Oral magnesium supplements reduce erythrocyte dehydration in patients with sickle cell disease.

Intracellular polymerization and sickling depend markedly on the cellular concentration of sickle hemoglobin (Hb S). A possible therapeutic strategy for sickle cell disease is based on reducing the cellular concentration of Hb S through prevention of erythrocyte dehydration. The K-Cl cotransporter i...

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Bibliographic Details
Main Authors: De Franceschi, L, Bachir, D, Galacteros, F, Tchernia, G, Cynober, T, Alper, S, Platt, O, Beuzard, Y, Brugnara, C
Format: Artigo
Language:Inglês
Published: 1997
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Research Article
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC508371/
https://ncbi.nlm.nih.gov/pubmed/9312186
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