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Journal Abstract Search

160 related items for PubMed ID: 15768554

  • 21. Thalassemias and other hemoglobinopathies in the Republic of Macedonia.
    Efremov GD.
    Hemoglobin; 2007; 31(1):1-15. PubMed ID: 17365000
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  • 22. A 21 Nucleotide Duplication on the α1- and α2-Globin Genes Involves a Variety of Hypochromic Microcytic Anemias, From Mild to Hb H Disease.
    Farashi S, Faramarzi Garous N, Zeinali F, Vakili S, Ashki M, Imanian H, Najmabadi H, Azarkeivan A, Tamaddoni A.
    Hemoglobin; 2015; 39(3):196-200. PubMed ID: 25976776
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  • 23. The levels of zeta, gamma, and delta chains in patients with Hb H disease.
    Kutlar F, Gonzalez-Redondo JM, Kutlar A, Gurgey A, Altay C, Efremov GD, Kleman K, Huisman TH.
    Hum Genet; 1989 May; 82(2):179-86. PubMed ID: 2566576
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  • 24. Misdiagnosis of Hb constant spring (alpha142, Term-->Gln, TAA-->CAA in alpha2) in a Hb H (beta4) disease child.
    Li D, Liao C, Li J.
    Hemoglobin; 2007 May; 31(1):105-8. PubMed ID: 17365012
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  • 25. Comparison of red blood cell hematology among normal, alpha-thalassemia-1 trait, and hemoglobin Bart's fetuses at mid-pregnancy.
    Srisupundit K, Piyamongkol W, Tongsong T.
    Am J Hematol; 2008 Dec; 83(12):908-10. PubMed ID: 18932192
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  • 27. Prenatal diagnosis of hemoglobin Bart's hydrops fetalis by HPLC analysis of hemoglobin in fetal blood samples.
    Sanguansermsri T, Thanaratanakorn P, Steger HF, Tongsong T, Sirivatanapa P, Wanapirak C, Sirichotiyakul S, Chanprapas P, Flatz G.
    Southeast Asian J Trop Med Public Health; 2001 Mar; 32(1):180-5. PubMed ID: 11485083
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  • 28. Common alpha-thalassemia deletions in transfusion-dependent thalassemia patients in the Southeast Asia region of Myanmar.
    Ne-Win, Harano K, Harano T, Thein-Thein-Myint, Rai-Mra, Aye-Aye-Myint, Shimono K, Okada S.
    Lab Hematol; 2006 Mar; 12(3):139-42. PubMed ID: 16950674
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  • 33. Fetal Anemia and Hydrops Fetalis Associated with Homozygous Hb Constant Spring (HBA2: c.427T > C).
    He Y, Zhao Y, Lou JW, Liu YH, Li DZ.
    Hemoglobin; 2016 Mar; 40(2):97-101. PubMed ID: 26757782
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  • 34. An alpha0-thalassemia-like mutation: Hb Suan-Dok [alpha109(G16)Leu-->Arg] carried by a recombinant -alpha(3.7) gene.
    Moradkhani K, Mazurier E, Giordano PC, Wajcman H, Préhu C.
    Hemoglobin; 2008 Mar; 32(4):419-24. PubMed ID: 18654893
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