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American Journal of Human Genetics|November 27, 2012
Exome sequencing reveals de novo WDR45 mutations causing a phenotypically distinct, X-linked dominant form of NBIATobias B Haack, Penelope Hogarth, Michael C Kruer, et al.
Brain : a Journal of Neurology|May 21, 2013
β-Propeller protein-associated neurodegeneration: a new X-linked dominant disorder with brain iron accumulationSusan J Hayflick, Michael C Kruer, Allison Gregory, et al.
Cell Reports|July 27, 2012
Mutations in the gene PRRT2 cause paroxysmal kinesigenic dyskinesia with infantile convulsionsHsien-Yang Lee, Yong Huang, Nadine Bruneau, et al.
Transplant International : Official Journal of the European Society for Organ Transplantation|November 28, 2025
The Variation in Practice of the Living Donor Kidney Transplant Pathway in the UK: Results of a National SurveyKatie Nightingale, Josh Stephenson, Rajesh Sivaprakasam, et al.
Journal of Parkinson'S Disease|April 17, 2026
Levodopa-Induced dyskinesia in Latin America: Prevalence and associated clinical factors in the LARGE-PD cohortHenry Mauricio Chaparro-Solano, Daniel Teixeira-Dos-Santos, Emily Waldo, et al.
Medrxiv : the Preprint Server for Health Sciences|September 5, 2025
EPIDEMIOLOGY OF LEVODOPA-INDUCED DYSKINESIA: PREVALENCE AND ASSOCIATED CLINICAL FACTORS IN LATIN AMERICAHenry Mauricio Chaparro-Solano, Daniel Teixeira-Dos-Santos, Emily Waldo, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 24, 2023
Embracing Monogenic Parkinson's Disease: The MJFF Global Genetic PD CohortEva-Juliane Vollstedt, Susen Schaake, Katja Lohmann, et al.
Brain : a Journal of Neurology|August 1, 2024
Relevance of genetic testing in the gene-targeted trial era: the Rostock Parkinson's disease studyAna Westenberger, Volha Skrahina, Tatiana Usnich, et al.
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