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PUBMED FOR HANDHELDS

Journal Abstract Search

176 related items for PubMed ID: 35303690

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  • 47. Genetic variants associated with fetal hemoglobin levels show the diverse ethnic origin in Colombian patients with sickle cell anemia.
    Fong C, Menzel S, Lizarralde MA, Barreto G.
    Biomedica; 2015; 35(3):437-43. PubMed ID: 26849705
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  • 49. Unique Polymorphisms at BCL11A, HBS1L-MYB and HBB Loci Associated with HbF in Kuwaiti Patients with Sickle Cell Disease.
    Akbulut-Jeradi N, Fernandez MJ, Al Khaldi R, Sukumaran J, Adekile A.
    J Pers Med; 2021 Jun 17; 11(6):. PubMed ID: 34204365
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  • 51. High fetal hemoglobin level is associated with increased risk of cerebral vasculopathy in children with sickle cell disease in Mayotte.
    Chamouine A, Saandi T, Muszlak M, Larmaraud J, Lambrecht L, Poisson J, Balicchi J, Pissard S, Elenga N.
    BMC Pediatr; 2020 Jun 20; 20(1):302. PubMed ID: 32563256
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  • 54. Effect of haplotypes of functional SNPs related to expression of fetal hemoglobin (HbF) on clinical prognosis of hematological malignancies.
    Sales RR, Luizon MR.
    Int J Hematol; 2023 Apr 20; 117(4):626-627. PubMed ID: 36847933
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  • 57. Genetic modifiers of fetal hemoglobin affect the course of sickle cell disease in patients treated with hydroxyurea.
    Allard P, Alhaj N, Lobitz S, Cario H, Jarisch A, Grosse R, Oevermann L, Hakimeh D, Tagliaferri L, Kohne E, Kopp-Schneider A, Kulozik AE, Kunz JB.
    Haematologica; 2022 Jul 01; 107(7):1577-1588. PubMed ID: 34706496
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  • 59. Genetic modifiers of sickle cell anemia in the BABY HUG cohort: influence on laboratory and clinical phenotypes.
    Sheehan VA, Luo Z, Flanagan JM, Howard TA, Thompson BW, Wang WC, Kutlar A, Ware RE, BABY HUG Investigators.
    Am J Hematol; 2013 Jul 01; 88(7):571-6. PubMed ID: 23606168
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