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Molecular Neurodegeneration|July 9, 2026
Understanding the genetic imperfections of Lewy body dementiaMolly M Watkins, Gisela Xhafkollari, Na Zhao, et al.Frontiers in Genetics|March 18, 2022
Current Status of Next-Generation Sequencing Approaches for Candidate Gene Discovery in Familial Parkinson´s DiseaseNikita Simone Pillay, Owen A Ross, Alan Christoffels, et al.Genes|September 23, 2022
A Novel Nonsense Variant in GRM1 Causes Autosomal Recessive Spinocerebellar Ataxia 13 in a Consanguineous Pakistani FamilyHammad Yousaf, Ambrin Fatima, Zafar Ali, et al.American Journal of Human Genetics|February 24, 2005
Identification of a novel LRRK2 mutation linked to autosomal dominant parkinsonism: evidence of a common founder across European populationsJennifer Kachergus, Ignacio F Mata, Mary Hulihan, et al.Frontiers in Aging Neuroscience|November 7, 2022
Genetic architecture of Parkinson's disease subtypes - Review of the literatureJarosław Dulski, Ryan J Uitti, Owen A Ross, et al.Annals of Clinical and Translational Neurology|February 5, 2025
Epigenome-wide association study, meta-analysis, and multiscore profiling of whole blood in Parkinson's diseaseIngeborg Haugesag Lie, Manuela M X Tan, Maren Stolp Andersen, et al.Journal of Neuroscience Research|March 28, 2007
MAPK-pathway activity, Lrrk2 G2019S, and Parkinson's diseaseLinda R White, Mathias Toft, Sylvia N Kvam, et al.American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|June 11, 2026
The EXPLAIN Study: Exploring Arthrogryposis Multiplex Congenita in Adults in Norway - A Description of Demographic, Medical, and Neurological FindingsMy Vuong Hermansen, Kristin Ørstavik, Unni Steen, et al.Brain : a Journal of Neurology|May 29, 2023
Lysosomal polygenic risk is associated with the severity of neuropathology in Lewy body diseaseJon-Anders Tunold, Manuela M X Tan, Shunsuke Koga, et al.Journal of Parkinson'S Disease|August 14, 2013
Found in transcription: accurate Parkinson's disease classification in peripheral bloodMagdalena Kauczynska Karlsson, Praveen Sharma, Jan Aasly, et al.Pageof 49