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Neuromelanin magnetic resonance imaging of locus ceruleus and substantia nigra in Parkinson??s diseaseMorphometrical reappraisal of motor neuron system of Pick's disease and amyotrophic lateral sclerosis with dementiaSporadic amyotrophic lateral sclerosis of long duration mimicking spinal progressive muscular atrophy exists: additional autopsy case with a clinical course of 19 yearsSporadic amyotrophic lateral sclerosis with circumscribed temporal atrophy: a report of an autopsy case without dementia and with ubiquitinated intraneuronal inclusions.IGFBP3 colocalizes with and regulates hypocretin (orexin)Progressive nonfluent aphasia: a rare clinical subtype of FTLD-TDP in Japan.Different immunoreactivities of the microtubule-binding region of tau and its molecular basis in brains from patients with Alzheimer's disease, Pick's disease, progressive supranuclear palsy and corticobasal degeneration.Pick body disease and Pick syndrome.Preservation of nigral neurons in Pick's disease with Pick bodies: a clinicopathological and morphometric study of five autopsy cases.Clinical heterogeneity in progressive supranuclear palsy: problems of clinical diagnostic criteria of NINDS-SPSP in a retrospective study of seven Japanese autopsy cases.Parkinson's disease mimicking senile dementia of the Alzheimer type: a clinicopathological study of four autopsy cases.Clinicopathological characterization of Pick's disease versus frontotemporal lobar degeneration with ubiquitin/TDP-43-positive inclusions.Coexistence of CJD and Alzheimer's disease: an autopsy case showing typical clinical features of CJD.Motor neuron disease group accompanied by inclusions of unidentified protein signaled by ubiquitin.The 28-amino acid form of an APLP1-derived Abeta-like peptide is a surrogate marker for Abeta42 production in the central nervous system.Constant and severe involvement of Betz cells in corticobasal degeneration is not consistent with pyramidal signs: a clinicopathological study of ten autopsy cases."Forme fruste" of amyotrophic lateral sclerosis with dementia: a report of five autopsy cases without dementia and with ubiquitinated intraneuronal inclusions.Posterior spinal artery syndrome showing marked swelling of the spinal cord: a clinico-pathological study.Phosphorylated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis.Phosphorylated and cleaved TDP-43 in ALS, FTLD and other neurodegenerative disorders and in cellular models of TDP-43 proteinopathy.Ubiquitin-positive frontotemporal lobar degeneration presenting with progressive Gogi (word-meaning) aphasia. A neuropsychological, radiological and pathological evaluation of a Japanese semantic dementia patient.Frontotemporal lobar degeneration with ubiquitin pathology: an autopsy case presenting with semantic dementia and upper motor neuron signs with a clinical course of 19 years.Clinicopathological characteristics of FTLD-TDP showing corticospinal tract degeneration but lacking lower motor neuron loss.The role of G-protein-coupled receptor kinase 5 in pathogenesis of sporadic Parkinson's disease.Fatal encephalitis in a case of hypereosinophilic syndrome: MRI and autopsy findings.[An autopsied case of schizophrenic patient who died from heat stroke].Increased expression of neuronal apolipoprotein E in human brain with cerebral infarction.An atypical autopsy case of Lewy body disease with clinically diagnosed major depression: a clinical, radiological and pathological study.Basal ganglia lesions in 'Pick complex': a topographic neuropathological study of 19 autopsy cases.Glial clusters and perineuronal glial satellitosis in the basal ganglia of neurofibromatosis type 1.Progressive supranuclear palsy combined with Alzheimer's disease: a clinicopathological study of two autopsy cases.Pick-body-like inclusions in corticobasal degeneration differ from Pick bodies in Pick's disease.TDP-43 M337V mutation in familial amyotrophic lateral sclerosis in Japan.Pathological features of FTLD-FUS in a Japanese population: analyses of nine cases.Frequency and clinicopathological characteristics of alcoholic cerebellar degeneration in Japan: a cross-sectional study of 1,509 postmortems.Prion disease causes less severe lesions in human hippocampus than other parts of brain.[123I] meta-iodobenzylguanidine myocardial scintigraphy differentiates corticobasal degeneration from Parkinson's disease.Microglial tau undergoes phosphorylation-independent modification after ischemia.Immunohistochemical study of tau accumulation in early stages of Alzheimer-type neurofibrillary lesions.14-3-3 proteins and zeta isoform containing neurofibrillary tangles in patients with Alzheimer's disease.
P50
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P50
name
Kuniaki Tsuchiya
@en
Kuniaki Tsuchiya
@nl
type
label
Kuniaki Tsuchiya
@en
Kuniaki Tsuchiya
@nl
prefLabel
Kuniaki Tsuchiya
@en
Kuniaki Tsuchiya
@nl