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2018 | 2 |
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Chronic Administration of Hydroxyurea (HU) Benefits Caucasian Patients with Sickle-Beta Thalassemia.
Int J Mol Sci. 2018 Feb 28;19(3):681. doi: 10.3390/ijms19030681.
Int J Mol Sci. 2018.
PMID: 29495591
Free PMC article.
Real-life experience with hydroxyurea in sickle cell disease: A multicenter study in a cohort of patients with heterogeneous descent.
Rigano P, De Franceschi L, Sainati L, Piga A, Piel FB, Cappellini MD, Fidone C, Masera N, Palazzi G, Gianesin B, Forni GL; Italian Multicenter Study of Hydroxyurea in Sickle Cell Anemia Investigators.
Rigano P, et al.
Blood Cells Mol Dis. 2018 Mar;69:82-89. doi: 10.1016/j.bcmd.2017.08.017. Epub 2017 Oct 9.
Blood Cells Mol Dis. 2018.
PMID: 29107441
Free article.
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