomenclature (2007) (344)
Amyloid: Toward terminology clarification Report from the Nomenclature Committee of the International Society of Amyloidosis (2005) (339)
Amyloid fibril protein nomenclature: 2010 recommendations from the nomenclature committee of the International Society of Amyloidosis (2010) (337)
Association of HTRA1 mutations and familial ischemic cerebral small-vessel disease. (2009) (300)
Amyloid fibril protein nomenclature: 2012 recommendations from the Nomenclature Committee of the International Society of Amyloidosis (2012) (294)
Liver Transplantation for Hereditary Transthyretin Amyloidosis: After 20 Years Still the Best Therapeutic Alternative? (2015) (244)
Hereditary ceruloplasmin deficiency with hemosiderosis: A clinicopathological study of a japanese family (1995) (243)
Amyloid Fibril Protein Nomenclature - 2002 (2002) (221)
Type I (transthyretin Met30) familial amyloid polyneuropathy in Japan: early- vs late-onset form. (2002) (220)
Familial transthyretin-type amyloid polyneuropathy in Japan: clinical and genetic heterogeneity. (2002) (211)
Diflunisal stabilizes familial amyloid polyneuropathy-associated transthyretin variant tetramers in serum against dissociation required for amyloidogenesis (2006) (141)
Pathogenesis of and therapeutic strategies to ameliorate the transthyretin amyloidoses. (2008) (141)
Morphology and distribution of plaque and related deposits in the brains of Alzheimer's disease and control cases. An immunohistochemical study using amyloid beta-protein antibody. (1989) (135)
Carpal tunnel syndrome: a common initial symptom of systemic wild-type ATTR (ATTRwt) amyloidosis (2016) (134)
High prevalence of wild-type transthyretin deposition in patients with idiopathic carpal tunnel syndrome: a common cause of carpal tunnel syndrome in the elderly. (2011) (125)
Energetic Characteristics of the New Transthyretin Variant A25T May Explain Its Atypical Central Nervous System Pathology (2003) (118)
Anti-neuronal autoantibody in Hashimoto's encephalopathy: neuropathological, immunohistochemical, and biochemical analysis of two patients (2004) (108)
Amyloid fibrils containing fragmented ATTR may be the standard fibril composition in ATTR amyloidosis (2013) (104)
Increased lipid peroxidation in the brains of aceruloplasminemia patients (2000) (100)
Clinical and genetic characterization of adult‐onset leukoencephalopathy with axonal spheroids and pigmented glia associated with CSF1R mutation (2016) (99)
Progression of dystrophic features and activation of mitogen‐activated protein kinases and calcineurin by physical exercise, in hearts of mdx mice (2002) (96)
Plasma Levels of amyloid β proteins Aβ1–40 and Aβ1–42(43) are elevated in Down's syndrome (1997) (96)
Rheumatoid meningitis: an autopsy report and review of the literature (2003) (96)
Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy. (2002) (96)
EARLY SENILE PLAQUES IN DOWN'S SYNDROME BRAINS SHOW A CLOSE RELATIONSHIP WITH CELL BODIES OF NEURONS (1989) (95)
Molecular analysis of the duchenne muscular dystrophy gene in patients with becker muscular dystrophy presenting with dilated cardiomyopathy (1993) (95)
Peripheral nerve pathological findings in familial amyloid polyneuropathy: A correlative study of proximal sciatic nerve and sural nerve lesions (1989) (94)
Type II (adult onset) citrullinaemia: clinical pictures and the therapeutic effect of liver transplantation (2001) (87)
Event based and time based prospective memory in Parkinson’s disease (2003) (86)
Thorn-shaped astrocytes: possibly secondarily induced tau-positive glial fibrillary tangles (2004) (86)
Activation and localization of matrix metalloproteinase-2 and -9 in the skeletal muscle of the muscular dystrophy dog (CXMDJ) (2007) (84)
Safety and efficacy of long-term diflunisal administration in hereditary transthyretin (ATTR) amyloidosis (2015) (83)
Exome sequencing reveals a homozygous SYT14 mutation in adult-onset, autosomal-recessive spinocerebellar ataxia with psychomotor retardation. (2011) (80)
Clinical and Genetic Features of Familial Mediterranean Fever in Japan (2009) (79)
Hypertrophic neuritis due to chronic inflammatory demyelinating polyradiculoneuropathy (CIDP): A postmortem pathological study (1996) (77)
Follow-up of three patients with a large in-frame deletion of exons 45–55 in the Duchenne muscular dystrophy (DMD) gene (2008) (76)
Schwann cell and endothelial cell damage in transthyretin familial amyloid polyneuropathy (2016) (75)
Matrix metalloproteinase-2 ablation in dystrophin-deficient mdx muscles reduces angiogenesis resulting in impaired growth of regenerated muscle fibers. (2011) (74)
A Case of Mitochondrial Cytopathy with a Typical Point Mutation for MELAS, Presenting with Severe Focal-Segmental Glomerulosclerosis as MainClinical Manifesta tion (1998) (74)
Spinal nerve root hypertrophy on MRI: clinical significance in the diagnosis of chronic inflammatory demyelinating polyradiculoneuropathy. (2008) (73)
Peripheral Sympathetic Nerve Dysfunction in Adolescent Japanese Girls Following Immunization with the Human Papillomavirus Vaccine. (2015) (72)
Genotype-phenotype correlation in Japanese patients with familial Mediterranean fever: differences in genotype and clinical features between Japanese and Mediterranean populations (2014) (68)
Extensive loss of arterial medial smooth muscle cells and mural extracellular matrix in cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL) (2008) (66)
Evidence of amyloid beta-protein immunoreactive early plaque lesions in Down's syndrome brains. (1989) (64)
Astrocytic Deformity and Globular Structures Are Characteristic of the Brains of Patients with Aceruloplasminemia (2002) (63)
Interstitial lung disease associated with amyopathic dermatomyositis: review of 18 cases. (2007) (62)
Increase in incidence of elderly-onset patients with myasthenia gravis in Nagano Prefecture, Japan. (2005) (61)
Cerebral amyloid angiopathy in posttransplant patients with hereditary ATTR amyloidosis (2016) (61)
Marked regression of abdominal fat amyloid in patients with familial amyloid polyneuropathy during long‐term follow‐up after liver transplantation (2008) (61)
Immunohistochemical and immunoelectron microscopical characterization of cerebrovascular and senile plaque amyloid in aged dogs' brains (1991) (60)
Vagus nerve and celiac ganglion lesions in generalized amyloidosis A correlative study of familial amyloid polyneuropathy and AL-amyloidosis (1987) (58)
Dystonia, mental deterioration, and dyschromatosis symmetrica hereditaria in a family with ADAR1 mutation (2006) (58)
Transthyretin‐derived amyloid deposition on the gastric mucosa in domino recipients of familial amyloid polyneuropathy liver (2007) (58)
Metabolic derangements in deficiency of citrin, a liver-type mitochondrial aspartate-glutamate carrier. (2005) (58)
Up-regulation of mitogen activated protein kinases in mdx skeletal muscle following chronic treadmill exercise. (2005) (58)
Clinical Characteristics of Aged Becker Muscular Dystrophy Patients with Onset after 30 Years (1999) (57)
Glial Fibrillary Acidic Protein is Greatly Modified by Oxidative Stress in Aceruloplasminemia Brain (2002) (57)
Peripheral sympathetic nerve dysfunction in adolescent Japanese girls following immunization with the human papillomavirus vaccine. (2014) (57)
Cerebral arterial pathology of CADASIL and CARASIL (Maeda syndrome) (2003) (57)
Safety and efficacy of thalidomide in patients with POEMS syndrome: a multicentre, randomised, double-blind, placebo-controlled trial (2016) (57)
Partial-Liver Transplantation To Treat Familial Amyloid Polyneuropathy: Follow-up of 11 Patients (1999) (56)
CPPD crystal deposition disease of the cervical spine: A common cause of acute neck pain encountered in the neurology department (2010) (55)
Immunohistochemical evidence for the derivation of a peptide ligand from the amyloid beta-protein precursor of Alzheimer disease. (1988) (54)
Hypersomnia and low CSF hypocretin-1 (orexin-A) concentration in a patient with multiple sclerosis showing bilateral hypothalamic lesions. (2003) (54)
Early identification of amyloid heart disease by technetium-99m-pyrophosphate scintigraphy: a study with familial amyloid polyneuropathy. (1987) (54)
Quantitative evaluation of expression of iron-metabolism genes in ceruloplasmin-deficient mice. (2002) (53)
Diagnostic criteria for adult‐onset leukoencephalopathy with axonal spheroids and pigmented glia due to CSF1R mutation (2018) (53)
Gastrointestinal amyloid deposition in familial amyloid polyneuropathy (1982) (53)
SELDI-TOF mass spectrometry evaluation of variant transthyretins for diagnosis and pathogenesis of familial amyloidotic polyneuropathy. (2009) (53)
Cyclosporin A in treatment of refractory patients with chronic inflammatory demyelinating polyradiculoneuropathy (2004) (52)
Effects of tafamidis treatment on transthyretin (TTR) stabilization, efficacy, and safety in Japanese patients with familial amyloid polyneuropathy (TTR-FAP) with Val30Met and non-Val30Met: A phase III, open-label study (2016) (52)
