Rare case of atypical parkinsonism: why family history is important.

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Rare case of atypical parkinsonism: why family history is important.

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年學術文章

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2017年學術文章

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Rare case of atypical parkinsonism: why family history is important.

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Rare case of atypical parkinsonism: why family history is important.

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Rare case of atypical parkinsonism: why family history is important.

@en

Rare case of atypical parkinsonism: why family history is important.

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Rare case of atypical parkinsonism: why family history is important.

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Rare case of atypical parkinsonism: why family history is important.

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P1476

Rare case of atypical parkinsonism: why family history is important.

@en

P2093

Donald G Grosset

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Naveed Malek

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Ravi Jampana

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P2860

Inherited prion disease with A117V mutation of the prion protein gene: a novel Hungarian family

A retrospective study of Creutzfeldt-Jakob disease in England and Wales 1970-79. I: Clinical features

Movement disorders and Creutzfeldt-Jakob disease: a review.

Inherited prion disease with an alanine to valine mutation at codon 117 in the prion protein gene.

Pro----leu change at position 102 of prion protein is the most common but not the sole mutation related to Gerstmann-Sträussler syndrome.

Involvement of the peripheral nervous system in human prion diseases including dural graft associated Creutzfeldt-Jakob disease

Creutzfeldt-Jakob disease in Sweden

The genetics of prion diseases.

Striatal [123I] FP-CIT SPECT demonstrates dopaminergic deficit in a sporadic case of Creutzfeldt-Jakob disease.

Codon 200 mutation of the prion gene: genotype-phenotype correlations.

P304

159-162

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P31

scholarly article

P356

10.1177/0036933017727966

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P433

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

P478

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P577

2017-01-01T00:00:00Z

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P698

29192564

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