Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Édis Belini-Júnior"'
Autor:
Lidiane S Torres, Jéssika V Okumura, Danilo G H Silva, Kallyne K O Mimura, Édis Belini-Júnior, Renan G Oliveira, Clarisse L C Lobo, Sonia M Oliani, Claudia R Bonini-Domingos
Publikováno v:
PLoS ONE, Vol 12, Iss 2, p e0172659 (2017)
[This corrects the article DOI: 10.1371/journal.pone.0165833.].
Externí odkaz:
https://doaj.org/article/c79e8c22c1374ca0b8edc4f7f9c44d6b
Autor:
Lidiane S Torres, Jéssika V Okumura, Danilo G H Silva, Kallyne K O Mimura, Édis Belini-Júnior, Renan G Oliveira, Clarisse L C Lobo, Sonia M Oliani, Claudia R Bonini-Domingos
Publikováno v:
PLoS ONE, Vol 11, Iss 11, p e0165833 (2016)
Sickle cell disease (SCD) is an inherited hemolytic anemia whose pathophysiology is driven by polymerization of the hemoglobin S (Hb S), leading to hemolysis and vaso-occlusive events. Inflammation is a fundamental component in these processes and a
Externí odkaz:
https://doaj.org/article/bf0bd5ef2c0b4b3a9b514473238841b2
Autor:
Diego A. Pereira-Martins, Igor F. Domingos, Edis Belini-Junior, Juan L. Coelho-Silva, Isabel Weinhäuser, Aderson S. Araújo, Clarisse L. Lobo, Claudia R. Bonini-Domingos, Marcos A. Bezerra, Antonio R. Lucena-Araujo
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 43, Iss 3, Pp 243-248 (2021)
Introduction: Sickle cell anemia (SCA) is a Mendelian disorder with a heterogeneous clinical course. The reasons for this phenotypic diversity are not entirely established, but it is known that high fetal hemoglobin levels lead to a milder course of
Externí odkaz:
https://doaj.org/article/b4f7b9e9364742d191c10f93c9d5a4c7
Publikováno v:
Revista Brasileira de Hematologia e Hemoterapia, Vol 34, Iss 1, Pp 68-68 (2012)
Externí odkaz:
https://doaj.org/article/e369481b098a4169ad2c6fe1076362f9