Early senile plaques in Alzheimer's disease demonstrated by histochemistry, immunocytochemistry, and electron microscopy. (1990) (51)
Hereditary diffuse leukoencephalopathy with axonal spheroids caused by R782H mutation in CSF1R: Case report (2012) (51)
Flow cytometric analysis of lymphocyte subpopulations and TH1/TH2 balance in patients with polymyositis and dermatomyositis. (2008) (51)
Complete neurological recovery of an adult patient with type II citrullinemia after living related partial liver transplantation. (1996) (50)
Risk of worsened encephalopathy after intravenous glycerol therapy in patients with adult-onset type II citrullinemia (CTLN2). (2005) (50)
Severe protein losing enteropathy with intractable diarrhea due to systemic AA amyloidosis, successfully treated with corticosteroid and octreotide (2005) (50)
A novel splicing mutation in the ceruloplasmin gene responsible for hereditary ceruloplasmin deficiency with hemosiderosis (1998) (49)
Ten years of experience with liver transplantation for familial amyloid polyneuropathy in Japan: outcomes of living donor liver transplantations. (2005) (49)
Steatogenesis in adult-onset type II citrullinemia is associated with down-regulation of PPARα. (2015) (48)
Clinical features of non‐hypertensive lobar intracerebral hemorrhage related to cerebral amyloid angiopathy (2010) (48)
Intravenous immunoglobulin (IVIg) with methylprednisolone pulse therapy for motor impairment of neuralgic amyotrophy: clinical observations in 10 cases. (2012) (47)
Diagnostic value of abdominal wall fat pad biopsy in senile systemic amyloidosis (2011) (47)
Neutropenia as a Complication of High-Dose Intravenous Immunoglobulin Therapy in Adult Patients With Neuroimmunologic Disorders (2003) (46)
Induction of AApoAII amyloidosis by various heterogeneous amyloid fibrils (2004) (44)
Clinical assessment of standing and gait in ataxic patients using a triaxial accelerometer (2015) (44)
Adult or late-onset triple A syndrome Case report and literature review (2010) (43)
Secretory form of Alzheimer amyloid precursor protein 695 in human brain lacks beta/A4 amyloid immunoreactivity. (1993) (43)
Feasibility of auxiliary partial orthotopic liver transplantation from living donors for patients with adult‐onset type II citrullinemia (2004) (43)
Clinical and pathological studies of cardiac amyloidosis in transthyretin type familial amyloid polyneuropathy (2003) (42)
Successful treatment with rituximab in a patient with stiff-person syndrome complicated by dysthyroid ophthalmopathy. (2010) (42)
Pneumatosis cystoides intestinalis in neuropsychiatric systemic lupus erythematosus with diabetes mellitus: case report and literature review (2011) (42)
Sarcoidosis with high serum levels of vascular endothelial growth factor (VEGF), showing RS3PE-like symptoms in extremities (2004) (41)
Comparison of the strain Doppler echocardiographic features of familial amyloid polyneuropathy (FAP) and light-chain amyloidosis. (2005) (41)
Expression of various glutamate receptors including N-methyl-D-aspartate receptor (NMDAR) in an ovarian teratoma removed from a young woman with anti-NMDAR encephalitis. (2010) (41)
Transthyretin-type cerebral amyloid angiopathy in type I familial amyloid polyneuropathy (2004) (41)
Usefulness of [123I]metaiodobenzylguanidine ([123I]MIBG) myocardial scintigraphy in differentiating between Alzheimer's disease and dementia with Lewy bodies. (2003) (41)
Plasma levels of amyloid β proteins did not differ between subjects taking statins and those not taking statins (2001) (41)
Peripheral Nerves Regenerated in Familial Amyloid Polyneuropathy after Liver Transplantation (1997) (41)
Pravastatin at 10 mg/day does not decrease plasma levels of either amyloid-β (Aβ) 40 or Aβ 42 in humans (2003) (40)
Nationwide Survey of 741 Patients with Systemic Amyloid Light-chain Amyloidosis in Japan (2017) (40)
The Diflunisal Trial: Study accrual and drug tolerance (2012) (40)
Plasma levels of amyloid beta proteins Abeta1-40 and Abeta1-42(43) are elevated in Down's syndrome. (1997) (39)
A Japanese patient with familial Mediterranean fever associated with compound heterozygosity for pyrin variant E148Q/M694I. (2005) (39)
Characterization of amyloid fibril protein from a case of cerebral amyloid angiopathy showing immunohistochemical reactivity for both β protein and cystatin C (1992) (39)
Suspected Adverse Effects After Human Papillomavirus Vaccination: A Temporal Relationship Between Vaccine Administration and the Appearance of Symptoms in Japan (2017) (38)
Identification of a novel transthyretin variant (Val30→Leu) associated with familial amyloidotic polyneuropathy (1992) (38)
Extensive brain pathology in a patient with aceruloplasminemia with a prolonged duration of illness. (2012) (38)
Ten-year follow-up of peripheral nerve function in patients with familial amyloid polyneuropathy after liver transplantation (2008) (37)
Relationship between clinical factors and neuropsychiatric manifestations in systemic lupus erythematosus (2005) (37)
Risk factors for hospital-acquired bacteremia. (2005) (37)
Analysis of an insertion mutation in a cohort of 94 patients with spinocerebellar ataxia type 31 from Nagano, Japan (2010) (36)
A novel frameshift mutation in the McLeod syndrome gene in a Japanese family (1999) (36)
Prevalence and clinical features of cough variant asthma in a general internal medicine outpatient clinic in Japan (2005) (35)
The significance of carpal tunnel syndrome in transthyretin Val30Met familial amyloid polyneuropathy (2009) (34)
Intractable skin necrosis and interstitial pneumonia in amyopathic dermatomyositis, successfully treated with cyclosporin A. (2003) (34)
Echocardiographic assessment of the cardiac amyloidoses. (2015) (34)
Familial amyloid polyneuropathy in Taiwan: Identification of transthyretin variant (Leu55 → Pro) (1994) (34)
Decrease in presynaptic inhibition on heteronymous monosynaptic Ia terminals in patients with Parkinson's disease (2000) (33)
Cardiac amyloidosis: heterogenous pathogenic backgrounds. (2004) (33)
VAD with or without subsequent high-dose melphalan followed by autologous stem cell support in AL amyloidosis: Japanese experience and criteria for patient selection (2004) (33)
Clinicopathologic and genetic features of early- and late-onset FAP type I (FAP ATTR Val30Met) in Japan (2003) (33)
Neuronal activity in the globus pallidus in chorea caused by striatal lacunar infarction (2001) (32)
Prevalence of Dementia ofAlzheimer Type and Apolipoprotein EPhenotypes in Aged Patients withDown’s Syndrome (1998) (32)
Soluble Aβ homeostasis in AD and DS: impairment of anti-amyloidogenic protection by lipoproteins (2004) (32)
Lack of modulation of Ib inhibition during antagonist contraction in spasticity (2006) (32)
Hepatocellular carcinoma in a case of adult-onset type II citrullinemia. (2003) (32)
Successful treatment with infliximab and low-dose methotrexate in a Japanese patient with familial Mediterranean fever. (2007) (32)
Markers for Guillain‐Barré syndrome with poor prognosis: a multi‐center study (2017) (31)
Adult onset leukoencephalopathy with axonal spheroids and pigmented glia (ALSP) and Nasu–Hakola disease: lesion staging and dynamic changes of axons and microglial subsets (2017) (31)
Unexpectedly high incidence of visceral AA-amyloidosis in slaughtered cattle in Japan (2005) (31)
Early involvement of the corpus callosum in a patient with hereditary diffuse leukoencephalopathy with spheroids carrying the de novo K793T mutation of CSF1R. (2013) (31)
Conventional diet therapy for hyperammonemia is risky in the treatment of hepatic encephalopathy associated with citrin deficiency. (2010) (31)
Progressive supranuclear palsy with asymmetric tau pathology presenting with unilateral limb dystonia (2002) (30)
Biochemical characteristics of variant transthyretins causing hereditary leptomeningeal amyloidosis (2005) (30)
A −16C>T substitution in the 5′ UTR of the puratrophin-1 gene is prevalent in autosomal dominant cerebellar ataxia in Nagano (2006) (30)
Successful treatment of fulminant pulmonary hemorrhage associated with systemic lupus erythematosus (2004) (30)
Immunogold labeling of cerebrovascular and neuritic plaque amyloid fibrils in Alzheimer's disease with an anti-beta protein monoclonal antibody. (1987) (29)
Upper limb neuropathy such as carpal tunnel syndrome as an initial manifestation of ATTR Val30Met familial amyloid polyneuropathy (2010) (29)
[Diagnosis and treatment in systemic amyloidosis]. (2008) (29)
Distribution of neprilysin and deposit patterns of Aβ subtypes in the brains of aged squirrel monkeys (Saimiri sciureus) (2010) (29)
Senile systemic amyloidosis presenting as bilateral carpal tunnel syndrome (2002) (29)
Autosomal-recessive complicated spastic paraplegia with a novel lysosomal trafficking regulator gene mutation (2014) (29)
AH amyloidosis associated with an immunoglobulin heavy chain variable region (VH1) fragment: a case report (2008) (29)
Clinical manifestations at diagnosis in Japanese patients with systemic AL amyloidosis: a retrospective study of 202 cases with a special attention to uncommon symptoms. (2014) (28)
