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Neurology. Genetics

Showing results (401-410 of 1,012) with videos related to

Pageof 102
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Neurology. Genetics|August 26, 2017
What does phenotype have to do with it?Stefan M Pulst
Neurology. Genetics|October 5, 2017
Genome-wide scan in Hispanics highlights candidate loci for brain white matter hyperintensitiesAshley Beecham, Chuanhui Dong, Clinton B Wright, et al.
Neurology. Genetics|October 4, 2017
ARHGEF28 p.Lys280Metfs40Ter in an amyotrophic lateral sclerosis family with a C9orf72 expansionSali M K Farhan, Tania F Gendron, Leonard Petrucelli, et al.
Neurology. Genetics|July 14, 2017
Loss-of-function variants of <i>SCN8A</i> in intellectual disability without seizuresJacy L Wagnon, Bryan S Barker, Matteo Ottolini, et al.
Neurology. Genetics|May 28, 2016
ABCA7 frameshift deletion associated with Alzheimer disease in African AmericansHolly N Cukier, Brian W Kunkle, Badri N Vardarajan, et al.
Neurology. Genetics|June 9, 2016
Next-generation profiling to identify the molecular etiology of Parkinson dementiaAdrienne Henderson-Smith, Jason J Corneveaux, Matthew De Both, et al.
Neurology. Genetics|January 31, 2018
1q21.1 Duplication syndrome and epilepsy: Case report and reviewIoulia Gourari, Romaine Schubert, Aparna Prasad
Neurology. Genetics|November 30, 2017
Genomic links between blast exposure, brain injury, and Alzheimer diseaseYvette P Conley, Ramon Diaz-Arrastia
Neurology. Genetics|December 22, 2017
<i>CDKL5</i> variants: Improving our understanding of a rare neurologic disorderRalph D Hector, Vera M Kalscheuer, Friederike Hennig, et al.
Neurology. Genetics|February 15, 2018
Erratum: Mutation of <i>TBCK</i> causes a rare recessive developmental disorder
Pageof 102

Showing results (401-410 of 1,012) with videos related to

Sort By:
Pageof 102
Neurology. Genetics|August 26, 2017
What does phenotype have to do with it?Stefan M Pulst
Neurology. Genetics|October 5, 2017
Genome-wide scan in Hispanics highlights candidate loci for brain white matter hyperintensitiesAshley Beecham, Chuanhui Dong, Clinton B Wright, et al.
Neurology. Genetics|October 4, 2017
ARHGEF28 p.Lys280Metfs40Ter in an amyotrophic lateral sclerosis family with a C9orf72 expansionSali M K Farhan, Tania F Gendron, Leonard Petrucelli, et al.
Neurology. Genetics|July 14, 2017
Loss-of-function variants of <i>SCN8A</i> in intellectual disability without seizuresJacy L Wagnon, Bryan S Barker, Matteo Ottolini, et al.
Neurology. Genetics|May 28, 2016
ABCA7 frameshift deletion associated with Alzheimer disease in African AmericansHolly N Cukier, Brian W Kunkle, Badri N Vardarajan, et al.
Neurology. Genetics|June 9, 2016
Next-generation profiling to identify the molecular etiology of Parkinson dementiaAdrienne Henderson-Smith, Jason J Corneveaux, Matthew De Both, et al.
Neurology. Genetics|January 31, 2018
1q21.1 Duplication syndrome and epilepsy: Case report and reviewIoulia Gourari, Romaine Schubert, Aparna Prasad
Neurology. Genetics|November 30, 2017
Genomic links between blast exposure, brain injury, and Alzheimer diseaseYvette P Conley, Ramon Diaz-Arrastia
Neurology. Genetics|December 22, 2017
<i>CDKL5</i> variants: Improving our understanding of a rare neurologic disorderRalph D Hector, Vera M Kalscheuer, Friederike Hennig, et al.
Neurology. Genetics|February 15, 2018
Erratum: Mutation of <i>TBCK</i> causes a rare recessive developmental disorder
Pageof 102