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Neurology. Genetics

Showing results (111-120 of 1,011) with videos related to

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Neurology. Genetics|March 27, 2018
Rare <i>ABCA7</i> variants in 2 German families with Alzheimer diseasePatrick May, Sabrina Pichler, Daniela Hartl, et al.
Neurology. Genetics|March 27, 2018
Twenty-year-old African American woman with prion disease associated with the G114V <i>PRNP</i> variantJason Margolesky, Mario Saporta
Neurology. Genetics|January 31, 2018
Alzheimer risk loci and associated neuropathology in a population-based study (Vantaa 85+)Mira Mäkelä, Karri Kaivola, Miko Valori, et al.
Neurology. Genetics|January 31, 2018
Homozygous <i>CAPN1</i> mutations causing a spastic-ataxia phenotype in 2 familiesCemile Kocoglu, Asli Gundogdu, Gulsen Kocaman, et al.
Neurology. Genetics|July 19, 2021
PARK7-Related Early Onset Parkinson Disease in the Setting of Complete Uniparental Isodisomy of Chromosome 1Changrui Xiao, Thomas Markello, Wadih M Zein, et al.
Neurology. Genetics|July 23, 2021
Disease Severity and Motor Impairment Correlate With Health-Related Quality of Life in AP-4-Associated Hereditary Spastic ParaplegiaCatherine Jordan, Gregory Geisel, Julian E Alecu, et al.
Neurology. Genetics|June 3, 2021
Chromosomal Microarray Analysis in Pregnancies With Corpus Callosum or Posterior Fossa AnomaliesLior Greenbaum, Idit Maya, Lena Sagi-Dain, et al.
Neurology. Genetics|June 25, 2021
<i>SMN1</i> Duplications Are Associated With Progressive Muscular Atrophy, but Not With Multifocal Motor Neuropathy and Primary Lateral SclerosisJeroen W Bos, Ewout J N Groen, Renske I Wadman, et al.
Neurology. Genetics|June 25, 2021
Adult-Onset Spinal Muscular Atrophy due to Mutations in the <i>VRK1</i> GeneAngela Sung, Paolo Moretti, Aziz Shaibani
Neurology. Genetics|June 7, 2021
Association of <i>HLA-DQA2</i> and <i>HLA-B</i> With Moyamoya Disease in the Chinese Han PopulationJiang Wan, Wei Ling, Zhang Zhengshan, et al.
Pageof 102

Showing results (111-120 of 1,011) with videos related to

Sort By:
Pageof 102
Neurology. Genetics|March 27, 2018
Rare <i>ABCA7</i> variants in 2 German families with Alzheimer diseasePatrick May, Sabrina Pichler, Daniela Hartl, et al.
Neurology. Genetics|March 27, 2018
Twenty-year-old African American woman with prion disease associated with the G114V <i>PRNP</i> variantJason Margolesky, Mario Saporta
Neurology. Genetics|January 31, 2018
Alzheimer risk loci and associated neuropathology in a population-based study (Vantaa 85+)Mira Mäkelä, Karri Kaivola, Miko Valori, et al.
Neurology. Genetics|January 31, 2018
Homozygous <i>CAPN1</i> mutations causing a spastic-ataxia phenotype in 2 familiesCemile Kocoglu, Asli Gundogdu, Gulsen Kocaman, et al.
Neurology. Genetics|July 19, 2021
PARK7-Related Early Onset Parkinson Disease in the Setting of Complete Uniparental Isodisomy of Chromosome 1Changrui Xiao, Thomas Markello, Wadih M Zein, et al.
Neurology. Genetics|July 23, 2021
Disease Severity and Motor Impairment Correlate With Health-Related Quality of Life in AP-4-Associated Hereditary Spastic ParaplegiaCatherine Jordan, Gregory Geisel, Julian E Alecu, et al.
Neurology. Genetics|June 3, 2021
Chromosomal Microarray Analysis in Pregnancies With Corpus Callosum or Posterior Fossa AnomaliesLior Greenbaum, Idit Maya, Lena Sagi-Dain, et al.
Neurology. Genetics|June 25, 2021
<i>SMN1</i> Duplications Are Associated With Progressive Muscular Atrophy, but Not With Multifocal Motor Neuropathy and Primary Lateral SclerosisJeroen W Bos, Ewout J N Groen, Renske I Wadman, et al.
Neurology. Genetics|June 25, 2021
Adult-Onset Spinal Muscular Atrophy due to Mutations in the <i>VRK1</i> GeneAngela Sung, Paolo Moretti, Aziz Shaibani
Neurology. Genetics|June 7, 2021
Association of <i>HLA-DQA2</i> and <i>HLA-B</i> With Moyamoya Disease in the Chinese Han PopulationJiang Wan, Wei Ling, Zhang Zhengshan, et al.
Pageof 102