Ceruloplasmin Protects Against Rotenone-Induced Oxidative Stress and Neurotoxicity (2011) (28)
Regional features of autosomal-dominant cerebellar ataxia in Nagano: clinical and molecular genetic analysis of 86 families (2004) (27)
[Alzheimer's disease and amyloid beta-protein]. (1989) (27)
Severe generalized dystonia as a presentation of a patient with aprataxin gene mutation (2003) (27)
Henoch–Schönlein purpura nephritis complicated by reversible posterior leukoencephalopathy syndrome (2007) (27)
The diflunisal trial: update on study drug tolerance and disease progression (2011) (27)
Spinocerebellar ataxia type 6 (SCA6): Clinical pilot trial with gabapentin (2009) (27)
A patient with severe renal amyloidosis associated with an immunoglobulin γ-heavy chain fragment (2004) (27)
Serum levels of free light chain before and after chemotherapy in primary systemic AL amyloidosis. (2005) (26)
Relationship between lobar intracerebral hemorrhage and leukoencephalopathy associated with cerebral amyloid angiopathy: Clinicopathological study of 64 Japanese patients (2003) (26)
Corpus callosum atrophy in patients with hereditary diffuse leukoencephalopathy with neuroaxonal spheroids: an MRI-based study. (2014) (26)
Systemic AL amyloidosis mimicking rheumatoid arthritis. (2008) (26)
Periodic alternating nystagmus and rebound nystagmus in spinocerebellar ataxia type 6 (2003) (26)
Distinctive features of degenerating Purkinje cells in spinocerebellar ataxia type 31 (2013) (26)
Phenotypic analysis of plasma cells in bone marrow using flow cytometry in AL amyloidosis (2003) (26)
Rituximab therapy in chronic inflammatory demyelinating polyradiculoneuropathy with anti-SGPG IgM antibody (2006) (26)
The safety of transcranial magnetic stimulation with deep brain stimulation instruments. (2010) (25)
Serum transthyretin monomer in patients with familial amyloid polyneuropathy (2001) (25)
A variant of Gerstmann-Sträussler-Scheinker disease with ß -protein epitopes and dystrophic neurites in the peripheral regions of PrP -immunoreactive amyloid plaques (1991) (25)
Recurrent gastric hemorrhaging with large submucosal hematomas in a patient with primary AL systemic amyloidosis: endoscopic and histopathological findings. (2004) (25)
Phenol Congo red staining enhances the diagnostic value of abdominal fat aspiration biopsy in reactive AA amyloidosis secondary to rheumatoid arthritis. (2003) (25)
Primary liver carcinoma exhibiting dual hepatocellular-biliary epithelial differentiations associated with citrin deficiency: a case report. (2008) (25)
Secretory cleavage site of Alzheimer amyloid precursor protein is heterogeneous in Down's syndrome brain (1994) (25)
Effective Use of Calcineurin Inhibitor in Combination Therapy for Interstitial Lung Disease in Patients With Dermatomyositis and Polymyositis (2017) (24)
Haplotype analysis in gelsoiin‐related amyloidosis reveals independent origin of identical mutation (G654A) of gelsolin in Finland and Japan (1995) (24)
Impaired left ventricular diastolic filling in patients with familial amyloid polyneuropathy: a pulsed Doppler echocardiographic study. (1989) (24)
Diagnostic value of abdominal fat tissue aspirate in familial amyloid polyneuropathy (1987) (24)
Brain SPECT with 123I-IMP for the early diagnosis of Creutzfeldt–Jakob disease (2001) (24)
Cortical petechial hemorrhage, subarachnoid hemorrhage and corticosteroid-responsive leukoencephalopathy in a patient with cerebral amyloid angiopathy (2008) (24)
Late-onset spastic ataxia phenotype in a patient with a homozygous DDHD2 mutation (2014) (24)
Adult GM1‐gangliosidosis (1985) (23)
Takayasu's arteritis in a patient with Crohn's disease: an unexpected association during infliximab therapy. (2010) (23)
Synovial deposition of wild-type transthyretin-derived amyloid in knee joint osteoarthritis patients (2013) (23)
A case of Mikulicz's disease complicated by malignant lymphoma: a postmortem histopathological finding. (2012) (23)
The characteristics of food intake in patients with type II citrullinemia. (2011) (23)
Increased vulnerability to rotenone-induced neurotoxicity in ceruloplasmin-deficient mice (2008) (23)
Characterization of deletion breakpoints in patients with dystrophinopathy carrying a deletion of exons 45–55 of the Duchenne muscular dystrophy (DMD) gene (2009) (23)
Hypertrophic pachymeningitis is a characteristic manifestation of granulomatosis with polyangiitis: A retrospective study of anti‐neutrophil cytoplasmic antibody‐associated vasculitis (2017) (23)
Efficacy of tacrolimus in treatment of polymyositis associated with myasthenia gravis (2004) (22)
Choroidal vascular lesions identified by ICG angiography in a case of familial amyloidotic polyneuropathy. (2003) (22)
Advantage of administering tacrolimus for improving prognosis of patients with polymyositis and dermatomyositis (2016) (22)
Natural History of Spinocerebellar Ataxia Type 31: a 4-Year Prospective Study (2017) (22)
Chronic pancreatitis associated with adult-onset type II citrullinemia: clinical and pathologic findings. (2004) (22)
Amyloid β protein species in cerebrospinal fluid and in brain from patients with Down's syndrome (1999) (22)
Pravastatin at 10 mg/day does not decrease plasma levels of either amyloid-beta (Abeta) 40 or Abeta 42 in humans. (2003) (22)
Partial liver transplantation from living donors in familial amyloid polyneuropathy (1997) (22)
Type III (chronic) GM1-gangliosidosis Histochemical and ultrastructural studies of rectal biopsy (1985) (22)
Postmortem findings in two familial amyloidosis patients with transthyretin variant Asp38Ala (2000) (22)
Systemic reactive amyloidosis associated with Castleman's disease: serial changes of the concentrations of acute phase serum amyloid A and interleukin 6 in serum. (1997) (22)
Tacrolimus in refractory patients with myasthenia gravis: Coadministration and tapering of oral prednisolone (2006) (21)
Coadministration of tacrolimus with corticosteroid accelerates recovery in refractory patients with polymyositis/ dermatomyositis: a retrospective study (2012) (21)
Clinical and serial MRI findings of a sialidosis type I patient with a novel missense mutation in the NEU1 gene. (2013) (21)
Amyloidogenic transthyretin Val30Met homozygote showing unusually early‐onset familial amyloid polyneuropathy (2008) (21)
[Cardiac involvement in systemic amyloidosis: myocardial scintigraphic evaluation]. (1985) (21)
Histopathological regression of systemic AA amyloidosis after surgical treatment of a localized Castleman's disease (2006) (21)
Wild-type transthyretin significantly contributes to the formation of amyloid fibrils in familial amyloid polyneuropathy patients with amyloidogenic transthyretin Val30Met. (2011) (21)
Coexistence of familial Mediterranean fever and Behçet's disease in a Japanese patient. (2006) (21)
Cerebrovascular amyloid in scrapie-affected sheep reacts with antibodies to prion protein (1988) (21)
Comparison of the histological and immunohistochemical features of the thymus in young- and elderly-onset myasthenia gravis without thymoma (2007) (21)
Nephrotic syndrome due to primary AL amyloidosis, successfully treated with VAD and subsequent high-dose melphalan followed by autologous peripheral blood stem cell transplantation. (2003) (20)
Serial CT and MRI findings in a patient with isolated angiitis of the central nervous system associated with cerebral amyloid angiopathy (2002) (20)
Stereotyped stepping associated with lesions in the bilateral medial frontoparietal cortices (2001) (20)
An 85-year-old case with Hashimoto's encephalopathy, showing spontaneous complete remission. (2007) (20)
A case of familial amyloid polyneuropathy treated with partial liver transplantation using a graft from a living related donor. (1995) (19)
Successful treatment of fulminant Wilson's disease without liver transplantation (2014) (19)
Periodic peritonitis due to familial Mediterranean fever in a patient with systemic lupus erythematosus. (2010) (19)
Slaughtered aged cattle might be one dietary source exhibiting amyloid enhancing factor activity (2009) (19)
Triple a syndrome in Japan (2013) (19)
Spinal form cerebrotendinous xanthomatosis patient with long spinal cord lesion (2016) (19)
Primary AL amyloid polyneuropathy successfully treated with high‐dose melphalan followed by autologous stem cell transplantation (2010) (19)
Cerebral amyloid angiopathy-related hemorrhage in a middle-aged patient with Down's syndrome (2008) (19)
p.E66Q mutation in the GLA gene is associated with a high risk of cerebral small‐vessel occlusion in elderly Japanese males (2014) (19)
Adult fucosidosis (1984) (19)
AL amyloidosis with spontaneous hepatic rupture: successful treatment by transcatheter hepatic artery embolization (2008) (19)
Nodular lung disease with five year survival and unilateral pleural effusion in AL amyloidosis. (1999) (18)
Transthyretin Thr60Ala Appalachian-type mutation in a Japanese family with familial amyloidotic polyneuropathy (2002) (18)
Imbalanced expression of dysfunctional regulatory T cells and T-helper cells relates to immunopathogenesis in polyarteritis nodosa (2017) (18)
