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Journal Abstract Search

125 related items for PubMed ID: 9299955

  • 1.
    ; . PubMed ID:
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  • 2. Chromatographic measurements of hemoglobin A2 in blood samples that contain sickle hemoglobin.
    Shokrani M, Terrell F, Turner EA, Aguinaga MD.
    Ann Clin Lab Sci; 2000 Apr; 30(2):191-4. PubMed ID: 10807164
    [Abstract] [Full Text] [Related]

  • 3. Chromatographic measurements of memoglobin A2 in blood samples containing sickle hemoglobin.
    Giordano PC, Harteveld CL.
    Ann Clin Lab Sci; 2000 Oct; 30(4):430-1. PubMed ID: 11045768
    [No Abstract] [Full Text] [Related]

  • 4. Rapid quantitation of hemoglobin S in sickle cell patients using the Variant II Turbo analyzer.
    Edwards HD, Sabio H, Shihabi ZK.
    Ann Clin Lab Sci; 2009 Oct; 39(1):32-7. PubMed ID: 19201738
    [Abstract] [Full Text] [Related]

  • 5. [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
    [Abstract] [Full Text] [Related]

  • 6. Hemoglobin SO-Arab and α-thalassemia diagnosed in an adult: A case-based review of the hemoglobinopathies.
    Zacharia G, Maronge GF, Brazda FW, Boulmay BC.
    Am J Med Sci; 2013 Oct 28; 346(4):325-7. PubMed ID: 23221516
    [Abstract] [Full Text] [Related]

  • 7. Automated HPLC screening of newborns for sickle cell anemia and other hemoglobinopathies.
    Eastman JW, Wong R, Liao CL, Morales DR.
    Clin Chem; 1996 May 28; 42(5):704-10. PubMed ID: 8653895
    [Abstract] [Full Text] [Related]

  • 8.
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  • 9. Prenatal and postnatal diagnoses of thalassemias and hemoglobinopathies by HPLC.
    Fucharoen S, Winichagoon P, Wisedpanichkij R, Sae-Ngow B, Sriphanich R, Oncoung W, Muangsapaya W, Chowthaworn J, Kanokpongsakdi S, Bunyaratvej A, Piankijagum A, Dewaele C.
    Clin Chem; 1998 Apr 28; 44(4):740-8. PubMed ID: 9554484
    [Abstract] [Full Text] [Related]

  • 10. [Sickle cell disease: laboratory and hemoglobin study].
    Wajcman H, Galacteros F.
    Bull Soc Pathol Exot; 2001 May 28; 94(2):80-4. PubMed ID: 11475032
    [Abstract] [Full Text] [Related]

  • 11. Use of an automated pyrosequencing technique for confirmation of sickle cell disease.
    de Martino CC, Alencar CS, Loureiro P, Carneiro-Proietti ABF, Máximo CA, Mota RA, Rodrigues DOW, Gaburo Junior N, Kelly S, Sabino EC, International Component of the NHLBI Recipient Epidemiology and Donor Evaluation Study (REDS-III).
    PLoS One; 2019 May 28; 14(12):e0216020. PubMed ID: 31830127
    [Abstract] [Full Text] [Related]

  • 12. [Drepanocytosis with alpha and beta(o) thalassemia: a case report].
    Désidéri-Vaillant C, Olivro J, Valéro E, Kerdoncuff C, Lafontaine Y, Laborde JP.
    Ann Biol Clin (Paris); 2009 May 28; 67(3):349-52. PubMed ID: 19411239
    [Abstract] [Full Text] [Related]

  • 13. New approach to accurate interpretation of sickle cell disease newborn screening by applying multiple of median cutoffs and ratios.
    Allaf B, Patin F, Elion J, Couque N.
    Pediatr Blood Cancer; 2018 Sep 28; 65(9):e27230. PubMed ID: 29781571
    [Abstract] [Full Text] [Related]

  • 14. Evaluation of high performance liquid chromatography (HPLC) pattern and prevalence of beta-thalassaemia trait among sickle cell disease patients in Lagos, Nigeria.
    Adeyemo T, Ojewunmi O, Oyetunji A.
    Pan Afr Med J; 2014 Sep 28; 18():71. PubMed ID: 25400838
    [Abstract] [Full Text] [Related]

  • 15. Detection of fetal hemoglobin in erythrocytes by flow cytometry.
    Campbell TA, Ware RE, Mason M.
    Ann N Y Acad Sci; 1998 Jun 30; 850():446-8. PubMed ID: 9668579
    [No Abstract] [Full Text] [Related]

  • 16. Hemoglobin A2 levels in healthy persons, sickle cell disease, sickle cell trait, and beta-thalassemia by capillary isoelectric focusing.
    Craver RD, Abermanis JG, Warrier RP, Ode DL, Hempe JM.
    Am J Clin Pathol; 1997 Jan 30; 107(1):88-91. PubMed ID: 8980373
    [Abstract] [Full Text] [Related]

  • 17. Analysis of fetal blood using capillary electrophoresis system: a simple method for prenatal diagnosis of severe thalassemia diseases.
    Srivorakun H, Fucharoen G, Sae-Ung N, Sanchaisuriya K, Ratanasiri T, Fucharoen S.
    Eur J Haematol; 2009 Jul 30; 83(1):57-65. PubMed ID: 19226360
    [Abstract] [Full Text] [Related]

  • 18. MALDI-MS in first-line screening of newborns for sickle cell disease: results from a prospective study in comparison to HPLC.
    El Osta M, Benoist JF, Naubourg P, Bonacorsi S, Messine R, Ducoroy P, Allaf B.
    Clin Chem Lab Med; 2024 May 27; 62(6):1149-1157. PubMed ID: 38353144
    [Abstract] [Full Text] [Related]

  • 19. [Hematological and clinical profile in sickle cell or thalassemic patients].
    Vilachá D, Salazar R.
    Rev Invest Clin; 2006 May 27; 58(2):94-100. PubMed ID: 16827261
    [Abstract] [Full Text] [Related]

  • 20. Red cell indices: differentiation between β-thalassemia trait and iron deficiency anemia and application to sickle-cell disease and sickle-cell thalassemia.
    Sahli CA, Bibi A, Ouali F, Fredj SH, Dakhlaoui B, Othmani R, Laouini N, Jouini L, Ouenniche F, Siala H, Touhami I, Becher M, Fattoum S, Toumi Nel H, Messaoud T.
    Clin Chem Lab Med; 2013 Nov 27; 51(11):2115-24. PubMed ID: 23800659
    [Abstract] [Full Text] [Related]

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