Shigeo Murayama

Neuropathologic analysis of Lewy-related α-synucleinopathy in olfactory mucosa.

[Argyrophilic grain dementia].

[Braak staging].

[Prognosis of amyotrophic lateral sclerosis in relation with pathological pattern of propagation].

Increased number of astrocytes and macrophages/microglial cells in the corpus callosum in amyotrophic lateral sclerosis.

ERBB4 mutations that disrupt the neuregulin-ErbB4 pathway cause amyotrophic lateral sclerosis type 19.

Imaging spectrum of sporadic cerebral amyloid angiopathy: multifaceted features of a single pathological condition.

Lack of genetic association between TREM2 and late-onset Alzheimer's disease in a Japanese population.

Alpha-synuclein immunohistochemistry of gastrointestinal and biliary surgical specimens for diagnosis of Lewy body disease.

Clinical features of genetic Creutzfeldt-Jakob disease with V180I mutation in the prion protein gene.

An aberrant sugar modification of BACE1 blocks its lysosomal targeting in Alzheimer's disease.

Sporadic Creutzfeldt-Jakob Disease MM1+2C and MM1 are Identical in Transmission Properties.

Variants associated with Gaucher disease in multiple system atrophy.

Identification of Neurexophilin 3 as a Novel Supportive Factor for Survival of Induced Pluripotent Stem Cell-Derived Dopaminergic Progenitors.

I2020T mutant LRRK2 iPSC-derived neurons in the Sagamihara family exhibit increased Tau phosphorylation through the AKT/GSK-3β signaling pathway.

The feasibility of white matter volume reduction analysis using SPM8 plus DARTEL for the diagnosis of patients with clinically diagnosed corticobasal syndrome and Richardson's syndrome.

Aging-related tau astrogliopathy (ARTAG): harmonized evaluation strategy.

Estradiol Facilitates Functional Integration of iPSC-Derived Dopaminergic Neurons into Striatal Neuronal Circuits via Activation of Integrin α5β1.

Prion-Seeding Activity Is widely Distributed in Tissues of Sporadic Creutzfeldt-Jakob Disease Patients.

Histopathologic Analysis of Cerebral Autosomal Recessive Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CARASIL): A Report of a New Genetically Confirmed Case and Comparison to 2 Previous Cases.

Simultaneous skin-nerve-muscle biopsy and abnormal mitochondrial inclusions in intranuclear hyaline inclusion body disease.

LRRK2 levels and phosphorylation in Parkinson's disease brain and cases with restricted Lewy bodies.

Excess APP O-glycosylation by GalNAc-T6 decreases Aβ production.

Serum microRNA miR-501-3p as a potential biomarker related to the progression of Alzheimer's disease.

Unusual tau pathology of the cerebellum in patients with amyotrophic lateral sclerosis/parkinsonism-dementia complex from the Kii Peninsula, Japan.

Prion-Like Seeding of Misfolded α-Synuclein in the Brains of Dementia with Lewy Body Patients in RT-QUIC.

Pathologic Study of Intracranial Large Artery Atherosclerosis in 7260 Autopsy Cases.

Optineurin pathology in the spinal cord of amyotrophic lateral sclerosis/parkinsonism-dementia complex patients in Kii Peninsula, Japan.

Does Parkinson's disease start in the gut?

DNA methylation level of the neprilysin promoter in Alzheimer's disease brains.

Spinocerebellar ataxia type 2 presenting with rapidly progressing muscle weakness and muscular atrophy.

Neuronal intranuclear hyaline inclusion disease presenting with childhood-onset night blindness associated with progressive retinal dystrophy.

Potent prion-like behaviors of pathogenic α-synuclein and evaluation of inactivation methods.

Soluble epoxide hydrolase plays a key role in the pathogenesis of Parkinson's disease.

TAR DNA-Binding Protein 43 and Disrupted in Schizophrenia 1 Coaggregation Disrupts Dendritic Local Translation and Mental Function in Frontotemporal Lobar Degeneration.

Distinct Incidence of Takotsubo Syndrome Between Amyotrophic Lateral Sclerosis and Synucleinopathies: A Cohort Study.