Shu‐ichi Ikeda
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Philosophy Biology
Shu‐ichi Ikeda's Degrees
- PhD Biochemistry Kyoto University
- Doctorate Medicine Kyoto University
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(Suggest an Edit or Addition)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)
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What Schools Are Affiliated With Shu‐ichi Ikeda?
Shu‐ichi Ikeda is affiliated with the following schools: