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440 related items for PubMed ID: 29343300

  • 1. Association between sickle cell and β-thalassemia genes and hemoglobin concentration and anemia in children and non-pregnant women in Sierra Leone: ancillary analysis of data from Sierra Leone's 2013 National Micronutrient Survey.
    Wirth JP, Ansumana R, Woodruff BA, Koroma AS, Hodges MH.
    BMC Res Notes; 2018 Jan 17; 11(1):43. PubMed ID: 29343300
    [Abstract] [Full Text] [Related]

  • 2. Prevalence of Inherited Hemoglobin Disorders and Relationships with Anemia and Micronutrient Status among Children in Yaoundé and Douala, Cameroon.
    Engle-Stone R, Williams TN, Nankap M, Ndjebayi A, Gimou MM, Oyono Y, Tarini A, Brown KH, Green R.
    Nutrients; 2017 Jul 03; 9(7):. PubMed ID: 28671630
    [Abstract] [Full Text] [Related]

  • 3. Sickle Cell and α+-Thalassemia Traits Influence the Association between Ferritin and Hepcidin in Rural Kenyan Children Aged 14-26 Months.
    Byrd KA, Williams TN, Lin A, Pickering AJ, Arnold BF, Arnold CD, Kiprotich M, Dentz HN, Njenga SM, Rao G, Colford JM, Null C, Stewart CP.
    J Nutr; 2018 Dec 01; 148(12):1903-1910. PubMed ID: 30517728
    [Abstract] [Full Text] [Related]

  • 4. Effect of α+ Thalassemia on the Severity of Plasmodium falciparum Malaria in Different Sickle Cell Genotypes in Indian Adults: A Hospital-Based Study.
    Purohit P, Mohanty PK, Panigrahi J, Das K, Patel S.
    Hemoglobin; 2023 Jan 01; 47(1):11-18. PubMed ID: 37122241
    [Abstract] [Full Text] [Related]

  • 5. Molecular biology of hemoglobin: its application to sickle cell anemia and thalassemia.
    Kan YW.
    Schweiz Med Wochenschr Suppl; 1991 Jan 01; 43():51-4. PubMed ID: 1726857
    [Abstract] [Full Text] [Related]

  • 6. Study of alpha hemoglobin stabilizing protein expression in patients with β thalassemia and sickle cell anemia and its impact on clinical severity.
    Mahmoud HM, Shoeib AA, Abd El Ghany SM, Reda MM, Ragab IA.
    Blood Cells Mol Dis; 2015 Dec 01; 55(4):358-62. PubMed ID: 26460260
    [Abstract] [Full Text] [Related]

  • 7. Genetic Background of the Sickle Cell Disease Pediatric Population of Dakar, Senegal, and Characterization of a Novel Frameshift β-Thalassemia Mutation [HBB: c.265_266del; p.Leu89Glufs*2].
    Gueye Tall F, Martin C, Malick Ndour EH, Déme Ly I, Renoux C, Chillotti L, Veyrenche N, Connes P, Madieye Gueye P, Ndiaye Diallo R, Lacan P, Diagne I, Amadou Diop P, Cissé A, Lopez Sall P, Joly P.
    Hemoglobin; 2017 Mar 01; 41(2):89-95. PubMed ID: 28670947
    [Abstract] [Full Text] [Related]

  • 8. Prevalence of hemoglobinopathy disorders in adult patients sent for diagnosis of anemia in saudi arabia.
    Alsaeed AH.
    Genet Test Mol Biomarkers; 2012 Jan 01; 16(1):25-9. PubMed ID: 21861712
    [Abstract] [Full Text] [Related]

  • 9. Risk factors for venous thromboembolism in adults with hemoglobin SC or Sβ(+) thalassemia genotypes.
    Yu TT, Nelson J, Streiff MB, Lanzkron S, Naik RP.
    Thromb Res; 2016 May 01; 141():35-8. PubMed ID: 26962984
    [Abstract] [Full Text] [Related]

  • 10. Premarital screening test results for β-thalassemia and sickle cell anemia trait in east Mediterranean region of Turkey.
    Guler E, Garipardic M, Dalkiran T, Davutoglu M.
    Pediatr Hematol Oncol; 2010 Nov 01; 27(8):608-13. PubMed ID: 20795773
    [Abstract] [Full Text] [Related]

