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This Month in Muscular Dystrophy

Nationwide Children's Hospital

This Month in Muscular Dystrophy

A Science and Medicine podcast
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This Month in Muscular Dystrophy

Nationwide Children's Hospital

This Month in Muscular Dystrophy

Episodes
This Month in Muscular Dystrophy

Nationwide Children's Hospital

This Month in Muscular Dystrophy

A Science and Medicine podcast
Good podcast? Give it some love!
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Episodes of This Month in Muscular Dystrophy

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Guest: Jerry Mendell, MD, is Director of the Center for Gene Therapy in The Research Institute, Director of the Paul D. Wellstone Muscular Dystrophy Cooperative Research Center, and Curran-Peters Chair of Pediatric Research at Nationwide Childr
Guest Host: Scott Harper, PhD, is a principal investigator in the Center for Gene Therapy in The Research Institute at Nationwide Children’s Hospital.Guest: Kevin Flanigan, MD, principal investigator in the Center for Gene Therapy, is also an
Guest: Louise Rodino-Klapac, PhD, is a principal investigator in the Center for Gene Therapy in The Research Institute at Nationwide Children’s Hospital. She is also an assistant professor in the Department of Pediatrics at The Ohio State Unive
Guest: Scott Harper, PhD, is a principal investigator in the Center for Gene Therapy in The Research Institute and the Neuromuscular Disorders program at Nationwide Children’s Hospital. He is also a faculty member for the Child Neurology Reside
Dr. Brian Kaspar Discusses a New Method for Studying ALS, with Potential to Test Therapeutics in Individual Patients :: April 2014Guest: Brian Kaspar, PhD, is a principal investigator in the Center for Gene Therapy and the first recipient of
Dr. Louis Chicoine Discusses the Effect of Plasmapheresis in Removal of AAV Antibodies for Gene Therapy :: November 2013Guest: Louis Chicoine, MD, principal investigator in the Center for Gene Therapy, The Research Institute at Nationwide Ch
Dr. Volker Straub Discusses the Use of Muscle MRI in Muscular DystrophyGuest: Volker Straub, MD, PhD, Harold Macmillan Professor of Medicine and Professor of neuromuscular genetics at the University of Newcastle upon Tyne in the United Kingdo
Dr. Jeff Chamberlain Discusses Gene and Cell Mediated Therapies for Muscular DystrophyGuest: Jeff Chamberlain, PhD, McCaw Chair in Muscular Dystrophy and Professor in the departments of neurology, medicine and biochemistry at the University o
Dr. Paul Martin Discusses Galgt2 Gene Therapy for Muscular DystrophyGuest: Paul T. Martin, principal investigator, Center for Gene Therapy and Neurosciences Center, The Research Institute at Nationwide Children’s Hospital.Access an abstract
Dr. Louise Rodino-Klapac Discusses Alpha 7 Integrin As A Therapeutic Approach to Muscular DystrophyGuest: Louise Rodino-Klapac, PhD, principal investigator, Center for Gene Therapy, The Research Institute at Nationwide Children’s Hospital.A
Dr. James Ervasti Discusses Stability of Therapeutic Forms of Dystrophin :: January 2013Guest: Dr. James Ervasti, PhD, Department of Biochemistry, Molecular Biology and Biophysics, University of MinnesotaAccess an abstract of this month’s f
Dr. Federica Montanaro Discusses New Cardiac Dystrophin Associated Proteins :: December 2012Guest: Dr. Federica Montanaro, PhD, principal investigator in the Center for Gene Therapy at The Research Institute at Nationwide Children’s Hospital
Professor Francesco Muntoni Discusses Congenital Muscular DystrophiesGuest: Professor Francesco Muntoni, Chair of Paediatric Neurology, United College London Institute of Child Health, Dubowitz Neuromuscular CentreAccess an abstract of this m
Dr. Louise Rodino-Klapac Discusses Advances in Dysferlin Gene TherapyGuest: Louise Rodino-Klapac, PhD, principal investigator, Center for Gene Therapy, The Research Institute at Nationwide Children’s HospitalAccess an abstract of this month’
Dr. Hugh Allen Discusses Cardiomyopathy in Duchenne Muscular DystrophyGuest: Hugh Allen, MD, principal investigator, Center for Gene TherapyAccess an abstract of this month’s featured research article: Effects of Angiotensin-Converting Enzy
Dr. Jerry Mendell Discusses Newborn Screening in Duchenne Muscular Dystrophy :: April 2012Guest: Jerry Mendell, MD, director, Center for Gene Therapy, The Research Institute at Nationwide Children’s Hospital.Access an abstract of this month
Dr. Thomas Voit Discusses Gamma Sarcoglycan Gene Therapy :: March 2012Guest: Thomas Voit, medical and scientific director, Institut de Myologie, Paris, FranceAccess an abstract of this month’s featured research article: A phase I trial of a
Dr. Arthur Burghes discusses antisense oligomer treatment in an SMA mouse modelGuest: Arthur Burghes, PhD, professor of Molecular and Cellular Biochemistry, Molecular Genetics and Neurology, The Ohio State University
Guest: Professor Steve Wilton, Australian Neuromuscular Research Institute, The University of Western AustraliaAccess an abstract of this month’s featured research article: Dystrophin isoform induction in vivo by antisense-mediated alternativ
Guest: Denis Guttridge, PhD, Associate Professor, Molecular Virology, Immunology and Medical Genetics, The Ohio State UniversityAccess an abstract of this month’s featured research articles: Improvement of cardiac contractile function by pep
Guest: Jill Rafael-Fortney, PhD, Department of Molecular and Cellular Biochemistry, The Ohio State UniversityAccess an abstract of this month’s featured research article: Early Treatment with Lisinopril and Spironolactone Preserves Cardiac
Guest: Valérie Allamand, PhD, the Institute of Myology, Paris, FranceAccess an abstract of this month’s featured research article: Satellite cell loss and impaired muscle regeneration in selenoprotein N deficiency. Hum Mol Genet. 2011 Feb 15;
Guest: Dr. Carsten Bonnemann, MD, Senior Investigator, Neurogenetics Branch, and Chief of Neuromuscular and Neurogenetic Disorders of Childhood Section, National Institutes of Neurological Disorders and Stroke, National Institutes of HealthAc
Guest: Paul Martin, PhD, principal investigator, Center for Gene Therapy, The Research Institute at Nationwide Children’s HospitalAccess an abstract of this month’s featured research article: A human-specific deletion in mouse Cmah increases d
Guest: Scott Harper, PhD, Nationwide Children's HospitalAccess an abstract of this Month's Featured Research Article: DUX4, a candidate gene for facioscapulohumeral muscular dystrophy, causes p53-dependent myopathy in vivo. Ann Neurol. 2010 O
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