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Journal Abstract Search

169 related items for PubMed ID: 31788855

  • 1. HbS/β+ thalassemia: Really a mild disease? A National survey from the AIEOP Sickle Cell Disease Study Group with genotype-phenotype correlation.
    Notarangelo LD, Agostini A, Casale M, Samperi P, Arcioni F, Gorello P, Perrotta S, Masera N, Barone A, Bertoni E, Bonetti E, Burnelli R, Casini T, Del Vecchio GC, Filippini B, Giona F, Giordano P, Gorio C, Marchina E, Nardi M, Petrone A, Colombatti R, Sainati L, Russo G.
    Eur J Haematol; 2020 Mar; 104(3):214-222. PubMed ID: 31788855
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  • 2. Hb S/β-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.
    Hemoglobin; 2020 Jan; 44(1):1-9. PubMed ID: 32172616
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  • 6. [Sickle cell syndrome. Association between hemoglobin S and β thalassemia].
    Gasparini NP, Agriello EE, Zanella MJ, Iommi MP, Maradei J, Sandoval MJ.
    Medicina (B Aires); 2016 Jan; 76(6):369-372. PubMed ID: 27959846
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  • 10. Genetic Modifiers of Sickle Cell Disease: A Genotype-Phenotype Relationship Study in a Cohort of 82 Children on Mayotte Island.
    Muszlak M, Pissard S, Badens C, Chamouine A, Maillard O, Thuret I.
    Hemoglobin; 2015 Jan; 39(3):156-61. PubMed ID: 25806420
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  • 11. New variants in beta globin gene among the Palestinian refugees with sickle cell disease in Lebanon.
    Moussa EY, Yassine NM, Borjac JM.
    Saudi Med J; 2018 Dec; 39(12):1253-1258. PubMed ID: 30520510
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  • 15. Sickle cell anemia--molecular diagnosis and prenatal counseling: SGPGI experience.
    Kumar R, Panigrahi I, Dalal A, Agarwal S.
    Indian J Pediatr; 2012 Jan; 79(1):68-74. PubMed ID: 21713598
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  • 16. β-globin gene cluster haplotypes in a cohort of 221 children with sickle cell anemia or Sβ⁰-thalassemia and their association with clinical and hematological features.
    Belisário AR, Martins ML, Brito AM, Rodrigues CV, Silva CM, Viana MB.
    Acta Haematol; 2010 Jan; 124(3):162-70. PubMed ID: 20938172
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