Cessation of cerebral hemorrhage recurrence associated with corticosteroid treatment in a patient with cerebral amyloid angiopathy (2000) (18)
Relation between changes in long-latency stretch reflexes and muscle stiffness in Parkinson's disease – comparison before and after unilateral pallidotomy (2001) (18)
Elevation of serum heat-shock protein levels in amyotrophic lateral sclerosis (2016) (18)
Adult GM1 gangliosidosis (1994) (18)
A Young Man with Anti-NMDAR Encephalitis following Guillain-Barré Syndrome (2011) (18)
Variability of beta-amyloid protein deposited lesions in Down's syndrome brains. (1994) (18)
Value of renal biopsy in the prognosis of liver transplantation in familial amyloid polyneuropathy ATTR Val30Met patients (2006) (18)
Abdominal fat aspiration biopsy and genotyping of serum amyloid A contribute to early diagnosis of reactive AA amyloidosis secondary to rheumatoid arthritis. (2003) (18)
Adult onset X-linked chronic granulomatous disease in a woman patient caused by a de novo mutation in paternal-origin CYBB gene and skewed inactivation of normal maternal X chromosome. (2008) (18)
Muscle CT scan findings in McLeod syndrome and chorea‐acanthocytosis (2000) (18)
A novel nonsense mutation in the TITF-1 gene in a Japanese family with benign hereditary chorea (2012) (18)
Identification of the N-Methyl-D-aspartate receptor (NMDAR)-related epitope, NR2B, in the normal human ovary: implication for the pathogenesis of anti-NMDAR encephalitis. (2013) (18)
Myasthenia gravis with anti-MuSK antibody, showing progressive muscular atrophy without blepharoptosis. (2005) (17)
Abnormal activity in the globus pallidus in off‐period dystonia (2001) (17)
Phenotypes of Peripheral Blood Lymphocytes and Cytokine Expression in Polymyositis and Dermatomyositis before Treatment and after Clinical Remission (2012) (17)
Acute respiratory distress syndrome due to systemic lupus erythematosus with hemophagocytic syndrome: an autopsy report (2005) (17)
Nonepisodic angioedema with eosinophilia: a report of two cases and a review of the literature (2006) (17)
Postmortem pathological findings in a Japanese patient with familial amyloidosis, Finnish type (FAF) (1996) (17)
Cerebral hemorrhage in Fabry's disease (2010) (17)
Lupus erythematosus profundus (lupus panniculitis) induced by interferon-β in a multiple sclerosis patient (2007) (17)
Churg-Strauss syndrome presenting as myositis following unaccustomed exercise (2009) (17)
Leukoencephalopathy induced by low-dose methotrexate in a patient with rheumatoid arthritis. (2011) (17)
Chronic inflammatory demyelinating polyradiculoneuropathy with autonomic involvement (2005) (17)
Multiple mitochondrial DNA deletions in a patient with mitochondrial myopathy and cardiomyopathy but no ophthalmoplegia (1995) (16)
Nodular cutaneous amyloidosis and carpal tDnnel syndrome due to the amyloidogenic transthyretin His 114 variant (2001) (16)
Static balance impairment and its change after pallidotomy in Parkinson's disease (2004) (16)
Abnormal conditioning effect of transcranial magnetic stimulation on soleus H-reflex during voluntary movement in Parkinson's disease (2002) (16)
Is familial amyloid polyneuropathy rare? (2007) (16)
Peripheral nerve function in patients with familial amyloid polyneuropathy after liver transplantation (2003) (16)
A Japanese case of SCA14 with the Gly128Asp mutation (2006) (16)
Clinical, endoscopic, and histopathological features of localized immunoglobulin light chain (AL) amyloidosis in the gastrointestinal tract (2015) (16)
Prednisolone (30–60 mg/day) for diseases other than AD decreases amyloid &bgr;-peptides in CSF (2002) (15)
Clinical and pathological findings of non-Val30Met TTR type familial amyloid polyneuropathy in Japan (2003) (15)
The first pure form of Ostertag-type amyloidosis in Japan: a sporadic case of hereditary fibrinogen Aα-chain amyloidosis associated with a novel frameshift variant (2015) (15)
Early cardiac involvement in senile systemic amyloidosis: a case report (2008) (15)
Cardiac positron-emission tomography images with an amyloid-specific tracer in familial transthyretin-related systemic amyloidosis. (2012) (15)
A primary Sjögren's syndrome patient with marked swelling of multiple exocrine glands and sclerosing pancreatitis. (2002) (15)
Characterization of a transthyretin-related amyloid fibril protein from cerebral amyloid angiopathy in type I familial amyloid polyneuropathy (1992) (15)
Pallidotomy for severe generalized chorea of juvenile-onset dentatorubral-pallidoluysian atrophy (2003) (15)
Brain Biopsy Is More Reliable than the DNA test for JC Virus in Cerebrospinal Fluid for the Diagnosis of Progressive Multifocal Leukoencephalopathy (2017) (15)
AH amyloidosis associated with lymphoplasmacytic lymphoma secreting a monoclonal gamma heavy chain carrying an unusual truncated D segment. (2006) (15)
Principal component analysis for ataxic gait using a triaxial accelerometer (2017) (15)
Isaacs’ syndrome associated with myasthenia gravis, showing remission after cytoreductive surgery of pleural recurrence of thymoma (2006) (15)
A 73-year-old patient with adult-onset type II citrullinemia successfully treated by sodium pyruvate and arginine (2013) (14)
Postmortem findings in a patient with cerebral amyloid angiopathy actively treated with corticosteroid (2012) (14)
Bilateral localized amyloidosis of the ureters: clinicopathology and therapeutic approaches in two cases (2004) (14)
Postmortem findings in a familial amyloid polyneuropathy patient with homozygosity of the mutant Val30Met transthyretin gene (2004) (14)
Clinical and radiological findings of a cerebrotendinous xanthomatosis patient with a novel p.A335V mutation in the CYP27A1 gene. (2014) (14)
Spinal intradural extramedullary cavernous angioma presenting with superficial siderosis and hydrocephalus: a case report and review of the literature. (2014) (14)
Liver dysfunction and thrombocytopenia diagnosed as intravascular large B-cell lymphoma using a timely and accurate transjugular liver biopsy. (2013) (14)
Regression of gastroduodenal amyloid deposition in systemic AL amyloidosis after intensive chemotherapies (2011) (14)
Thalamic Stimulation for Disabling Tremor in a Patient with Spinocerebellar Degeneration (2005) (14)
Osmotic demyelination syndrome: reversible MRI findings in bilateral cortical lesions. (2003) (14)
Severity and Progression Rate of Cerebellar Ataxia in 16q-linked Autosomal Dominant Cerebellar Ataxia (16q-ADCA) in the Endemic Nagano Area of Japan (2009) (14)
Distinctive clinicopathological features of 2 large families with amyotrophic lateral sclerosis having L106V mutation in SOD1 gene (2012) (14)
Japanese POEMS syndrome with Thalidomide (J-POST) Trial: study protocol for a phase II/III multicentre, randomised, double-blind, placebo-controlled trial (2015) (13)
Liver Transplantation: An Effective Treatment For Familial ATTR Amyloidosis (2002) (13)
Calciphylaxis as a Catastrophic Complication in a Patient with POEMS Syndrome (2009) (13)
Senile systemic amyloidosis starting as bilateral carpal and left ulnar tunnel syndrome. (2003) (13)
Follow-up nationwide survey on predictive genetic testing for late-onset hereditary neurological diseases in Japan (2013) (13)
Histochemical study of rectal aminergic nerves in type I familial amyloid polyneuropathy (1983) (13)
Effects of unilateral pallidotomy on voluntary movement, and simple and choice reaction times in Parkinson's disease (2003) (13)
A Japanese case of familial Mediterranean fever with homozygosity for the pyrin E148Q mutation. (2005) (13)
Non‐senile wild‐type transthyretin systemic amyloidosis presenting as bilateral carpal tunnel syndrome (2008) (13)
Gerstmann-Sträussler-Scheinker disease showing β-protein type cerebellar and cerebral amyloid angiopathy (2004) (13)
Hypertrophic Pachymeningitis as an Early Manifestation of Relapsing Polychondritis: Case Report and Review of the Literature (2016) (13)
Pathological changes long after liver transplantation in a familial amyloidotic polyneuropathy patient (2012) (13)
Serum amyloid A as a potent therapeutic marker in a refractory patient with polymyalgia rheumatica. (2005) (13)
AL amyloidosis manifesting as systemic lymphadenopathy (2008) (12)
A Physician's Guide to Transthyretin Amyloidosis (2008) (12)
Peripheral mechanisms in tremor after traumatic neck injury (2002) (12)
Mixed connective tissue disease with interstitial pneumonia in HTLV-1 carrier: case report and review of the literature (2004) (12)
Malignant lymphoma associated with rheumatoid arthritis, developing shortly after initiation of oral methotrexate. (2004) (12)
Multiple sclerosis with secondary syringomyelia An autopsy report (2001) (12)
Seronegative Sjögren syndrome with asymptomatic autoimmune sclerosing pancreatitis (2007) (11)
[Therapeutic approaches for patients with adult-onset type II citrullinemia (CTLN2): effectiveness of treatment with low-carbohydrate diet and sodium pyruvate]. (2010) (11)
Recurrent cerebral embolism in a familial amyloid polyneuropathy patient who received partial liver transplantation from a living donor. (2001) (11)
