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Neurology. Genetics

Showing results (641-650 of 842) with videos related to

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Neurology. Genetics|December 8, 2021
Novel Variations in the <i>KDM5C</i> Gene Causing X-Linked Intellectual DisabilityPo-Ming Wu, Wen-Hao Yu, Chi-Wu Chiang, et al.
Neurology. Genetics|March 10, 2021
Cumulative Genetic Risk and <i>APOE ε4</i> Are Independently Associated With Dementia Status in a Multiethnic, Population-Based CohortKelly M Bakulski, Harita S Vadari, Jessica D Faul, et al.
Neurology. Genetics|October 31, 2022
Clinical and Metabolic Signature of <i>UNC13A</i> rs12608932 Variant in Amyotrophic Lateral SclerosisAndrea Calvo, Antonio Canosa, Cristina Moglia, et al.
Neurology. Genetics|September 1, 2022
<i>RFC1</i>-Related Disease: Molecular and Clinical InsightsKayli Davies, David J Szmulewicz, Louise A Corben, et al.
Neurology. Genetics|September 1, 2022
Genetic Evidence for Protective Effects of Angiotensin-Converting Enzyme Against Alzheimer Disease But Not Other Neurodegenerative Diseases in European PopulationsDavid K Ryan, Ville Karhunen, Bowen Su, et al.
Neurology. Genetics|March 4, 2021
New recessive mutations in <i>SYT2</i> causing severe presynaptic congenital myasthenic syndromesStéphanie Bauché, Alain Sureau, Damien Sternberg, et al.
Neurology. Genetics|September 30, 2022
Long-Surviving Adult Siblings With Joubert Syndrome Harboring a Novel Compound Heterozygous <i>CPLANE1</i> VariantKento Matoba, Norio Chihara, Wataru Satake, et al.
Neurology. Genetics|September 30, 2022
Erratum: Epilepsy Course and Developmental Trajectories in <i>STXBP1</i>-DEE
Neurology. Genetics|April 12, 2016
CHCHD10 variant p.(Gly66Val) causes axonal Charcot-Marie-Tooth diseaseMari Auranen, Emil Ylikallio, Maria Shcherbii, et al.
Neurology. Genetics|April 12, 2016
Phenotypic and molecular analyses of primary lateral sclerosisHiroshi Mitsumoto, Peter L Nagy, Chris Gennings, et al.
Pageof 85

Showing results (641-650 of 842) with videos related to

Sort By:
Pageof 85
Neurology. Genetics|December 8, 2021
Novel Variations in the <i>KDM5C</i> Gene Causing X-Linked Intellectual DisabilityPo-Ming Wu, Wen-Hao Yu, Chi-Wu Chiang, et al.
Neurology. Genetics|March 10, 2021
Cumulative Genetic Risk and <i>APOE ε4</i> Are Independently Associated With Dementia Status in a Multiethnic, Population-Based CohortKelly M Bakulski, Harita S Vadari, Jessica D Faul, et al.
Neurology. Genetics|October 31, 2022
Clinical and Metabolic Signature of <i>UNC13A</i> rs12608932 Variant in Amyotrophic Lateral SclerosisAndrea Calvo, Antonio Canosa, Cristina Moglia, et al.
Neurology. Genetics|September 1, 2022
<i>RFC1</i>-Related Disease: Molecular and Clinical InsightsKayli Davies, David J Szmulewicz, Louise A Corben, et al.
Neurology. Genetics|September 1, 2022
Genetic Evidence for Protective Effects of Angiotensin-Converting Enzyme Against Alzheimer Disease But Not Other Neurodegenerative Diseases in European PopulationsDavid K Ryan, Ville Karhunen, Bowen Su, et al.
Neurology. Genetics|March 4, 2021
New recessive mutations in <i>SYT2</i> causing severe presynaptic congenital myasthenic syndromesStéphanie Bauché, Alain Sureau, Damien Sternberg, et al.
Neurology. Genetics|September 30, 2022
Long-Surviving Adult Siblings With Joubert Syndrome Harboring a Novel Compound Heterozygous <i>CPLANE1</i> VariantKento Matoba, Norio Chihara, Wataru Satake, et al.
Neurology. Genetics|September 30, 2022
Erratum: Epilepsy Course and Developmental Trajectories in <i>STXBP1</i>-DEE
Neurology. Genetics|April 12, 2016
CHCHD10 variant p.(Gly66Val) causes axonal Charcot-Marie-Tooth diseaseMari Auranen, Emil Ylikallio, Maria Shcherbii, et al.
Neurology. Genetics|April 12, 2016
Phenotypic and molecular analyses of primary lateral sclerosisHiroshi Mitsumoto, Peter L Nagy, Chris Gennings, et al.
Pageof 85