RARECast
Podcast autorstwa RARECast - Czwartki
548 Odcinki
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How One Drugmaker Reaches out to Communities at Greater Risk for Rare Heart Condition
Opublikowany: 3.03.2023 -
A Next-Generation RNA Therapy Targets Telomere Disorders
Opublikowany: 3.03.2023 -
BridgeBio Advances Therapy for Limb-Girdle Muscular Dystrophy that Started with Two Patient Families
Opublikowany: 24.02.2023 -
Translating Urgency into Science
Opublikowany: 16.02.2023 -
Empowering Ultra-Rare Disease Patients to Pursue the Discovery of Treatments
Opublikowany: 10.02.2023 -
Why a Topical Cannabidiol Gel May Help Treat the Behavioral Symptoms of Fragile X
Opublikowany: 2.02.2023 -
An Ultra-Rare Disease Drug Developer Tries to Navigate Regulatory Uncertainty
Opublikowany: 26.01.2023 -
Powering Cells in People with Rare Mitochondrial Diseases
Opublikowany: 19.01.2023 -
Powering Weakened and Stressed Cells in ALS to Function Better with Nanocrystal Therapy
Opublikowany: 12.01.2023 -
Developing a New Class of Therapies Based on a Natural Cargo Carrier
Opublikowany: 5.01.2023 -
Reaching Beyond the Limits of Enzyme Replacement Therapies with Gene Therapies
Opublikowany: 29.12.2022 -
One Woman’s Journey as a Caregiver to a Husband with Frontotemporal Dementia
Opublikowany: 22.12.2022 -
Treating Rare Endocrine Disorders with Therapeutic Peptides
Opublikowany: 15.12.2022 -
Tackling the Pricing Challenges for Advanced Therapies for Rare Diseases
Opublikowany: 8.12.2022 -
Addressing the Current Limitations of AAV Gene Therapies
Opublikowany: 1.12.2022 -
Examining the Legislative Landscape for Rare Disease Drug Development
Opublikowany: 24.11.2022 -
How a Drug Setback Became a Patient Community’s Gain
Opublikowany: 18.11.2022 -
Helping Regulators and Drug Developers Understand the Challenges of Living with Fabry Disease
Opublikowany: 10.11.2022 -
Addressing Racial Disparities in a Rare Blood Cancer
Opublikowany: 3.11.2022 -
How New Sequencing Technology Promises to Alter the Diagnostic Odyssey
Opublikowany: 27.10.2022
RARECast is a Global Genes podcast hosted by award-winning journalist Daniel Levine. It focuses on the intersection of rare disease with business, science, and policy.