BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

155 related articles for article (PubMed ID: 27164532)

  • 21. Rapid quantitation of hemoglobin S by isoelectric focusing.
    Reddy MN; Franciosi RA
    Ann Clin Lab Sci; 1994; 24(5):401-6. PubMed ID: 7529472
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Sickling syndromes in children.
    Honig GR
    Adv Pediatr; 1976; 23():271-313. PubMed ID: 795281
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Antenatal diagnosis of haemoglobinopathies by Biorex chromatography of haemoglobin.
    Blouquit Y; Beuzard Y; Varnavides L; Chabret C; Dumez Y; John PN; Rodeck C; White JM
    Br J Haematol; 1982 Jan; 50(1):7-15. PubMed ID: 6173058
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Accuracy of cord blood screening for sickle hemoglobinopathies. Three- to five-year follow-up.
    Kramer MS; Rooks Y; Johnston D; Pearson HA
    JAMA; 1979 Feb; 241(5):485-6. PubMed ID: 759662
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [Diagnosis of hemoglobinopathies in the clinical laboratory].
    Hopmeier P
    Wien Klin Wochenschr; 1983 Nov; 95(22):797-804. PubMed ID: 6199903
    [TBL] [Abstract][Full Text] [Related]  

  • 26. [Separation of hemoglobins F, Fac, S, C, A1c and determination of hemoglobin F using high performance liquid chromatography].
    Pic P; Ducrocq R; Girot R
    Ann Biol Clin (Paris); 1994; 52(2):129-32. PubMed ID: 7528482
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Prenatal diagnosis of hemoglobinopathies: detection of alpha-thalassemia trait and of sickle cell disease in utero.
    Alter BP; Nathan DG; Modell CB; Fairweather D; Mahoney MJ; Hobbins JC
    Hemoglobin; 1977; 1(4):395-400. PubMed ID: 893137
    [No Abstract]   [Full Text] [Related]  

  • 29. Prevalence of hemoglobinopathy disorders in adult patients sent for diagnosis of anemia in saudi arabia.
    Alsaeed AH
    Genet Test Mol Biomarkers; 2012 Jan; 16(1):25-9. PubMed ID: 21861712
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Prenatal diagnosis of thalassemia and Hb S syndromes in Greece: an evaluation of 1500 cases.
    Loukopoulos D; Karababa P; Antsaklis A; Panourgias J; Boussiou M; Karayannopoulos K; Politis J; Rombou D; Kaltsoya-Tassiopoulou A; Fessas P
    Ann N Y Acad Sci; 1985; 445():357-75. PubMed ID: 2409876
    [No Abstract]   [Full Text] [Related]  

  • 31. Liquid chromatography in diagnosis of rare hemoglobin variant (Hb Chicago) and its combination with HB S: Hb Chicago/S trait and Hb Chicago/sickle cell disease.
    Ou CN; Rognerud CL
    Clin Chem; 1996 May; 42(5):774-6. PubMed ID: 8653909
    [No Abstract]   [Full Text] [Related]  

  • 32. The presence of F cells with a fetal phenotype in adults with hemoglobinopathies limits the utility of flow cytometry for quantitation of fetomaternal hemorrhage.
    Othman J; Orellana D; Chen LS; Russell M; Khoo TL
    Cytometry B Clin Cytom; 2018 Jul; 94(4):695-698. PubMed ID: 29072803
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Simultaneous diagnosis of severe SARS-CoV-2 infection and sickle cell disease in two infants.
    Parodi E; Voi V; Vania B; Lonardi P; Saracco P; Longobardo A; Grassitelli S; Peruzzi L; Scolfaro C; Piga A
    Blood Transfus; 2021 Mar; 19(2):120-123. PubMed ID: 33539288
    [No Abstract]   [Full Text] [Related]  

  • 34. Pneumococcal septicemia and meningitis in an infant with Hb S/D-Los Angeles disease: a failure of neonatal hemoglobinopathy screening.
    Abhyankar SH; Miller ST; Rao SP; Brown AB; Pass KA
    Hemoglobin; 1991; 15(1-2):119-23. PubMed ID: 1717404
    [No Abstract]   [Full Text] [Related]  

  • 35. Sickle-cell anemia and other hemoglobinopathies. Procedures and strategy for screening employing spots of blood on filter paper as specimens.
    Garrick MD; Dembure P; Guthrie R
    N Engl J Med; 1973 Jun; 288(24):1265-8. PubMed ID: 4703315
    [No Abstract]   [Full Text] [Related]  

  • 36. Survey of Haryana children for abnormal hemoglobins.
    Aggarwal VP; Dhatt PS; Singh H
    Indian Pediatr; 1983 Apr; 20(4):255-8. PubMed ID: 6194111
    [No Abstract]   [Full Text] [Related]  

  • 37. [Flowcharts for the diagnosis and the molecular characterization of hemoglobinopathies].
    Aguilar-Martinez P; Badens C; Bonello-Palot N; Cadet E; Couque N; Ducrocq R; Elion J; Francina A; Joly P; Pissard S; Rochette J;
    Ann Biol Clin (Paris); 2010; 68(4):455-64. PubMed ID: 20650741
    [TBL] [Abstract][Full Text] [Related]  

  • 38. The determinants of irreversibly sickled cells in homozygous sickle cell disease.
    Serjeant GR; Serjeant BE; Desai P; Mason KP; Sewell A; England JM
    Br J Haematol; 1978 Nov; 40(3):431-8. PubMed ID: 749928
    [TBL] [Abstract][Full Text] [Related]  

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

  • 40. Sickle cell trait/hereditary persistence of fetal hemoglobin trait. Misdiagnosis as sickle cell anemia by newborn screening.
    Rubin EM; Rowley PT
    Am J Dis Child; 1979 Dec; 133(12):1248-50. PubMed ID: 517474
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.