Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Laura Delvasto-Nuñez"'
Autor:
Inge Baas, Laura Delvasto-Nuñez, Peter Ligthart, Conny Brouwer, Claudia Folman, Edimara S. Reis, Daniel Ricklin, John D. Lambris, Diana Wouters, Masja de Haas, Ilse Jongerius, Sacha S. Zeerleder
Publikováno v:
Haematologica, Vol 105, Iss 2 (2020)
Externí odkaz:
https://doaj.org/article/080d337720a34853a8f979a034075c99
Autor:
Esther Catharina Wilhelmina De Boer, Marit Jalink, Laura Delvasto-Nuñez, Elisabeth Meulenbroek, Inge Baas, Susanne R. Janssen, Claudia C. Folman, Kyra A. Gelderman, Diana Wouters, Marije D. Engel, Masja de Haas, Marie José Kersten, Ilse Jongerius, Sacha Zeerleder, Josephine M.I. Vos
Complement-mediated autoimmune hemolytic anemia (CM-AIHA) is characterized by destruction of red blood cells (RBCs) by autoantibodies that activate the classical complement pathway. These antibodies also reduce transfusion efficacy via lysis of donor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5f5186d3b43c978e049dde3c71a3aba6
http://hdl.handle.net/10029/626572
http://hdl.handle.net/10029/626572
Autor:
Ilse Jongerius, Sacha Zeerleder, Laura Delvasto-Nuñez, Kamran Bakhtiari, Joost C. M. Meijers, Dorina Roem, Gerard van Mierlo
Publikováno v:
Delvasto, Laura; Roem, Dorina; Bakhtiari, Kamran; van Mierlo, Gerard J; Meijers, Joost; Jongerius, Ilse; Zeerleder, Sacha S (2022). Iron-driven alterations on red blood cell-derived microvesicles amplify coagulation during hemolysis via the intrinsic tenase complex. Thrombosis and haemostasis, 122(1), pp. 80-91. Thieme 10.1055/a-1497-9573
Thrombosis and haemostasis. Schattauer GmbH
Thrombosis and haemostasis. Schattauer GmbH
Hemolytic disorders characterized by complement-mediated intravascular hemolysis, such as autoimmune hemolytic anemia and paroxysmal nocturnal hemoglobinuria, are often complicated by life-threatening thromboembolic complications. Severe hemolytic ep
Publikováno v:
ISBT Science Series. 15:91-101
Publikováno v:
Blood reviews. 50
Thromboembolic events represent the most common complication of hemolytic anemias characterized by complement-mediated hemolysis such as paroxysmal nocturnal hemoglobinuria and autoimmune hemolytic anemia. Similarly, atypical hemolytic uremic syndrom
Autor:
Conny Brouwer, Peter C. Ligthart, Diana Wouters, Ilse Jongerius, John D. Lambris, Daniel Ricklin, Inge O. Baas, Laura Delvasto-Nuñez, Masja de Haas, Edimara S. Reis, Sacha S. Zeerleder, Claudia C. Folman
Publikováno v:
Haematologica, 105(2), e57-e60. Ferrata Storti Foundation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::70da4b8f765adc20fbdbbeba247963d8
https://europepmc.org/articles/PMC7012486/
https://europepmc.org/articles/PMC7012486/
Autor:
Manfred Wuhrer, Diana Wouters, Gerard van Mierlo, Dorina Roem, Ruchira Engel, Laura Delvasto-Nuñez, Agnes L. Hipgrave Ederveen, Stephanie Holst, Sacha Zeerleder, Jaap D. van Buul
Publikováno v:
Thrombosis and Haemostasis
Thrombosis and haemostasis, 118(12), 2134-2144. Schattauer GmbH
Thrombosis and haemostasis, 118(12), 2134-2144. Schattauer GmbH
Background C1-inhibitor (C1-inh) therapeutics can reduce neutrophil activity in various inflammatory conditions. This ‘novel’ anti-inflammatory effect of C1-inh is attributed to the tetrasaccharide sialyl LewisX (SLeX) present on its N-glycans. V