Clinical and pathological features of familial frontotemporal dementia caused by C9ORF72 mutation on chromosome 9p

By Hsiung Ging-Yuek R.  

Brain, Vol. 135, Iss. 3, 2012-04 ,pp. : 709-722

Oxford University Press

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Characterization of frontotemporal dementia and/or amyotrophic lateral sclerosis associated with the GGGGCC repeat expansion in C9ORF72

By Boeve Bradley F.  

Brain, Vol. 135, Iss. 3, 2012-04 ,pp. : 765-783

Oxford University Press

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The clinical and pathological phenotype of C9ORF72 hexanucleotide repeat expansions

By Simn-Snchez Javier  

Brain, Vol. 135, Iss. 3, 2012-04 ,pp. : 723-735

Oxford University Press

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Clinical characteristics of patients with familial amyotrophic lateral sclerosis carrying the pathogenic GGGGCC hexanucleotide repeat expansion of C9ORF72

By Chi Adriano  

Brain, Vol. 135, Iss. 3, 2012-04 ,pp. : 784-793

Oxford University Press

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Enlarging the clinical spectrum associated with C9orf 72 repeat expansions: Findings in an Italian cohort of patients with Parkinsonian syndromes and relevance for genetic counselling

By Origone Paola  

Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, Vol. 14, Iss. 5-6, 2013-09 ,pp. : 479-480

Informa Healthcare

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