Diversity of Cognitive Phenotypes Associated with C9ORF72 Hexanucleotide Expansion.

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Diversity of Cognitive Phenotypes Associated with C9ORF72 Hexanucleotide Expansion.

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2016 nî lūn-bûn

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2016年の論文

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2016年論文

@yue

2016年論文

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2016年論文

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2016年論文

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2016年論文

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2016年论文

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Diversity of Cognitive Phenotypes Associated with C9ORF72 Hexanucleotide Expansion.

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Diversity of Cognitive Phenotypes Associated with C9ORF72 Hexanucleotide Expansion.

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prefLabel

Diversity of Cognitive Phenotypes Associated with C9ORF72 Hexanucleotide Expansion.

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P1476

Diversity of Cognitive Phenotypes Associated with C9ORF72 Hexanucleotide Expansion

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P2093

Cristina Prieto-Jurczynska

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Estrella Gómez-Tortosa

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Jesús Gallego

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Laura Olivié

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María José Sainz

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María José Trujillo-Tiebas

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Rosa Guerrero-López

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Soledad Serrano

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P2860

Classification of primary progressive aphasia and its variants

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Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study

C9orf72 expansions are the most common genetic cause of Huntington disease phenocopies

Frontotemporal dementia with the C9ORF72 hexanucleotide repeat expansion: clinical, neuroanatomical and neuropathological features

Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS

Atypical, slowly progressive behavioural variant frontotemporal dementia associated with C9ORF72 hexanucleotide expansion

A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD

Comparison of family histories in FTLD subtypes and related tauopathies

Autosomal dominant frontotemporal lobar degeneration due to the C9ORF72 hexanucleotide repeat expansion: late-onset psychotic clinical presentation.

P304

25-31

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P31

scholarly article

P356

10.3233/JAD-150922

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P433

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P478

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P577

2016-02-01T00:00:00Z

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P698

26967212

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