Showing results (881-890 of 902) with videos related to
Sort By:
Pageof 91
JAMA Neurology|November 29, 2017
Neurologic Phenotypes Associated With Mutations in RTN4IP1 (OPA10) in Children and Young AdultsMajida Charif, Alessia Nasca, Kyle Thompson, et al.Neurology|September 16, 2016
A genome-wide association study in multiple system atrophyAnna Sailer, Sonja W Scholz, Michael A Nalls, et al.Nature Genetics|July 31, 2007
C-terminal truncations in human 3'-5' DNA exonuclease TREX1 cause autosomal dominant retinal vasculopathy with cerebral leukodystrophyAnna Richards, Arn M J M van den Maagdenberg, Joanna C Jen, et al.Nature Genetics|November 17, 2009
Genome-wide association study reveals genetic risk underlying Parkinson's diseaseJavier Simón-Sánchez, Claudia Schulte, Jose M Bras, et al.Nature Genetics|July 28, 2014
Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's diseaseMike A Nalls, Nathan Pankratz, Christina M Lill, et al.Neuron|November 26, 2020
Pathogenic Huntingtin Repeat Expansions in Patients with Frontotemporal Dementia and Amyotrophic Lateral SclerosisRamita Dewan, Ruth Chia, Jinhui Ding, et al.American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|November 30, 2020
The demise of islet allotransplantation in the United States: A call for an urgent regulatory updatePiotr Witkowski, Louis H Philipson, Dixon B Kaufman, et al.The Lancet. Neurology|November 9, 2019
Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studiesMike A Nalls, Cornelis Blauwendraat, Costanza L Vallerga, et al.Journal of Neurology|June 27, 2024
A multi-centre longitudinal study analysing multiple sclerosis disease-modifying therapy prescribing patterns during the COVID-19 pandemicAnoushka P Lal, Yi Chao Foong, Paul G Sanfilippo, et al.Cell Genomics|June 30, 2023
Genome-wide structural variant analysis identifies risk loci for non-Alzheimer's dementiasKarri Kaivola, Ruth Chia, Jinhui Ding, et al.Pageof 91