Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Lívia Netto Chaer"'
Autor:
Valter Romão de Souza, Ana Beatriz Cavalcante de Oliveira, Ana Maria Vanderlei, Amanda Queiroz da Mota Silveira Aroucha, Bruna Pontes Duarte, Aureli Nunes Machado, Lívia Netto Chaer, Cláudia Wanderley de Barros Correia, Maria da Conceição de Barros Correia, Manuela Freire Hazin Costa
Publikováno v:
Journal of Medical Case Reports, Vol 12, Iss 1, Pp 1-6 (2018)
Abstract Background Thrombotic thrombocytopenic purpura is a very rare hereditary blood deficiency disorder of ADAMTS13 (von Willebrand factor-cleaving protease) and a life-threatening thrombotic microangiopathy characterized by thrombocytopenia and
Externí odkaz:
https://doaj.org/article/b9f4d7364fec4bd99f52bedc64c078ac
Autor:
Diego Vinicius Santinelli-Pestana, Livia Netto Chaer, Livia Mariano, Leonardo Jun Otuyama, Alfredo Medrone Junior, Vanderson Rocha
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 46, Iss 3, Pp 256-260 (2024)
Introduction: Autologous hematopoietic stem cell transplantation (ASCT) is the long-term consolidation treatment for various hematological malignancies. The collection of hematopoietic stem cell yield is critical to successful ASCTs, but not always a
Externí odkaz:
https://doaj.org/article/dbe12a40f6554623925c2f5399a3c081
Autor:
Ana Beatriz Cavalcante de Oliveira, Manuela Freire Hazin Costa, Amanda Queiroz da Mota Silveira Aroucha, Aureli Nunes Machado, Valter Romão de Souza, Lívia Netto Chaer, Cláudia Wanderley de Barros Correia, Maria da Conceição de Barros Correia, Ana Maria Vanderlei, B.P. Duarte
Publikováno v:
Journal of Medical Case Reports, Vol 12, Iss 1, Pp 1-6 (2018)
Journal of Medical Case Reports
Journal of Medical Case Reports
Background Thrombotic thrombocytopenic purpura is a very rare hereditary blood deficiency disorder of ADAMTS13 (von Willebrand factor-cleaving protease) and a life-threatening thrombotic microangiopathy characterized by thrombocytopenia and microangi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5b12441e8cb76bbc68ddecde7e875c34
http://link.springer.com/article/10.1186/s13256-017-1545-3
http://link.springer.com/article/10.1186/s13256-017-1545-3