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Plos One|October 11, 2014
The extracellular domain of myelin oligodendrocyte glycoprotein elicits atypical experimental autoimmune encephalomyelitis in rat and Macaque speciesAlan D Curtis, Najla Taslim, Shaun P Reece, et al.The Journal of Infectious Diseases|April 1, 1991
Safety and pharmacokinetics of 566C80, a hydroxynaphthoquinone with anti-Pneumocystis carinii activity: a phase I study in human immunodeficiency virus (HIV)-infected menW T Hughes, W Kennedy, J L Shenep, et al.JIMD Reports|October 8, 2013
Cystinosis with sclerotic bone lesionsS Sirrs, P Munk, P I Mallinson, et al.Current Neurovascular Research|February 2, 2019
Basilar Apex Aneurysms in the Setting of Carotid Artery Stenosis: Case Series and Angiographic Anatomic StudyMihael D Rosenbaum, Daniel M Heiferman, Osama A Raslan, et al.Journal of Medical Toxicology : Official Journal of the American College of Medical Toxicology|December 4, 2014
Acute Methylenedioxypyrovalerone ToxicityBlake A Froberg, Michael Levine, Michael C Beuhler, et al.American Journal of Medical Genetics|February 25, 2000
No evidence for a major susceptibility locus for juvenile myoclonic epilepsy on chromosome 15qM Durner, S Shinnar, S R Resor, et al.The Journal of Rheumatology|December 15, 2025
Examination of HLA-DRB1*15-linked candidate antigens in Still's disease with and without lung disease and features of drug hypersensitivityDale M Kobrin, D Garrett Brown, Peter D Burbelo, et al.Arthritis & Rheumatology (Hoboken, N.J.)|February 11, 2026
Type I interferon signature associates with lung disease, drug-associated immune reactions, and genetic variation in interferon-linked pathways in Still's diseaseMariana Correia Marques, Zuoming Deng, Navid Chowdhury, et al.Clinical Pharmacology and Therapeutics|May 25, 2007
The bradykinin type 2 receptor BE1 polymorphism and ethnicity influence systolic blood pressure and vascular resistanceM M Pretorius, J V Gainer, G P Van Guilder, et al.American Journal of Human Genetics|March 21, 2000
Reproducibility and complications in gene searches: linkage on chromosome 6, heterogeneity, association, and maternal inheritance in juvenile myoclonic epilepsyD A Greenberg, M Durner, M Keddache, et al.Pageof 24