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Journal Abstract Search

440 related items for PubMed ID: 29343300

  • 21. Adverse clinical and obstetric outcomes among pregnant women with different sickle cell disease genotypes.
    Silva FAC, Ferreira ALCG, Hazin-Costa MF, Dias MLG, Araújo AS, Souza AI.
    Int J Gynaecol Obstet; 2018 Oct; 143(1):89-93. PubMed ID: 30030929
    [Abstract] [Full Text] [Related]

  • 22. Haemoglobin genotypes: a prevalence study and implications for reproductive health in Uyo, Nigeria.
    Umoh AV, Abah GM, Ekanem TI, Essien EM.
    Niger J Med; 2010 Oct; 19(1):36-41. PubMed ID: 20232754
    [Abstract] [Full Text] [Related]

  • 23. Screening for inherited thrombophilia might be warranted among Eastern Mediterranean sickle-beta-0 thalassemia patients.
    Isma'eel H, Arnaout MS, Shamseddeen W, Mahfouz R, Zeineh N, Jradi O, Taher A.
    J Thromb Thrombolysis; 2006 Oct; 22(2):121-3. PubMed ID: 17008978
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  • 24. [From gene to disease; from hemoglobin genes to thalassemia and sickle cell anemia].
    Giordano PC, Breuning MH.
    Ned Tijdschr Geneeskd; 2000 Sep 30; 144(40):1910-3. PubMed ID: 11045138
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  • 25. Molecular analysis of beta-thalassemia and sickle cell anemia in Antalya.
    Keser I, Sanlioglu AD, Manguoglu E, Guzeloglu Kayisli O, Nal N, Sargin F, Yesilipek A, Simsek M, Mendilcioglu I, Canatan D, Luleci G.
    Acta Haematol; 2004 Sep 30; 111(4):205-10. PubMed ID: 15153712
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  • 28. Study on the Role of Polymorphisms of the SOX-6 and MYB Genes and Fetal Hemoglobin Levels in Sicilian Patients with β-Thalassemia and Sickle Cell Disease.
    Listì F, Sclafani S, Agrigento V, Barone R, Maggio A, D'Alcamo E.
    Hemoglobin; 2018 Mar 30; 42(2):103-107. PubMed ID: 30200835
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  • 30. Extended therapy with intravenous arginine butyrate in patients with beta-hemoglobinopathies.
    Sher GD, Ginder GD, Little J, Yang S, Dover GJ, Olivieri NF.
    N Engl J Med; 1995 Jun 15; 332(24):1606-10. PubMed ID: 7753139
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  • 31. Future prospects for treatment of hemoglobinopathies.
    Stamatoyannopoulos JA.
    West J Med; 1992 Dec 15; 157(6):631-6. PubMed ID: 1282285
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  • 33. Studies on abnormal hemoglobins. XIII. Hemoglobin S-thalassemia disease and hemoglobin C-thalassemia disease in siblings.
    SINGER K, JOSEPHSON AM, SINGER L, HELLER P, ZIMMERMAN HJ.
    Blood; 1957 Jul 15; 12(7):593-602. PubMed ID: 13436515
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  • 34. Phenotype and genotype frequency of β-thalassemia and sickle cell disease carriers in Halkidiki, Northern Greece.
    Kalleas C, Anagnostopoulos K, Sinopoulou K, Delaki E, Margaritis D, Bourikas G, Tsatalas C, Kortsaris A, Tentes I.
    Hemoglobin; 2012 Jul 15; 36(1):64-72. PubMed ID: 22188117
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  • 35. [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 Jul 15; 76(6):369-372. PubMed ID: 27959846
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  • 37. Hemoglobin Disorders Among Anemic Patients: a Cross-Sectional Study from Jeddah City, Western Saudi Arabia.
    Alzahrani M, Felimban R, Alzahrani F, Qadah T.
    Clin Lab; 2020 Dec 01; 66(12):. PubMed ID: 33337829
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  • 40. Osteonecrosis of the humeral head in sickle cell disease.
    Milner PF, Kraus AP, Sebes JI, Sleeper LA, Dukes KA, Embury SH, Bellevue R, Koshy M, Moohr JW, Smith J.
    Clin Orthop Relat Res; 1993 Apr 01; (289):136-43. PubMed ID: 8472404
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