These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

503 related items for PubMed ID: 2086380

  • 1. Beta-, delta beta-thalassemia and Hb lepore among Yugoslav, Bulgarian, Turkish and Albanian.
    Efremov GD.
    Haematologica; 1990; 75 Suppl 5():31-41. PubMed ID: 2086380
    [Abstract] [Full Text] [Related]

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

  • 3. Hemoglobinopathies in Yugoslavia: an update.
    Efremov GD.
    Hemoglobin; 1992; 16(6):531-44. PubMed ID: 1487426
    [Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6. The molecular pathology of beta-thalassemia in Turkey: the Boğaziçi university experience.
    Basak AN.
    Hemoglobin; 2007; 31(2):233-41. PubMed ID: 17486506
    [Abstract] [Full Text] [Related]

  • 7. Molecular basis of beta-thalassemia and other hemoglobinopathies in Bulgaria: an update.
    Petkov GH, Efremov GD.
    Hemoglobin; 2007; 31(2):225-32. PubMed ID: 17486505
    [Abstract] [Full Text] [Related]

  • 8. Hemoglobinopathies among the Gond tribal groups of central India; interaction of alpha- and beta-thalassemia with beta chain variants.
    Gupta RB, Tiwary RS, Pande PL, Kutlar F, Oner C, Oner R, Huisman TH.
    Hemoglobin; 1991; 15(5):441-58. PubMed ID: 1802886
    [Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10. Dominantly Inherited beta-Thalassemia.
    Efremov GD.
    Hemoglobin; 2007; 31(2):193-207. PubMed ID: 17486503
    [Abstract] [Full Text] [Related]

  • 11. Molecular basis of thalassemia syndromes in Serbia and Montenegro.
    Pavlovic S, Urosevic J, Poznanic J, Perisic LJ, Petrucev B, Tosic N, Krivokapic-Dokmanovic L, Janic D, Cvorkov-Drazic M, Bunjevacki G.
    Acta Haematol; 2005; 113(3):175-80. PubMed ID: 15870487
    [Abstract] [Full Text] [Related]

  • 12. 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]

  • 13. Thalassemia syndromes in Serbia: an update.
    Radmilovic M, Zukic B, Stankovic B, Karan-Djurasevic T, Stojiljkovic M, Spasovski V, Tosic N, Dokmanovic L, Janic D, Pavlovic S.
    Hemoglobin; 2010 Nov; 34(5):477-85. PubMed ID: 20854122
    [Abstract] [Full Text] [Related]

  • 14. Diversity of the 5' beta-globin haplotype of four beta-thalassemia mutations in the Mexican population.
    Morales KR, Magaña MT, Ibarra B, Perea FJ.
    Hemoglobin; 2009 Nov; 33(1):66-71. PubMed ID: 19205976
    [Abstract] [Full Text] [Related]

  • 15. Beta-thalassemia in Yugoslavia.
    Dimovski A, Efremov DG, Jankovic L, Juricic D, Zisovski N, Stojanovski N, Nikolov N, Petkov GT, Reese AL, Stoming TA.
    Hemoglobin; 1990 Nov; 14(1):15-24. PubMed ID: 2200761
    [Abstract] [Full Text] [Related]

  • 16. Molecular basis of β-thalassemia in the United Arab Emirates.
    Baysal E.
    Hemoglobin; 2011 Nov; 35(5-6):581-8. PubMed ID: 22074124
    [Abstract] [Full Text] [Related]

  • 17. Sickle cell disease in the Kurdish population of northern Iraq.
    Al-Allawi NA, Jalal SD, Nerwey FF, Al-Sayan GO, Al-Zebari SS, Alshingaly AA, Markous RD, Jubrael JM, Hamamy H.
    Hemoglobin; 2012 Nov; 36(4):333-42. PubMed ID: 22686351
    [Abstract] [Full Text] [Related]

  • 18. Molecular characterization of beta-thalassemia in the Dohuk region of Iraq.
    Al-Allawi NA, Jubrael JM, Hughson M.
    Hemoglobin; 2006 Nov; 30(4):479-86. PubMed ID: 16987803
    [Abstract] [Full Text] [Related]

  • 19. Study of beta-Thalassemia mutations using the polymerase chain reaction-amplification refractory mutation system and direct DNA sequencing techniques in a group of Egyptian Thalassemia patients.
    El-Gawhary S, El-Shafie S, Niazi M, Aziz M, El-Beshlawy A.
    Hemoglobin; 2007 Nov; 31(1):63-9. PubMed ID: 17365006
    [Abstract] [Full Text] [Related]

  • 20. Interactions of hemoglobin Lepore (deltabeta hybrid hemoglobin) with various hemoglobinopathies: A molecular and hematological characteristics and differential diagnosis.
    Chaibunruang A, Srivorakun H, Fucharoen S, Fucharoen G, Sae-ung N, Sanchaisuriya K.
    Blood Cells Mol Dis; 2010 Mar 15; 44(3):140-5. PubMed ID: 20022270
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 26.