Sidra Medicine, a member of Qatar Foundation, has established a gene therapy centre to treat rare genetic diseases such as ...
KOCHI: Residents of Cherai are rallying to support two-and-a-half-year-old Adharv, who is suffering from Spinal Muscular ...
Thiruvananthapuram, A registry for rare disease patients in the state will become a reality this year, State Health Minister ...
The announcement was made at Arab Health 2025 where Sidra Medicine will highlight its international patient service programmes ...
The health activists argue that the government is empowered with effective law and policy tools and therefore should ...
Health activists demand government action to reduce the cost of SMA medicines, citing constitutional obligations and ...
Biogen has announced that the European Medicines Agency (EMA) and US Food and Drug Administration (FDA) have started ...
Application is supported by results from the DEVOTE study, which suggested that two doses of Spinraza (nusinerse) 50 mg taken ...
Thiruvananthapuram: The Kerala government is planning to launch a registry for rare diseases and set up a treatment clinic in ...
Centre abdicates its constitutional obligation, criticises patients and experts on SMA issue: Our Bureau, New Delhi Friday, January 24, 2025, 18:15 Hrs [IST] Patients and public h ...