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Acta Haematol ; 85(4): 212-6, 1991.
Artigo em Inglês | MEDLINE | ID: mdl-1853685

RESUMO

Hb Regina was identified in a 58-year-old German male and 2 of his 3 children. All affected subjects presented moderate erythrocytosis and the whole blood exhibited increased oxygen affinity (P50:17.5 mm Hg). This hemoglobinopathy was undetectable with the conventional electrophoretic methods. It was, however, separated and quantified by cation-exchange and reverse-phase high-performance liquid chromatography. Hb Regina accounted for 30-35% of the total Hb. No significant clinical symptoms were found to be related to this hemoglobinopathy. This is the first known instance in Germany, and so far the second case reported.


Assuntos
Hemoglobinas Anormais/análise , Oxigênio/sangue , Policitemia/sangue , 2,3-Difosfoglicerato , Cromatografia Líquida de Alta Pressão , Ácidos Difosfoglicéricos/sangue , Alemanha , Humanos , Leucina , Masculino , Pessoa de Meia-Idade , Policitemia/genética , Valina
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