Platelet Disorder Support Association – Empowering ITP Patients – Research
Platelet Disorder Support Association – Empowering ITP Patients. Comprehensive information and support for those concerned about ITP, immune thrombocytopenia.
Platelet Disorder Support Association – Empowering ITP Patients. Comprehensive information and support for those concerned about ITP, immune thrombocytopenia.
QUINCY, MA, May 1, 2024—The National Organization for Rare Disorders (NORD) announced today that Pamela K. Gavin has been named CEO effective immediately. She
Treatment with NALL for 12 weeks yields better neurological status than placebo among patients with Niemann-Pick disease type C.
Cat Lutz, PhD, MBA, VP at JAX Rare Disease Translational Center, discusses rare disease research’s impact on understanding common diseases.
Philips has reached a $1 billion settlement in the U.S. related its Respironics ventilators, and backed its full-year guidance.
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There are a total of 12 candidates in mid to late-stage trials for ALS poised to enter the market in the next five years.
From the original Broadway production of “Camelot” ; together with the song is a slideshow of several photos of the production starring Julie Andrews, Richar…
Tambourine is a private grantmaking foundation founded by Ben Silbermann and his wife Divya Silbermann. Ben Silbermann is a billionaire donor and former technology executive…
The Living Rare, Living Stronger NORD Patient and Family Forum will be a truly patient first event. Through it all, we will maintain our objectives:…
This very special event will celebrate NORD’s legacy and achievements, and honor those individuals and organizations doing remarkable work on behalf of the rare disease…