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Journal Abstract Search

374 related items for PubMed ID: 19556751

  • 1. A pilot beta-thalassaemia screening program in the Albanian population for a health planning program.
    Baghernajad-Salehi L, D'Apice MR, Babameto-Laku A, Biancolella M, Mitre A, Russo S, Di Daniele N, Sangiuolo F, Mokini V, Novelli G.
    Acta Haematol; 2009; 121(4):234-8. PubMed ID: 19556751
    [Abstract] [Full Text] [Related]

  • 2. Spectrum of beta-globin gene mutations among thalassemia patients in the West Bank region of Palestine.
    Darwish HM, El-Khatib FF, Ayesh S.
    Hemoglobin; 2005; 29(2):119-32. PubMed ID: 15921164
    [Abstract] [Full Text] [Related]

  • 3. Prenatal diagnosis of beta-thalassaemia and sickle cell anaemia in Turkey.
    Tüzmen S, Tadmouri GO, Ozer A, Baig SM, Ozçelik H, Başaran S, Başak AN.
    Prenat Diagn; 1996 Mar; 16(3):252-8. PubMed ID: 8710780
    [Abstract] [Full Text] [Related]

  • 4. Mutational spectrum of delta-globin gene in the Portuguese population.
    Morgado A, Picanço I, Gomes S, Miranda A, Coucelo M, Seuanes F, Seixas MT, Romão L, Faustino P.
    Eur J Haematol; 2007 Nov; 79(5):422-8. PubMed ID: 17916081
    [Abstract] [Full Text] [Related]

  • 5. Prenatal diagnosis of beta-thalassaemia by reverse dot-blot hybridization.
    Winichagoon P, Saechan V, Sripanich R, Nopparatana C, Kanokpongsakdi S, Maggio A, Fucharoen S.
    Prenat Diagn; 1999 May; 19(5):428-35. PubMed ID: 10360511
    [Abstract] [Full Text] [Related]

  • 6. Prevalence of beta-thalassaemia and sickle cell traits in premarital screening in Al-Qassim, Saudi Arabia.
    El-Tayeb EN, Yaqoob M, Abdur-Rahim K, Gustavson KH.
    Genet Couns; 2008 May; 19(2):211-8. PubMed ID: 18618996
    [Abstract] [Full Text] [Related]

  • 7. Student screening for inherited blood disorders in Bahrain.
    Al-Arrayed S, Hafadh N, Amin S, Al-Mukhareq H, Sanad H.
    East Mediterr Health J; 2003 May; 9(3):344-52. PubMed ID: 15751927
    [Abstract] [Full Text] [Related]

  • 8. The molecular analysis of beta-thalassemia mutations in Lorestan Province, Iran.
    Kiani AA, Mortazavi Y, Zeinali S, Shirkhani Y.
    Hemoglobin; 2007 May; 31(3):343-9. PubMed ID: 17654071
    [Abstract] [Full Text] [Related]

  • 9. Beta-thalassaemia mutations and the underlying beta gene cluster haplotypes in the Greek population.
    Kollia P, Karababa PH, Sinopoulou K, Voskaridou E, Boussiou M, Papadakis M, Loukopoulos D.
    Gene Geogr; 1992 May; 6(1-2):59-70. PubMed ID: 1299316
    [Abstract] [Full Text] [Related]

  • 10. [Most frequent beta-thalassemia mutations in the Argentinian population].
    Varela V, Abreu S, Rossetti LC, Targovnik H.
    Sangre (Barc); 1996 Apr; 41(2):137-40. PubMed ID: 9045354
    [Abstract] [Full Text] [Related]

  • 11. [Screening of hemoglobinopathies and molecular analysis of beta-thalassemia in Central Tunisia].
    Chebil-Laradi S, Pousse H, Khelif A, Ghanem N, Martin J, Kortas M, Ennabli S, Mehdouani K, B'Chir N, Kharrat H.
    Arch Pediatr; 1994 Dec; 1(12):1100-5. PubMed ID: 7849895
    [Abstract] [Full Text] [Related]

  • 12. Carrier diagnostics and prevention of hemoglobinopathies in early pregnancy in The Netherlands: a pilot study.
    Giordano PC, Plancke A, Van Meir CA, Janssen CA, Kok PJ, Van Rooijen-Nijdam IH, Tanis BC, van Huisseling JC, Versteegh FG.
    Prenat Diagn; 2006 Aug; 26(8):719-24. PubMed ID: 16752436
    [Abstract] [Full Text] [Related]

  • 13. Molecular analysis of beta-thalassemia and sickle cell anemia in Antalya.
    Keser I, Sanlioglu AD, Manguoglu E, Guzeloglu Kayisli O, Nal N, Sargin F, Yesilipek A, Simsek M, Mendilcioglu I, Canatan D, Luleci G.
    Acta Haematol; 2004 Aug; 111(4):205-10. PubMed ID: 15153712
    [Abstract] [Full Text] [Related]

  • 14. Thalassaemia and glucose-6-phosphate dehydrogenase screening in 13- to 14-year-old students of the Sardinian population: preliminary findings.
    Cao A, Congiu R, Sollaino MC, Desogus MF, Demartis FR, Loi D, Cau M, Galanello R.
    Community Genet; 2008 Aug; 11(3):121-8. PubMed ID: 18376107
    [Abstract] [Full Text] [Related]

  • 15. The clinical significance of the spectrum of interactions of CAP+1 (A-->C), a silent beta-globin gene mutation, with other beta-thalassemia mutations and globin gene modifiers in north Indians.
    Garewal G, Das R, Awasthi A, Ahluwalia J, Marwaha RK.
    Eur J Haematol; 2007 Nov; 79(5):417-21. PubMed ID: 17900295
    [Abstract] [Full Text] [Related]

  • 16. 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]

  • 17. Molecular heterogeneity of beta-thalassemia alleles in Spain and its importance in the diagnosis and prevention of beta-thalassemia major and sickle cell disorders.
    Pereira Mdel M, Dalmau AC, Corrons JL.
    Hemoglobin; 2009 Nov; 33(3):226-34. PubMed ID: 19657837
    [Abstract] [Full Text] [Related]

  • 18. Preventation of thalassemia in Australia.
    Hendy J.
    Southeast Asian J Trop Med Public Health; 1999 Nov; 30 Suppl 2():94-6. PubMed ID: 11400797
    [Abstract] [Full Text] [Related]

  • 19. Thalassemias and other hemoglobinopathies in the Republic of Macedonia.
    Efremov GD.
    Hemoglobin; 2007 Nov; 31(1):1-15. PubMed ID: 17365000
    [Abstract] [Full Text] [Related]

  • 20. Variable haematological and clinical presentation of β-thalassaemia carriers and homozygotes with the Poly A (T→C) mutation in the Indian population.
    Italia K, Sawant P, Surve R, Wadia M, Nadkarni A, Ghosh K, Colah R.
    Eur J Haematol; 2012 Aug; 89(2):160-4. PubMed ID: 22690826
    [Abstract] [Full Text] [Related]

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