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Journal Abstract Search

233 related items for PubMed ID: 31071550

  • 1. The Growth Differentiation Factor-15 (GDF-15) levels are increased in patients with compound heterozygous sickle cell and beta-thalassemia (HbS/βthal), correlate with markers of hemolysis, iron burden, coagulation, endothelial dysfunction and pulmonary hypertension.
    Larissi K, Politou M, Margeli A, Poziopoulos C, Flevari P, Terpos E, Papassotiriou I, Voskaridou E.
    Blood Cells Mol Dis; 2019 Jul; 77():137-141. PubMed ID: 31071550
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  • 2. Growth differentiation factor-15 in young sickle cell disease patients: relation to hemolysis, iron overload and vascular complications.
    Tantawy AA, Adly AA, Ismail EA, Darwish YW, Ali Zedan M.
    Blood Cells Mol Dis; 2014 Dec; 53(4):189-93. PubMed ID: 25065856
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  • 3. Activin-A is elevated in patients with thalassemia major and double heterozygous sickle cell/beta-thalassemia and correlates with markers of hemolysis and bone mineral density.
    Voskaridou E, Ntanasis-Stathopoulos I, Christoulas D, Dimopoulou M, Komninaka V, Repa K, Papatheodorou A, Terpos E.
    Ann Hematol; 2019 Jul; 98(7):1583-1592. PubMed ID: 31041514
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  • 5. The German sickle cell disease registry reveals a surprising risk of acute splenic sequestration and an increased transfusion requirement in patients with compound heterozygous sickle cell disease HbS/β-thalassaemia and no or low HbA expression.
    Allard P, Tagliaferri L, Weru V, Cario H, Lobitz S, Grosse R, Bleeke M, Oevermann L, Hakimeh D, Jarisch A, Kopp-Schneider A, Kulozik AE, Kunz JB, German Sickle Cell Disease Study Group, Lassay L.
    Eur J Haematol; 2024 Oct; 113(4):501-509. PubMed ID: 38946051
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  • 6. Growth differentiation factor-15 in children and adolescents with thalassemia intermedia: Relation to subclinical atherosclerosis and pulmonary vasculopathy.
    Tantawy AA, Adly AA, Ismail EA, Youssef OI, Ali ME.
    Blood Cells Mol Dis; 2015 Aug; 55(2):144-50. PubMed ID: 26142330
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  • 10. Thrombophilic mutations among Southern Iranian patients with sickle cell disease: high prevalence of factor V Leiden.
    Rahimi Z, Vaisi-Raygani A, Nagel RL, Muniz A.
    J Thromb Thrombolysis; 2008 Jun; 25(3):288-92. PubMed ID: 17619828
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  • 11. N-terminal natriuretic peptide and ventilation-perfusion lung scan in sickle cell disease and thalassemia patients with pulmonary hypertension.
    Mokhtar GM, Adly AA, El Alfy MS, Tawfik LM, Khairy AT.
    Hemoglobin; 2010 Jun; 34(1):78-94. PubMed ID: 20113292
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  • 17. Transforming growth factor 15 increased in severe aplastic anemia patients.
    Shao Y, Wang H, Liu C, Cao Q, Fu R, Wang H, Wang T, Qi W, Shao Z.
    Hematology; 2017 Oct; 22(9):548-553. PubMed ID: 28385068
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  • 19. Circulating platelet and erythrocyte microparticles in young children and adolescents with sickle cell disease: Relation to cardiovascular complications.
    Tantawy AA, Adly AA, Ismail EA, Habeeb NM, Farouk A.
    Platelets; 2013 Oct; 24(8):605-14. PubMed ID: 23249216
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  • 20. Genetic Regulation of Redox Balance in β-Thalassemia Trait.
    Terán MM, Mónaco ME, Lazarte SS, Haro C, Ledesma Achem E, Asensio NA, Issé BA.
    Hemoglobin; 2020 Mar; 44(2):122-127. PubMed ID: 32448013
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