A study of the morphology and distribution of amyloid β protein immunoreactive plaque and related lesions in the brains of Alzheimer's disease and adult Down's syndrome (1989) (11)
MRI analysis on a patient with the V30M mutation is characteristic of leptomeningeal amyloid (2004) (11)
Long-term follow-up of plasma cells in bone marrow and serum free light chains in primary systemic AL amyloidosis. (2008) (11)
A patient with severe renal amyloidosis associated with an immunoglobulin gamma-heavy chain fragment. (2004) (11)
Comparison of the standard and speckle tracking echocardiographic features of wild-type and mutated transthyretin cardiac amyloidoses. (2016) (10)
Amyloid beta protein and its 3-kDa fragment are present in the axoplasm fraction of the white matter in human brain. (1996) (10)
High prevalence of ATTR amyloidosis in endomyocardial biopsy-proven cardiac amyloidosis patients (2013) (10)
Paraneoplastic Sensorimotor Neuropathy and Encephalopathy Associated with Anti-α-Enolase Antibody in a Case of Gastric Adenocarcinoma (2004) (10)
Transthyretin Met 30 familial amyloid polyneuropathy in China. Usefulness of mass spectrometry for screening a variant TTR in serum (1997) (10)
Postpartum Anti-N-methyl-D-aspartate Receptor Encephalitis: A Case Report and Literature Review (2017) (10)
Significant deposition of wild type transthyretin-derived amyloid in the gastrointestinal tract of aged individuals (2009) (10)
Marked intrafamilial phenotypic variation in a family with SOD1 C111Y mutation (2012) (10)
A rare lung nodule consisting of adenocarcinoma and amyloid deposition in a patient with primary systemic AL amyloidosis. (2011) (10)
Nonparaneoplastic, Nonherpetic Limbic Encephalitis with Severe Episodic Hypothermia: A Case Report (2005) (10)
Left ventricular deformation and torsion assessed by speckle-tracking echocardiography in patients with mutated transthyretin-associated cardiac amyloidosis and the effect of diflunisal on myocardial function☆ (2015) (10)
Steady turnover of amyloid fibril proteins in gastric mucosa after liver transplantation in familial amyloid polyneuropathy (2013) (10)
Marked and rapid regression of hepatic amyloid deposition in a patient with systemic light chain (AL) amyloidosis after high-dose melphalan therapy with stem cell transplantation. (2014) (10)
An Adolescent Case of Citrin Deficiency With Severe Anorexia Mimicking Anorexia Nervosa (2015) (10)
Two Japanese cases with aspartylglycosaminuria: clinical and morphological features (1991) (10)
Bilirubin adsorption therapy and subsequent liver transplantation cured severe bilirubin encephalopathy in a long-term survival patient with Crigler-Najjar disease type I. (2000) (10)
Secretory cleavage of β-amyloid precursor protein in the cerebral white matter produces amyloidogenic carboxyl-terminal fragments (1995) (10)
Ultrasonography of Thymoma with Pathologic Correlation (1994) (10)
Herpes simplex virus type-1 meningoencephalitis showing disseminated cortical lesions. (2007) (9)
A case with rheumatoid arthritis and systemic reactive AA amyloidosis showing rapid regression of amyloid deposition on gastroduodenal mucosa after a combined therapy of corticosteroid and etanercept (2011) (9)
Effect of synovial transthyretin amyloid deposition on preoperative symptoms and postoperative recovery of median nerve function among patients with idiopathic carpal tunnel syndrome (2014) (9)
Coexistence of Copper in the Iron-Rich Particles of Aceruloplasminemia Brain (2016) (9)
Long-term follow-up of systemic reactive AA amyloidosis secondary to rheumatoid arthritis: successful treatment with intermediate-dose corticosteroid. (2002) (9)
Reversible extensive leukoencephalopathy in Sweet disease: A case report (2008) (9)
Nationwide survey on predictive genetic testing for late-onset, incurable neurological diseases in Japan (2007) (9)
Secretory form of β-amyloid precursor protein is much abundantly contained in the cerebral white matter in human brain (1994) (9)
Prostate amyloid tumor is a clue leading to the diagnosis of systemic AL amyloidosis (2013) (9)
Retrospective analyses of clinical features and therapeutic outcomes in thymectomized patients with myasthenia gravis at Shinshu University. (2004) (9)
Arterial thromboembolism in senile systemic amyloidosis: report of two cases (2012) (9)
Temporary Auxiliary Partial Orthotopic Liver Transplantation Using a Small Graft for Familial Amyloid Polyneuropathy (2012) (9)
Mechanism for increased hepatic glycerol synthesis in the citrin/mitochondrial glycerol-3-phosphate dehydrogenase double-knockout mouse: Urine glycerol and glycerol 3-phosphate as potential diagnostic markers of human citrin deficiency. (2015) (9)
Three patients with isolated adrenocorticotropin deficiency presenting with neuroleptic malignant syndrome-like symptoms. (2001) (9)
An autopsy case with adult onset type II citrullinemia showing myelopathy (2007) (9)
No association between apolipoprotein E ϵ4 allele and the age of onset in type I familial amyloid polyneuropathy (1996) (9)
ANCA-associated vasculitis with central retinal artery occlusion developing during treatment with methimazole. (2012) (8)
Clinical Picture and Outcome of Transthyretin-Related Familial Amyloid Polyneuropathy (FAP) in Japanese Patients (2002) (8)
Electrophysiological features of familial amyloid polyneuropathy in endemic area (2011) (8)
Noradrenergic nerve fibers of the rectal mucosa in autonomic disorders: comparison of histochemical study with clinical severity and changes in plasma noradrenaline induced by standing (1991) (8)
Simultaneous exacerbation and remission of central and peripheral demyelination (2000) (8)
Hemophagocytic syndrome associated with rheumatoid arthritis. (2007) (8)
Squatting-induced bilateral peroneal nerve palsy in a sewer pipe worker. (2017) (8)
Successful Treatment with Alpha-Interferon of a Patient with Chronic Measles Infection of the Brain and Parkinsonism (2000) (8)
Hereditary renal amyloidosis caused by a heterozygous G654A gelsolin mutation: a report of two cases (2013) (8)
Spontaneous pneumoperitoneum: an unusual complication of systemic reactive AA amyloidosis secondary to rheumatoid arthritis (2003) (8)
Characteristic spinal MRI findings of HIV-associated myelopathy in an AIDS patient. (2005) (8)
Adult onset leukoencephalopathy with axonal spheroids and pigmented glia (ALSP) and Nasu-Hakola disease: Lesion staging and dynamic changes of axons and microglial subsets (2017) (8)
Coadministration of Cyclosporin A with Prednisolone in Acute Interstitial Pneumonia Complicating Polymyositis/Dermatomyositis (2012) (8)
Fatal acute pancreatitis with cystic formation in reactive systemic AA amyloidosis secondary to rheumatoid arthritis. (2003) (8)
The pathological and biochemical identification of possible seed‐lesions of transmitted transthyretin amyloidosis after domino liver transplantation (2016) (8)
Therapeutic outcome of cyclic VAD (vincristine, doxorubicin and dexamethasone) therapy in primary systemic AL amyloidosis patients. (2008) (8)
A novel nonsense mutation in a Japanese family with ataxia with oculomotor apraxia type 2 (AOA2) (2009) (8)
Transthyretin Tyr69-to-Ile mutation (doublenucleotide substitution in codon 69) in a Japanese familial amyloidosis patient with cardiomyopathy and carpal tunnel syndrome (2003) (8)
Transthyretin Val30Met familial amyloid polyneuropathy: a considerably different clinical picture and natural course in endemic and non-endemic areas (2012) (8)
An unusual case of Klippel-Trénaunay-Weber syndrome presenting with portosystemic encephalopathy. (2008) (8)
Liver Transplantation Is a Potential Treatment Option for Systemic Light Chain Amyloidosis Patients with Dominant Hepatic Involvement: A Case Report and Analytical Review of the Literature. (2016) (8)
Treatment of Autonomic Dysfunction with L-Threo-3,4-Dihydroxyphenylserine in Patients with Familial Amyloidotic Polyneuropathy: A Multicenter Study (1988) (7)
Multifocal Fibrosclerosis with Hypertrophic Pachymeningitis and a Soft Tissue Mass around the Thoracic Vertebral Bodies: A Case Report with Review of the Literature. (2015) (7)
Slowly progressing lower motor neuron disease caused by a novel duplication mutation in exon 1 of the SOD1 gene (2014) (7)
Nephrotic syndrome due to primary systemic AL amyloidosis, successfully treated with VAD (vincristine, doxorubicin and dexamethasone) alone. (2008) (7)
First two cases of adult‐onset type II citrullinemia successfully treated by deceased‐donor liver transplantation in Japan (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)
Fasciitis in mixed connective tissue disease successfully treated with high-dose intravenous immunoglobulin. (2003) (7)
[Two patients with different types of vasculitic neuropathy--a comparison between cutaneous polyarteritis nodosa and nonsystemic vasculitic neuropathy]. (2003) (7)
High-dose melphalan followed by autologous stem cell support in primary systemic AL amyloidosis with multiple organ involvement. (2005) (7)
Severe amyloid deposition in mammary glands of familial amyloid polyneuropathy patients (2007) (7)
