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Parkinson'S Disease|April 2, 2016
Altered Mitochondrial Respiration and Other Features of Mitochondrial Function in Parkin-Mutant Fibroblasts from Parkinson's Disease PatientsWilliam Haylett, Chrisna Swart, Francois van der Westhuizen, et al.
Scientific Reports|May 29, 2019
Ocean predation and mortality of adult Atlantic salmonJohn Fredrik Strøm, Audun Håvard Rikardsen, Steven E Campana, et al.
Clinical Genetics|April 29, 2024
Best practice guidelines on genetic diagnostics of facioscapulohumeral muscular dystrophy: Update of the 2012 guidelinesEmiliano Giardina, Pilar Camaño, Sarah Burton-Jones, et al.
British Journal of Sports Medicine|November 10, 2017
Chronic inflammation is a feature of Achilles tendinopathy and ruptureStephanie Georgina Dakin, Julia Newton, Fernando O Martinez, et al.
European Journal of Human Genetics : EJHG|June 14, 2025
Structural variation in nebulin and its impact on phenotype and inheritance: establishing a dominant distal phenotype caused by large deletionsLydia Sagath, Kirsi Kiiski, Kireshnee Naidu, et al.
Medrxiv : the Preprint Server for Health Sciences|January 13, 2025
Structural variation in nebulin and its implications on phenotype and inheritance: establishing a dominant distal phenotype caused by large deletionsLydia Sagath, Kirsi Kiiski, Kireshnee Naidu, et al.
Discover Mental Health|October 20, 2023
RNA-seq analysis of gene expression profiles in posttraumatic stress disorder, Parkinson's disease and schizophrenia identifies roles for common and distinct biological pathwaysSian M J Hemmings, Patricia Swart, Jacqueline S Womersely, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 7, 2018
PTRHD1 Loss-of-function mutation in an african family with juvenile-onset Parkinsonism and intellectual disabilityDemy J S Kuipers, Jonathan Carr, Soraya Bardien, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 8, 2009
GCH1 in early-onset Parkinson's diseaseStephanie A Cobb, Christian Wider, Owen A Ross, et al.
BMC Medical Genetics|February 6, 2020
Targeted next-generation sequencing identifies novel variants in candidate genes for Parkinson's disease in Black South African and Nigerian patientsOluwafemi G Oluwole, Helena Kuivaniemi, Shameemah Abrahams, et al.
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