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Annals of Neurology|March 9, 2018
Recessive mutations in VPS13D cause childhood onset movement disordersJulie Gauthier, Inge A Meijer, Davor Lessel, et al.Neuroinformatics|May 18, 2021
The C-BIG Repository: an Institution-Level Open Science PlatformSamir Das, Rida Abou-Haidar, Henri Rabalais, et al.Nature Genetics|January 10, 2017
Impaired H3K36 methylation defines a subset of head and neck squamous cell carcinomasSimon Papillon-Cavanagh, Chao Lu, Tenzin Gayden, et al.Neuromuscular Disorders : NMD|January 17, 2023
Myositis with prominent B cell aggregates may meet classification criteria for sporadic inclusion body myositisAlain Meyer, Yves Troyanov, Pat Korathanakhun, et al.Nature Communications|April 7, 2016
Spatial and temporal homogeneity of driver mutations in diffuse intrinsic pontine gliomaHamid Nikbakht, Eshini Panditharatna, Leonie G Mikael, et al.Neurology. Genetics|October 30, 2023
mTOR Pathway Somatic Pathogenic Variants in Focal Malformations of Cortical Development: Novel Variants, Topographic Mapping, and Clinical OutcomesEric Krochmalnek, Andrea Accogli, Judith St-Onge, et al.Journal of Parkinson'S Disease|December 24, 2019
The Quebec Parkinson Network: A Researcher-Patient Matching Platform and Multimodal BiorepositoryZiv Gan-Or, Trisha Rao, Etienne Leveille, et al.Cancer Discovery|September 24, 2020
H3.3 G34W Promotes Growth and Impedes Differentiation of Osteoblast-Like Mesenchymal Progenitors in Giant Cell Tumor of BoneSima Khazaei, Nicolas De Jay, Shriya Deshmukh, et al.Arthritis Research & Therapy|January 10, 2020
Statin-induced anti-HMGCR myopathy: successful therapeutic strategies for corticosteroid-free remission in 55 patientsAlain Meyer, Yves Troyanov, Julie Drouin, et al.Frontiers in Neuroinformatics|January 24, 2017
Cyberinfrastructure for Open Science at the Montreal Neurological InstituteSamir Das, Tristan Glatard, Christine Rogers, et al.Pageof 7