Irreversibly sickled erythrocytes: a consequence of the heterogeneous distribution of hemoglobin types in sickle-cell anemia

The amount of fetal hemoglobin (Hb F) in erythrocytes of patients with sickle cell anemia (Hb SS disease) was measured by two methods: (a) photometry of individual cells stained for Hb F by the Kleihauer-Betke technique; and (b) chemical assay of alkali-resistant hemoglobin in cells distributed acco...

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Veröffentlicht in:	J Clin Invest
Hauptverfasser:	Bertles, John F., Milner, Paul F. A.
Format:	Artigo
Sprache:	Inglês
Veröffentlicht:	American Society for Clinical Investigation 1968
Schlagworte:	Articles
Online-Zugang:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC297333/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/5666109/ https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI105863
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