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Neurology. Genetics

Showing results (31-40 of 1,009) with videos related to

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Neurology. Genetics|October 4, 2017
Autosomal recessive inheritance of <i>ADCY5</i>-related generalized dystonia and myoclonusMatthew J Barrett, Eli S Williams, Chelsea Chambers, et al.
Neurology. Genetics|March 31, 2017
Phenotypes, genotypes, and prevalence of congenital myopathies older than 5 years in DenmarkNanna Witting, Ulla Werlauff, Morten Duno, et al.
Neurology. Genetics|March 31, 2017
Establishing prevalence in rare neuromuscular diseases: A lesson from congenital myopathiesAhmed K Bamaga, Conrad C Weihl
Neurology. Genetics|April 5, 2017
<i>CNTNAP1</i> mutations cause CNS hypomyelination and neuropathy with or without arthrogryposisHolger Hengel, Alex Magee, Muhammad Mahanjah, et al.
Neurology. Genetics|October 5, 2019
Epidemiology of DYT1 dystonia: Estimating prevalence via genetic ascertainmentJoseph Park, Scott M Damrauer, Aris Baras, et al.
Neurology. Genetics|February 12, 2021
Can Anti-β-amyloid Monoclonal Antibodies Work in Autosomal Dominant Alzheimer Disease?Bruno P Imbimbo, Ugo Lucca, Mark Watling
Neurology. Genetics|February 12, 2021
V374A KCND3 Pathogenic Variant Associated With Paroxysmal Ataxia ExacerbationsMartin Paucar, Richard Ågren, Tianyi Li, et al.
Neurology. Genetics|February 18, 2017
Microangiopathy in primary familial brain calcification: Evidence from skin biopsiesGaël Nicolas, Florent Marguet, Annie Laquerrière, et al.
Neurology. Genetics|January 5, 2026
Immune Cell Mitochondrial Phenotypes Are Largely Preserved in Mitochondrial Diseases and Do Not Reflect Disease SeverityCynthia C Liu, Mangesh Kurade, Anna S Monzel, et al.
Neurology. Genetics|June 16, 2025
Genotype-Phenotype Association for 14 <i>GFAP</i> Variants in Alexander DiseaseAlbee Messing, Amy Tara Waldman, Daniel M Bolt
Pageof 101

Showing results (31-40 of 1,009) with videos related to

Sort By:
Pageof 101
Neurology. Genetics|October 4, 2017
Autosomal recessive inheritance of <i>ADCY5</i>-related generalized dystonia and myoclonusMatthew J Barrett, Eli S Williams, Chelsea Chambers, et al.
Neurology. Genetics|March 31, 2017
Phenotypes, genotypes, and prevalence of congenital myopathies older than 5 years in DenmarkNanna Witting, Ulla Werlauff, Morten Duno, et al.
Neurology. Genetics|March 31, 2017
Establishing prevalence in rare neuromuscular diseases: A lesson from congenital myopathiesAhmed K Bamaga, Conrad C Weihl
Neurology. Genetics|April 5, 2017
<i>CNTNAP1</i> mutations cause CNS hypomyelination and neuropathy with or without arthrogryposisHolger Hengel, Alex Magee, Muhammad Mahanjah, et al.
Neurology. Genetics|October 5, 2019
Epidemiology of DYT1 dystonia: Estimating prevalence via genetic ascertainmentJoseph Park, Scott M Damrauer, Aris Baras, et al.
Neurology. Genetics|February 12, 2021
Can Anti-β-amyloid Monoclonal Antibodies Work in Autosomal Dominant Alzheimer Disease?Bruno P Imbimbo, Ugo Lucca, Mark Watling
Neurology. Genetics|February 12, 2021
V374A KCND3 Pathogenic Variant Associated With Paroxysmal Ataxia ExacerbationsMartin Paucar, Richard Ågren, Tianyi Li, et al.
Neurology. Genetics|February 18, 2017
Microangiopathy in primary familial brain calcification: Evidence from skin biopsiesGaël Nicolas, Florent Marguet, Annie Laquerrière, et al.
Neurology. Genetics|January 5, 2026
Immune Cell Mitochondrial Phenotypes Are Largely Preserved in Mitochondrial Diseases and Do Not Reflect Disease SeverityCynthia C Liu, Mangesh Kurade, Anna S Monzel, et al.
Neurology. Genetics|June 16, 2025
Genotype-Phenotype Association for 14 <i>GFAP</i> Variants in Alexander DiseaseAlbee Messing, Amy Tara Waldman, Daniel M Bolt
Pageof 101