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Neurology. Genetics

Showing results (141-150 of 1,011) with videos related to

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Neurology. Genetics|October 5, 2018
DRESS after IV phenytoin associated with cytochrome P450 CYP2C9*3 homozygosityMette S Nissen, Christoph P Beier
Neurology. Genetics|October 5, 2018
<i>AP4S1</i> splice-site mutation in a case of spastic paraplegia type 52 with polymicrogyriaSusana Carmona, Clara Marecos, Marta Amorim, et al.
Neurology. Genetics|May 24, 2019
Muscular dystrophy with arrhythmia caused by loss-of-function mutations in <i>BVES</i>Willem De Ridder, Isabelle Nelson, Bob Asselbergh, et al.
Neurology. Genetics|May 24, 2019
Antisense oligonucleotides: A primerDaniel R Scoles, Eric V Minikel, Stefan M Pulst
Neurology. Genetics|May 24, 2019
First <i>TMEM126A</i> missense mutation in an Italian proband with optic atrophy and deafnessChiara La Morgia, Leonardo Caporali, Francesca Tagliavini, et al.
Neurology. Genetics|June 14, 2019
Brain-derived neurotrophic factor, epigenetics in stroke skeletal muscle, and exercise trainingAlice S Ryan, Huichun Xu, Frederick M Ivey, et al.
Neurology. Genetics|June 14, 2019
Novel pathogenic <i>VPS13A</i> gene mutations in Japanese patients with chorea-acanthocytosisYoshiaki Nishida, Masayuki Nakamura, Yuka Urata, et al.
Neurology. Genetics|June 14, 2019
Novel mutation in <i>TNPO3</i> causes congenital limb-girdle myopathy with slow progressionAnna Vihola, Johanna Palmio, Olof Danielsson, et al.
Neurology. Genetics|April 24, 2023
Clinical Features and Classification of Neuronal Intranuclear Inclusion DiseaseHongfei Tai, An Wang, Yumei Zhang, et al.
Neurology. Genetics|April 24, 2023
Erratum: Expanding the Allelic Heterogeneity of ANO10-Associated Autosomal Recessive Cerebellar Ataxia
Pageof 102

Showing results (141-150 of 1,011) with videos related to

Sort By:
Pageof 102
Neurology. Genetics|October 5, 2018
DRESS after IV phenytoin associated with cytochrome P450 CYP2C9*3 homozygosityMette S Nissen, Christoph P Beier
Neurology. Genetics|October 5, 2018
<i>AP4S1</i> splice-site mutation in a case of spastic paraplegia type 52 with polymicrogyriaSusana Carmona, Clara Marecos, Marta Amorim, et al.
Neurology. Genetics|May 24, 2019
Muscular dystrophy with arrhythmia caused by loss-of-function mutations in <i>BVES</i>Willem De Ridder, Isabelle Nelson, Bob Asselbergh, et al.
Neurology. Genetics|May 24, 2019
Antisense oligonucleotides: A primerDaniel R Scoles, Eric V Minikel, Stefan M Pulst
Neurology. Genetics|May 24, 2019
First <i>TMEM126A</i> missense mutation in an Italian proband with optic atrophy and deafnessChiara La Morgia, Leonardo Caporali, Francesca Tagliavini, et al.
Neurology. Genetics|June 14, 2019
Brain-derived neurotrophic factor, epigenetics in stroke skeletal muscle, and exercise trainingAlice S Ryan, Huichun Xu, Frederick M Ivey, et al.
Neurology. Genetics|June 14, 2019
Novel pathogenic <i>VPS13A</i> gene mutations in Japanese patients with chorea-acanthocytosisYoshiaki Nishida, Masayuki Nakamura, Yuka Urata, et al.
Neurology. Genetics|June 14, 2019
Novel mutation in <i>TNPO3</i> causes congenital limb-girdle myopathy with slow progressionAnna Vihola, Johanna Palmio, Olof Danielsson, et al.
Neurology. Genetics|April 24, 2023
Clinical Features and Classification of Neuronal Intranuclear Inclusion DiseaseHongfei Tai, An Wang, Yumei Zhang, et al.
Neurology. Genetics|April 24, 2023
Erratum: Expanding the Allelic Heterogeneity of ANO10-Associated Autosomal Recessive Cerebellar Ataxia
Pageof 102