Showing results (501-510 of 2,687) with videos related to
Sort By:
Pageof 269
Journal of Molecular and Cellular Cardiology|October 1, 1987
Eicosanoids and susceptibility to ventricular arrhythmias during myocardial ischaemia and reperfusionJ R Parratt, S J Coker, C L WainwrightPediatric Research|September 25, 2020
APS/SPR Virtual Chat: race, racism, and child health equity in academic pediatricsTumaini Rucker Coker, David Keller, Stephanie Davis, et al.Journal of Health, Population, and Nutrition|March 12, 2008
Salmonellosis in Lagos, Nigeria: incidence of Plasmodium falciparum-associated co-infection, patterns of antimicrobial resistance, and emergence of reduced susceptibility to fluoroquinolonesKabir O Akinyemi, Babajide S Bamiro, Akitoye O CokerCancer Letters|June 12, 2019
New insights and therapeutic implication of gut microbiota in non-alcoholic fatty liver disease and its associated liver cancerNiama Ezzaidi, Xiang Zhang, Olabisi Oluwabukola Coker, et al.Archives of Otolaryngology--Head & Neck Surgery|February 1, 1986
Facial paralysis as the initial presentation of an internal carotid artery aneurysmT W Brandt, H A Jenkins, N J CokerNutrients|January 23, 2020
Essential Amino Acid Supplement Lowers Intrahepatic Lipid despite Excess Alcohol ConsumptionMelynda S Coker, Kaylee R Ladd, Jimin Kim, et al.Aperito Journal of Cellular and Molecular Biology|December 1, 2015
Senile transthyretin cardiac amyloidosis in patients with plasma cell dyscrasias: importance of cardiac biopsy for making the correct diagnosisLogan Roof, Woodrow J Coker, John Lazarchick, et al.Journal of Immunology (Baltimore, Md. : 1950)|January 1, 1985
Subsets of Lyt-2+ cells defined by differential expression of the 9F3 antigen: alterations in mice of the lpr/lpr genotypeF J Dumont, R C Habbersett, L Z CokerArchives of Otolaryngology--Head & Neck Surgery|October 1, 1986
Hereditary congenital cholesteatoma. A variant of branchio-oto dysplasiaA F Lipkin, N J Coker, H A JenkinsArchivos Argentinos De Pediatria|January 24, 2022
Severe perinatal hypophosphatasia case with a novel mutationHavva Yazici, Ebru Canda, Sema Kalkan Ucar, et al.Pageof 269