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pro vyhledávání: '"Natália Durazzo"'
Autor:
Caroline Gabe, Karen Chinoca Ziza, Natália Durazzo, Flavia M. Pagani, Valéria Brito Oliveira, Marina-C.A.V. Conrado, Marcia R. Dezan, Alfredo Mendrone, Paula Ribeiro Villaça, Carla Luana Dinardo, Vanderson Rocha
Publikováno v:
Hematology, transfusion and cell therapy.
The Glanzmann Thrombasthenia (GT) and Bernard-Soulier Syndrome (BSS) are rare hereditary disorders of platelet function. Their treatment often requires platelet transfusion, which can lead to the development of alloantibodies.In this study, we aim to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e613878e275c84347eb453f03fc98f66
https://pubmed.ncbi.nlm.nih.gov/36114116
https://pubmed.ncbi.nlm.nih.gov/36114116
