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Seminars in Neurology|August 27, 2002
Progress toward gene therapy of Duchenne muscular dystrophyD Hartigan-O'Connor, J S ChamberlainCurrent Topics in Developmental Biology|February 3, 2009
The value of mammalian models for duchenne muscular dystrophy in developing therapeutic strategiesGlen B Banks, Jeffrey S ChamberlainBiological Psychiatry|November 1, 1990
A novel biochemical model linking dysfunctions in brain melatonin, proopiomelanocortin peptides, and serotonin in autismR S Chamberlain, B H HermanThe American Surgeon|January 9, 2015
Surgeons and their tools: a history of surgical instruments and their innovators. Part III: the medical student's best friend—retractorsAbraham El-Sedfy, Ronald S ChamberlainJournal of Neurology, Neurosurgery, and Psychiatry|February 1, 1980
Lipids and lipoproteins in Friedreich's ataxiaJ L Walker, S Chamberlain, N RobinsonJournal of Pediatric Surgery|July 29, 2015
Probiotic administration can prevent necrotizing enterocolitis in preterm infants: A meta-analysisChristine S M Lau, Ronald S ChamberlainMolecular Therapy. Nucleic Acids|December 2, 2025
Genetic strategies for therapy of Duchenne muscular dystrophyAgnieszka Łoboda, Jeffrey S Chamberlain, Józef DulakGene|August 6, 1999
Insertion of expanded CAG trinucleotide repeat motifs into a yeast artificial chromosome containing the human Machado-Joseph disease geneC K Cemal, C Huxley, S ChamberlainClinical Breast Cancer|June 13, 2017
Disease Severity, Presentation, and Clinical Outcomes Among Adolescents With Malignant Breast Neoplasms: A 20-Year Population-Based Outcomes Study From the SEER Database (1973-2009)Vijayashree Murthy, Shonali Pawar, Ronald S ChamberlainAnnals of Neurology|July 1, 1980
Failure to detect abnormal fatty acid profiles in serum lipoproteins in Friedreich's ataxiaJ L Walker, S Chamberlain, N RobinsonPageof 45