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Neurology. Genetics

Showing results (321-330 of 1,012) with videos related to

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Neurology. Genetics|May 27, 2022
Erratum: Multigene Panel Testing in a Large Cohort of Adults With Epilepsy: Diagnostic Yield and Clinically Actionable Genetic Findings
Neurology. Genetics|May 27, 2022
Clinical Evidence for Variegated Silencing in Patients With Friedreich AtaxiaLayne N Rodden, Christian Rummey, Yi Na Dong, et al.
Neurology. Genetics|May 27, 2022
Erratum: Migraine, Stroke, and Cervical Arterial Dissection: Shared Genetics for a Triad of Brain Disorders With Vascular Involvement
Neurology. Genetics|May 27, 2022
A New Case With Cortical Malformation Caused by Biallelic Variants in <i>LAMC3</i>Kazuo Abe, Kumiko Ando, Mitsuhiro Kato, et al.
Neurology. Genetics|June 25, 2021
Novel <i>TUBA4A</i> Variant Associated With Familial Frontotemporal DementiaMerel O Mol, Tsz H Wong, Shamiram Melhem, et al.
Neurology. Genetics|March 23, 2018
<i>ACO2</i> mutations: A novel phenotype associating severe optic atrophy and spastic paraplegiaCecilia Marelli, Christian Hamel, Melanie Quiles, et al.
Neurology. Genetics|December 21, 2018
Rare genetic variation implicated in non-Hispanic white families with Alzheimer diseaseGary W Beecham, Badri Vardarajan, Elizabeth Blue, et al.
Neurology. Genetics|December 21, 2018
Leigh syndrome followed by parkinsonism in an adult with homozygous c.626C>T mutation in <i>MTFMT</i>Dimitri M Hemelsoet, Arnaud V Vanlander, Joél Smet, et al.
Neurology. Genetics|December 26, 2018
Amyloid- and tau-PET imaging in a familial prion kindredDavid T Jones, Ryan A Townley, Jonathan Graff-Radford, et al.
Neurology. Genetics|December 26, 2018
Brain somatic mutations in <i>SLC35A2</i> cause intractable epilepsy with aberrant N-glycosylationNam Suk Sim, Youngsuk Seo, Jae Seok Lim, et al.
Pageof 102

Showing results (321-330 of 1,012) with videos related to

Sort By:
Pageof 102
Neurology. Genetics|May 27, 2022
Erratum: Multigene Panel Testing in a Large Cohort of Adults With Epilepsy: Diagnostic Yield and Clinically Actionable Genetic Findings
Neurology. Genetics|May 27, 2022
Clinical Evidence for Variegated Silencing in Patients With Friedreich AtaxiaLayne N Rodden, Christian Rummey, Yi Na Dong, et al.
Neurology. Genetics|May 27, 2022
Erratum: Migraine, Stroke, and Cervical Arterial Dissection: Shared Genetics for a Triad of Brain Disorders With Vascular Involvement
Neurology. Genetics|May 27, 2022
A New Case With Cortical Malformation Caused by Biallelic Variants in <i>LAMC3</i>Kazuo Abe, Kumiko Ando, Mitsuhiro Kato, et al.
Neurology. Genetics|June 25, 2021
Novel <i>TUBA4A</i> Variant Associated With Familial Frontotemporal DementiaMerel O Mol, Tsz H Wong, Shamiram Melhem, et al.
Neurology. Genetics|March 23, 2018
<i>ACO2</i> mutations: A novel phenotype associating severe optic atrophy and spastic paraplegiaCecilia Marelli, Christian Hamel, Melanie Quiles, et al.
Neurology. Genetics|December 21, 2018
Rare genetic variation implicated in non-Hispanic white families with Alzheimer diseaseGary W Beecham, Badri Vardarajan, Elizabeth Blue, et al.
Neurology. Genetics|December 21, 2018
Leigh syndrome followed by parkinsonism in an adult with homozygous c.626C>T mutation in <i>MTFMT</i>Dimitri M Hemelsoet, Arnaud V Vanlander, Joél Smet, et al.
Neurology. Genetics|December 26, 2018
Amyloid- and tau-PET imaging in a familial prion kindredDavid T Jones, Ryan A Townley, Jonathan Graff-Radford, et al.
Neurology. Genetics|December 26, 2018
Brain somatic mutations in <i>SLC35A2</i> cause intractable epilepsy with aberrant N-glycosylationNam Suk Sim, Youngsuk Seo, Jae Seok Lim, et al.
Pageof 102