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Neurogenetics|April 3, 2013
The p.A382T TARDBP gene mutation in Sardinian patients affected by Parkinson's disease and other degenerative parkinsonismsAntonino Cannas, Giuseppe Borghero, Gian Luca Floris, et al.
Neurobiology of Aging|February 9, 2010
FUS mutations in sporadic amyotrophic lateral sclerosisShiao-Lin Lai, Yevgeniya Abramzon, Jennifer C Schymick, et al.
Neurobiology of Aging|July 16, 2015
HFE p.H63D polymorphism does not influence ALS phenotype and survivalAdriano Chiò, Gabriele Mora, Mario Sabatelli, et al.
Neurobiology of Aging|March 2, 2015
CHCH10 mutations in an Italian cohort of familial and sporadic amyotrophic lateral sclerosis patientsAdriano Chiò, Gabriele Mora, Mario Sabatelli, et al.
Neurobiology of Aging|January 7, 2016
ATNX2 is not a regulatory gene in Italian amyotrophic lateral sclerosis patients with C9ORF72 GGGGCC expansionAdriano Chiò, Gabriele Mora, Mario Sabatelli, et al.
Neurobiology of Aging|September 20, 2011
Chromosome 9 ALS and FTD locus is probably derived from a single founderKin Mok, Bryan J Traynor, Jennifer Schymick, et al.
Human Molecular Genetics|November 16, 2013
No evidence for shared genetic basis of common variants in multiple sclerosis and amyotrophic lateral sclerosisAn Goris, Jessica van Setten, Frank Diekstra, et al.
Neuron|December 15, 2010
Exome sequencing reveals VCP mutations as a cause of familial ALSJanel O Johnson, Jessica Mandrioli, Michael Benatar, et al.
Neurobiology of Aging|May 20, 2014
Analysis of the KIFAP3 gene in amyotrophic lateral sclerosis: a multicenter survival studyPerry T C van Doormaal, Nicola Ticozzi, Cinzia Gellera, et al.
Brain : a Journal of Neurology|February 28, 2012
Clinical characteristics of patients with familial amyotrophic lateral sclerosis carrying the pathogenic GGGGCC hexanucleotide repeat expansion of C9ORF72Adriano Chiò, Giuseppe Borghero, Gabriella Restagno, et al.
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