Rezultati pretraživanja
  1. 16. ruj 2018.

    We've reached a big milestone--100 known cases of GAND.

  2. 18. velj 2015.
    Odgovor korisniku/ci

    yeaaaa!!!! rare gene mutations and deletions!!!

  3. 4. stu 2018.
  4. 4. lis 2018.

    Well done, ! You did it again! Another amazing filled with , , , , , , and - allowing us to live in the moment! Thank you!!

  5. 22. sij

    Now online in : GATAD2B-associated Neurodevelopmental Disorder (GAND): Clinical and Molecular Insights Into a NuRD-related Disorder

  6. 6. stu 2019.

    So is gonna be able to cure my boys ? Anyone? in kids

  7. 16. ruj 2019.
  8. 21. kol 2019.

    HHFG is now a proud member organization of the National Organization for Rare Disorders ()! We are excited for this opportunity to better represent GAND in the broader rare disease community and to learn from fellow patient advocacy organizations.

  9. 16. ožu 2019.
  10. 28. velj 2019.
  11. 27. stu 2018.

    Happy ! We are seeking to raise $100 in honor of each of the 100+ people diagnosed with GAND. On this global day of giving, make an impact in the community.

  12. 4. lis 2018.

    Thank you for your passion and for sharing your story! I am grateful for you and your help to raise awareness about !

  13. 3. lis 2018.
    Odgovor korisnicima

    She's a doll. I have a rare disease, too! And I've been getting treatment for almost 30 years. Thanks for giving me an opportunity to read about .

  14. 21. kol 2018.
  15. 6. tra 2017.

    :Having an Ultra-Rare disease= odessey of doctor's appointments,(mis)diagnosis,isolation

  16. 1. tra 2017.

    Mooie, leerzame dag in over achter de rug!

  17. 27. velj 2017.

    Vandaag de internationale dag van de zeldzame ziekten: Wereldwijd gaat het om 7.000 aandoeningen, waaronder

  18. 9. pro 2016.

    Does anyone know more about the ?

  19. 23. ruj 2016.
  20. 29. velj 2016.

Čini se da učitavanje traje već neko vrijeme.

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