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Neurology|December 1, 2012
Ataxin-1 and ataxin-2 intermediate-length PolyQ expansions in amyotrophic lateral sclerosisFrancesca L Conforti, Rossella Spataro, William Sproviero, et al.Human Molecular Genetics|July 13, 2016
Loss-of-function mutations in the SIGMAR1 gene cause distal hereditary motor neuropathy by impairing ER-mitochondria tethering and Ca2+ signallingElisa Gregianin, Giorgia Pallafacchina, Sofia Zanin, et al.Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|July 9, 2008
Further evidence that D90A-SOD1 mutation is recessively inherited in ALS patients in ItalyFrancesca Luisa Conforti, Teresa Sprovieri, Rosalucia Mazzei, et al.Neurobiology of Aging|November 8, 2011
FUS mutations in sporadic amyotrophic lateral sclerosis: clinical and genetic analysisWilliam Sproviero, Vincenzo La Bella, Rosalucia Mazzei, et al.Journal of the Neurological Sciences|December 17, 2008
Spastic paraplegia with thinning of the corpus callosum and white matter abnormalities: further mutations and relative frequency in ZFYVE26/SPG15 in the Italian populationPaola S Denora, Maria Muglia, Carlo Casali, et al.Neuroscience Letters|November 3, 2004
Could mitochondrial haplogroups play a role in sporadic amyotrophic lateral sclerosis?Michelangelo Mancuso, Francesca Luisa Conforti, Anna Rocchi, et al.Pageof 4