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Dystonia (Lausanne, Switzerland)|October 17, 2022
Clinical Features and Evolution of Blepharospasm: A Multicenter International Cohort and Systematic Literature ReviewLaura M Scorr, Hyun Joo Cho, Gamze Kilic-Berkmen, et al.Journal of Neurology|March 21, 2023
COVID19-associated new-onset movement disorders: a follow-up studySusanne A Schneider, Soaham Desai, Onanong Phokaewvarangkul, et al.Nature Genetics|June 9, 2016
Identification of TMEM230 mutations in familial Parkinson's diseaseHan-Xiang Deng, Yong Shi, Yi Yang, et al.American Journal of Human Genetics|March 6, 2003
Mitochondrial polymorphisms significantly reduce the risk of Parkinson diseaseJoelle M van der Walt, Kristin K Nicodemus, Eden R Martin, et al.Archives of Neurology|July 23, 2003
Association study of Parkin gene polymorphisms with idiopathic Parkinson diseaseSofia A Oliveira, William K Scott, Martha A Nance, et al.European Journal of Neurology|July 23, 2021
Predictive modeling of spread in adult-onset isolated dystonia: Key properties and effect of tremor inclusionMeng Wang, Tolulope Sajobi, Francesca Morgante, et al.Human Molecular Genetics|October 23, 2003
Glutathione S-transferase omega-1 modifies age-at-onset of Alzheimer disease and Parkinson diseaseYi-Ju Li, Sofia A Oliveira, Puting Xu, et al.American Journal of Human Genetics|March 5, 2002
Age at onset in two common neurodegenerative diseases is genetically controlledYi-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 DiseaseLara 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 DiseaseLara M Lange, Zih-Hua Fang, Laurel Screven, et al.Pageof 59