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Orphanet Journal of Rare Diseases|July 31, 2016
Nosological delineation of congenital ocular motor apraxia type Cogan: an observational studySarah Wente, Simone Schröder, Johannes Buckard, et al.
Plos One|January 5, 2012
Reduced food intake and body weight in mice deficient for the G protein-coupled receptor GPR82Kathrin M Y Engel, Kristin Schröck, Daniel Teupser, et al.
Human Molecular Genetics|December 17, 2013
Recessive and dominant mutations in COL12A1 cause a novel EDS/myopathy overlap syndrome in humans and miceYaqun Zou, Daniela Zwolanek, Yayoi Izu, et al.
Vaccines|May 28, 2022
Differences in Immunogenicity of Three Different Homo- and Heterologous Vaccination Regimens against SARS-CoV-2Robert Daniel Heinrich Markewitz, David Juhl, Daniela Pauli, et al.
Journal of Clinical Medicine|June 28, 2023
A Multidimensional Approach to Assessing Factors Impacting Health-Related Quality of Life after Pediatric Traumatic Brain InjuryNicole von Steinbuechel, Ugne Krenz, Fabian Bockhop, et al.
Academic Radiology|November 8, 2025
Deep Learning Denoising Algorithm for Improved Assessment of Coronary Arteries in Transcatheter Aortic Valve Implantation CT ImagingLudovica R M Lanzafame, Sebastian Steinmetz, Tommaso D'Angelo, et al.
International Journal of Molecular Sciences|September 5, 2019
Ceritinib-Induced Regression of an Insulin-Like Growth Factor-Driven Neuroepithelial Brain TumorAlexandra Russo, Claudia Paret, Francesca Alt, et al.
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