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The Lancet. Neurology|January 14, 2012
Subthalamic deep brain stimulation with a constant-current device in Parkinson's disease: an open-label randomised controlled trialMichael S Okun, Bruno V Gallo, George Mandybur, et al.Movement Disorders Clinical Practice|February 11, 2022
Current Guidelines for Classifying and Diagnosing Cervical Dystonia: Empirical Evidence and RecommendationsGamze Kilic-Berkmen, Sarah Pirio Richardson, Joel S Perlmutter, et al.Brain : a Journal of Neurology|February 2, 2026
Mapping the causal chain from genetic risk variants to lipid dysmetabolism in Parkinson's diseaseRuth B De-Paula, Jonggeol Kim, Herve Rhinn, et al.Movement Disorders : Official Journal of the Movement Disorder Society|September 2, 2017
Treatable inherited rare movement disordersH A Jinnah, Alberto Albanese, Kailash P Bhatia, et al.Movement Disorders : Official Journal of the Movement Disorder Society|November 23, 2006
Screening for Lrrk2 G2019S and clinical comparison of Tunisian and North American Caucasian Parkinson's disease familiesLianna Ishihara, Rachel A Gibson, Liling Warren, et al.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.Dystonia (Lausanne, Switzerland)|November 8, 2024
Tremor in cervical dystoniaSinem Balta Beylergil, Krishna Nikhil Mukunda, Mohamed Elkasaby, 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.Pageof 58