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Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|June 18, 2015
A common functional allele of the Nogo receptor gene, reticulon 4 receptor (RTN4R), is associated with sporadic amyotrophic lateral sclerosis in a French populationMaïté Amy, Oliver Staehlin, Frédérique René, et al.Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|January 26, 2011
Identification of novel FUS mutations in sporadic cases of amyotrophic lateral sclerosisVeronique V Belzil, Hussein Daoud, Judith St-Onge, et al.JIMD Reports|September 26, 2015
Detailed Biochemical and Bioenergetic Characterization of FBXL4-Related Encephalomyopathic Mitochondrial DNA DepletionGhadi Antoun, Skye McBride, Jason R Vanstone, et al.Human Genetics|November 18, 2008
Haploinsufficiency of the GPD2 gene in a patient with nonsyndromic mental retardationHussein Daoud, Nicolas Gruchy, Jean-Marc Constans, et al.Neurobiology of Aging|January 1, 2013
Investigation of C9orf72 repeat expansions in Parkinson's diseaseHussein Daoud, Anne Noreau, Daniel Rochefort, et al.American Journal of Medical Genetics. Part A|April 23, 2015
Resolution of refractory hypotension and anuria in a premature newborn with loss-of-function of ACEJulie Richer, Hussein Daoud, Pavel Geier, et al.European Journal of Human Genetics : EJHG|July 23, 2015
Exome sequencing identifies recessive CDK5RAP2 variants in patients with isolated agenesis of corpus callosumLoubna Jouan, Bouchra Ouled Amar Bencheikh, Hussein Daoud, et al.Journal of Medical Genetics|September 18, 2015
Identification of a pathogenic FTO mutation by next-generation sequencing in a newborn with growth retardation and developmental delayHussein Daoud, Dong Zhang, Fiona McMurray, et al.Biological Psychiatry|January 18, 2011
De novo SYNGAP1 mutations in nonsyndromic intellectual disability and autismFadi F Hamdan, Hussein Daoud, Amélie Piton, et al.Plos Genetics|October 31, 2014
De novo mutations in moderate or severe intellectual disabilityFadi F Hamdan, Myriam Srour, Jose-Mario Capo-Chichi, et al.Pageof 7