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kw.\*:("Familial ALS")

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Severe familial ALS with a novel exon 4 mutation (L106F) in the SOD1 geneBATTISTINI, Stefania; RICCI, Claudia; LOTTI, Enrico Maria et al.Journal of the neurological sciences. 2010, Vol 293, Num 1-2, pp 112-115, issn 0022-510X, 4 p.Article

Measures of bulbar and spinal motor function, muscle innervation, and mitochondrial function in ALS ratsSMITTKAMP, Susan E; SPALDING, Heather N; BROWN, Jordan W et al.Behavioural brain research. 2010, Vol 211, Num 1, pp 48-57, issn 0166-4328, 10 p.Article

Corticomotoneuronal function in asymptomatic SOD-1 mutation carriersVUCIC, Steve; WINHAMMAR, Jennica M. C; ROWE, Dominic B et al.Clinical neurophysiology. 2010, Vol 121, Num 10, pp 1781-1785, issn 1388-2457, 5 p.Article

A novel codon4 mutation (A4F) in the SOD1gene in familial amyotrophic lateral sclerosisBAEK, Wonki; KOH, Seong-Ho; JIN SEOK PARK et al.Journal of the neurological sciences. 2011, Vol 306, Num 1-2, pp 157-159, issn 0022-510X, 3 p.Article

Cortical hyperexcitability may precede the onset of familial amyotrophic lateral sclerosisVUCIC, Steve; NICHOLSON, Garth A; KIERNAN, Matthew C et al.Brain. 2008, Vol 131, pp 1540-1550, issn 0006-8950, 11 p., 6Article

Clinical characteristics of patients with familial amyotrophic lateral sclerosis carrying the pathogenic GGGGCC hexanucleotide repeat expansion of C9ORF72CHIO, Adriano; BORGHERO, Giuseppe; PUGLIATTI, Maura et al.Brain. 2012, Vol 135, pp 784-793, issn 0006-8950, 10 p., 3Article

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