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Ruth H Walker

Showing results (81-90 of 126) with videos related to

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Human Mutation|July 25, 2016
Identification of a Large DNAJB2 Deletion in a Family with Spinal Muscular Atrophy and ParkinsonismElena Sanchez, Hossein Darvish, Roxana Mesias, et al.
Journal of the Neurological Sciences|April 6, 2011
Two McLeod patients with novel mutations in XKPatrycja M Dubielecka, Nelson Hwynn, Cenk Sengun, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 1, 2011
Genetic diagnosis of neuroacanthocytosis disorders using exome sequencingRuth H Walker, Vincent P Schulz, Irina R Tikhonova, et al.
Parkinsonism & Related Disorders|June 12, 2018
Movement disorders in non-encephalopathic Hashimoto's thyroiditisMarcelo Miranda, M Leonor Bustamante, Mario Campero, et al.
The American Journal of Pathology|January 11, 2014
Giant axon formation in mice lacking Kell, XK, or Kell and XK: animal models of McLeod neuroacanthocytosis syndromeXiang Zhu, Eun-Sook Cho, Quan Sha, et al.
Journal of Clinical Movement Disorders|April 18, 2017
Presentation and care of a family with Huntington disease in a resource-limited communityJarmal Charles, Lindyann Lessey, Jennifer Rooney, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 8, 2006
Developments in neuroacanthocytosis: expanding the spectrum of choreatic syndromesRuth H Walker, Adrian Danek, Carol Dobson-Stone, et al.
Archives of Neurology|October 12, 2011
Chorea-acanthocytosis genotype in the original critchley kentucky neuroacanthocytosis kindredAntonio Velayos-Baeza, Elke Holinski-Feder, Birgit Neitzel, et al.
Neuroscience|November 1, 2019
A Novel Transgenic Mouse Model to Investigate the Cell-Autonomous Effects of torsinA(ΔE) Expression in Striatal Output NeuronsPedro Gonzalez-Alegre, Genevieve Beauvais, Janine Martin, et al.
Tremor and Other Hyperkinetic Movements (New York, N.Y.)|December 12, 2017
Absence of Acanthocytosis in Huntington's Disease-like 2: A Prospective Comparison with Huntington's DiseaseDavid G Anderson, Sergio Carmona, Kubendran Naidoo, et al.
Pageof 13

Showing results (81-90 of 126) with videos related to

Sort By:
Pageof 13
Human Mutation|July 25, 2016
Identification of a Large DNAJB2 Deletion in a Family with Spinal Muscular Atrophy and ParkinsonismElena Sanchez, Hossein Darvish, Roxana Mesias, et al.
Journal of the Neurological Sciences|April 6, 2011
Two McLeod patients with novel mutations in XKPatrycja M Dubielecka, Nelson Hwynn, Cenk Sengun, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 1, 2011
Genetic diagnosis of neuroacanthocytosis disorders using exome sequencingRuth H Walker, Vincent P Schulz, Irina R Tikhonova, et al.
Parkinsonism & Related Disorders|June 12, 2018
Movement disorders in non-encephalopathic Hashimoto's thyroiditisMarcelo Miranda, M Leonor Bustamante, Mario Campero, et al.
The American Journal of Pathology|January 11, 2014
Giant axon formation in mice lacking Kell, XK, or Kell and XK: animal models of McLeod neuroacanthocytosis syndromeXiang Zhu, Eun-Sook Cho, Quan Sha, et al.
Journal of Clinical Movement Disorders|April 18, 2017
Presentation and care of a family with Huntington disease in a resource-limited communityJarmal Charles, Lindyann Lessey, Jennifer Rooney, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 8, 2006
Developments in neuroacanthocytosis: expanding the spectrum of choreatic syndromesRuth H Walker, Adrian Danek, Carol Dobson-Stone, et al.
Archives of Neurology|October 12, 2011
Chorea-acanthocytosis genotype in the original critchley kentucky neuroacanthocytosis kindredAntonio Velayos-Baeza, Elke Holinski-Feder, Birgit Neitzel, et al.
Neuroscience|November 1, 2019
A Novel Transgenic Mouse Model to Investigate the Cell-Autonomous Effects of torsinA(ΔE) Expression in Striatal Output NeuronsPedro Gonzalez-Alegre, Genevieve Beauvais, Janine Martin, et al.
Tremor and Other Hyperkinetic Movements (New York, N.Y.)|December 12, 2017
Absence of Acanthocytosis in Huntington's Disease-like 2: A Prospective Comparison with Huntington's DiseaseDavid G Anderson, Sergio Carmona, Kubendran Naidoo, et al.
Pageof 13