Latest News
Read the latest news articles featuring the LSDSS and the latest topics and developments related to Lysosomal Storage Disorders in India!
- Rare-disease patients urge health minister to release funds - The Times of Indiaon December 18, 2024
- Patients suffering from rare disease await funds for treatment after exhausting Rs 50L given by govt - ETHealthWorldon December 2, 2024
- India News - LatestLYon December 1, 2024
- Petition sent to Union Health Minister seeking sustainable treatment support for Gaucher Disease - The Hinduon October 19, 2024
- How heel-prick can save an infant’s life - The Times of Indiaon June 4, 2024
- Rare disease patients seek inclusion in BJP’s manifesto for funding - The Hinduon April 6, 2024
- Lysosomal storage disorders identified in adult population from India: Experience of a tertiary genetic centre and review of literature - Wiley Online Libraryon January 2, 2024
- Early Screening Crucial to Manage Rare Genetic Disorders - ETHealthWorldon December 5, 2023
- Rare diseases: Funds use by AIIMS rarer - The Times of Indiaon July 29, 2023
- Tackling Rare Disease in India - Inside Precision Medicineon June 5, 2023
- Despite availability of funds, patients with rare Fabry Disease yet to be given treatment, says support society - The Hinduon April 29, 2023
- Fabry Awareness Month: Five-point recommendation to decision makers of India - ETHealthWorldon April 27, 2023
- Rare Diseases Need Not Be Neglected Anymore - BSI bureauon February 28, 2023
- We remain committed to delivering new options for people with rare diseases: Anil Raina, Sanofi - ETHealthWorldon February 28, 2023
- The Indian scenario of rare Lysosomal Storage Disorders, diagnostic and treatment approaches - Express Pharmaon January 16, 2023
- Lysosomal storage disorders: from biology to the clinic with reference to India - The Lanceton November 20, 2022
- Newborn Screening in India: An overview on challenges and opportunities to improve public health - Express Healthcareon October 7, 2022
- Takeda India reaffirms commitment on World Rare Disease Day - BSI bureauon March 2, 2020
- Health Minister expedites process of rare disease policy formation - BSI bureauon June 27, 2019
- 'Indians at a higher risk of rare genetic diseases' - The Times of Indiaon August 1, 2018
- Sanofi Genzyme reaffirms its support towards rare diseases in India - BSI bureauon February 26, 2018
- Ignored so far, rare genetic disorders continue to face neglect - BSI bureauon September 1, 2014