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Pediatrics|December 1, 1990
Diagnosis and management of infantile marfan syndromeR P Morse, S Rockenmacher, R E Pyeritz, et al.
The American Journal of Drug and Alcohol Abuse|July 26, 2014
An open-label pilot trial of N-acetylcysteine and varenicline in adult cigarette smokersErin A McClure, Nathaniel L Baker, Cassandra D Gipson, et al.
Annals of Neurology|November 15, 2001
Human herpesvirus 6 limbic encephalitis after stem cell transplantationM S Wainwright, P L Martin, R P Morse, et al.
Archives of Neurology|June 15, 2011
Neuropathy in a human without the PMP22 geneMario Andre Saporta, Istvan Katona, Xuebao Zhang, et al.
Prostate Cancer and Prostatic Diseases|June 13, 2012
A randomized phase II study of pomegranate extract for men with rising PSA following initial therapy for localized prostate cancerC J Paller, X Ye, P J Wozniak, et al.
Neurology|July 24, 2002
Autosomal recessive inheritance of RYR1 mutations in a congenital myopathy with coresH Jungbluth, C R Müller, B Halliger-Keller, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 5, 2001
Recombinant human acid alpha-glucosidase enzyme therapy for infantile glycogen storage disease type II: results of a phase I/II clinical trialA Amalfitano, A R Bengur, R P Morse, et al.
Human Mutation|August 10, 2013
MTO1 mutations are associated with hypertrophic cardiomyopathy and lactic acidosis and cause respiratory chain deficiency in humans and yeastEnrico Baruffini, Cristina Dallabona, Federica Invernizzi, et al.
Neurology|January 26, 2011
Muscle histology vs MRI in Duchenne muscular dystrophyM Kinali, V Arechavala-Gomeza, S Cirak, et al.
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