Progressive supranuclear palsy: clinical and pathological diagnosis.

about

FMR1 gray-zone alleles: association with Parkinson's disease in women?Clinical Phenotype of Adult Fragile X Gray Zone Allele Carriers: a Case Series.Further extension of the H1 haplotype associated with progressive supranuclear palsy

P2860

Q37601806-EC3D9772-0A71-4F3D-88AA-27E4B4B90765 Q46018564-5A3D0B51-8969-4EA1-A2CF-111C6ADD92D0 Q57814754-2EEDBEA2-10A6-47F7-98FA-C45547867DE6

P2860

Progressive supranuclear palsy: clinical and pathological diagnosis.

Item

http://www.wikidata.org/entity/Q38166808

description

article científic

@ca

article scientifique

@fr

articol științific

@ro

articolo scientifico

@it

artigo científico

@gl

artigo científico

@pt

artigo científico

@pt-br

artikel ilmiah

@id

artikull shkencor

@sq

artículo científico

@es

name

Progressive supranuclear palsy: clinical and pathological diagnosis.

@en

type

Item

label

Progressive supranuclear palsy: clinical and pathological diagnosis.

@en

prefLabel

Progressive supranuclear palsy: clinical and pathological diagnosis.

@en

P1476

Progressive supranuclear palsy: clinical and pathological diagnosis.

@en

P2093

E Tolosa

http://www.w3.org/2001/XMLSchema#string

F Cruz-Sánchez

http://www.w3.org/2001/XMLSchema#string

F Valldeoriola

http://www.w3.org/2001/XMLSchema#string

P2860

Morphological overlap between corticobasal degeneration and Pick's disease: a clinicopathological report

Ubiquitin is associated with abnormal cytoplasmic filaments characteristic of neurodegenerative diseases.

A case of progressive subcortical gliosis presenting clinically as Steele-Richardson-Olszewski syndrome.

Progressive supranuclear palsy: neuropathologically based diagnostic clinical criteria.

Differential distribution of neurofibrillary tangles in the cerebral cortex of dementia pugilistica and Alzheimer's disease cases.

PROGRESSIVE SUPRANUCLEAR PALSY. A HETEROGENEOUS DEGENERATION INVOLVING THE BRAIN STEM, BASAL GANGLIA AND CEREBELLUM WITH VERTICAL GAZE AND PSEUDOBULBAR PALSY, NUCHAL DYSTONIA AND DEMENTIA.

Neuronal loss in the pedunculopontine tegmental nucleus in Parkinson disease and in progressive supranuclear palsy

Progressive supranuclear palsy: neuropathologic and clinical heterogeneity.

Argyrophilic grains: characteristic pathology of cerebral cortex in cases of adult onset dementia without Alzheimer changes.

Parkinsonism-dementia complex, an endemic disease on the island of Guam. II. Pathological features.

P304

259-273

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1111/J.1468-1331.1995.TB00129.X

http://www.w3.org/2001/XMLSchema#string

P433

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P577

1995-09-01T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P698

24283678

http://www.w3.org/2001/XMLSchema#string

Progressive supranuclear palsy: clinical and pathological diagnosis.

about

P2860

P2860

Progressive supranuclear palsy: clinical and pathological diagnosis.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P698

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P698