Gene Therapy Cure for Beta Thalassemia @ucsf
Gene Therapy Cure for Beta Thalassemia  @ucsf
Uploaded October 2023 | Updated September 2026, 1 week ago
Nine-year-old Ada is the very first patient on the West Coast to receive a life-changing curative therapy for beta thalassemia, a rare blood disorder. UCSF Benioff Children’s Hospital Oakland led clinical trials of this innovative therapy, which recently received FDA approval. Now 90% of patients, including Ada, are free from monthly six-hour blood transfusions to manage their blood disorder.
Gene Therapy Cure for Beta Thalassemia2023 year in YouTube #shortsA 17-Year-Old Beat a Massive #Stroke and Now Helps Others3d Spine Surgery #ucsf‘Extremely Personal’: Why a Physician is Determined to Serve, Mentor the UnderrepresentedWhy a UCSF Associate Professor Found a Calling in Sub-Saharan Africa2023: UCSF Year in ImagesNew DBS Brain Pacemaker Improves Movement for People with ParkinsonsWhat hooked you on Science? #ucsfThe Power of Deep Rest2023 Last Lecture with Dr. Kai KennedyThis Stool is Taken – UCSF Postdoc Slam 2023, Jay Moltzau Anderson, PhD
UC San Francisco (UCSF) |

Gene Therapy Cure for Beta Thalassemia

SHARE TO X SHARE TO REDDIT SHARE TO FACEBOOK WALLPAPER