Showing results (971-980 of 2,404) with videos related to
Sort By:
Pageof 241
International Journal of Molecular Sciences|December 19, 2018
Histone H3 lysine 9 acetylation is downregulated in GDM Placentas and Calcitriol supplementation enhanced this effectPaula Hepp, Stefan Hutter, Julia Knabl, et al.Retina (Philadelphia, Pa.)|December 13, 2017
THEORETICAL GAS CONCENTRATIONS ACHIEVING 100% FILL OF THE VITREOUS CAVITY IN THE POSTOPERATIVE PERIOD: A Gas Eye Model StudyTom H Williamson, Jean-Yves Guillemaut, Sheldon K Hall, et al.AJR. American Journal of Roentgenology|January 1, 1983
Contrast-medium-induced electrocardiographic abnormalities: comparison of bolus and infusion of methylglucamine iodamide and methylglucamine/sodium diatrizoateR C Pfister, A M Hutter, J H Newhouse, et al.The American Journal of Cardiology|January 1, 1981
Predicting cardiac morbidity based on risk factors and coronary angiographic findingsJ E Dimsdale, J Gilbert, A M Hutter, et al.Journal of Biotechnology|December 19, 2016
Biotransformation of prednisone and dexamethasone by cytochrome P450 based systems - Identification of new potential drug candidatesNatalia Putkaradze, Flora Marta Kiss, Daniela Schmitz, et al.Vector Borne and Zoonotic Diseases (Larchmont, N.Y.)|August 14, 2019
Leptospira Seroprevalence Detection and Rabies Virus Absence in an Urban Raccoon (Procyon lotor) Population in a Highly Populated Area, Costa RicaMario Baldi, Gabriela Hernández-Mora, Carlos Jimenez, et al.Heliyon|March 30, 2019
Hepatic and neuronal phenotype of NPC1-/- miceEstibaliz Santiago-Mujica, Stefanie Flunkert, Roland Rabl, et al.The American Journal of Cardiology|October 1, 1978
Type A personality and extent of coronary atherosclerosisJ E Dimsdale, T P Hackett, A M Hutter, et al.Child Neuropsychology : a Journal on Normal and Abnormal Development in Childhood and Adolescence|February 24, 2004
Math weaknesses in survivors of acute lymphoblastic leukemia compared to healthy childrenKris L Kaemingk, Marissa E Carey, Ida M Moore, et al.Neurogenetics|March 14, 2009
Ashkenazi Parkinson's disease patients with the LRRK2 G2019S mutation share a common founder dating from the second to fifth centuriesAnat Bar-Shira, Carolyn M Hutter, Nir Giladi, et al.Pageof 241