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American Journal of Human Genetics|October 23, 2012
A mutation in PNPT1, encoding mitochondrial-RNA-import protein PNPase, causes hereditary hearing lossSimon von Ameln, Geng Wang, Redouane Boulouiz, et al.
The International Journal of Artificial Organs|May 12, 2018
Antithrombotic therapy in pediatric ventricular assist devices: Multicenter survey of the European EXCOR Pediatric Investigator GroupOliver Miera, Katharina L Schmitt, Hakan Akintuerk, et al.
European Journal of Cancer (Oxford, England : 1990)|June 14, 2024
Understanding quality of life issues in patients with advanced melanoma: Phase 1 and 2 in the development of the EORTC advanced melanoma moduleM D Egeler, M van Leeuwen, J Lai-Kwon, et al.
Oncotarget|April 4, 2012
Stratification of Wilms tumor by genetic and epigenetic analysisRichard H Scott, Anne Murray, Linda Baskcomb, et al.
Circulation Research|July 22, 2015
Adrenergic Repression of the Epigenetic Reader MeCP2 Facilitates Cardiac Adaptation in Chronic Heart FailureSandra C Mayer, Ralf Gilsbach, Sebastian Preissl, et al.
American Journal of Medicine Open|April 1, 2025
Returning Individual-Level Urgent or Emergent Research Results to Participants: The Project Baseline Health Study ExperienceNeha Pagidipati, Brooke Heidenfelder, Lydia Coulter Kwee, et al.
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