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Alpha thalassemia changes erythrocyte heterogeneity in sickle cell disease.

Homozygous alpha-thalassemia has the beneficial effect in sickle cell anemia of reducing the hemolytic severity while changing several other hematological parameters. We examined in detail the cellular basis of some of these hematologic alterations. We find that the broad distribution in erythrocyte...

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Detalhes bibliográficos
Main Authors: Noguchi, C T, Dover, G J, Rodgers, G P, Serjeant, G R, Antonarakis, S E, Anagnou, N P, Higgs, D R, Weatherall, D J, Schechter, A N
Formato: Artigo
Idioma:Inglês
Publicado em: 1985
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC425505/
https://ncbi.nlm.nih.gov/pubmed/2581999
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