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American Journal of Human Genetics
|
March 5, 2002
Age at onset in two common neurodegenerative diseases is genetically controlled
Yi-Ju Li, William K Scott, Dale J Hedges, et al.
Medrxiv : the Preprint Server for Health Sciences
|
July 17, 2025
Rare but Relevant: Assessing Variants in Dystonia-linked Genes in Parkinson's Disease
Lara M Lange, Zih-Hua Fang, Laurel Screven, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
October 11, 2025
Rare but Relevant? Assessing Variants in Dystonia-Linked Genes in Parkinson's Disease
Lara M Lange, Zih-Hua Fang, Laurel Screven, et al.
Movement Disorders Clinical Practice
|
October 11, 2025
Segmental and Multifocal Isolated Dystonias: Similarities and Differences
Hyder A Jinnah, Vittorio Velucci, Daniele Belvisi, et al.
Neurology
|
October 13, 2020
Dystonia and Tremor: A Cross-Sectional Study of the Dystonia Coalition Cohort
Aasef G Shaikh, Sinem Balta Beylergil, Laura Scorr, et al.
Cell Reports
|
July 27, 2012
Mutations in the gene PRRT2 cause paroxysmal kinesigenic dyskinesia with infantile convulsions
Hsien-Yang Lee, Yong Huang, Nadine Bruneau, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
April 9, 2019
Parkinson's disease age at onset genome-wide association study: Defining heritability, genetic loci, and α-synuclein mechanisms
Cornelis Blauwendraat, Karl Heilbron, Costanza L Vallerga, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
March 1, 2020
Outcome measurement in functional neurological disorder: a systematic review and recommendations
Susannah Pick, David G Anderson, Ali A Asadi-Pooya, et al.
JAMA Neurology
|
January 4, 2022
Association of Essential Tremor With Novel Risk Loci: A Genome-Wide Association Study and Meta-analysis
Calwing Liao, Charles-Etienne Castonguay, Karl Heilbron, et al.
The Lancet. Neurology
|
November 9, 2019
Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies
Mike A Nalls, Cornelis Blauwendraat, Costanza L Vallerga, et al.
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of 58
Search research articles
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Showing results (551-560 of 574) with videos related to
Sort By:
Page
of 58
American Journal of Human Genetics
|
March 5, 2002
Age at onset in two common neurodegenerative diseases is genetically controlled
Yi-Ju Li, William K Scott, Dale J Hedges, et al.
Medrxiv : the Preprint Server for Health Sciences
|
July 17, 2025
Rare but Relevant: Assessing Variants in Dystonia-linked Genes in Parkinson's Disease
Lara M Lange, Zih-Hua Fang, Laurel Screven, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
October 11, 2025
Rare but Relevant? Assessing Variants in Dystonia-Linked Genes in Parkinson's Disease
Lara M Lange, Zih-Hua Fang, Laurel Screven, et al.
Movement Disorders Clinical Practice
|
October 11, 2025
Segmental and Multifocal Isolated Dystonias: Similarities and Differences
Hyder A Jinnah, Vittorio Velucci, Daniele Belvisi, et al.
Neurology
|
October 13, 2020
Dystonia and Tremor: A Cross-Sectional Study of the Dystonia Coalition Cohort
Aasef G Shaikh, Sinem Balta Beylergil, Laura Scorr, et al.
Cell Reports
|
July 27, 2012
Mutations in the gene PRRT2 cause paroxysmal kinesigenic dyskinesia with infantile convulsions
Hsien-Yang Lee, Yong Huang, Nadine Bruneau, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
April 9, 2019
Parkinson's disease age at onset genome-wide association study: Defining heritability, genetic loci, and α-synuclein mechanisms
Cornelis Blauwendraat, Karl Heilbron, Costanza L Vallerga, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
March 1, 2020
Outcome measurement in functional neurological disorder: a systematic review and recommendations
Susannah Pick, David G Anderson, Ali A Asadi-Pooya, et al.
JAMA Neurology
|
January 4, 2022
Association of Essential Tremor With Novel Risk Loci: A Genome-Wide Association Study and Meta-analysis
Calwing Liao, Charles-Etienne Castonguay, Karl Heilbron, et al.
The Lancet. Neurology
|
November 9, 2019
Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies
Mike A Nalls, Cornelis Blauwendraat, Costanza L Vallerga, et al.
Page
of 58