Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Louis, Aledort"'
Autor:
Karin Berger, Roxy H. O’Rourke, Matteo Nicola Dario Di Minno, Angelika Batorova, Kaan Kavakli, Pier Mannuccio Mannucci, Wolfgang Schramm, Rhonda L. Bohn, Louis Aledort
Publikováno v:
Haematologica, Vol 999, Iss 1 (2024)
The treatment landscape for haemophilia continues to rapidly develop, and expectations for future treatment success are high. There is limited information on the challenges to accessing new and innovative therapies. The aim of this study was to explo
Externí odkaz:
https://doaj.org/article/af4046fe78af487687f795c7a684cdf0
Publikováno v:
Expert Review of Hematology. :1-17
Autor:
Giovanni Di Minno, Pier Mannuccio Mannucci, James W. Ironside, Carlo Federico Perno, Lutz Gürtler, Louis Aledort
Publikováno v:
Haematologica, Vol 105, Iss 12 (2020)
Externí odkaz:
https://doaj.org/article/9197447f8135490d95f2eae9bb195666
Autor:
Karin, Berger, Angelika, Batorova, Rhonda, Bohn, Matteo, di Minno, Pier Mannuccio, Mannucci, Kaan, Kavakli, Wolfgang, Schramm, Louis, Aledort
Publikováno v:
Haemophilia : the official journal of the World Federation of Hemophilia. 28(6)
Publikováno v:
Haemophilia : the official journal of the World Federation of Hemophilia. 27(6)
Autor:
Silvia Ferrari, Kristina Palavra, Bernadette Gruber, Johanna A. Kremer Hovinga, Paul Knöbl, Claudine Caron, Caroline Cromwell, Louis Aledort, Barbara Plaimauer, Peter L. Turecek, Hanspeter Rottensteiner, Friedrich Scheiflinger
Publikováno v:
Haematologica, Vol 99, Iss 4 (2014)
Anti-ADAMTS13 autoantibodies are the main cause of acquired thrombotic thrombocytopenic purpura. Binding of these antibodies to ADAMTS13 eventually results in the formation of antigen-antibody immune complexes. Circulating ADAMTS13-specific immune co
Externí odkaz:
https://doaj.org/article/6088089c03124975a2c1d1ed3b9c8981
Autor:
Daniel B. Aruch, Louis Aledort
Publikováno v:
Journal of Hematology & Thromboembolic Diseases.
Here we describe the case of an unfortunate 26 year old woman who developed a fatal combination of autoimmune hemolytic anemia (AIHA), hemophagocytic lymphohistiocytosis (HLH), and thrombotic thrombocytopenic purpura (TTP). Her initial clinical pictu
Autor:
Louis Aledort
Publikováno v:
American Journal of Hematology. 47:208-217
The development of inhibitor antibodies is a long-standing, well-documented complication of coagulation factor replacement therapy and is difficult to treat. Previous estimates of 5-15% of patients developing inhibitors may be low, since newer data s
Publikováno v:
The American Journal of Gastroenterology. 97:187-189
A 53-yr-old man with a 33-yr history of Crohn's ileocolitis, complicated by arthritis and cologastric fistulization, was diagnosed with GI amyloidosis at the time of proctocolectomy. He had marked proteinuria (4.2 g/24 h) and moderate renal insuffici