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Movement Disorders : Official Journal of the Movement Disorder Society
|
March 4, 2011
The c.-237_236GA>TT THAP1 sequence variant does not increase risk for primary dystonia
Jianfeng Xiao, Yu Zhao, Robert W Bastian, et al.
Human Genetics
|
April 14, 2011
Novel human pathological mutations. Gene symbol: THAP1. Disease: dystonia 6
Jianfeng Xiao, Yu Zhao, Robert W Bastian, et al.
Human Genetics
|
April 14, 2011
Novel human pathological mutations. Gene symbol: THAP1. Disease: dystonia 6
Jianfeng Xiao, Yu Zhao, Robert W Bastian, et al.
Human Genetics
|
April 14, 2011
Novel human pathological mutations. Gene symbol: THAP1. Disease: dystonia 6
Jianfeng Xiao, Y Zhao, Robert W Bastian, et al.
Human Genetics
|
April 14, 2011
Novel human pathological mutations. Gene symbol: THAP1. Disease: dystonia 6
Jianfeng Xiao, Yu Zhao, Robert W Bastian, et al.
Neurology
|
January 20, 2010
Novel THAP1 sequence variants in primary dystonia
J Xiao, Y Zhao, R W Bastian, et al.
Cell Metabolism
|
August 2, 2011
Deletion of the mammalian INDY homolog mimics aspects of dietary restriction and protects against adiposity and insulin resistance in mice
Andreas L Birkenfeld, Hui-Young Lee, Fitsum Guebre-Egziabher, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
July 1, 2026
Longitudinal Dynamics of Polyglutamine-Expanded ATXN3 in Biofluids of Spinocerebellar Ataxia Type 3
Jordan Bartfield, Lukasz Milanowski, Karen R Jansen-West, et al.
Parkinsonism & Related Disorders
|
July 24, 2021
Urine levels of the polyglutamine ataxin-3 protein are elevated in patients with spinocerebellar ataxia type 3
Yuka Koike, Karen R Jansen-West, Rana Hanna Al-Shaikh, et al.
Journal of the Neurological Sciences
|
October 8, 2021
Consensus on the treatment of dysphagia in Parkinson's disease
Antonio Schindler, Nicole Pizzorni, Emanuele Cereda, et al.
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of 73
Search research articles
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Showing results (711-720 of 728) with videos related to
Sort By:
Page
of 73
Movement Disorders : Official Journal of the Movement Disorder Society
|
March 4, 2011
The c.-237_236GA>TT THAP1 sequence variant does not increase risk for primary dystonia
Jianfeng Xiao, Yu Zhao, Robert W Bastian, et al.
Human Genetics
|
April 14, 2011
Novel human pathological mutations. Gene symbol: THAP1. Disease: dystonia 6
Jianfeng Xiao, Yu Zhao, Robert W Bastian, et al.
Human Genetics
|
April 14, 2011
Novel human pathological mutations. Gene symbol: THAP1. Disease: dystonia 6
Jianfeng Xiao, Yu Zhao, Robert W Bastian, et al.
Human Genetics
|
April 14, 2011
Novel human pathological mutations. Gene symbol: THAP1. Disease: dystonia 6
Jianfeng Xiao, Y Zhao, Robert W Bastian, et al.
Human Genetics
|
April 14, 2011
Novel human pathological mutations. Gene symbol: THAP1. Disease: dystonia 6
Jianfeng Xiao, Yu Zhao, Robert W Bastian, et al.
Neurology
|
January 20, 2010
Novel THAP1 sequence variants in primary dystonia
J Xiao, Y Zhao, R W Bastian, et al.
Cell Metabolism
|
August 2, 2011
Deletion of the mammalian INDY homolog mimics aspects of dietary restriction and protects against adiposity and insulin resistance in mice
Andreas L Birkenfeld, Hui-Young Lee, Fitsum Guebre-Egziabher, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
July 1, 2026
Longitudinal Dynamics of Polyglutamine-Expanded ATXN3 in Biofluids of Spinocerebellar Ataxia Type 3
Jordan Bartfield, Lukasz Milanowski, Karen R Jansen-West, et al.
Parkinsonism & Related Disorders
|
July 24, 2021
Urine levels of the polyglutamine ataxin-3 protein are elevated in patients with spinocerebellar ataxia type 3
Yuka Koike, Karen R Jansen-West, Rana Hanna Al-Shaikh, et al.
Journal of the Neurological Sciences
|
October 8, 2021
Consensus on the treatment of dysphagia in Parkinson's disease
Antonio Schindler, Nicole Pizzorni, Emanuele Cereda, et al.
Page
of 73