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American Journal of Human Genetics|July 1, 1981
HLA linkage and B14, DR1, BfS haplotype association with the genes for late onset and cryptic 21-hydroxylase deficiencyM S Pollack, L S Levine, G J O'Neill, et al.Journal of the American College of Surgeons|February 18, 2018
Venous Thromboembolism after Inpatient Surgery in Administrative Data vs NSQIP: A Multi-Institutional StudyDavid A Etzioni, Cynthia Lessow, Liliana G Bordeianou, et al.Annals of Surgery|March 1, 2019
Concordance Between Registry and Administrative Data in the Determination of Comorbidity: A Multi-institutional StudyDavid A Etzioni, Cynthia Lessow, Liliana G Bordeianou, et al.JCI Insight|November 16, 2023
Spatial transcriptomics identifies candidate stromal drivers of benign prostatic hyperplasiaAnna S Pollack, Christian A Kunder, Noah Brazer, et al.The American Journal of Cardiology|November 1, 1982
Comparison of oral propranolol and verapamil for combined systemic hypertension and angina pectoris. A placebo-controlled double-blind randomized crossover trialW H Frishman, N A Klein, P Klein, et al.The American Journal of Cardiology|November 1, 1982
Comparative effects of abrupt withdrawal of propranolol and verapamil in angina pectorisW H Frishman, N Klein, J Strom, et al.Biology of Blood and Marrow Transplantation : Journal of the American Society for Blood and Marrow Transplantation|September 18, 2002
Phase II study of a moderate-intensity preparative regimen with allogeneic peripheral blood stem cell transplantation for hematologic diseases: the Texas Transplant Consortium experienceP J Shaughnessy, D Ornstein, D Ririe, et al.Oncogenesis|February 12, 2019
Most canine ameloblastomas harbor HRAS mutations, providing a novel large-animal model of RAS-driven cancerPersiana S Saffari, Natalia Vapniarsky, Anna S Pollack, et al.Ophthalmic Surgery, Lasers & Imaging Retina|November 24, 2020
Baseline Visual Acuity at Wet AMD Diagnosis Predicts Long-Term Vision Outcomes: An Analysis of the IRIS RegistryAllen C Ho, David M Kleinman, Flora C Lum, et al.American Journal of Human Genetics|February 1, 1988
Uniparental disomy as a mechanism for human genetic diseaseJ E Spence, R G Perciaccante, G M Greig, et al.Pageof 62