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Journal Abstract Search

270 related items for PubMed ID: 16533721

  • 1. Hb Bronovo, a new globin gene mutation at alpha2 103 (His->Leu) associated with an alpha thalassemia phenotype.
    Harteveld CL, Steen G, Vlasveld LT, van Delft P, Giordano PC.
    Haematologica; 2006 Apr; 91(4):570-1. PubMed ID: 16533721
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  • 2. Hb Bleuland [alpha108(G15)Thr-->Asn, ACC-->AAC (alpha2)]: a new abnormal hemoglobin associated with a mild alpha-thalassemia phenotype.
    Harteveld CL, Versteegh FG, Kok PJ, van Rooijen-Nijdam IH, van Delft P, Giordano PC.
    Hemoglobin; 2006 Apr; 30(3):349-54. PubMed ID: 16840225
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  • 3. A novel mutation of the alpha2-globin causing alpha(+)-thalassemia: Hb Plasencia [alpha125(H8)Leu--Arg (alpha2).
    Martin G, Villegas A, González FA, Ropero P, Hojas R, Polo M, Mateo M, Salvador M, Benavente C.
    Hemoglobin; 2005 Apr; 29(2):113-7. PubMed ID: 15921163
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  • 7. A rare thalassemic syndrome caused by interaction of Hb Adana [alpha59(E8)Gly-->Asp] with an alpha+-thalassemia deletion: clinical aspects in two cases.
    Douna V, Papassotiriou I, Garoufi A, Georgouli E, Ladis V, Stamoulakatou A, Metaxotou-Mavrommati A, Kanavakis E, Traeger-Synodinos J.
    Hemoglobin; 2008 Apr; 32(4):361-9. PubMed ID: 18654886
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  • 9. Hb St. Jozef, A Val-->Leu N-terminal mutation leading to retention of the methionine, and partial acetylation found in the globin gene in Cis with a -alpha3.7 thalassemia deletion.
    Harteveld CL, Versteegh FG, van Leer EH, Starreveld JS, Kok PJ, van Rooijen-Nijdam I, van Delft P, Zanella-Cleon I, Becchi M, Wajcman H, Giordano PC.
    Hemoglobin; 2007 Apr; 31(3):313-23. PubMed ID: 17654068
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  • 13. Unstable and thalassemic alpha chain hemoglobin variants: a cause of Hb H disease and thalassemia intermedia.
    Wajcman H, Traeger-Synodinos J, Papassotiriou I, Giordano PC, Harteveld CL, Baudin-Creuza V, Old J.
    Hemoglobin; 2008 Apr; 32(4):327-49. PubMed ID: 18654884
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  • 15. Complex interaction of hemoglobin (Hb) Nakhon Ratchasima [α63(E12)Ala→Val], a novel α2-globin chain variant with Hb E [β26(B8)Glu→Lys] and a deletional α(+)-thalassemia.
    Srivorakun H, Fucharoen G, Puangplruk R, Kheawon N, Fucharoen S.
    Eur J Haematol; 2011 Jul; 87(1):68-72. PubMed ID: 21447006
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  • 17. Laboratory diagnosis of a compound heterozygosity for Hb Hekinan [alpha27(B8) Glu-Asp] and a deletional alpha-thalassaemia 2 in Thailand.
    Chunpanich S, Ayukarn K, Sanchaisuriya K, Fucharoen G, Fucharoen S.
    Clin Lab Haematol; 2004 Oct; 26(5):355-8. PubMed ID: 15485467
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  • 18. Codon 24 (TAT>TAG) and codon 32 (ATG>AGG) (Hb Rotterdam): two novel alpha2 gene mutations associated with mild alpha-thalassemia found in the same family after newborn screening.
    Giordano PC, Cnossen MH, Joosten AM, Jansen CA, Hakvoort TE, Bakker-Verweij M, Arkesteijn SG, van Delft P, Waye JS, Bouva MJ, Harteveld CL.
    Hemoglobin; 2010 Oct; 34(4):354-65. PubMed ID: 20642333
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