Видео ютуба по тегу Rare Disease India

Children With Rare Diseases Die Waiting For Treatment Despite Govt Policy Assuring Aid
Children With Rare Diseases Die Waiting For Treatment Despite Govt Policy Assuring Aid
Rare Disease Diagnosis & Treatment in India: Girls Father Helps Thousands | The Better India
Rare Disease Diagnosis & Treatment in India: Girls Father Helps Thousands | The Better India
14 Year Old Suffering Rare Disease, Needs 48 Lakhs Rupees To Cure
14 Year Old Suffering Rare Disease, Needs 48 Lakhs Rupees To Cure
Rare genetic diseases in India: An overview and experiences from one centre
Rare genetic diseases in India: An overview and experiences from one centre
How a Journalist Revealed Failures in India’s Rare Disease Plan
How a Journalist Revealed Failures in India’s Rare Disease Plan
Dr. Radha Rama Devi Discusses Rare Diseases in India: Challenges & Government Support
Dr. Radha Rama Devi Discusses Rare Diseases in India: Challenges & Government Support
Five-Year-Old Yunus Battles Rare Muscular Disease DMD | India Today News
Five-Year-Old Yunus Battles Rare Muscular Disease DMD | India Today News
Status of Rare Diseases Today
Status of Rare Diseases Today
Government’s big decision- Treatment to rare diseases
Government’s big decision- Treatment to rare diseases
“Current Scenario of Genetic Rare Diseases in India” by Dr. Suvarna Magar
“Current Scenario of Genetic Rare Diseases in India” by Dr. Suvarna Magar
Dr. L Swasticharan: Rare Disease India - Indo US Bridging RARE Summit 2023
Dr. L Swasticharan: Rare Disease India - Indo US Bridging RARE Summit 2023
Organization For Rare Diseases India
Organization For Rare Diseases India
#RareDisease | IORD | Rare Diseases in India Impact, Initiatives & Challenges
#RareDisease | IORD | Rare Diseases in India Impact, Initiatives & Challenges
Rare Disease Consultation: Blueprint for Rare Diseases in India (North)
Rare Disease Consultation: Blueprint for Rare Diseases in India (North)
Raregivers™: India & US Rare Disease: AI, Multi-lingual in India with Dr. Harsha Rajasimha
Raregivers™: India & US Rare Disease: AI, Multi-lingual in India with Dr. Harsha Rajasimha
Infantile Systemic Hyalinosis | Rare Disease | Organization For Rare Disease in India | Karnataka
Infantile Systemic Hyalinosis | Rare Disease | Organization For Rare Disease in India | Karnataka