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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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| 出版年: | J Clin Invest |
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| 主要な著者: | , , , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
American Society for Clinical Investigation
1997
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| 主題: | |
| オンライン・アクセス: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC508371/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/9312186/ https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI119713 |
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