Marked biochemical difference in amyloid proportion between intra- and extraocular tissues in a liver-transplanted patient with hereditary ATTR amyloidosis (2017) (7)
ULTRASTRUCTURAL FINDINGS OF RECTAL AND SKIN BIOPSIES IN ADULT GM1‐GANGLIOSIDOSIS (1986) (7)
Autoantibodies against Autonomic Nerve Receptors in Adolescent Japanese Girls after Immunization with Human Papillomavirus Vaccine (2019) (7)
Severe cranial nerve involvement in a patient with monoclonal anti-MAG/SGPG IgM antibody and localized hard palate amyloidosis (2006) (7)
Hypothalamic encephalitis with bradycardia. (2001) (7)
Liver transplantation as treatment for neurological disorders (2003) (7)
Superficial siderosis associated with aceruloplasminemia. Case report (2014) (7)
[Pathogenesis and treatment of brachial plexus neuritis]. (2013) (7)
Crossed Cerebellar Diaschisis in Status Epilepticus. (2016) (7)
Hemolysis, elevated liver enzymes and low platelet (HELLP) syndrome associated with systemic lupus erythematosus. (2003) (7)
Suspected adverse effects after human papillomavirus vaccination: a temporal relationship (2018) (7)
Delayed domino liver transplantation: use of the remnant liver of a recipient of a temporary auxiliary orthotopic liver transplant as a liver graft for another patient. (2004) (7)
Polyarteritis nodosa with central nervous system involvement mimicking relapsing–remitting multiple sclerosis (2012) (7)
Diagnosis of familial amyloidotic polyneuropathy (1987) (7)
Presenilin-1 exists in the axoplasm fraction in the brains of aged Down's syndrome subjects and non-demented individuals (1999) (6)
Argentinian patients of European ancestry with familial amyloid polyneuropathy (1994) (6)
Prevalence of Fabry disease and GLA c.196G>C variant in Japanese stroke patients (2017) (6)
Pathologic basis of the preferential thinning of thecorpus callosum in adult-onset leukoencephalopathy with axonal spheroids and pigmented glia (ALSP) (2021) (6)
Laryngo-tracheo-bronchial amyloidosis presenting severe airway stenosis. (2006) (6)
Klüver–Bucy syndrome following status epilepticus associated with hepatic encephalopathy (2008) (6)
Biopsy-proven tuberculous meningitis mimicking CNS sarcoidosis. (2007) (6)
On the occurrence of neuronal sprouting in the frontal cortex of a patient with Down’s syndrome (1999) (6)
Coexistence of hemidystonia and hemiballism in a diabetic patient with striatal hyperintensity on T1-weighted MRI (2001) (6)
Senile systemic amyloidosis in an aged savannah monkey (Cercopithecus aethiops) with tenosynovial degeneration. (2010) (6)
Proteomic analysis of leptomeningeal amyloid fibril extracts of cerebral amyloid angiopathy (CAA) patients with or without corticosteroid therapy (2013) (6)
Sjögren syndrome-related plasma cell disorder and multifocal nodular AL amyloidosis: clinical picture and pathological findings (2019) (6)
Congenital fibrosis of the extraocular muscles (CFEOM) syndrome associated with progressive cerebellar ataxia (2007) (6)
[Survey on the attitude toward genetic testing of neurologists certified by the Japanese Society of Neurology]. (2013) (6)
Reactive arthritis due to asymptomatic infection of Chlamydia trachomatis. (2005) (6)
IgM AL amyloidosis due to B cell lymphoproliferative disorder: efficacy of high-dose melphalan followed by autologous stem cell transplantation (2004) (6)
Pictures in clinical medicine. Spinal epidural abscess with osteomyelitis as a cause of bacterial meningitis. (2008) (6)
A study of the morphology and distribution of amyloid beta protein immunoreactive plaque and related lesions in the brains of Alzheimer's disease and adult Down's syndrome. (1989) (6)
Bortezomib–dexamethasone versus high-dose melphalan for Japanese patients with systemic light-chain (AL) amyloidosis: a retrospective single-center study (2017) (6)
Size variance of motor evoked potential at initiation of voluntary contraction in palsy of conversion disorder (2008) (6)
Late-onset autosomal recessive limb-girdle muscular dystrophy with rimmed vacuoles (2004) (6)
Buerger's disease manifesting nodular erythema with livedo reticularis. (2007) (6)
Non-herpetic fulminant meningoencephalitis with periodic lateralised epileptiform discharges (2002) (6)
Isolated autonomic failure without evident somatic polyneuropathy in AL amyloidosis (2014) (5)
Phenotypical analysis of lymphocytes using flow cytometry in dermatomyositis with and without interstitial pneumonia (2006) (5)
Familial amyloid polyneuropathy in Korea: The first case report with a proven ATTR Lys35Asn gene (2005) (5)
Evaluation of intensive chemotherapy in AL amyloidosis: usefulness of flow cytometric analysis of plasma cells in bone marrow (2003) (5)
Discriminative clinical and neuroimaging features of motor-predominant hereditary diffuse leukoencephalopathy with axonal spheroids and primary progressive multiple sclerosis: A preliminary cross-sectional study. (2019) (5)
Pure red cell aplasia developing after treatment of pleural recurrence of thymoma, successfully treated with cyclosporin A but not with tacrolimus. (2006) (5)
Pathological, biochemical, and biophysical characteristics of the transthyretin variant Y114H (p.Y134H) explain its very mild clinical phenotype (2015) (5)
EEG–EMG polygraphic study of dystonia and myoclonus in a case of Creutzfeldt–Jakob disease☆ (2015) (5)
[Localization of NMDAR-related epitopes in ovarian teratoma: comparison between patients and controls]. (2012) (5)
Unilateral oculomotor nerve palsy induced by combination therapy of interferon-alpha2b and ribavirin. (2005) (5)
Correlation between serum levels of free light chain and phenotype of plasma cells in bone marrow in primary AL amyloidosis (2005) (5)
[Hereditary diffuse leukoencephalopathy with axonal spheroids (HDLS): its clinical concept and the review of the previously reported cases]. (2012) (5)
Lip biopsy in Mikulicz's disease phenotype IgG4-related disease. (2013) (5)
[Cerebral amyloid angiopathy with familial transthyretin-derived oculoleptomeningeal amyloidosis]. (2013) (5)
Paradoxical modulation of tendon tap reflex during voluntary contraction in Parkinson's disease (2005) (5)
Patient with adult‐onset type II citrullinemia beginning 2 years after operation for duodenal malignant somatostatinoma: Indication for liver transplantation (2013) (5)
Intestinal angina due to atherosclerosis in a 45-year-old systemic lupus erythematosus patient. (2010) (5)
Expression of N-methyl-D-aspartate receptor subunits in the bovine ovum: ova as a potential source of autoantigens causing anti-NMDAR encephalitis. (2015) (4)
[Diagnostic significance of technetium-99m-pyrophosphate, technetium-99m-methylene diphosphonate and gallium-67-citrate scintigraphy in amyloid heart disease--a study with AL amyloidosis and familial amyloid polyneuropathy]. (1986) (4)
Adalimumab Monotherapy in a Patient with Psoriatic Arthritis Associated with Chronic Renal Failure on Hemodialysis: A Case Report and Literature Review (2012) (4)
[A clinically diagnosed lymphocytic hypophysitis presenting as recurrent meningitis]. (2007) (4)
Senile systemic amyloidosis: clinical pictures and diagnostic criteria (2011) (4)
Marked intrafamilial phenotypic variation in a family with SOD1 C111Y mutation (2012) (4)
[Neurologic Complications in HPV Vaccination]. (2015) (4)
Japanese family with an autosomal dominant chromosome instability syndrome: a new neurodegenerative disease? (2000) (4)
A New procedure for temporary auxiliary partial liver transplantation using living donor graft for patients with familial amyloid polyneuropathy (2012) (4)
A novel RNA splice site mutation in the C1 inhibitor gene of a patient with type I hereditary angioedema. (2004) (4)
Cytomegalovirus-induced infectious mononucleosis-like syndrome in a rheumatoid arthritis patient treated with methotrexate and infliximab. (2010) (4)
Clinical Trial for Ttr Amyloidosis Using Diflunisal (2007) (4)
[Analysis of 14 individuals who requested predictive genetic testing for hereditary neuromuscular diseases]. (2002) (4)
[Lower urinary tract dysfunction and neuropathological findings of the neural circuits controlling micturition in familial amyotrophic lateral sclerosis with L106V mutation in the SOD1 gene]. (2016) (4)
Clinical and Pathological Studies of Familial Amyloid Polyneuropathy (FAP), with Special Reference to Nephropathy and Cardiopathy (1986) (3)
Tafamidis dramatically improved severe proteinuria in a patient with TTR V30M hereditary ATTR amyloidosis (2019) (3)
Clinicopathological Studies on Nephropathy of Familial Amyloid Polyneuropathy in Japan (1988) (3)
Extremely early onset hereditary ATTR amyloidosis with G47R (p.G67R) mutation (2016) (3)
Recurrent steroid-responsive trismus and painful ophthalmoplegia (1999) (3)
Evaluation of Variant Transthyretins for Diagnosis and Pathogenesis of Familial Amyloidotic Polyneuropathy (2009) (3)
[Liver transplantation in metabolic diseases]. (1995) (3)
Marked shrinkage of amyloid lymphadenopathy after an intensive chemotherapy in a patient with IgM-associated AL amyloidosis (2009) (3)
Coexistence of IgA nephropathy and undifferentiated spondyloarthropathy in a female patient (2006) (3)
