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Peter Hedera

Showing results (121-130 of 134) with videos related to

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Neurology|July 1, 2018
Effects of deep brain stimulation on rest tremor progression in early stage Parkinson diseaseMallory L Hacker, Mahlon R DeLong, Maxim Turchan, et al.
American Journal of Human Genetics|August 24, 2004
Mutations in the slow skeletal muscle fiber myosin heavy chain gene (MYH7) cause laing early-onset distal myopathy (MPD1)Christopher Meredith, Ralf Herrmann, Cheryl Parry, et al.
American Journal of Human Genetics|April 7, 2009
Autosomal-dominant distal myopathy associated with a recurrent missense mutation in the gene encoding the nuclear matrix protein, matrin 3Jan Senderek, Sean M Garvey, Michael Krieger, et al.
Molecular Genetics & Genomic Medicine|June 18, 2014
A rare sequence variant in intron 1 of THAP1 is associated with primary dystoniaSatya R Vemula, Jianfeng Xiao, Yu Zhao, et al.
BMC Medical Genetics|March 17, 2009
High-throughput mutational analysis of TOR1A in primary dystoniaJianfeng 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 cohortMark S LeDoux, Satya R Vemula, Jianfeng Xiao, et al.
Human Genetics|April 14, 2011
Novel human pathological mutations. Gene symbol: THAP1. Disease: dystonia 6Jianfeng Xiao, Robert W Bastian, Joel S Perlmutter, et al.
Human Genetics|April 14, 2011
Novel human pathological mutations. Gene symbol: THAP1. Disease: dystonia 6Jianfeng Xiao, Yu Zhao, Robert W Bastian, et al.
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 dystoniaJianfeng Xiao, Yu Zhao, Robert W Bastian, et al.
Human Genetics|April 14, 2011
Novel human pathological mutations. Gene symbol: THAP1. Disease: dystonia 6Jianfeng Xiao, Yu Zhao, Robert W Bastian, et al.
Pageof 14

Showing results (121-130 of 134) with videos related to

Sort By:
Pageof 14
Neurology|July 1, 2018
Effects of deep brain stimulation on rest tremor progression in early stage Parkinson diseaseMallory L Hacker, Mahlon R DeLong, Maxim Turchan, et al.
American Journal of Human Genetics|August 24, 2004
Mutations in the slow skeletal muscle fiber myosin heavy chain gene (MYH7) cause laing early-onset distal myopathy (MPD1)Christopher Meredith, Ralf Herrmann, Cheryl Parry, et al.
American Journal of Human Genetics|April 7, 2009
Autosomal-dominant distal myopathy associated with a recurrent missense mutation in the gene encoding the nuclear matrix protein, matrin 3Jan Senderek, Sean M Garvey, Michael Krieger, et al.
Molecular Genetics & Genomic Medicine|June 18, 2014
A rare sequence variant in intron 1 of THAP1 is associated with primary dystoniaSatya R Vemula, Jianfeng Xiao, Yu Zhao, et al.
BMC Medical Genetics|March 17, 2009
High-throughput mutational analysis of TOR1A in primary dystoniaJianfeng 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 cohortMark S LeDoux, Satya R Vemula, Jianfeng Xiao, et al.
Human Genetics|April 14, 2011
Novel human pathological mutations. Gene symbol: THAP1. Disease: dystonia 6Jianfeng Xiao, Robert W Bastian, Joel S Perlmutter, et al.
Human Genetics|April 14, 2011
Novel human pathological mutations. Gene symbol: THAP1. Disease: dystonia 6Jianfeng Xiao, Yu Zhao, Robert W Bastian, et al.
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 dystoniaJianfeng Xiao, Yu Zhao, Robert W Bastian, et al.
Human Genetics|April 14, 2011
Novel human pathological mutations. Gene symbol: THAP1. Disease: dystonia 6Jianfeng Xiao, Yu Zhao, Robert W Bastian, et al.
Pageof 14