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Parkinsonism & Related Disorders|August 22, 2019
Late-onset phenotype associated with a homozygous GJC2 missense mutation in a Turkish familyDemy J S Kuipers, Zeynep Tufekcioglu, Başar Bilgiç, et al.Journal of Alzheimer'S Disease : JAD|June 30, 2020
Clinical and Pathological Phenotypes of LRP10 Variant Carriers with DementiaLeonie J M Vergouw, Hanneke Geut, Guido Breedveld, 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.BMC Medical Education|March 6, 2024
The co-development and evaluation of an e-learning course on spinal cord injury physical activity counselling: a randomized controlled trialFemke Hoekstra, Heather L Gainforth, Rogier Broeksteeg, et al.Neurobiology of Aging|June 13, 2020
LRP10 variants in progressive supranuclear palsyLeonie J M Vergouw, Shamiram Melhem, Laura Donker Kaat, et al.JACC. Advances|January 20, 2026
Lipoprotein(a) and the Early Diagnosis, Complexity, and Extent of Coronary Artery Disease and Myocardial InfarctionCasper F Coerkamp, Victor A Verpalen, Kaoutar Bouhbouh, et al.Parkinsonism & Related Disorders|December 10, 2021
WARS2 mutations cause dopa-responsive early-onset parkinsonism and progressive myoclonus ataxiaMatej Skorvanek, Irena Rektorova, Wim Mandemakers, et al.Brain : a Journal of Neurology|September 8, 2022
PTPA variants and impaired PP2A activity in early-onset parkinsonism with intellectual disabilityChristina Fevga, Christelle Tesson, Ana Carreras Mascaro, et al.Brain Communications|July 20, 2022
A multiplex pedigree with pathologically confirmed multiple system atrophy and Parkinson's disease with dementiaAlessandra Fanciulli, Fabian Leys, Fabienne Lehner, et al.Annals of Neurology|November 25, 2020
EIF2AK2 Missense Variants Associated with Early Onset Generalized DystoniaDemy J S Kuipers, Wim Mandemakers, Chin-Song Lu, et al.Pageof 8