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Journal Abstract Search

153 related items for PubMed ID: 10203101

  • 1. Hemoglobin S/O(Arab): thirteen new cases and review of the literature.
    Zimmerman SA, O'Branski EE, Rosse WF, Ware RE.
    Am J Hematol; 1999 Apr; 60(4):279-84. PubMed ID: 10203101
    [Abstract] [Full Text] [Related]

  • 2. Hemoglobin SO Arab and hemoglobin CO Arab diseases. Clinical and laboratory study.
    Maeda K, Kini RK, Saeed SM, Rucknagel DL.
    Am J Pediatr Hematol Oncol; 1983 Apr; 5(2):127-31. PubMed ID: 6614393
    [Abstract] [Full Text] [Related]

  • 3. Hemoglobin C and hemoglobin O-Arab variants can be diagnosed using the Bio-Rad Variant II high-performance liquid chromatography system without further confirmatory tests.
    Joutovsky A, Nardi M.
    Arch Pathol Lab Med; 2004 Apr; 128(4):435-9. PubMed ID: 15043463
    [Abstract] [Full Text] [Related]

  • 4. [Hemoglobin O Arab in Ivory Coast and western Africa].
    Sangare A, Sanogo I, Meite M, Ambofo Y, Abesopie V, Segbena A, Tolo A.
    Med Trop (Mars); 1992 Apr; 52(2):163-7. PubMed ID: 1328806
    [Abstract] [Full Text] [Related]

  • 5. The clinical and laboratory spectrum of Hb C [β6(A3)Glu→Lys, GAG>AAG] disease.
    Cook CM, Smeltzer MP, Mortier NA, Kirk SE, Despotovic JM, Ware RE, Hankins JS.
    Hemoglobin; 2013 Apr; 37(1):16-25. PubMed ID: 23297836
    [Abstract] [Full Text] [Related]

  • 6. Hb O-Tibesti [beta121(GH4)Glu-->Lys; beta11(A8)Val-->Ile], a hemoglobin variant carrying in the same beta chain the substitutions of Hb O-Arab and Hb Hamilton, found in combination with Hb S [beta6(A3)Glu-->Val].
    Préhu C, Riou J, Sartelet I, Promé D, Claparols C, Denier M, Motte J, Galactéros F, Wajcman H.
    Hemoglobin; 2002 Feb; 26(1):13-20. PubMed ID: 11939508
    [Abstract] [Full Text] [Related]

  • 7. Hemoglobin O arab in four negro families and its interaction with hemoglobin S and hemoglobin C.
    Milner PF, Miller C, Grey R, Seakins M, DeJong WW, Went LN.
    N Engl J Med; 1970 Dec 24; 283(26):1417-25. PubMed ID: 5481775
    [No Abstract] [Full Text] [Related]

  • 8. [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]

  • 9. Diagnosis of a novel hemoglobinopathy of compound heterozygosity of hemoglobin S/hemoglobin Q India.
    Parab S, Sakhare S, Sengupta C, Velumani A.
    Clin Chim Acta; 2015 Mar 10; 442():33-5. PubMed ID: 25576799
    [Abstract] [Full Text] [Related]

  • 10. 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 10; 346(4):325-7. PubMed ID: 23221516
    [Abstract] [Full Text] [Related]

  • 11. Diagnosis and characterization of Hb C/Hb Iowa: a rare but easily misidentified compound heterozygous condition.
    Somjee S, Yu LC, Hagar AF, Hempe JM.
    Hemoglobin; 2004 Feb 10; 28(1):7-13. PubMed ID: 15008260
    [Abstract] [Full Text] [Related]

  • 12. Aplastic crisis revealing the diagnosis of Hb Evans [alpha62(E11)Val-->Met, GTG-->ATG (alpha2)] in a Hispanic kindred: case report and review.
    Steiner LA, Van Hoff J, Kutlar F, Gallagher PG.
    Hemoglobin; 2007 Feb 10; 31(4):409-16. PubMed ID: 17994374
    [Abstract] [Full Text] [Related]

  • 13. Globin synthesis in subjects doubly heterozygous for hemoglobin G-Philadelphia and hemoglobin S or C.
    McCurdy PR, Sherman AS, Kamuzora H, Lehmann H.
    J Lab Clin Med; 1975 Jun 10; 85(6):891-7. PubMed ID: 1138022
    [Abstract] [Full Text] [Related]

  • 14.
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  • 15. Severe Drug-Induced Hemolysis in a Patient with Compound Heterozygosity for Hb Peterborough (HBB: c.334G>T) and Hb Lepore-Boston-Washington (NG_000007.3: g.63632_71046del).
    Agbuduwe C, Rugless M, Asba N, Proven M, Sivakumaran M.
    Hemoglobin; 2019 Jan 10; 43(1):56-59. PubMed ID: 31060398
    [Abstract] [Full Text] [Related]

  • 16. HbSD-Punjab: clinical and hematological profile of a rare hemoglobinopathy.
    Oberoi S, Das R, Trehan A, Ahluwalia J, Bansal D, Malhotra P, Marwaha RK.
    J Pediatr Hematol Oncol; 2014 Apr 10; 36(3):e140-4. PubMed ID: 24276032
    [Abstract] [Full Text] [Related]

  • 17. Modification of hemoglobin H disease by sickle trait.
    Matthay KK, Mentzer WC, Dozy AM, Kan YW, Bainton DF.
    J Clin Invest; 1979 Oct 10; 64(4):1024-32. PubMed ID: 479366
    [Abstract] [Full Text] [Related]

  • 18. Asymptomatic child heterozygous for hemoglobin S and hemoglobin Pôrto Alegre.
    Lojo L, Santiago-Borrero P, Rivera E, Renta J, Cadilla CL.
    Pediatr Blood Cancer; 2011 Mar 10; 56(3):458-9. PubMed ID: 21225927
    [Abstract] [Full Text] [Related]

  • 19. [Hemoglobin O Arab: about 20 cases].
    Hafsia R, Gouider E, Ben Moussa S, Ben Salah N, Elborji W, Hafsia A.
    Tunis Med; 2007 Aug 10; 85(8):637-40. PubMed ID: 18254282
    [Abstract] [Full Text] [Related]

  • 20. [Clinical and hematological profile of Lepore Hemoglobin in Ivory Coast].
    Sangare A, Sanogo I, Meite M, Segbena A, Toure AH, Elenga JP, Siransy L, Allangba O.
    Med Trop (Mars); 1994 Aug 10; 54(1):43-6. PubMed ID: 8196525
    [Abstract] [Full Text] [Related]

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