PRNP P39L Variant is a Rare Cause of Frontotemporal Dementia in Italian Population.

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Mutational analysis of PRNP in Alzheimer's disease and frontotemporal dementia in China.Hereditary Human Prion Diseases: an Update.Characterization of mutations in (prion) gene and their possible roles in neurodegenerative diseases

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PRNP P39L Variant is a Rare Cause of Frontotemporal Dementia in Italian Population.

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2016 nî lūn-bûn

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2016年の論文

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2016年学术文章

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2016年学术文章

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2016年学术文章

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2016年学术文章

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2016年學術文章

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2016年學術文章

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PRNP P39L Variant is a Rare Cause of Frontotemporal Dementia in Italian Population.

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PRNP P39L Variant is a Rare Cause of Frontotemporal Dementia in Italian Population.

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PRNP P39L Variant is a Rare Cause of Frontotemporal Dementia in Italian Population.

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PRNP P39L Variant is a Rare Cause of Frontotemporal Dementia in Italian Population.

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PRNP P39L Variant is a Rare Cause of Frontotemporal Dementia in Italian Population.

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PRNP P39L Variant is a Rare Cause of Frontotemporal Dementia in Italian Population.

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P1476

PRNP P39L Variant is a Rare Cause of Frontotemporal Dementia in Italian Population

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P2093

Chiara Fenoglio

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Claudio Mariani

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Devan Bursey

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Emanuela Oldoni

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Giulia Grande

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Giuseppe Bruno

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Giuseppina Talarico

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Innocenzo Rainero

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John S Kauwe

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Lorenzo Pinessi

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Sensitivity of revised diagnostic criteria for the behavioural variant of frontotemporal dementia

Frontotemporal lobar degeneration: a consensus on clinical diagnostic criteria

Clinical and pathological diagnosis of frontotemporal dementia: report of the Work Group on Frontotemporal Dementia and Pick's Disease.

Huntington disease phenocopy is a familial prion disease.

Nonsense mutation in PRNP associated with clinical Alzheimer's disease

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

Psychiatric symptoms in frontotemporal dementia: epidemiology, phenotypes, and differential diagnosis.

Updated clinical diagnostic criteria for sporadic Creutzfeldt-Jakob disease.

Atypical presentation of Creutzfeldt-Jakob disease: the first Italian case associated with E196K mutation in the PRNP gene.

The cerebrospinal fluid "Alzheimer profile": easily said, but what does it mean?

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An Eadailt

PRNP P39L Variant is a Rare Cause of Frontotemporal Dementia in Italian Population.

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P2860

P2860

PRNP P39L Variant is a Rare Cause of Frontotemporal Dementia in Italian Population.

description

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P1433

P1476

P2093

P2860

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P698

P921

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P2860

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P433

P478

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P921