Inadequate Modulation of Excitability With Voluntary Dorsiflexion in Parkinson's Disease (2014) (3)
Surgical removal of amyloid-laden lymph nodes: a possible therapeutic approach in a primary systemic AL amyloidosis patient with focal lymphadenopathy (2011) (3)
A survey of epidemiology, clinical picture, and current treatments for elderly-onset (≥ 65) patients with myasthenia gravis in Nagano Prefecture, Japan (2017) (3)
On the errors in assessment of severity of involuntary movements using surface EMG. (2005) (3)
Paraneoplastic neurologic syndrome associated with small breast cancer: diagnostic value of FDG-PET for detection of underlying malignancy. (2005) (3)
[A case of Guillain-Barré syndrome starting from severe upper back pain]. (2003) (3)
Presurgical Factors Affecting Patient Satisfaction with Pallidal Surgery in Parkinson’s Disease (2006) (3)
Unusual clinical manifestations of primary systemic AL amyloidosis: are myasthenic symptoms and dilated cardiomyopathy caused by muscular or myocardial amyloid angiopathy? (2006) (3)
Intractable Cutaneous Nontuberculous Mycobacteriosis (Mycobacterium abscessus) during Treatment for Systemic Lupus Erythematosus (2017) (3)
Cancer-associated retinopathy in a patient with seminoma. (2011) (3)
Human Papillomavirus (HPV) Vaccination: Just the Facts. (2015) (2)
Regression of localized ureter amyloidosis after treatment with steroids suggested by Tc-99 m pyrophosphate scintigraphy (2015) (2)
Amyloid neuropathy and autonomic dysfunction (2022) (2)
Rituximab therapy in nephrotic syndrome due to AH amyloidosis (2009) (2)
Extrinsic and Intrinsic Nerve Lesions of the Intestine in Type I Familial Amyloid Polyneuropathy (1991) (2)
[Two patients with pseudogout manifested by severe neck pain]. (2002) (2)
Human Papillomavirus (HPV) Vaccination Safety Assessment: The Methods Matter. (2015) (2)
[Adult-onset citrullinemia]. (2007) (2)
[Cerebral amyloid angiopathy]. (2011) (2)
Motor Branch Biopsy of the Pronator Teres Muscle in a Patient with Painful Forearm Neuropathy (2014) (2)
Successful Pharmacotherapy for an Adult Case with Prolonged Symptoms of Postganglionic Cholinergic Dysautonomia (2004) (2)
Huntington’s disease with onset ages greater than 60 years (2007) (2)
[Autonomic dysfunction in FAP: its therapeutic effect by liver transplantation]. (2006) (2)
[Diagnosis of familial amyloid polyneuropathy--gene analysis with primer-directed enzymatic amplification of DNA, isolation of plasma variant prealbumin and immunohistochemical identification of tissue amyloid protein]. (1991) (2)
[Neuropsychiatric systemic lupus erythematosus associated with anti-phospholipid syndrome, showing massive intracranial calcifications]. (2003) (2)
Coexistence of familial transthyretin amyloidosis ATTR Val30Met and spinocerebellar ataxia type 1 in a Japanese family – A follow-up autopsy report (2004) (2)
Massive mesenteric edema in a patient with type I hereditary angioedema (2005) (2)
No association between apolipoprotein E epsilon4 allele and the age of onset in type I familial amyloid polyneuropathy. (1996) (2)
Localized amyloidogenic immunoglobulin light chain-derived amyloidosis in a young boy and an adolescent girl (2017) (2)
[Therapeutic strategy for familial amyloid polyneuropathy (FAP)]. (2009) (1)
An Abnormal MRI Signal in Both Lateral Geniculate Bodies Is a Diagnostic Indicator for Patients with Behçet's Disease (2014) (1)
Elevated serum levels of heat-shock protein (HSP) 70 and 90 in patients with ALS (2015) (1)
[Metabolic turn over of amyloid fibrils and post-treatment regression of amyloid deposits in systemic amyloidosis with polyneuropathy]. (2011) (1)
Migrating osteoarthralgia: a rare initial manifestation of adult leukemia. (2006) (1)
[Dropped head sign and tongue atrophy in systemic sclerosis-associated myopathy: a case report]. (2010) (1)
[A 36-year-old woman with primary central nervous system lymphoma diagnosed by twice brain biopsies, showing relapsing and remitting brain lesions]. (2018) (1)
The urinary glycosaminoglycans in pachydermoperiostosis. (1974) (1)
[Identification of NMDA receptor in normal bovine ovary and ovum]. (2014) (1)
A Long-Term Observation on the Possible Adverse Effects in Japanese Adolescent Girls after Human Papillomavirus Vaccination (2021) (1)
[Familial amyloidosis with polyneuropathy presenting restrictive cardiomyopathy as its main manifestation]. (1984) (1)
[Adult-onset citrullinemia]. (2007) (1)
[Upper gastrointestinal lesions in familial polyposis of the colon]. (1975) (1)
Impaired left ventricular diastolic filling inpatients withfamilial amyloid polyneuropathy: apulsed Doppler echocardiographic study (1989) (1)
Hereditary amyloid polyneuropathy-related destructive arthropathy in a hip joint (2017) (1)
Life-threatening orthostatic hypotension in a case with bulbo-myelo-radiculo-neuropathy (2001) (1)
Development of High-Grade Ventricular Arrhythmias in Familial Amyloid Polyneuropathy (1988) (1)
Marked shrinkage of amyloid lymphadenopathy after an intensive chemotherapy in a patient with IgM-associated AL amyloidosis (2009) (1)
Disruption of blood–nerve barriers in hereditary transthyretin (ATTR) amyloidosis (2017) (1)
[Autonomic nerve disorders in generalized amyloidosis]. (1992) (1)
Prealbumin type cerebral amyloid angiopathy in familial amyloid polyneuropathy (1991) (1)
[Current status of the predictive genetic testing for hereditary neurological diseases in Shinshu University Hospital]. (2013) (1)
[A Case of Microscopic Polyangiitis with Hypertrophic Pachymeningitis and Diabetes Insipidus]. (2015) (1)
Protein-losing Gastroenteropathy Related to Mixed Connective Tissue Disease: A Case Report of a Successful Outcome and Literature Review (2017) (1)
[Dementia due to sarcoidosis]. (2004) (1)
[A case progressive dementia developed after repeated head trauma]. (1991) (1)
CEREBRAL AMYLOID AND ALZHEIMER'S DISEASE — EVIDENCE FOR THE DERIVATION OF A PEPTIDE LIGAND FROM THE β PROTEIN PRECURSOR (1988) (1)
Acknowledgment to reviewers (2013) (1)
Monoarthropathy or Polyarthritis in Adolescent Japanese Girls Who Received Immunization with the Human Papillomavirus Vaccine (2016) (1)
Unexpected Occurrence of Fetal Hemophagocytic Syndrome in a Patient with Hereditary Diffuse Leukoencephalopathy with Spheroids (2016) (1)
Painful ophthalmoplegia due to inflammation of the cavernous sinus in a patient with familial Mediterranean fever (2017) (1)
Evidence for the derivation of a peptide ligand from the amyloid beta-protein precursor of Alzheimer's disease. (1989) (1)
Baseline nutritional status in symptomatic patients in the transthyretin amyloidosis outcomes survey (thaos) (2011) (1)
Cerebral Amyloid Angiopathy-related Microbleeds: Radiology versus Pathology. (2016) (1)
Recurrent Cerebral Infarctions caused by Intravascular Lymphoma Diagnosed by Brain Biopsy : A Case Report (2012) (1)
[Can prion-like propagation occur in neurodegenerative diseases?: in view of transmissible systemic amyloidosis]. (2012) (1)
[Peripartum cardiomyopathy of multiple pregnancy]. (1996) (1)
A pedigree analysis withminimised ascertainment biasshowsanticipation inMet3O-transthyre tin related familial amyloid polyneuropathy (1998) (0)
472 Cerebral white matter pathology in Down's syndrome patients with Alzheimer type dementia (1996) (0)
Biochemical analysis of deposited amyloid fibrils—Analysis of amyloid protein extracted from small biopsy samples (2010) (0)
Long-term Follow-up Studies of Posterior Fusion of the Upper Spine in Rheumatoid Arthritis (2005) (0)
longitudinally within the dural space and invades into the vertebral bone. 1 These images clearly show a rarely (2013) (0)
Table 2. [Phenotypes Associated with Familial Transthyretin Amyloidosis]. (2012) (0)
Clinical Management of AntiN-Methyl-D-Aspartate Receptor(NMDAR)Encephalitis Localization of NMDAR-related epitopes in ovarian teratoma : comparison between patients and controls (2012) (0)
[Barth syndrome (X linked cardioskeletal myopathy and neutropenia)]. (2002) (0)
[Liver transplantation for familial amyloidosis]. (2006) (0)
P-126 Diagnosis of Cardiac Amyloidosis with Quantitative Analysis of Myocardial Technetium-99m-Pyrophosphate Scintigraphy (2009) (0)
[Mohr-Tranebjaerg syndrome]. (2002) (0)
4. Vasculitis Syndrome (2010) (0)
[Tuberculous pleuritis and tuberculous empyema]. (1994) (0)
Tuberculous Cold Abscess in the Axillary Lymph Nodes (2012) (0)
17. Inadequate spinal inhibitory control in a patient with Stiff-person syndrome (2009) (0)
Noninvasive Evaluation of Left Ventricular Systolic and Diastolic Time Intervals in Familial Amyloid Polyneuropathy (1988) (0)
The Author Reply: A Truly Unusual Vascular Overgrowth Syndrome (2009) (0)
Coexistence of type i familial amyloid polyneuropathy and spinocerebellar ataxia type i. Pathological study and gene analysis of a Japanese family (1996) (0)
Influence of prednisolone on β-secretase enzyme activity in vitro (2003) (0)
P37.2 The safety of transcranial magnetic stimulation in patients treaded with deep brain stimulation (2006) (0)
Lupus erythematosus profundus ( lupus panniculitis ) induced by interferon-β in a patient with multiple sclerosis (2007) (0)
