Medical Bulletin 04 January/ 2025 Dr. Bhumika Maikhuri4 Jan 2025 3:00 PM ISTHere are the top medical news for the dayUnderstanding Duchenne Muscular Dystrophy: Study Unveils Critical Protein Interactions A new study has shed...
Study Highlights Critical Protein Interactions In Duchenne Muscular Dystrophy Dr. Bhumika Maikhuri4 Jan 2025 8:00 AM ISTA new study has shed light on the complex interactions between dystrophin, a protein critical to muscle stability, and its partner protein,...
Sarepta says its experimental Duchenne drug more effective than older medicine Kajal Rajput30 Jan 2024 11:30 AM ISTNew Delhi: Sarepta Therapeutics' experimental drug produced higher levels of a specific protein deficient in some patients with Duchenne muscular...
Odisha: Rs 10 lakh aid for each Duchenne Muscular Dystrophy patient Kajal Rajput8 May 2023 1:30 PM ISTBhubaneswar: Extending financial support to the patients suffering from Duchenne Muscular Dystrophy (DMD), the state government has allowed one-time...
Daily steroids improve motor and pulmonary function in kids with Duchenne muscular dystrophy: JAMA Dr. Kamal Kant Kohli6 May 2022 8:30 PM ISTNew research published in JAMA recommends daily steroid doses for children with Duchenne muscular dystrophy (DMD), marking a significant change in how...
FDA Approves Viltolarsen for Rare Duchenne Muscular Dystrophy Mutation Dr. Kamal Kant Kohli13 Aug 2020 10:00 AM ISTThe U.S. Food and Drug Administration has pgranted accelerated approval to Viltepso (viltolarsen) injection for the treatment of Duchenne muscular...
Gene editing tool to help treat muscular dystrophy savita thakur thakur2 Jan 2016 11:06 AM ISTWASHINGTON: Scientists, including one of Indian-origin, have successfully used a gene editing tool to treat a genetic disease in a fully developed...
FDA delays BioMarin drug approval, gives investors hope savita thakur thakur20 Dec 2015 11:44 AM ISTBy Vidya L NathanThe U.S. Food and Drug Administration pushed back its deadline to decide on drug developer BioMarin Pharmaceutical Inc's lead drug,...
Indian-origin boy denied Duchenne muscular dystrophy treatment in UK Meghna A Singhania20 Oct 2015 11:24 AM ISTLondon, Oct 19: Six children, including a 6-year-old Indian-origin boy, have been denied life-saving treatment from a rare disease due to high costs...
