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Journal Abstract Search

525 related items for PubMed ID: 21861712

  • 1. 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
    [Abstract] [Full Text] [Related]

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

  • 3. 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 Jul; 18():71. PubMed ID: 25400838
    [Abstract] [Full Text] [Related]

  • 4. Prevalence of Hemoglobinopathies (β-Thalassemia and Sickle Cell Trait) in the Adult Population of Al Majma'ah, Saudi Arabia.
    Mir SA, Alshehri BM, Alaidarous M, Banawas SS, Dukhyil AAAB, Alturki MK.
    Hemoglobin; 2020 Jan; 44(1):47-50. PubMed ID: 32091272
    [Abstract] [Full Text] [Related]

  • 5. [Hemoglobinopathies in Tunisia. An updated review of the epidemiologic and molecular data].
    Fattoum S.
    Tunis Med; 2006 Nov; 84(11):687-96. PubMed ID: 17294892
    [Abstract] [Full Text] [Related]

  • 6. Prevalence and Regional Distribution of Beta-Hemoglobin Variants in Saudi Arabia: Insights from the National Premarital Screening Program".
    Aljabry M, Sulimani S, Alotaibi G, Aljabri H, Alomary S, Aljabri O, Sallam M, Alsultan A.
    J Epidemiol Glob Health; 2024 Sep; 14(3):1242-1248. PubMed ID: 39073533
    [Abstract] [Full Text] [Related]

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

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  • 9. Microcytic hypochromic anemia: should high performance liquid chromatography be used routinely for screening anemic and antenatal patients?
    Philip J, Sarkar RS, Kushwaha N.
    Indian J Pathol Microbiol; 2013 Sep; 56(2):109-13. PubMed ID: 24056645
    [Abstract] [Full Text] [Related]

  • 10. 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]

  • 11. 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; 27(8):608-13. PubMed ID: 20795773
    [Abstract] [Full Text] [Related]

  • 12. Appraisal of sickle-cell and thalassaemia genes in Saudi Arabia.
    el-Hazmi MA, Warsy AS.
    East Mediterr Health J; 1999 Nov; 5(6):1147-53. PubMed ID: 11924103
    [Abstract] [Full Text] [Related]

  • 13. Incidence of hemoglobinopathies and thalassemias in Northern Alberta. Establishment of reference intervals for HbF and HbA2.
    Rodriguez-Capote K, Higgins TN.
    Clin Biochem; 2015 Jul; 48(10-11):698-702. PubMed ID: 25869492
    [Abstract] [Full Text] [Related]

  • 14. Epidemiology of Hemoglobinopathies in the Huzhou Region, Zhejiang Province, Southeast China.
    Ding ZY, Shen GS, Zhang S, He PY.
    Hemoglobin; 2016 Sep; 40(5):304-309. PubMed ID: 27615034
    [Abstract] [Full Text] [Related]

  • 15. Prenatal diagnosis of hemoglobinopathies in Hacettepe University, Turkey.
    Beksac MS, Gumruk F, Gurgey A, Cakar N, Mumusoglu S, Ozyuncu O, Altay C.
    Pediatr Hematol Oncol; 2011 Feb; 28(1):51-5. PubMed ID: 20863160
    [Abstract] [Full Text] [Related]

  • 16. Six-year outcome of the national premarital screening and genetic counseling program for sickle cell disease and β-thalassemia in Saudi Arabia.
    Memish ZA, Saeedi MY.
    Ann Saudi Med; 2011 Feb; 31(3):229-35. PubMed ID: 21623050
    [Abstract] [Full Text] [Related]

  • 17. Clinical and molecular characterization of Hb Hofu in eastern India.
    Purohit P, Mashon RS, Patel S, Dehury S, Pattanayak C, Das K, Nair S, Italia K, Bag S, Colah R, Patel DK.
    Int J Lab Hematol; 2014 Feb; 36(1):71-6. PubMed ID: 23889802
    [Abstract] [Full Text] [Related]

  • 18. [Beta-thalassemia and Hb D in patients with anemia].
    Troĭtskaia OV, Antonova LA, Lozhechnik IG, Toshchan OV.
    Klin Lab Diagn; 1998 Mar; (3):16-23. PubMed ID: 9575728
    [Abstract] [Full Text] [Related]

  • 19. Measurement of HbA₂ by capillary electrophoresis for diagnosing β-thalassemia/HbE disease in patients with low HbF.
    Prasing W, Pornprasert S.
    Lab Med; 2014 Mar; 45(3):226-30. PubMed ID: 25051074
    [Abstract] [Full Text] [Related]

  • 20. Fibrocongestive splenomegaly in sickle cell disease: a distinct clinicopathological entity in the Eastern province of Saudi Arabia.
    Chopra R, Al-Mulhim AR, Al-Baharani AT.
    Am J Hematol; 2005 Jul; 79(3):180-6. PubMed ID: 15981225
    [Abstract] [Full Text] [Related]

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