Latest News
Read the latest news articles featuring the LSDSS and the latest topics and developments related to Lysosomal Storage Disorders in India!
- Scientists develop novel way to diagnose genetic disorders - The Times of Indiaon June 3, 2024
- Include funding for rare disease treatment in BJP manifesto: PAGs - The Times of Indiaon April 15, 2024
- Rare disease patients seek inclusion in BJP’s manifesto for funding - The Hinduon April 6, 2024
- Big jolt for kids with rare genetic disorder - The Times of Indiaon December 26, 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 disease: Advocacy group seeks Health Ministry's intervention - The Economic Timeson 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
- The Indian scenario of rare Lysosomal Storage Disorders, diagnostic and treatment approaches - Express Pharmaon January 16, 2023
- Rare disease patients yet to receive financial help promised by Centre, flags MP Varun Gandhi - Down To Earth Magazineon January 10, 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
- Rare Disease India Foundation writes to Centre for funds - Hindustan Timeson March 1, 2022
- Takeda launches mobile app for management of genetic diseases - ETHealthWorldon February 26, 2021
- Covid-19 pose additional challenges for patients with Gaucher - Social News XYZon October 28, 2020
- Tamil Nadu government to form panel to devise cheap Lysosomal Storage Disorder management - The New Indian Expresson August 29, 2019
- Takeda Pharmaceutical expands portfolio of rare disease therapies in India - Moneycontrolon July 15, 2019
- 'Indians at a higher risk of rare genetic diseases' - The Times of Indiaon August 1, 2018
- The diagnosis of Lysosomal Storage Disorders is challenging: Dr. Madhulika Kabra - ETHealthWorldon August 21, 2017
- India's first white paper on rare inherited disorders released - Down To Earth Magazineon March 2, 2015