Clinicopathological Correlates in a PRNP P102L Mutation Carrier with Rapidly Progressing Parkinsonism-dystonia

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Clinicopathological Correlates in a PRNP P102L Mutation Carrier with Rapidly Progressing Parkinsonism-dystonia

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article científic

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article scientifique

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articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on 18 February 2016

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vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

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Clinicopathological Correlates ...... gressing Parkinsonism-dystonia

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Clinicopathological Correlates ...... ressing Parkinsonism-dystonia.

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Clinicopathological Correlates ...... gressing Parkinsonism-dystonia

@en

Clinicopathological Correlates ...... ressing Parkinsonism-dystonia.

@nl

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Clinicopathological Correlates ...... gressing Parkinsonism-dystonia

@en

Clinicopathological Correlates ...... ressing Parkinsonism-dystonia.

@nl

P1476

Clinicopathological Correlates ...... gressing Parkinsonism-dystonia

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P2093

Bernardino Ghetti

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Chizoba C Umeh

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Michael K Greenberg

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Pierluigi Gambetti

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Silvio Notari

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Yvonne Cohen

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Zoltan Mari

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P2860

Validation of the new consensus criteria for the diagnosis of corticobasal degeneration

Neuropathology of Gerstmann-Sträussler-Scheinker disease.

Corticobasal syndrome: Five new things.

Hereditary prion protein amyloidoses.

Different patterns of truncated prion protein fragments correlate with distinct phenotypes in P102L Gerstmann-Sträussler-Scheinker disease.

Prion protein amyloidosis.

Linkage of a prion protein missense variant to Gerstmann-Sträussler syndrome.

Phenotypic variability of Gerstmann-Sträussler-Scheinker disease is associated with prion protein heterogeneity.

Phenotypic heterogeneity in inherited prion disease (P102L) is associated with differential propagation of protease-resistant wild-type and mutant prion protein.

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355-358

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scholarly article

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10.1002/MDC3.12307

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English

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P478

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P50

Piyush Kalakoti

Adrian L. Oblak

P577

2016-02-18T00:00:00Z

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P698

27617269

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P921

Parkinson's disease

P932

5015693

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