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Pathological, clinical and genetic heterogeneity in progressive supranuclear palsy.

Pathological, clinical and genetic heterogeneity in progressive supranuclear palsy.

http://www.wikidata.org/entity/Q33183604

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Hypokinesia without decrement distinguishes progressive supranuclear palsy from Parkinson's disease Differentiation of progressive supranuclear palsy: clinical, imaging and laboratory tools.Characteristics of two distinct clinical phenotypes in pathologically proven progressive supranuclear palsy: Richardson's syndrome and PSP-parkinsonism.Clinical outcomes of progressive supranuclear palsy and multiple system atrophy.Saccade abnormalities in autopsy-confirmed frontotemporal lobar degeneration and Alzheimer disease.Voxel-based morphometry in autopsy proven PSP and CBD Gray matter atrophy in progressive supranuclear palsy: meta-analysis of voxel-based morphometry studies.The phenotypic spectrum of progressive supranuclear palsy: a retrospective multicenter study of 100 definite cases.Transcranial brain sonography findings in two main variants of progressive supranuclear palsy.Clinical outcomes of two main variants of progressive supranuclear palsy and multiple system atrophy: a prospective natural history study.In vivo evaluation of white matter pathology in patients of progressive supranuclear palsy using TBSS.Microtubule defects in mesenchymal stromal cells distinguish patients with Progressive Supranuclear Palsy.Progressive parkinsonism, oculomotor abnormalities and autonomic dysfunction: clinicopathological case.MRI measurements of brainstem structures in patients with Richardson's syndrome, progressive supranuclear palsy-parkinsonism, and Parkinson's disease Characterisation of tau in the human and rodent enteric nervous system under physiological conditions and in tauopathy Variation at the TRIM11 locus modifies progressive supranuclear palsy phenotype

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P2860

Pathological, clinical and genetic heterogeneity in progressive supranuclear palsy.

http://www.wikidata.org/entity/Q33183604

description

2002 nî lūn-bûn

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2002 թուականի Մայիսին հրատարակուած գիտական յօդուած

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Pathological, clinical and genetic heterogeneity in progressive supranuclear palsy.

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Pathological, clinical and genetic heterogeneity in progressive supranuclear palsy.

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Pathological, clinical and genetic heterogeneity in progressive supranuclear palsy.

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Pathological, clinical and genetic heterogeneity in progressive supranuclear palsy.

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Pathological, clinical and genetic heterogeneity in progressive supranuclear palsy.

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Pathological, clinical and genetic heterogeneity in progressive supranuclear palsy.

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Pathological, clinical and genetic heterogeneity in progressive supranuclear palsy.

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Anderton BH

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P2860

Cleavage of structural proteins during the assembly of the head of bacteriophage T4

Association of missense and 5'-splice-site mutations in tau with the inherited dementia FTDP-17

New phosphorylation sites identified in hyperphosphorylated tau (paired helical filament-tau) from Alzheimer's disease brain using nanoelectrospray mass spectrometry

The Consortium to Establish a Registry for Alzheimer's Disease (CERAD). Part II. Standardization of the neuropathologic assessment of Alzheimer's disease

Association between early-onset Parkinson's disease and mutations in the parkin gene

Neurodegenerative tauopathies

Neuropathological features of Alzheimer's disease in non-demented parkinsonian patients.

Neurofibrillary tangle parkinsonian disorders--tau pathology and tau genetics.

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

Clinical research criteria for the diagnosis of progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome): report of the NINDS-SPSP international workshop.

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969-975

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10.1093/BRAIN/AWF109

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Pt 5

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125

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Andrew John Lees

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