Showing results (2311-2320 of 2,942) with videos related to
Sort By:
Pageof 295
Nature|August 23, 2013
Germline mitochondrial DNA mutations aggravate ageing and can impair brain developmentJaime M Ross, James B Stewart, Erik Hagström, et al.JIMD Reports|August 26, 2015
Safety and Efficacy of Chronic Extended Release Cornstarch Therapy for Glycogen Storage Disease Type IKatalin M Ross, Laurie M Brown, Michelle M Corrado, et al.Journal of Pain and Symptom Management|November 18, 2018
Destination Therapy: Standardizing the Role of Palliative Medicine and Delineating the DT-LVAD JourneyJennifer L Woodburn, Linda L Staley, Sara E Wordingham, et al.American Journal of Physiology. Regulatory, Integrative and Comparative Physiology|November 16, 2012
Effect of chronic perinatal hypoxia on the role of rho-kinase in pulmonary artery contraction in newborn lambsArlin B Blood, Michael H Terry, Travis A Merritt, et al.The Journal of Asthma : Official Journal of the Association for the Care of Asthma|July 15, 2024
Patient and clinician preferences for biologic treatments for severe uncontrolled asthma: a discrete choice experiment (DCE)Melissa M Ross, Yen Chung, Tara Carr, et al.Molecular Pharmaceutics|July 18, 2023
Targeting Acute Myeloid Leukemia Using Sphingosine Kinase 1 Inhibitor-Loaded LiposomesThao M Nguyen, Manasi Jambhrunkar, Sook S Wong, et al.BMC Infectious Diseases|June 9, 2023
Frequency of HIV serodifferent couples within TB-affected households in a setting with a high burden of HIV-associated TBGodwin Anguzu, Amanda J Gupta, Emmanuel Ochom, et al.Drug and Alcohol Dependence|June 14, 2002
Decreased activity of brain phospholipid metabolic enzymes in human users of cocaine and methamphetamineBrian M Ross, Anna Moszczynska, Frank J Peretti, et al.The New England Journal of Medicine|November 15, 1984
Exercise radionuclide ventriculographic responses in hypertensive patients with chest painA G Wasserman, R J Katz, P J Varghese, et al.American Journal of Human Genetics|July 27, 1999
Identification of a mutation cluster in mevalonate kinase deficiency, including a new mutation in a patient of Mennonite ancestryD D Hinson, R M Ross, S Krisans, et al.Pageof 295