Buscar
Mostrando ítems 1-10 de 117
HB D Los Angeles in a Brazilian family
(Associação Brasileira de Hematologia e Hemoterapia e daSociedade Brasileira de Transplante de Medula Óssea, 2001-09-01)
As doenças hereditária da hemoglobina são as mais comuns doenças monogênicas e atualmente bem conhecidas do ponto de vista molecular, fato este que propiciou um avanço no seu controle e manuseio. A população brasileira ...
Abnormal hemoglobin phenotypes in carriers of mild anemia in Latin America.
(2010-05-26)
We looked for abnormal hemoglobins in blood samples sent for diagnosis of anemia. Identification of the hemoglobins was made using electrophoretic, chromatographic and molecular procedures. The 2020 blood samples were of ...
Hemoglobin D-Punjab: origin, distribution and laboratory diagnosis
(Elsevier B. V., 2015)
This review discusses hemoglobin D-Punjab, also known as hemoglobin D-Los Angeles, one of the most common hemoglobin variants worldwide. It is derived from a point mutation in the beta-globin gene (HBB: c.364G>C; rs33946267) ...
Electrophoretic and chromatographic profile for S-like hemoglobin
(Funpec-editora, 2006-01-01)
Hemoglobin variants originate mainly by simple amino acid substitutions, the result of nucleotide sequence changes. Recently, the number of known abnormal hemoglobins has increased due to improvement in analysis methodologies; ...
Hemoglobin (Hb) Val de Marne (Hb Footscray) in Brazil: the first case report
(Funpec-editora, 2016-01-01)
Hemoglobin (Hb) variants involving alpha-chains are less common in the global population than Hb variants resulting from beta-chain alterations. Generally, alpha-chain Hb variants are caused by point mutations affecting ...
Identificação de variantes de hemoglobina em doadores de sangue
(Associação Brasileira de Hematologia e Hemoterapia e Terapia Celular, 2004-03)
Hemoglobinopathies are the most common genetic diseases and affect a great number of individuals in the world, with diverse clinical complications ranging from the almost unnoticeable to lethal consequences. In Brazil the ...
O laboratório clínico na investigação dos distúrbios da hemoglobinaThe clinical laboratory in the investigation of hemoglobin disorders
(Sociedade Brasileira de Patologia ClínicaSociedade Brasileira de PatologiaSociedade Brasileira de CitopatologiaBrasil, 2011)
O laboratório clínico na investigação dos distúrbios da hemoglobina
(Sociedade Brasileira de Patologia ClínicaSociedade Brasileira de PatologiaSociedade Brasileira de Citopatologia, 2011)
As alterações na síntese da hemoglobina resultam em um grupo de distúrbios hereditários, os quais podem ser classificados como hemoglobina variante, se a alteração tiver origem em uma mutação no gene da hemoglobina, ...
Utilization of different methodologies for the characterization of Hb Hasharon heterozygotes
(2006-03-09)
Hb Hasharon has an electrophoretic mobility similar to that of Hb S in cellulose acetate and a mobility between Hb S and C at acid pH. In high-performance liquid chromatography, Hb Hasharon shows a distinct chromatographic ...