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Human Mutation|July 13, 2005
Dysferlin mutations in LGMD2B, Miyoshi myopathy, and atypical dysferlinopathiesKarine Nguyen, Guillaume Bassez, Rafaëlle Bernard, et al.
Canadian Liver Journal|March 13, 2023
Disparities in health utilities among hepatitis C patients receiving care in different settingsYasmin A Saeed, Kate Mason, Nicholas Mitsakakis, et al.
Intellectual and Developmental Disabilities|October 1, 2019
Data Linkage: Canadian and Australian Perspectives on a Valuable Methodology for Intellectual and Developmental Disability ResearchRobert Balogh, Helen Leonard, Jenny Bourke, et al.
Muscle & Nerve|April 10, 2014
Entire CAPN3 gene deletion in a patient with limb-girdle muscular dystrophy type 2AOihane Jaka, Margarita Azpitarte, Coro Paisán-Ruiz, et al.
JACC. Clinical Electrophysiology|February 3, 2025
Cardioverter-Defibrillator Implantation as a Risk Factor For Motor Vehicle CrashJohn A Staples, Daniel Daly-Grafstein, Isaac Robinson, et al.
The Canadian Journal of Cardiology|April 30, 2005
Long-term outcome of cardiac resynchronization therapy in patients with severe congestive heart failureDarryl R Davis, Andrew D Krahn, Anthony S L Tang, et al.
Nucleic Acids Research|December 15, 2023
tRNA shape is an identity element for an archaeal pyrrolysyl-tRNA synthetase from the human gutNatalie Krahn, Jingji Zhang, Sergey V Melnikov, et al.
Nature Communications|November 9, 2022
Cryo-EM reveals the architecture of the PELP1-WDR18 molecular scaffoldJacob Gordon, Fleur L Chapus, Elizabeth G Viverette, et al.
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