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Movement Disorders : Official Journal of the Movement Disorder Society
|
April 13, 2018
Genotype-Phenotype Relations for the Parkinson's Disease Genes Parkin, PINK1, DJ1: MDSGene Systematic Review
Meike Kasten, Corinna Hartmann, Jennie Hampf, et al.
Environmental Health Perspectives
|
January 29, 2011
Rotenone, paraquat, and Parkinson's disease
Caroline M Tanner, Freya Kamel, G Webster Ross, et al.
Frontiers in Aging Neuroscience
|
July 23, 2016
Prodromal Markers in Parkinson's Disease: Limitations in Longitudinal Studies and Lessons Learned
Sebastian Heinzel, Benjamin Roeben, Yoav Ben-Shlomo, et al.
Genes
|
October 24, 2017
Functional Characterization of Rare RAB12 Variants and Their Role in Musician's and Other Dystonias
Eva Hebert, Friederike Borngräber, Alexander Schmidt, et al.
JAMA Neurology
|
February 19, 2014
Mutations in GNAL: a novel cause of craniocervical dystonia
Kishore R Kumar, Katja Lohmann, Ikuo Masuho, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
April 9, 2020
Rare Variants in Specific Lysosomal Genes Are Associated With Parkinson's Disease
Franziska Hopfner, Stefanie H Mueller, Silke Szymczak, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
April 18, 2018
Clustering of motor and nonmotor traits in leucine-rich repeat kinase 2 G2019S Parkinson's disease nonparkinsonian relatives: A multicenter family study
Tiago A Mestre, Claustre Pont-Sunyer, Farah Kausar, et al.
NPJ Parkinson'S Disease
|
August 1, 2025
Large-scale copy number variant analysis in genes linked to Parkinson´s disease
Zied Landoulsi, Katja Lohmann, Eva-Juliane Vollstedt, et al.
Annals of Neurology
|
April 19, 2013
Whispering dysphonia (DYT4 dystonia) is caused by a mutation in the TUBB4 gene
Katja Lohmann, Robert A Wilcox, Susen Winkler, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
January 12, 2024
Large-Scale Screening: Phenotypic and Mutational Spectrum in Isolated and Combined Dystonia Genes
Mirja Thomsen, Katrin Marth, Sebastian Loens, et al.
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of 10
Search research articles
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Showing results (81-90 of 98) with videos related to
Sort By:
Page
of 10
Movement Disorders : Official Journal of the Movement Disorder Society
|
April 13, 2018
Genotype-Phenotype Relations for the Parkinson's Disease Genes Parkin, PINK1, DJ1: MDSGene Systematic Review
Meike Kasten, Corinna Hartmann, Jennie Hampf, et al.
Environmental Health Perspectives
|
January 29, 2011
Rotenone, paraquat, and Parkinson's disease
Caroline M Tanner, Freya Kamel, G Webster Ross, et al.
Frontiers in Aging Neuroscience
|
July 23, 2016
Prodromal Markers in Parkinson's Disease: Limitations in Longitudinal Studies and Lessons Learned
Sebastian Heinzel, Benjamin Roeben, Yoav Ben-Shlomo, et al.
Genes
|
October 24, 2017
Functional Characterization of Rare RAB12 Variants and Their Role in Musician's and Other Dystonias
Eva Hebert, Friederike Borngräber, Alexander Schmidt, et al.
JAMA Neurology
|
February 19, 2014
Mutations in GNAL: a novel cause of craniocervical dystonia
Kishore R Kumar, Katja Lohmann, Ikuo Masuho, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
April 9, 2020
Rare Variants in Specific Lysosomal Genes Are Associated With Parkinson's Disease
Franziska Hopfner, Stefanie H Mueller, Silke Szymczak, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
April 18, 2018
Clustering of motor and nonmotor traits in leucine-rich repeat kinase 2 G2019S Parkinson's disease nonparkinsonian relatives: A multicenter family study
Tiago A Mestre, Claustre Pont-Sunyer, Farah Kausar, et al.
NPJ Parkinson'S Disease
|
August 1, 2025
Large-scale copy number variant analysis in genes linked to Parkinson´s disease
Zied Landoulsi, Katja Lohmann, Eva-Juliane Vollstedt, et al.
Annals of Neurology
|
April 19, 2013
Whispering dysphonia (DYT4 dystonia) is caused by a mutation in the TUBB4 gene
Katja Lohmann, Robert A Wilcox, Susen Winkler, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
January 12, 2024
Large-Scale Screening: Phenotypic and Mutational Spectrum in Isolated and Combined Dystonia Genes
Mirja Thomsen, Katrin Marth, Sebastian Loens, et al.
Page
of 10