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Neurobiology of Aging|November 26, 2020
Association study of DNAJC13, UCHL1, HTRA2, GIGYF2, and EIF4G1 with Parkinson's diseasePrabhjyot Saini, Uladzislau Rudakou, Eric Yu, et al.Parkinsonism & Related Disorders|March 31, 2015
Genetic markers of Restless Legs Syndrome in Parkinson diseaseZiv Gan-Or, Roy N Alcalay, Anat Bar-Shira, et al.Nature Communications|November 5, 2020
Systematic elucidation of neuron-astrocyte interaction in models of amyotrophic lateral sclerosis using multi-modal integrated bioinformatics workflowVartika Mishra, Diane B Re, Virginia Le Verche, et al.Movement Disorders : Official Journal of the Movement Disorder Society|September 24, 2020
Analysis of Heterozygous PRKN Variants and Copy-Number Variations in Parkinson's DiseaseEric Yu, Uladzislau Rudakou, Lynne Krohn, et al.Brain : a Journal of Neurology|August 23, 2015
Closing the tau loop: the missing tau mutationAllan McCarthy, Roisin Lonergan, Diana A Olszewska, et al.Biorxiv : the Preprint Server for Biology|November 28, 2024
Single-cell transcriptomic landscape of the neuroimmune compartment in amyotrophic lateral sclerosis brain and spinal cordJohn F Tuddenham, Masashi Fujita, Anthony Khairallah, et al.Neurology. Genetics|February 12, 2020
Analysis of common and rare VPS13C variants in late-onset Parkinson diseaseUladzislau Rudakou, Jennifer A Ruskey, Lynne Krohn, et al.Neurobiology of Aging|May 7, 2020
Variants in the Niemann-Pick type C gene NPC1 are not associated with Parkinson's diseaseBouchra Ouled Amar Bencheikh, Konstantin Senkevich, Uladzislau Rudakou, et al.Medrxiv : the Preprint Server for Health Sciences|March 30, 2023
Association of rare variants in ARSA with Parkinson's diseaseKonstantin Senkevich, Mariia Beletskaia, Aliza Dworkind, et al.Movement Disorders : Official Journal of the Movement Disorder Society|June 29, 2023
Association of Rare Variants in ARSA with Parkinson's DiseaseKonstantin Senkevich, Mariia Beletskaia, Aliza Dworkind, et al.Pageof 28