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Sickle cell disease: a comprehensive program of care from birth.
de Montalembert M, Tshilolo L, Allali S. de Montalembert M, et al. Among authors: allali s. Hematology Am Soc Hematol Educ Program. 2019 Dec 6;2019(1):490-495. doi: 10.1182/hematology.2019000053. Hematology Am Soc Hematol Educ Program. 2019. PMID: 31808910 Free PMC article. Review.
Management of iron overload in hemoglobinopathies.
Allali S, de Montalembert M, Brousse V, Chalumeau M, Karim Z. Allali S, et al. Transfus Clin Biol. 2017 Sep;24(3):223-226. doi: 10.1016/j.tracli.2017.06.008. Epub 2017 Jun 30. Transfus Clin Biol. 2017. PMID: 28673501 Review.
Plasma histamine elevation in a large cohort of sickle cell disease patients.
Allali S, Lionnet F, Mattioni S, Callebert J, Stankovic Stojanovic K, Bachmeyer C, Arlet JB, Brousse V, de Montalembert M, Chalumeau M, Grateau G, Maciel TT, Launay JM, Hermine O, Georgin-Lavialle S. Allali S, et al. Br J Haematol. 2019 Jul;186(1):125-129. doi: 10.1111/bjh.15900. Epub 2019 Mar 28. Br J Haematol. 2019. PMID: 30924132 Free article.
Innate-like T cells in children with sickle cell disease.
Allali S, Dietrich C, Machavoine F, Rignault-Bricard R, Brousse V, de Montalembert M, Hermine O, Maciel TT, Leite-de-Moraes M. Allali S, et al. PLoS One. 2019 Jun 28;14(6):e0219047. doi: 10.1371/journal.pone.0219047. eCollection 2019. PLoS One. 2019. PMID: 31251783 Free PMC article.
76 results