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Cerebellum (London, England)
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October 14, 2016
Current Opinions and Areas of Consensus on the Role of the Cerebellum in Dystonia
Vikram G Shakkottai, Amit Batla, Kailash Bhatia, et al.
Molecular Genetics & Genomic Medicine
|
June 18, 2014
A rare sequence variant in intron 1 of THAP1 is associated with primary dystonia
Satya R Vemula, Jianfeng Xiao, Yu Zhao, et al.
Human Molecular Genetics
|
February 16, 2018
A recurrent de novo missense mutation in UBTF causes developmental neuroregression
Camilo Toro, Roderick T Hori, May Christine V Malicdan, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
August 27, 2020
Clinical and Demographic Characteristics of Upper Limb Dystonia
Scott A Norris, Hyder A Jinnah, Christine Klein, et al.
Human Molecular Genetics
|
January 5, 2018
A recurrent de novo missense mutation in UBTF causes developmental neuroregression
Camilo Toro, Roderick T Hori, May Christine V Malicdan, et al.
BMC Medical Genetics
|
March 17, 2009
High-throughput mutational analysis of TOR1A in primary dystonia
Jianfeng Xiao, Robert W Bastian, Joel S Perlmutter, et al.
Neurology. Genetics
|
April 29, 2016
Clinical and genetic features of cervical dystonia in a large multicenter cohort
Mark S LeDoux, Satya R Vemula, Jianfeng Xiao, et al.
Human Genetics
|
April 14, 2011
Novel human pathological mutations. Gene symbol: THAP1. Disease: dystonia 6
Jianfeng Xiao, Robert W Bastian, Joel S Perlmutter, 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.
Page
of 22
Search research articles
Search
Showing results (181-190 of 214) with videos related to
Sort By:
Page
of 22
Cerebellum (London, England)
|
October 14, 2016
Current Opinions and Areas of Consensus on the Role of the Cerebellum in Dystonia
Vikram G Shakkottai, Amit Batla, Kailash Bhatia, et al.
Molecular Genetics & Genomic Medicine
|
June 18, 2014
A rare sequence variant in intron 1 of THAP1 is associated with primary dystonia
Satya R Vemula, Jianfeng Xiao, Yu Zhao, et al.
Human Molecular Genetics
|
February 16, 2018
A recurrent de novo missense mutation in UBTF causes developmental neuroregression
Camilo Toro, Roderick T Hori, May Christine V Malicdan, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
August 27, 2020
Clinical and Demographic Characteristics of Upper Limb Dystonia
Scott A Norris, Hyder A Jinnah, Christine Klein, et al.
Human Molecular Genetics
|
January 5, 2018
A recurrent de novo missense mutation in UBTF causes developmental neuroregression
Camilo Toro, Roderick T Hori, May Christine V Malicdan, et al.
BMC Medical Genetics
|
March 17, 2009
High-throughput mutational analysis of TOR1A in primary dystonia
Jianfeng Xiao, Robert W Bastian, Joel S Perlmutter, et al.
Neurology. Genetics
|
April 29, 2016
Clinical and genetic features of cervical dystonia in a large multicenter cohort
Mark S LeDoux, Satya R Vemula, Jianfeng Xiao, et al.
Human Genetics
|
April 14, 2011
Novel human pathological mutations. Gene symbol: THAP1. Disease: dystonia 6
Jianfeng Xiao, Robert W Bastian, Joel S Perlmutter, 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.
Page
of 22