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Decreased Hepcidin Levels Are Associated with Low Steady-state Hemoglobin in Children With Sickle Cell Disease in TanzaniaResearch in Context by Nathaniel Lee, Julie Makani, Furahini Tluway, Abel Makubi, Andrew E. Armitage, Sant-Rayn Pasricha, Hal Drakesmith, Andrew M. Prentice, Sharon E. Cox
Published 2018-08-01
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Hematological and Biochemical Reference Ranges for the Population with Sickle Cell Disease at Steady State in Tanzania by Anna Daniel Fome, Raphael Z. Sangeda, Emmanuel Balandya, Josephine Mgaya, Deogratius Soka, Furahini Tluway, Upendo Masamu, Siana Nkya, Julie Makani, Bruno P. Mmbando
Published 2022-01-01
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