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Event Details
CureDuchenne
2010
Breakfast with the DMD Experts
On Saturday March 20th, CureDuchenne’s Scientific Advisory Board will be available to answer questions and present the latest DMD research. Please join us in Newport Beach, CA for breakfast to meet these researchers as well as meet Southern CA physical therapist, Jennifer Wallace, who specializes in Duchenne.
CureDuchenne's Scientific Advisory Board
Barry J. Byrne, MD, PhD, University of Florida
Professor and Associate Chair of Research,
Department of Pediatrics and Microbiology & Molecular Genetics.
Kevin Campbell, PhD, University of Iowa
Roy J. Carver Biomedical Research Chair in Molecular Physiology and Biophysics
Jeffrey Chamberlain, PhD, University of Washington School of Medicine
Principle Investigator of the Chamberlain Lab in the Dept. of Nuerology
Eric Hoffman, PhD, Chairman, Department of Integrative Systems Biology, George Washington
University School of Medicine, Clark Chair and Director, Research Center for Genetic Medicine,
Children’s National Medical Center in Washington DC
Edward Kaye, M.D.
Group VP Clinical Research at Genzyme
Douglas Macdonald, PhD
Director Drug Discovery at CHDI Foundation, Inc.
Carrie Miceli, PhD, UCLA
Professor in the Dept. of Microbiology, Immunology & Molecular Genetics
Stanley Nelson, MD, UCLA
Professor in the Departments of Psychiatry & Biobehavioral Sciences & Human Genetics
Pier Lorenzo Puri, MD/PhD, Burnham Institute San Diego Ca.
Assistant Professor at the Burnham Institute
Brian Tseng, MD/PhD, Massachusetts General Hospital Harvard Medical School
Assistant Professor & Director at Pediatric Neuromuscular Clinic
Where
Newport Beach Marriott
900 Newport Center Drive
Newport Beach,
CA 92660
Other Maps:
Hosted By
CureDuchenne
CureDuchenne is fighting for the lives of the 1 in every 3500 boys who are stricken with Duchenne Muscular Dystrophy. Most of these boys will not live past their teens. Their muscle cells will die and won't regenerate. It can happen in any family. But finally, thanks to recent scientific breakthroughs, THERE IS HOPE!
CureDuchenne is a not-for-profit organization founded by Corona del Mar (California) parents of a Duchenne boy. Unlike other organizations that simply fund research, CureDuchenne demands more. They are fighting to bring the most promising research out of the labs and into clinical trials that can save THIS generation of Duchenne boys. YOU can help us bring lifesaving treatments to market and give them a chance for a life.
