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Journal of Neuro-Oncology|January 12, 2013
A very rare cancer in Down syndrome: medulloblastoma. Epidemiological data from 13 countriesDaniel Satgé, Charles A Stiller, Stefan Rutkowski, et al.
Der Radiologe|August 29, 2020
[Microvascular changes in COVID-19]W L Wagner, K Hellbach, M O Fiedler, et al.
Basic Research in Cardiology|November 13, 2020
Functional investigation of the coronary artery disease gene SVEP1Michael J Winkler, Philipp Müller, Amin M Sharifi, et al.
British Journal of Sports Medicine|July 28, 2018
Concussion management in combat sports: consensus statement from the Association of Ringside PhysiciansJohn Neidecker, Nitin K Sethi, Randolph Taylor, et al.
Human Molecular Genetics|September 3, 2010
A point mutation in the dynein heavy chain gene leads to striatal atrophy and compromises neurite outgrowth of striatal neuronsKerstin E Braunstein, Judith Eschbach, Krisztina Ròna-Vörös, et al.
Circulation Research|September 7, 2023
ADAMTS-7 Modulates Atherosclerotic Plaque Formation by Degradation of TIMP-1M Amin Sharifi, Michael Wierer, Tan An Dang, et al.
Nature Genetics|November 10, 2015
Mutations in the transcriptional repressor REST predispose to Wilms tumorShazia S Mahamdallie, Sandra Hanks, Kristen L Karlin, et al.
Human Molecular Genetics|March 7, 2003
Transgenic rat model of Huntington's diseaseStephan von Hörsten, Ina Schmitt, Huu Phuc Nguyen, et al.
Critical Care (London, England)|December 6, 2014
Expert consensus and recommendations on safety criteria for active mobilization of mechanically ventilated critically ill adultsCarol L Hodgson, Kathy Stiller, Dale M Needham, et al.
Molecular Cell|October 16, 2012
eIF2γ mutation that disrupts eIF2 complex integrity links intellectual disability to impaired translation initiationGuntram Borck, Byung-Sik Shin, Barbara Stiller, et al.
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