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Journal of Medical Systems|August 28, 2019
Profile of Educational Technology Use by Medical Students and Evaluation of a New Mobile Application Designed for the Study of Human PhysiologyErica Y Oliveira, Nathalia I Crosewski, André L M Silva, et al.The Cochrane Database of Systematic Reviews|March 11, 2015
Standard (head-down tilt) versus modified (without head-down tilt) postural drainage in infants and young children with cystic fibrosisDiana A Freitas, Fernando A L Dias, Gabriela S S Chaves, et al.American Journal of Physiology. Heart and Circulatory Physiology|July 12, 2011
Effects of nicotine administration in a mouse model of familial hypertrophic cardiomyopathy, α-tropomyosin D175NRobert D Gaffin, Shamim A K Chowdhury, Marco S L Alves, et al.The Cochrane Database of Systematic Reviews|September 24, 2013
Chest physiotherapy for pneumonia in childrenGabriela S S Chaves, Guilherme A F Fregonezi, Fernando A L Dias, et al.Journal of Molecular and Cellular Cardiology|June 30, 2006
The effect of myosin regulatory light chain phosphorylation on the frequency-dependent regulation of cardiac functionFernando A L Dias, Lori A Walker, Grace M Arteaga, et al.Journal of Molecular and Cellular Cardiology|August 16, 2011
Long-term rescue of a familial hypertrophic cardiomyopathy caused by a mutation in the thin filament protein, tropomyosin, via modulation of a calcium cycling proteinRobert D Gaffin, James R Peña, Marco S L Alves, et al.Cardiovascular Pathology : the Official Journal of the Society for Cardiovascular Pathology|May 28, 2017
Exercise training ameliorates matrix metalloproteinases 2 and 9 messenger RNA expression and mitigates adverse left ventricular remodeling in streptozotocin-induced diabetic ratsFlávio S Silva, Raul H Bortolin, Diego N Araújo, et al.Circulation. Cardiovascular Genetics|March 4, 2014
Desensitization of myofilaments to Ca2+ as a therapeutic target for hypertrophic cardiomyopathy with mutations in thin filament proteinsMarco L Alves, Fernando A L Dias, Robert D Gaffin, et al.Pageof 2