Skip to content
Care-for-Rare Foundation for children with rare diseases

Care-for-Rare Foundation for children with rare diseases

Help us to help the orphans of medicine!

Menu

  • About us
    • Our vision
    • Our team
    • Our partners
    • Frequently asked questions
  • Our activities
    • Success
  • Take action
    • Donate
    • Support
  • Media library and press
  • Blog
  • Contact
  • Deutsch

Who does research at Dr. von Hauner Children’s Hospital? Our current fellows

Who does research at Dr. von Hauner Children’s Hospital? Our current fellows

We show the scientist in the research building Kubus of the Comprehensive Childhood Research Center and introduce our current fellows: Chonlatis Srichumpuang from Chulalongkorn University in Bangkok specializes in haemophilia and congenital blood clotting disorders (thrombophilia), which can lead to strokes

c4r-admin January 9, 2024March 20, 2024 Read more

Recent Posts

  • Better future for pediatric medicine
  • Latest film on genome research
  • Who does research at Dr. von Hauner Children’s Hospital? Our current fellows
  • International Care-for-Rare IBD Alliance for children with inflammatory bowel disease
  • Please support the Care-for-Rare Foundation in general

Our funding lines

>  Academy

>  Aid

>  Alliance

>  Awards

>  Awareness

Care-for-Rare Foundation
Foundation for children with Rare Diseases
Administrative Office
Dr. von Hauner Children’s Hospital
Lindwurmstraße 4
80337 München

 

 

   

Our donations account:
Care-for-Rare Foundation
Sparkasse Ulm

IBAN: DE93 6305 0000 0000 0035 33
SWIFT-BIC: SOLADES1ULM

 

Subscribe to our newsletter (in German)
Stay up to date!
We will inform you regularly about current projects and new foundation developments by e-mail.

Care-for-Rare Foundation für Kinder mit seltenen Erkrankungen

Care-for-Rare Foundation für Kinder mit seltenen Erkrankungen

 

 

 

 

 

 

 

 

Media library & press             Newsletter        Jobs        Imprint        Privacy

Copyright © 2025 Care-for-Rare Foundation for children with rare diseases