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Journal Abstract Search

121 related items for PubMed ID: 10506456

  • 1. Laboratory recognition of a rare hemoglobinopathy: hemoglobins SS and SG(Philadelphia) associated with alpha-thalassemia-2.
    Kirk CM, Papadea CN, Lazarchick J.
    Arch Pathol Lab Med; 1999 Oct; 123(10):963-6. PubMed ID: 10506456
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  • 2. HPLC-ESI-MS/MS analysis of hemoglobin peptides in tryptic digests of dried-blood spot extracts detects HbS, HbC, HbD, HbE, HbO-Arab, and HbG-Philadelphia mutations.
    Haynes CA, Guerra SL, Fontana JC, DeJesús VR.
    Clin Chim Acta; 2013 Sep 23; 424():191-200. PubMed ID: 23796846
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  • 3. Usefulness of HPLC methodology for the characterization of combinations of the common beta chain variants Hbs S, C, and O-Arab, and the alpha chain variant Hb G-Philadelphia.
    Kutlar F, Kutlar A, Nuguid E, Prchal J, Huisman TH.
    Hemoglobin; 1993 Feb 23; 17(1):55-66. PubMed ID: 8454470
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  • 4. Modification of hemoglobin H disease by sickle trait.
    Matthay KK, Mentzer WC, Dozy AM, Kan YW, Bainton DF.
    J Clin Invest; 1979 Oct 23; 64(4):1024-32. PubMed ID: 479366
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  • 5. Pitfalls in newborn hemoglobinopathy screening: failure to detect beta(+)-thalassemia.
    Strickland DK, Ware RE, Kinney TR.
    J Pediatr; 1995 Aug 23; 127(2):304-8. PubMed ID: 7636661
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  • 9. [Hemoglobin Boumerdès alpha 2(37) (C2) Pro----Arg beta 2: a new variant of the alpha chain associated with hemoglobin S in an Algerian family].
    Dahmane-Arbane M, Blouquit Y, Arous N, Bardakdjian J, Benamani M, Riou J, Benabadji M, Rosa J, Galacteros F.
    Nouv Rev Fr Hematol (1978); 1987 Aug 23; 29(5):317-20. PubMed ID: 3438164
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  • 13. Hematological and Molecular Characterization of a Novel Hb A2 Variant with Homozygous α-Thalassemia-2 in a Southern Thai Individual.
    Nuinoon M, Jeenduang N, Kesornsit A, Horpet D, Plyduang T.
    Hemoglobin; 2017 May 23; 41(3):213-215. PubMed ID: 28795619
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  • 17. [Diagnosis of thalassemias and hemoglobinopathies by HPLC (high performance liquid chromatography): study of 627 patients].
    Sabo G, Brodbeck U, Cardile N, Viollier AF, Scheurmann T, Knecht H.
    Schweiz Med Wochenschr; 1999 Aug 28; 129(34):1196-200. PubMed ID: 10486859
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  • 18. Laboratory investigation of hemoglobinopathies and thalassemias: review and update.
    Clarke GM, Higgins TN.
    Clin Chem; 2000 Aug 28; 46(8 Pt 2):1284-90. PubMed ID: 10926923
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  • 19. Rapid and accurate quantitation of Hb Bart's and Hb H using weak cation exchange high performance liquid chromatography: correlation with the alpha-thalassemia genotype.
    Papassotiriou I, Traeger-Synodinos J, Vlachou C, Karagiorga M, Metaxotou A, Kanavakis E, Stamoulakatou A.
    Hemoglobin; 1999 Aug 28; 23(3):203-11. PubMed ID: 10490132
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  • 20. Sickle haemoglobin and haemoglobin Stanleyville II: possible confusion with sickle cell-haemoglobin C disease.
    Serjeant GR, Wild B, Tebasulwa S, Mason KP, Serjeant BE, Ndugwa CM.
    East Afr Med J; 2005 Jul 28; 82(7):367-70. PubMed ID: 16167711
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