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Neurology|February 5, 1999
A double mutation (A8296G and G8363A) in the mitochondrial DNA tRNA (Lys) gene associated with myoclonus epilepsy with ragged-red fibersJ Arenas, Y Campos, B Bornstein, et al.American Heart Journal|July 6, 2010
The impact of combined health factors on cardiovascular disease mortalityJonathan A Mitchell, Daniel B Bornstein, Xuemei Sui, et al.Cancer|October 1, 1996
Relationship of tumor grade to other pathologic features and to treatment outcome of patients with early stage breast carcinoma treated with breast-conserving therapyA J Nixon, S J Schnitt, R Gelman, et al.Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|June 17, 1998
Family history and treatment outcome in young women after breast-conserving surgery and radiation therapy for early-stage breast cancerE Chabner, A Nixon, R Gelman, et al.International Journal of Radiation Oncology, Biology, Physics|July 1, 1997
Locally advanced rectal carcinoma: pelvic control and morbidity following preoperative radiation therapy, resection, and intraoperative radiation therapyH K Kim, J M Jessup, C J Beard, et al.Journal of Public Health Management and Practice : JPHMP|January 11, 2018
Which US States Pose the Greatest Threats to Military Readiness and Public Health? Public Health Policy Implications for a Cross-sectional Investigation of Cardiorespiratory Fitness, Body Mass Index, and Injuries Among US Army RecruitsDaniel B Bornstein, George L Grieve, Morgan N Clennin, et al.Neurology|October 10, 2001
Mitochondrial dysfunction associated with a mutation in the Notch3 gene in a CADASIL familyP de la Peña, B Bornstein, P del Hoyo, et al.Human Mutation|March 26, 2003
Mutation analysis in 16 patients with mtDNA depletionR Carrozzo, B Bornstein, S Lucioli, et al.Science Robotics|November 7, 2020
AEGIS autonomous targeting for ChemCam on Mars Science Laboratory: Deployment and results of initial science team useR Francis, T Estlin, G Doran, et al.Annals of Neurology|September 18, 2001
Early-onset multisystem mitochondrial disorder caused by a nonsense mutation in the mitochondrial DNA cytochrome C oxidase II geneY Campos, A García-Redondo, M A Fernández-Moreno, et al.Pageof 13