«The fact that the medical research of a son of the Mississippi Delta, born in Louise, MS in 1929, is being continued by a team of researchers all over the world, still excites me!»
The Hereditary TTP Registry participated in the first-in-human study evaluating a recombinant human ADAMTS13 as therapeutic option in the treatment of congenital TTP
Primer on TTP to download Our Primer on TTP is shown on the NATURE home page this month (www.nature.com/nrdp/)
Our Primer on TTP is shown on the NATURE home page this month (www.nature.com/nrdp/) and is free to download…
28.01.2019
newsletter_december-2018.pdf Newsletter December 2018 Dear Colleagues, the end of the year is approaching soon, and we are looking back on a successful year for the Hereditary TTP Registry with some key achievements. In the…
11.01.2019
First Newsletter 2018 The first annual Newsletter of the Hereditary TTP Registry is available.
To read or to sign up, see on the right side of this page.
International TTP Day in Bern was a Success! Dear All!
Thank you for your support and contribution at the International TTP Day.
The TTP Team Bern has collected $899.95 to support the Answering T.T.P Foundation and TTP research. This is 257%…
16.09.2018
International TTP Day in Bern on 16.09.2018 SAVE THE DATE
International TTP Day in Bern will take place on SUNDAY, SEPTEMBER 16, 2018
Please support us in our quest to help answer TTP!
International TTP Day is Saturday September 15,…
Best abstract at the GTH 2018 in Vienna, Austria The groups' abstract on iTTP was nominated as one of the four "best abstracts" at the 62nd Annual Meeting Society of Thrombosis and Haemostasis Research in Vienna, Wien
In the category…
