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Showing results (51-60 of 64) with videos related to

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Journal of Neuromuscular Diseases|November 18, 2016
Sexual Reassignment Fails to Prevent Kennedy's DiseaseTyler A Lanman, Dara Bakar, Nisha M Badders, et al.
Neuromuscular Disorders : NMD|July 23, 2014
Early onset and novel features in a spinal and bulbar muscular atrophy patient with a 68 CAG repeatChristopher Grunseich, Ilona R Kats, Laura C Bott, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 2, 2021
α-Synuclein Deposition in Sympathetic Nerve Fibers in Genetic Forms of Parkinson's DiseaseRisa Isonaka, David S Goldstein, William Zhu, et al.
Annals of Clinical and Translational Neurology|August 15, 2015
A randomized controlled trial of exercise in spinal and bulbar muscular atrophyJoseph A Shrader, Ilona Kats, Angela Kokkinis, et al.
Brain : a Journal of Neurology|May 31, 2022
Heterozygous PRKN mutations are common but do not increase the risk of Parkinson's diseaseWilliam Zhu, Xiaoping Huang, Esther Yoon, et al.
Molecular Cell|February 4, 2018
Senataxin Mutation Reveals How R-Loops Promote Transcription by Blocking DNA Methylation at Gene PromotersChristopher Grunseich, Isabel X Wang, Jason A Watts, et al.
Neurology|July 15, 2011
Dominant GDAP1 mutations cause predominantly mild CMT phenotypesM Zimoń, J Baets, G M Fabrizi, et al.
The Lancet. Neurology|January 11, 2011
Efficacy and safety of dutasteride in patients with spinal and bulbar muscular atrophy: a randomised placebo-controlled trialLindsay E Fernández-Rhodes, Angela D Kokkinis, Michelle J White, et al.
The Journal of Infectious Diseases|January 19, 2010
A phase 1/2 study of a multiclade HIV-1 DNA plasmid prime and recombinant adenovirus serotype 5 boost vaccine in HIV-Uninfected East Africans (RV 172)Hannah Kibuuka, Robert Kimutai, Leonard Maboko, et al.
Human Mutation|September 11, 2014
Mosaicism for dominant collagen 6 mutations as a cause for intrafamilial phenotypic variabilitySandra Donkervoort, Ying Hu, Tanya Stojkovic, et al.
Pageof 7

Showing results (51-60 of 64) with videos related to

Sort By:
Pageof 7
Journal of Neuromuscular Diseases|November 18, 2016
Sexual Reassignment Fails to Prevent Kennedy's DiseaseTyler A Lanman, Dara Bakar, Nisha M Badders, et al.
Neuromuscular Disorders : NMD|July 23, 2014
Early onset and novel features in a spinal and bulbar muscular atrophy patient with a 68 CAG repeatChristopher Grunseich, Ilona R Kats, Laura C Bott, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 2, 2021
α-Synuclein Deposition in Sympathetic Nerve Fibers in Genetic Forms of Parkinson's DiseaseRisa Isonaka, David S Goldstein, William Zhu, et al.
Annals of Clinical and Translational Neurology|August 15, 2015
A randomized controlled trial of exercise in spinal and bulbar muscular atrophyJoseph A Shrader, Ilona Kats, Angela Kokkinis, et al.
Brain : a Journal of Neurology|May 31, 2022
Heterozygous PRKN mutations are common but do not increase the risk of Parkinson's diseaseWilliam Zhu, Xiaoping Huang, Esther Yoon, et al.
Molecular Cell|February 4, 2018
Senataxin Mutation Reveals How R-Loops Promote Transcription by Blocking DNA Methylation at Gene PromotersChristopher Grunseich, Isabel X Wang, Jason A Watts, et al.
Neurology|July 15, 2011
Dominant GDAP1 mutations cause predominantly mild CMT phenotypesM Zimoń, J Baets, G M Fabrizi, et al.
The Lancet. Neurology|January 11, 2011
Efficacy and safety of dutasteride in patients with spinal and bulbar muscular atrophy: a randomised placebo-controlled trialLindsay E Fernández-Rhodes, Angela D Kokkinis, Michelle J White, et al.
The Journal of Infectious Diseases|January 19, 2010
A phase 1/2 study of a multiclade HIV-1 DNA plasmid prime and recombinant adenovirus serotype 5 boost vaccine in HIV-Uninfected East Africans (RV 172)Hannah Kibuuka, Robert Kimutai, Leonard Maboko, et al.
Human Mutation|September 11, 2014
Mosaicism for dominant collagen 6 mutations as a cause for intrafamilial phenotypic variabilitySandra Donkervoort, Ying Hu, Tanya Stojkovic, et al.
Pageof 7