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Neurology. Genetics

Showing results (91-100 of 1,011) with videos related to

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Neurology. Genetics|June 9, 2018
Erratum: Expanding the global prevalence of spinocerebellar ataxia type 42
Neurology. Genetics|May 31, 2018
<i>ANXA11</i> mutations prevail in Chinese ALS patients with and without cognitive dementiaKang Zhang, Qing Liu, Keqiang Liu, et al.
Neurology. Genetics|May 31, 2018
Determining the incidence of familiality in ALS: A study of temporal trends in Ireland from 1994 to 2016Marie Ryan, Mark Heverin, Mark A Doherty, et al.
Neurology. Genetics|May 31, 2018
Chorea-acanthocytosis: Homozygous 1-kb deletion in <i>VPS13A</i> detected by whole-genome sequencingSusan Walker, Rubina Dad, Bhooma Thiruvahindrapuram, et al.
Neurology. Genetics|November 9, 2016
Peripheral neuropathy in patients with CPEO associated with single and multiple mtDNA deletionsDiana Lehmann, Malte E Kornhuber, Carolina Clajus, et al.
Neurology. Genetics|November 9, 2016
<i>SORL1</i> mutations in early- and late-onset Alzheimer diseaseMichael L Cuccaro, Regina M Carney, Yalun Zhang, et al.
Neurology. Genetics|November 19, 2020
Primary mitochondrial myopathy: Clinical features and outcome measures in 118 cases from ItalyVincenzo Montano, Francesco Gruosso, Valerio Carelli, et al.
Neurology. Genetics|November 2, 2020
Integrative analysis identifies the association between <i>CASZ1</i> methylation and ischemic strokeXing-Bo Mo, Huan Zhang, Ai-Li Wang, et al.
Neurology. Genetics|November 2, 2020
KCNQ2 encephalopathy manifesting with Rett-like features: A follow-up into adulthoodMario Mastrangelo, Filippo Manti, Maria Teresa Giannini, et al.
Neurology. Genetics|November 2, 2020
Identification of a novel mutation in <i>ATP13A2</i> associated with a complicated form of hereditary spastic paraplegiaYasuko Odake, Kishin Koh, Yoshihisa Takiyama, et al.
Pageof 102

Showing results (91-100 of 1,011) with videos related to

Sort By:
Pageof 102
Neurology. Genetics|June 9, 2018
Erratum: Expanding the global prevalence of spinocerebellar ataxia type 42
Neurology. Genetics|May 31, 2018
<i>ANXA11</i> mutations prevail in Chinese ALS patients with and without cognitive dementiaKang Zhang, Qing Liu, Keqiang Liu, et al.
Neurology. Genetics|May 31, 2018
Determining the incidence of familiality in ALS: A study of temporal trends in Ireland from 1994 to 2016Marie Ryan, Mark Heverin, Mark A Doherty, et al.
Neurology. Genetics|May 31, 2018
Chorea-acanthocytosis: Homozygous 1-kb deletion in <i>VPS13A</i> detected by whole-genome sequencingSusan Walker, Rubina Dad, Bhooma Thiruvahindrapuram, et al.
Neurology. Genetics|November 9, 2016
Peripheral neuropathy in patients with CPEO associated with single and multiple mtDNA deletionsDiana Lehmann, Malte E Kornhuber, Carolina Clajus, et al.
Neurology. Genetics|November 9, 2016
<i>SORL1</i> mutations in early- and late-onset Alzheimer diseaseMichael L Cuccaro, Regina M Carney, Yalun Zhang, et al.
Neurology. Genetics|November 19, 2020
Primary mitochondrial myopathy: Clinical features and outcome measures in 118 cases from ItalyVincenzo Montano, Francesco Gruosso, Valerio Carelli, et al.
Neurology. Genetics|November 2, 2020
Integrative analysis identifies the association between <i>CASZ1</i> methylation and ischemic strokeXing-Bo Mo, Huan Zhang, Ai-Li Wang, et al.
Neurology. Genetics|November 2, 2020
KCNQ2 encephalopathy manifesting with Rett-like features: A follow-up into adulthoodMario Mastrangelo, Filippo Manti, Maria Teresa Giannini, et al.
Neurology. Genetics|November 2, 2020
Identification of a novel mutation in <i>ATP13A2</i> associated with a complicated form of hereditary spastic paraplegiaYasuko Odake, Kishin Koh, Yoshihisa Takiyama, et al.
Pageof 102