Trusted Resources: People & Places
Healthcare providers, researchers, and advocates
Megan A Waldrop, MD
Healthcare Professionals Assistant Professor
Nationwide Children’s Hospital
700 Childrens Drive
Columbus, Ohio, United States
Megan Waldrop, MD, is a Pediatric Neurologist at Nationwide Children’s Hospital and an Assistant Professor of Pediatrics and Neurology at The Ohio State University College of Medicine. She completed her Pediatrics and Child Neurology training at the Children’s Hospital of Orange County/University of California, Irvine School of Medicine. She completed a Neuromuscular Medicine Fellowship at Ohio State University/Nationwide Children’s Hospital and a Neuromuscular Genetics Therapeutics Fellowship at Nationwide Children’s Hospital.
She is board certified in Neuromuscular Medicine and Neurology with special qualifications in Child Neurology. Her clinical and research interests include muscular dystrophy, congenital myopathy and spinal muscular atrophy, with a particular interest in diagnosing rare neuromuscular diseases.
Representative Publications:
Overview of Gene Therapy in Spinal Muscular Atrophy and Duchenne Muscular Dystrophy
Current Treatment Options in Neurology-SMA Therapeutics
The Genotypic and Phenotypic Spectrum of BICD2 Variants in Spinal Muscular Atrophy
Related Content
-
Kathie Bishop, PhDKathie Bishop is a Ph.D level neuroscien...
-
New Gene Therapy Transforms SMA (Spinal Muscular Atrophy)https://www.youtube.com/watch?v=C5Dl3iMv...
-
Assessment of Cerebral Spinal Fluid Biomarkers and microRNA-Mediated Disease Mechanisms in Spinal Muscular Atrophy P...Cerebral spinal fluid (CSF) is a promisi...
-
Thomas Crawford, MDDr. Tom Crawford has been a member of th...
-
Basil Darras, MDDr. Basil Darras serves as an expert in ...
-
Pharmacological and Clinical Profile of Onasemnogene Aveparvovec, the First Gene Therapy for Spinal Muscular Atrophy...Onasemnogene abeparvovec (Zolgensma; for...
-
A Dallas Startup Aims to Build a Big Business—and Transform Lives—by Curing Rare DiseasesBabies born with spinal muscular atrophy...