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hemoglobin S-beta thalassemia 相关文献:
Exagamglogene Autotemcel: First Approval.
Hoy SM.
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Sickle Cell Disease.
Bender MA, Carlberg K.
2003 Sep 15 [updated 2025 Feb 13]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2025.
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Hb S/beta-Thalassemia in the REDS-III Brazil Sickle Cell Disease Cohort: Clinical, Laboratory and Molecular Characteristics.
Belisário AR, Carneiro-Proietti AB, Sabino EC, Araújo A, Loureiro P, Máximo C, Flor-Park MV, Rodrigues DDOW, Ozahata MC, McClure C, Mota RA, Gomes Moura IC, Custer B, Kelly S; Recipient Epidemiology and Donor Evaluation Study (REDS-III) International Component Brazil.
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Falsely elevated hemoglobin A1c due to S-beta+-thalassemia interference in Bio-Rad Variant II Turbo HbA1c assay.
Zhu Y, Williams LM.
Clin Chim Acta. 2009 Nov;409(1-2):18-20. doi: 10.1016/j.cca.2009.08.009. Epub 2009 Aug 19.
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Hb S (HBB: c.20A>T) and alpha- and beta-Thalassemia Coinheritance in Iranian Patients.
Azarkeivan A, Cohan N, Niazkar HR, Azizi A, Rad F.
Hemoglobin. 2020 Mar;44(2):109-112. doi: 10.1080/03630269.2020.1757462. Epub 2020 May 6.
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Sickle Cell Trait.
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Compound Heterozygosity of beta-Thalassemia and the Sickle Cell Hemoglobin in Various Populations of Chhattisgarh State, India.
Jha AN, Mishra H, Verma HK, Pandey I, Lakkakula BVKS.
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Molecular characterization of Hb S(C) beta-thalassemia in American blacks.
Gonzalez-Redondo JM, Kutlar A, Kutlar F, McKie VC, McKie KM, Baysal E, Huisman TH.
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Clinical, laboratory, and molecular characteristics of a cohort of children with hemoglobinopathy S/beta-thalassemia.
Oliveira ÉL, Belisário AR, Silva NP, Rezende PV, Muniz MB, Oliveira LMM, Velloso-Rodrigues C, Viana MB.
Hematol Transfus Cell Ther. 2024 Apr-Jun;46(2):167-175. doi: 10.1016/j.htct.2023.11.002. Epub 2023 Dec 19.
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Beta-thalassemia, HB S-beta-thalassemia and sickle cell anemia among Tunisians.
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