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Neuromuscular Disorders : NMD|September 1, 1995
Identification of three novel mutations in the gene for Cu/Zn superoxide dismutase in patients with familial amyotrophic lateral sclerosisP C Sapp, D R Rosen, B A Hosler, et al.Neurology|September 11, 2002
Survival in transgenic ALS mice does not vary with CNS glutathione peroxidase activityM E Cudkowicz, K A Pastusza, P C Sapp, et al.Neuroscience Letters|December 7, 2007
SOD1A4V-mediated ALS: absence of a closely linked modifier gene and origination in AsiaW J Broom, D V Johnson, K E Auwarter, et al.Neurology|September 11, 2009
Analysis of FUS gene mutation in familial amyotrophic lateral sclerosis within an Italian cohortN Ticozzi, V Silani, A L LeClerc, et al.American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|March 26, 2011
Mutational analysis reveals the FUS homolog TAF15 as a candidate gene for familial amyotrophic lateral sclerosisN Ticozzi, C Vance, A L Leclerc, et al.Neurogenetics|May 18, 1999
Refined mapping and characterization of the recessive familial amyotrophic lateral sclerosis locus (ALS2) on chromosome 2q33B A Hosler, P C Sapp, R Berger, et al.JAMA|October 4, 2000
Linkage of familial amyotrophic lateral sclerosis with frontotemporal dementia to chromosome 9q21-q22B A Hosler, T Siddique, P C Sapp, et al.Neuromuscular Disorders : NMD|October 1, 1996
Three novel mutations and two variants in the gene for Cu/Zn superoxide dismutase in familial amyotrophic lateral sclerosisB A Hosler, G A Nicholson, P C Sapp, et al.Neurology|March 7, 2008
New VAPB deletion variant and exclusion of VAPB mutations in familial ALSJ E Landers, A L Leclerc, L Shi, et al.Science (New York, N.Y.)|March 3, 2009
Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosisT J Kwiatkowski, D A Bosco, A L Leclerc, et al.Pageof 1