News
13d
First Alert 4 on MSNNew gene therapy considered cure for Sickle Cell Disease being administered at St. Louis Children’s HospitalA gene therapy recently approved by the FDA to treat patients with Sickle Cell Anemia is now being administered in St. Louis.
The one-off treatment highlights the promise of a new type of gene editing and the challenges of using it to treat extremely ...
1d
Tribune Online on MSNNew medical advances offer fresh hope for sickle cell patientsExperts make case for early testing, prevention and care In this report, VINCENT KURAUN explores the groundbreaking ...
Family overjoyed correction to DNA defect that causes metabolic disorder has given KJ Muldoon a new lease of life ...
The technique used on a 9½-month-old boy with a rare condition has the potential to help people with thousands of other ...
Editas Medicine reports successful gene editing levels in stem cells, supporting potential treatment for sickle cell disease and beta thalassemia. Editas Medicine announced promising new data on ...
A Delaware County infant with a rare metabolic disease, CPS1 deficiency, was treated at CHOP with a custom CRISPR therapy.
A baby born with a rare and dangerous genetic disease is growing and thriving after getting an experimental gene editing ...
Health camp certifies 35 sickle cell patients for disability benefits, emphasizing prevention, early detection, and community support.
A team of doctors and scientists have successfully treated a rare genetic condition with the first-ever personalized ...
In June, the Centers for Medicare & Medicaid Services (CMS) will name the participating states for the agency’s new Cell and ...
3don MSN
A team of doctors at the Children's Hospital of Philadelphia and Penn Medicine treated a baby with a gene editing technology ...
Results that may be inaccessible to you are currently showing.
Hide inaccessible results