  • 11. Abnormal hemoglobins; clinical disorders resulting from various combinations.
    LAWRENCE JS, VALENTINE WN.
    Calif Med; 1955 Jan 01; 82(1):1-5. PubMed ID: 13230906
    [Abstract] [Full Text] [Related]

  • 12. Splenic function in Omani children with sickle cell disease: correlation with severity index, hemoglobin phenotype, iron status, and alpha-thalassemia trait.
    Wali YA, Al-Lamki Z, Hussein SS, Bererhi H, Kumar D, Wasifuddin S, Zachariah M, Ghosh K.
    Pediatr Hematol Oncol; 2002 Jan 01; 19(7):491-500. PubMed ID: 12217195
    [Abstract] [Full Text] [Related]

  • 13. β-globin gene cluster haplotypes in a cohort of 221 children with sickle cell anemia or Sβ⁰-thalassemia and their association with clinical and hematological features.
    Belisário AR, Martins ML, Brito AM, Rodrigues CV, Silva CM, Viana MB.
    Acta Haematol; 2010 Jan 01; 124(3):162-70. PubMed ID: 20938172
    [Abstract] [Full Text] [Related]

  • 14. Genetic Blood Disorders Survey in the Sultanate of Oman.
    Al-Riyami A, Ebrahim GJ.
    J Trop Pediatr; 2003 Jul 01; 49 Suppl 1():i1-20. PubMed ID: 12934793
    [Abstract] [Full Text] [Related]

  • 15. [From gene to disease; from hemoglobin genes to thalassemia and sickle cell anemia].
    de Jong A, de Wert G.
    Ned Tijdschr Geneeskd; 2000 Dec 16; 144(51):2480-1. PubMed ID: 11151663
    [No Abstract] [Full Text] [Related]

  • 16. Frequencies and phenotypic consequences of association of α- and β-thalassemia alleles with sickle-cell disease in Bahrain.
    Abuamer S, Shome DK, Jaradat A, Radhi A, Bapat JP, Sharif KA, Al-Touq J, Al-Asheeri A, Al-Ajami A.
    Int J Lab Hematol; 2017 Feb 16; 39(1):76-83. PubMed ID: 27981798
    [Abstract] [Full Text] [Related]

  • 17. Anemia, micronutrient deficiencies, malaria, hemoglobinopathies and malnutrition in young children and non-pregnant women in Ghana: Findings from a national survey.
    Wegmüller R, Bentil H, Wirth JP, Petry N, Tanumihardjo SA, Allen L, Williams TN, Selenje L, Mahama A, Amoaful E, Steiner-Asiedu M, Adu-Afarwuah S, Rohner F.
    PLoS One; 2020 Feb 16; 15(1):e0228258. PubMed ID: 31999737
    [Abstract] [Full Text] [Related]

  • 18. THE FIRST OBSERVATION OF HOMOZYGOUS HEMOGLOBIN S-ALPHA THALASSEMIA DISEASE AND TWO TYPES OF SICKLE CELL THALASSEMIA DISEASE: (A) SICKLE CELL-ALPHA THALASSEMIA DISEASE, (B) SICKLE CELL-BETA THALASSEMIA DISEASE.
    AKSOY M.
    Blood; 1963 Dec 16; 22():757-69. PubMed ID: 14084634
    [No Abstract] [Full Text] [Related]

  • 19. A family with S and C hemoglobins and the hereditary persistence of F hemoglobin. A comparison of C thalassemia disease with the CF syndrome.
    SCHNEIDER RG, LEVIN WC, EVERETT C.
    N Engl J Med; 1961 Dec 28; 265():1278-83. PubMed ID: 13908956
    [No Abstract] [Full Text] [Related]

  • 20. Genetic predisposition to β-thalassemia and sickle cell anemia in Turkey: a molecular diagnostic approach.
    Basak AN, Tuzmen S.
    Methods Mol Biol; 2011 Dec 28; 700():291-307. PubMed ID: 21204041
    [Abstract] [Full Text] [Related]

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