Alpha-Adrenergic Receptors in Familial Amyloidotic Polyneuropathy (1988) (0)
[Two cases with chronic inflammatory demyelinating polyneuropathy showing high signal and enlargement of the brachial plexus in short TI inversion recovery of MRI]. (1999) (0)
Therapuetic approaches to the intractable diseases: Chairman's remark (2001) (0)
Shinshu Brain Resource Net (2016) (0)
Apolipoprotein e genotype and familial amyloidotic polyneuropathy type I (1996) (0)
[Serial brain MRI findings of a patient with thrombotic thrombocytopenic purpura complicated by malignant hypertension and reversible posterior leukoencephalopathy syndrome]. (2004) (0)
A Case with XXXX Syndrome Who Was Incidentally Diagnosed during Examination for Suspected Post-Human Papillomavirus Vaccination Syndrome (2019) (0)
[Recent advances of the treatment in metabolic disorders]. (2000) (0)
Editorial Amyloid fibril protein (2002) (0)
A Histochemical, Immunohistochemical, Ultrastructural and Immunoelectron Microscopical Characterization of Cerebrovascular Amyloid and Diffuse Plaques in Autopsied Aged Dogs (1991) (0)
Table 5. [TTR Variants and Their Phenotypes]. (2012) (0)
[Development by researchers in academia of disease modifying drugs for neurological disorders]. (2010) (0)
Proposed Diagnostic Criteria for Adult-onset Leukoencephalopathy with Axonal Spheroids and Pigmented Glia (P2.238) (2016) (0)
Lesions in nerve ganglia of the rectum in type 1 familial amyloid polyneuropathy. Histochemical and immunohistochemical study (1992) (0)
[Kinetics of inflammatory cytokines during hyperacute phase of ischemic stroke]. (2006) (0)
Renal lesions in Cockyne's syndrome (1966) (0)
Clinic of familial amyloid polyneuropathy. (1992) (0)
A Case of Pectoral Fasciitis with Spontaneous Remission (2000) (0)
6. Response property of soleus motoneuron pool to inhibitory input in Parkinson’s disease (2010) (0)
Advantage of administering tacrolimus for improving the prognosis in polymyositis and dermatomyositis (2018) (0)
[May-white syndrome (myoclonus, ataxia, deafness)]. (2002) (0)
Clinical assessment of standing and gait in ataxic patients using a triaxial accelerometer (2015) (0)
Dynamic changes of axons and microglial subsets in corpus callosum in patients with adult onset leukoencephalopathy with axonal spheroids and pigmented glia (ALSP) (2017) (0)
155. Nerve conduction in symptomatic patients in the transthyretin amyloidosis outcomes survey (2012) (0)
The unique characteristics of spasticity in a patient with Type II (adult onset) citrullinaemia (2007) (0)
A survey on transition from pediatric to adult care for patients with Wilson disease (2020) (0)
[Neuroleptoanalgesic methods]. (1968) (0)
Tacrolimus Related Brady and Tachyarrhythmias in a Familial Amyloid Polyneuropathy Patient who Underwent Partial Liver Transplantation (2001) (0)
Subject Index Vol. 51, 2004 (2004) (0)
[The pathogenesis of Alzheimer's disease demonstrated by immunocytochemistry with anti-beta-protein antibody]. (1992) (0)
497 Alzheimer-type dementia and apolipoprotein E phenotypes in Japanese patients with down's syndrome (1996) (0)
FOCUS REVIEWS ON IMAGING : Echocardiographic Assessment of the Cardiac Amyloidoses (2015) (0)
Peptide histidine methionine- and substance P-immunoreactive nerves in endoscopic biopsies of human rectal mucosa (1990) (0)
M-MODE AND TWO-DIMENSIONAL ECHOCARDIOGRAPHIC FEATURES OF FAMILIAL AMYLOID POLYNEUROPATHY : PROCEEDINGS OF THE 47th ANNUAL SCIENTIFIC MEETING OF THE JAPANESE CIRCULATION SOCIETY : Cardiomyopathy (1983) (0)
New criteria of suspected adverse symptoms related human papillomavirus vaccination (2017) (0)
Acknowledgement to Referees (2017) (0)
Principal component analysis for ataxic gait using a triaxial accelerometer (2017) (0)
Hemophagocytic syndrome associated with rheumatoid arthritis : A case report and review of the literature (2008) (0)
A STUDY OF THE DISTRIBUTION OF AMYLOID B PROTEIN IMMUNOREACTIVITY IN ALZHEIMER'S DISEASE AND NON‐ALZHEIMER CONTROLS (1988) (0)
40th Annual Meeting of the Japanese Society of Neuropathology 3–5 June 1999 Pacifico Yokohama, JapanPresident: Kenji Kosaka (1999) (0)
[Cervical myelopathy in a patient with congenital cervico-cerebral vascular malformation]. (2004) (0)
Early Detection of Amyloid Heart Disease by Technetium-99M-Pyrophosphate Single-Photon Emission-Computed Tomography : A Study with Familial Amyloid Polyneuropathy (1988) (0)
[Clinicopathological conference: a case presenting symptoms of cognition disorder and spasm and resulting in sudden death due to gastrointestinal hemorrhage]. (1973) (0)
Familial Amyloid Polyneuropathy and the Treatment by Plasmapheresis or Liver Transplantation (2001) (0)
Doppler echocardiographic study . amyloid polyneuropathy : a pulsed filling in patients with familial Impaired left ventricular diastolic (2005) (0)
Crystal Deposition Disease of the Cervical Spine : A Common Cause of Acute Neck Pain Encountered in the Neurology (2013) (0)
[The 40th scientific meeting: perspectives of internal medicine; present situation and future extension of organ transplantation in Japan 9. Summary]. (2013) (0)
Table 1. [Summary of Molecular Genetic Testing Used in Familial Transthyretin Amyloidosis]. (2012) (0)
[Hereditary amyloidosis]. (2000) (0)
Living-related liver transplantation for the patients with familial amyloid polyneuropathy (1996) (0)
Clinical Status and Daily-Life Activity of Patients with Amyotrophic Lateral Sclerosis in Nagano Prefecture (2007) (0)
Alpha 2-adrenergic receptor in familial amyloidotic polyneuropathy. (1987) (0)
Trientine increases fecal copper excretion in Wilson's disease: A case report (2001) (0)
Contents Vol. 51, 2004 (2004) (0)
[Table, GeneReview Scope]. (2012) (0)
Coexistence of Copper in the Iron-Rich Particles of Aceruloplasminemia Brain (2016) (0)
A 67‐Year‐Old Man with Leg Weakness and Hypertrophic Cardiomyopathy (2020) (0)
Long-term Trial of Corticosteroid Therapy for the Recurrence of Cerebral Amyloid Angiopathy-related Hemorrhages : A Case Study Using [11C] BF-227 Amyloid-PET (2014) (0)
Amyloid β-protein pathology (in Japanese) (1990) (0)
[Cardiac tamponade, dyspnea, edema and ascites (thoracic radiography and echocardiography): (mediastinal tumor suggestive of yolk sac tumor)]. (1977) (0)
Presymptomatic gene testing and genetic counselling of familial amyloid polyneuropathy. A trial on Japanese kindreds (1996) (0)
Living donor liver transplantation using a graft with periportal fibrosis (2015) (0)
[Gene diagnosis of hereditary neurological disorders]. (1994) (0)
P37.1 Transcranial magnetic stimulation in hysterical palsy (2006) (0)
[Prion disease in animals and experimental prion disease]. (1997) (0)
Impaired Left Ventricular Diastolic Properties in Patients with Familial Amyloid Polyneuropathy : A Study by Computerized M-Mode Echocardiography (1988) (0)
Table 4. [Other Hereditary Amyloidoses]. (2012) (0)
[Amyloid neuropathy]. (2002) (0)
The 31st Neuropathological Meeting of Joh‐shin‐etsu District 29 October 2005 (2006) (0)
Communication support project for patients with an intractable neurological disease (2017) (0)
Natural History of Spinocerebellar Ataxia Type 31: a 4-Year Prospective Study (2016) (0)
[Pathophysiological variability and its cause of familial amyloid polyneuropathy]. (1994) (0)
Bullous formation in a patient with familial amyloid polyneuropathy type I (2013) (0)
[Characterization of amyloidosis]. (2014) (0)
Phosphorylated MTOR in the spinal anterior horn cells of patients with sporadic amyotrophic lateral sclerosis (2017) (0)
Semiquantitative estimation of severity of immunoreactive lesions in the cases with Down ' s syndrome (2006) (0)
[Chronic inflammatory demyelinating polyradiculoneuropathy(CIDP): Treatment and prognosis]. (2015) (0)
Table 3. [Symptoms at Presentation of Familial Amyloid Polyneuropathy]. (2012) (0)
Safety and Efficacy of Long-Term Diflunisal Administration in Familial Amyloid Polyneuropathy (PD1.009) (2013) (0)
Treatment of autonomic disorders in familial amyloid polyneuropathy with l-threo-3,4-dihydroxyphenilserine (1987) (0)
[Basal cell nevus syndrome]. (1977) (0)
Introduction (2003) (0)
Anticipation and multiple origins in familial amyloid polyneuropathy with transthyretin-Met30 in Japan (1996) (0)
Subject Index Vol. 32, 1992 (1992) (0)
Consultants for the American Journal aof Nephrology 1998 (1998) (0)
Immunohistochemical studies of cerebrovascular amyloid deposits in brains with cerebral amyloid angiopathy (1989) (0)
[Neuralgic amyotrophy]. (2014) (0)
[The 40th scientific meeting: perspectives of internal medicine; present situation and future extension of organ transplantation in Japan; 7. Liver transplanation for hereditary diseases]. (2013) (0)

This paper list is powered by the following services:

What Schools Are Affiliated With Shu‐ichi Ikeda?

Shu‐ichi Ikeda is affiliated with the following schools:

Shu‐ichi Ikeda's Academic­Influence.com Rankings

Shu‐ichi Ikeda's Degrees

Why Is Shu‐ichi Ikeda Influential?

Shu‐ichi Ikeda's Published Works

Published Works

What Schools Are Affiliated With Shu‐ichi Ikeda?

Shu‐ichi Ikeda's AcademicInfluence.com Rankings