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Neurogenetics

Showing results (601-610 of 949) with videos related to

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Neurogenetics|December 30, 2009
Hereditary spastic paraplegia and amyotrophy associated with a novel locus on chromosome 19K G Meilleur, M Traoré, M Sangaré, et al.
Neurogenetics|October 31, 2009
Isolated eyelid closure myotonia in two families with sodium channel myotoniaB C Stunnenberg, H B Ginjaar, J Trip, et al.
Neurogenetics|December 16, 2014
Migraine genetics: current findings and future lines of researchA M Persico, M Verdecchia, V Pinzone, et al.
Neurogenetics|October 25, 2014
The LITAF/SIMPLE I92V sequence variant results in an earlier age of onset of CMT1A/HNPP diseasesElena Sinkiewicz-Darol, Andressa Ferreira Lacerda, Anna Kostera-Pruszczyk, et al.
Neurogenetics|September 24, 2015
Clinical heterogeneity associated with KCNA1 mutations include cataplexy and nonataxic presentationsCatherine A Brownstein, Alan H Beggs, Lance Rodan, et al.
Neurogenetics|October 15, 2015
Transgenic rescue of phenotypic deficits in a mouse model of alternating hemiplegia of childhoodGreer S Kirshenbaum, James Dachtler, John C Roder, et al.
Neurogenetics|September 25, 2017
Molecular genetic and clinical characterization of myotonic dystrophy type 1 patients carrying variant repeats within DMPK expansionsJovan Pešović, S Perić, M Brkušanin, et al.
Neurogenetics|February 10, 2018
Clinical and neuroimaging features of autosomal recessive spastic paraplegia 35 (SPG35): case reports, new mutations, and brief literature reviewFrancesco Mari, Beatrice Berti, Alessandro Romano, et al.
Neurogenetics|March 29, 2018
Genetic test utilization and diagnostic yield in adult patients with neurological disordersTanya M Bardakjian, Ingo Helbig, Colin Quinn, et al.
Neurogenetics|May 15, 2009
Epidemiological, clinical, paraclinical and molecular study of a cohort of 102 patients affected with autosomal recessive progressive cerebellar ataxia from Alsace, Eastern France: implications for clinical managementM Anheim, M Fleury, B Monga, et al.
Pageof 95

Showing results (601-610 of 949) with videos related to

Sort By:
Pageof 95
Neurogenetics|December 30, 2009
Hereditary spastic paraplegia and amyotrophy associated with a novel locus on chromosome 19K G Meilleur, M Traoré, M Sangaré, et al.
Neurogenetics|October 31, 2009
Isolated eyelid closure myotonia in two families with sodium channel myotoniaB C Stunnenberg, H B Ginjaar, J Trip, et al.
Neurogenetics|December 16, 2014
Migraine genetics: current findings and future lines of researchA M Persico, M Verdecchia, V Pinzone, et al.
Neurogenetics|October 25, 2014
The LITAF/SIMPLE I92V sequence variant results in an earlier age of onset of CMT1A/HNPP diseasesElena Sinkiewicz-Darol, Andressa Ferreira Lacerda, Anna Kostera-Pruszczyk, et al.
Neurogenetics|September 24, 2015
Clinical heterogeneity associated with KCNA1 mutations include cataplexy and nonataxic presentationsCatherine A Brownstein, Alan H Beggs, Lance Rodan, et al.
Neurogenetics|October 15, 2015
Transgenic rescue of phenotypic deficits in a mouse model of alternating hemiplegia of childhoodGreer S Kirshenbaum, James Dachtler, John C Roder, et al.
Neurogenetics|September 25, 2017
Molecular genetic and clinical characterization of myotonic dystrophy type 1 patients carrying variant repeats within DMPK expansionsJovan Pešović, S Perić, M Brkušanin, et al.
Neurogenetics|February 10, 2018
Clinical and neuroimaging features of autosomal recessive spastic paraplegia 35 (SPG35): case reports, new mutations, and brief literature reviewFrancesco Mari, Beatrice Berti, Alessandro Romano, et al.
Neurogenetics|March 29, 2018
Genetic test utilization and diagnostic yield in adult patients with neurological disordersTanya M Bardakjian, Ingo Helbig, Colin Quinn, et al.
Neurogenetics|May 15, 2009
Epidemiological, clinical, paraclinical and molecular study of a cohort of 102 patients affected with autosomal recessive progressive cerebellar ataxia from Alsace, Eastern France: implications for clinical managementM Anheim, M Fleury, B Monga, et al.
Pageof 95