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Journal Abstract Search

82 related items for PubMed ID: 433978

  • 21. Laboratory screening of hemoglobinopathies.
    Chan MS, Schneider NJ.
    Health Lab Sci; 1975 Apr; 12(2):91-9. PubMed ID: 1052518
    [Abstract] [Full Text] [Related]

  • 22. Hb SE disease: a clinico-hematological profile.
    Mishra P, Pati HP, Chatterjee T, Dixit A, Choudhary DR, Srinivas MU, Mahapatra M, Choudhry VP.
    Ann Hematol; 2005 Oct; 84(10):667-70. PubMed ID: 15947927
    [Abstract] [Full Text] [Related]

  • 23. Newborn screening for sickle cell and other hemoglobinopathies: a Canadian pilot study.
    Yorke D, Mitchell J, Clow C, Nuguid E, Cadogan R, Sinclair D, Luscombe S, Rozen R, Meredith P, Esseltine D.
    Clin Invest Med; 1992 Aug; 15(4):376-83. PubMed ID: 1516295
    [Abstract] [Full Text] [Related]

  • 24. Differential diagnosis of adult hemoglobin A, F, and S conditions. A case of G gamma-beta(+)-hereditary persistence of fetal hemoglobin.
    Carter DK, Lucia MS, Winter SD.
    Arch Pathol Lab Med; 1991 May; 115(5):533-6. PubMed ID: 1708658
    [Abstract] [Full Text] [Related]

  • 25. A rapid test for sickle hemoglobin.
    Asakura T, Segal ME, Friedman S, Schwartz E.
    JAMA; 1975 Jul 14; 233(2):156-6. PubMed ID: 1173442
    [Abstract] [Full Text] [Related]

  • 26. Novel method for screening for the presence of haemoglobin S in blood.
    Higgins TN, Ridley B, Clarke G.
    Transfus Med; 2005 Dec 14; 15(6):493-7. PubMed ID: 16359421
    [Abstract] [Full Text] [Related]

  • 27. [Diagnosis and screening of sickle cell disease].
    Wajcman H.
    Rev Prat; 2004 Sep 30; 54(14):1543-7. PubMed ID: 15558963
    [Abstract] [Full Text] [Related]

  • 28. [Development of a method of screening for hemoglobin S for the purpose of genetic consultation in Cuba. Results of an analysis of 24,000 blood samples].
    Eredero L, Granda I, Al'tland K.
    Genetika; 1978 Jun 30; 14(6):1079-84. PubMed ID: 680558
    [Abstract] [Full Text] [Related]

  • 29. Haemoglobin S in Malays and Indians: association of Hb CoSp and Hb S in a Malay family.
    Saidi HT, Duraisamy G.
    Trop Geogr Med; 1978 Mar 30; 30(1):103-8. PubMed ID: 675819
    [Abstract] [Full Text] [Related]

  • 30. Biochemical diagnosis in sickle cell disease.
    Isaacs WA.
    Ghana Med J; 1971 Mar 30; 10(1):40-3. PubMed ID: 5173734
    [Abstract] [Full Text] [Related]

  • 31. Pitfalls in the genetic diagnosis of Hb S.
    Moradkhani K, Riou J, Wajcman H.
    Clin Biochem; 2013 Mar 30; 46(4-5):291-9. PubMed ID: 22995479
    [Abstract] [Full Text] [Related]

  • 32. [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 Mar 30; 29(5):317-20. PubMed ID: 3438164
    [Abstract] [Full Text] [Related]

  • 33. Hemoglobin variant detection from dried blood specimens by high performance liquid chromatography.
    Roa PD, Turner EA, Aguinaga Mdel P.
    Ann Clin Lab Sci; 1993 Mar 30; 23(6):433-8. PubMed ID: 7507311
    [Abstract] [Full Text] [Related]

  • 34. Unusual sickle cell disease observed for the first time in Italy: Hb S-Hb D Los Angeles.
    Samperi P, Dibenedetto SP, di Cataldo A, Mancuso GR, Schilirò G.
    Haematologica; 1990 Mar 30; 75(5):464-6. PubMed ID: 2097263
    [Abstract] [Full Text] [Related]

  • 35. A simplified screening strategy for thalassaemia and haemoglobin E in rural communities in south-east Asia.
    Fucharoen G, Sanchaisuriya K, Sae-ung N, Dangwibul S, Fucharoen S.
    Bull World Health Organ; 2004 May 30; 82(5):364-72. PubMed ID: 15298227
    [Abstract] [Full Text] [Related]

  • 36. Hb S-São Paulo: a new sickling hemoglobin with stable polymers and decreased oxygen affinity.
    Jorge SE, Petruk AA, Kimura EM, Oliveira DM, Caire L, Suemasu CN, Silveira PA, Albuquerque DM, Costa FF, Skaf MS, Martínez L, Sonati Mde F.
    Arch Biochem Biophys; 2012 Mar 01; 519(1):23-31. PubMed ID: 22244832
    [Abstract] [Full Text] [Related]

  • 37. Proportion of hemoglobin S in blood, as determined from solubility measurements.
    Bowie LJ, Dohnal JC.
    Clin Chem; 1983 Feb 01; 29(2):325-8. PubMed ID: 6821938
    [Abstract] [Full Text] [Related]

  • 38. Preliminary Evaluation of a Point-of-Care Testing Device (SickleSCAN™) in Screening for Sickle Cell Disease.
    Nwegbu MM, Isa HA, Nwankwo BB, Okeke CC, Edet-Offong UJ, Akinola NO, Adekile AD, Aneke JC, Okocha EC, Ulasi T, Abjah U, Ugwu NI, Okolo AA, Madu A, Emodi I, Girei A, Balogun TM, Diaku-Akinwumi IN, Ohiaeri C, Brown BJ, Olaniyi JA, Hassan A, Awwalu S, Okoh DA, Nnodu OE.
    Hemoglobin; 2017 Mar 01; 41(2):77-82. PubMed ID: 28617057
    [Abstract] [Full Text] [Related]

  • 39. [Perioperative monitoring of hemoglobin fractions in homozygous sickle cell disease].
    Frietsch T, Segiet W, Schütz P, Haux P, Lorentz A.
    Anaesthesist; 1999 Apr 01; 48(4):231-5. PubMed ID: 10352787
    [Abstract] [Full Text] [Related]

  • 40. Effect of HbS in the determination of HbA2 with the Menarini HA-8160 analyzer and comparison with other instruments.
    Anagnostopoulos K, Tentes I, Kalleas C, Margaritis D, Toli A, Pendilas D, Bourikas G, Tsatalas C, Kortsaris AH.
    Int J Lab Hematol; 2009 Dec 01; 31(6):665-72. PubMed ID: 18691341
    [Abstract] [Full Text] [Related]

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