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76: An Interview With Julie Parsons, MD, Co-Director of the Neuromuscular Clinic at Children's Hospital Colorado
Manage episode 362468426 series 3302577
Content provided by Rare Care Podcast. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by Rare Care Podcast or their podcast platform partner. If you believe someone is using your copyrighted work without your permission, you can follow the process outlined here https://ro.player.fm/legal.
Larry Luxner, senior correspondent for Rare Disease Advisor, interviews pediatric neurologist Julie Parsons, MD, of Children's Hospital Colorado in Denver. An expert on both muscular atrophy (SMA) and Duchenne muscular dystrophy (DMD), Dr. Parsons discusses how the nation's healthcare system must prepare for an avalanche of Duchenne patients if and when Sarepta's gene therapy wins final approval in May 2023.
133 episoade
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Manage episode 362468426 series 3302577
Content provided by Rare Care Podcast. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by Rare Care Podcast or their podcast platform partner. If you believe someone is using your copyrighted work without your permission, you can follow the process outlined here https://ro.player.fm/legal.
Larry Luxner, senior correspondent for Rare Disease Advisor, interviews pediatric neurologist Julie Parsons, MD, of Children's Hospital Colorado in Denver. An expert on both muscular atrophy (SMA) and Duchenne muscular dystrophy (DMD), Dr. Parsons discusses how the nation's healthcare system must prepare for an avalanche of Duchenne patients if and when Sarepta's gene therapy wins final approval in May 2023.
133 episoade
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Similar cu Rare Care Podcast
Help me fill in the blanks of the practice of ED Critical Care. In this podcast, we discuss all things related to the crashing, critically ill patient in the Emergency Department. Find the show notes at emcrit.org.
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continue reading
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