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「"Gelpi E "[Author]」の検索結果

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Anti-IGLON5 disease: A new case without neuropathologic evidence of brainstem tauopathy.

Teaching case 1-2020: Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia - An unusual cause of dementia.

Validation of the movement disorder society criteria for the diagnosis of 4-repeat tauopathies.

A unique common ancestor introduced P301L mutation in MAPT gene in frontotemporal dementia patients from Barcelona (Baix Llobregat, Spain).

p.V363I mutation: A rare cause of corticobasal degeneration.

Susceptibility-Weighted MR Imaging Hypointense Rim in Progressive Multifocal Leukoencephalopathy: The End Point of Neuroinflammation and a Potential Outcome Predictor.

Teaching case 3-2019: Are nuclear clefts or invaginations the niche of intranuclear inclusions in FTLD-TDP?

Nanoscale structure of amyloid-β plaques in Alzheimer's disease.

Combined Transcriptomics and Proteomics in Frontal Cortex Area 8 in Frontotemporal Lobar Degeneration Linked to C9ORF72 Expansion.

FXTAS: regional decrease of mitochondrial DNA copy number relates to clinical manifestations.

How to apply the movement disorder society criteria for diagnosis of progressive supranuclear palsy.

Brain tyrosinase overexpression implicates age-dependent neuromelanin production in Parkinson's disease pathogenesis.

Accumulation of prion protein in the vagus nerve in Creutzfeldt-Jakob disease.

Co-morbid demyelinating lesions and atypical clinical features in a patient with Parkinson's disease.

Teaching case 2-2019: Macrophagic scavenging of Aβ.

Lymphomatosis cerebri and anti-NMDAR antibodies: A unique constellation.

Myoclonus-Dominant Corticobasal Degeneration.

An Integrative Study of Protein-RNA Condensates Identifies Scaffolding RNAs and Reveals Players in Fragile X-Associated Tremor/Ataxia Syndrome.

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