Etiology of anemia of blood donor candidates deferred by hematologic screening

Autor: Michel Alves da Silva, Renata Andréia Volpe de Souza, Aline Meneses Carlos, Sheila Soares, Helio Moraes-Souza, Gilberto de Araujo Pereira

Publikováno v: Revista Brasileira de Hematologia e Hemoterapia, Vol 34, Iss 5, Pp 356-360 (2012)

OBJECTIVE: Iron deficiency is the most common cause of anemia and one of the main factors in the clinical deferral of blood donors. This fact prompted the current study that aimed to determine the prevalence and etiology of anemia in blood donor cand

Externí odkaz: https://doaj.org/article/b60d198719d84a99b165d65b2c257b0f

Etiology of anemia of blood donor candidates deferred by hematologic screening

Autor: Aline Meneses Carlos, Sheila Soares, Michel Alves da Silva, Renata Andréia Volpe de Souza, Gilberto de Araujo Pereira, Helio Moraes-Souza

Publikováno v: Revista Brasileira de Hematologia e Hemoterapia, Vol 34, Iss 5, Pp 356-360 (2012)
Revista Brasileira de Hematologia e Hemoterapia v.34 n.5 2012
Revista brasileira de hematologia e hemoterapia
Associação Brasileira de Hematologia e Hemoterapia e Terapia Celular (ABHHTC)
instacron:ABHHTC
Revista Brasileira de Hematologia e Hemoterapia, Volume: 34, Issue: 5, Pages: 356-360, Published: 2012
Revista Brasileira de Hematologia e Hemoterapia

Objective: Iron deficiency is the most common cause of anemia and one of the main factors in the clinical deferral of blood donors. This fact prompted the current study that aimed to determine the prevalence and etiology of anemia in blood donor cand

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ba57fc90bffb4690cc4b2f19c793e26f
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1516-84842012000500012

Α-Thalassemia: Genotypic Profile Associated with Ethnicity and Hematological Differentiation of Iron Deficiency Anemia in the Region of Uberaba, Minas Gerais, Brazil

Autor: Helio Moraes-Souza, Cibele Velloso Rodrigues, Bruna Maria Bereta de Souza, Aline Menezes Carlos, Gilberto de Araujo Pereira, Renata Andréia Volpe de Souza

Publikováno v: Hemoglobin. 39(4)

α-Thalassemia (α-thal) is a hereditary hemoglobinopathy characterized by microcytic anemia due to impaired production of α chains of human globin. Brazilian studies show that the most common genotype is an -α(3.7) deletion with the loss of one or

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e302f9da10a1da0a6c93507af4a238b7
https://pubmed.ncbi.nlm.nih.gov/26182338