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Journal Abstract Search

349 related items for PubMed ID: 21194265

  • 1. Co-inheritance of hemoglobin D and β-thalassemia traits in three Iranian families: clinical relevance.
    Taghavi Basmanj M, Karimipoor M, Amirian A, Jafarinejad M, Katouzian L, Valaei A, Bayat F, Kordafshari A, Zeinali S.
    Arch Iran Med; 2011 Jan; 14(1):61-3. PubMed ID: 21194265
    [Abstract] [Full Text] [Related]

  • 2. First report on the co-inheritance of beta-globin IVS-I-5 (G-->C) thalassemia with delta globin CD12 {Asn-->Lys (AAT-->AAA)}HbA₂-NYU in Iran.
    Amirian A, Karimipoor M, Jafarinejad M, Taghavi M, Kordafshari A, Fathi Azar S, Mohammadi MS, Zeinali S.
    Arch Iran Med; 2011 Jan; 14(1):8-11. PubMed ID: 21194254
    [Abstract] [Full Text] [Related]

  • 3. 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]

  • 4. Hb D-Punjab [beta 121 (GH4) Glu-->Gln]/beta0-thalassemia [IVSII.1(G-->A)] in two cases from an Iranian family: first report.
    Rahimi Z, Akramipour R, Korani S, Nagel RL.
    Am J Hematol; 2006 Apr; 81(4):302-3. PubMed ID: 16550524
    [No Abstract] [Full Text] [Related]

  • 5. Identification of IVS-I (-1) (G > C) or Hb Monroe as a report on the beta-globin gene with a beta-thalassemia minor phenotype in south of Iran.
    Hamid M, Shariati G, Saberi A, Kaikhaei B, Galehdari H, Mohammadi-Anaei M.
    Arch Iran Med; 2013 Sep; 16(9):563-4. PubMed ID: 23981164
    [Abstract] [Full Text] [Related]

  • 6. Heterozygous Hb Hope [beta136(H14)Gly --> Asp] in association with heterozygous beta0-thalassemia with apparent homozygous expression, in a Spanish patient.
    Beneitez D, Carrera A, Duran-Suárez JR, Paz V, León A, García Talavera J.
    Hemoglobin; 2006 Sep; 30(1):45-9. PubMed ID: 16540415
    [Abstract] [Full Text] [Related]

  • 7. [The association of beta zero-thalassemia and Hb D Punjab in a family of Indian origin. The second case reported in Spain].
    Ropero P, González FA, Sánchez J, Armada B, Martí E, Valdés B, Mora A, Villegas A.
    Med Clin (Barc); 1997 Mar 15; 108(10):385-8. PubMed ID: 9139146
    [Abstract] [Full Text] [Related]

  • 8. Hb Knossos (HBB: c.82G > T), β-globin CD 5 (-CT) (HBB: c.17_18delCT) and δ-globin CD 59 (-a) (HBD: c.179delA) mutations in a Syrian patient with β-thalassemia intermedia.
    Moassas F, Nweder MS, Murad H.
    BMC Pediatr; 2019 Feb 18; 19(1):61. PubMed ID: 30777047
    [Abstract] [Full Text] [Related]

  • 9. Comprehensive spectrum of the β-Thalassemia mutations in Khuzestan, southwest Iran.
    Galehdari H, Salehi B, Azmoun S, Keikhaei B, Zandian KM, Pedram M.
    Hemoglobin; 2010 Feb 18; 34(5):461-8. PubMed ID: 20854120
    [Abstract] [Full Text] [Related]

  • 10. Compound heterozygosity of Hb D(Iran) (beta(22) Glu-->Gln) and beta(0)-thalassemia (619 bp-deletion) in India.
    Agrawal MG, Bhanushali AA, Dedhia P, Jeswani KD, Dayanand S, Dasgupta A, Das BR.
    Eur J Haematol; 2007 Sep 18; 79(3):248-50. PubMed ID: 17655708
    [Abstract] [Full Text] [Related]

  • 11. Detection of a Hb A2 -Melbourne (HBD: c.130G>A) combined with β-thalassemia in a Chinese individual.
    Li Y, Huang T, Mao T, Zhang X, Liang L, Meng M.
    J Clin Lab Anal; 2020 Sep 18; 34(9):e23401. PubMed ID: 32770585
    [Abstract] [Full Text] [Related]

  • 12. Known and new hemoglobin A2 variants in Thailand and implication for β-thalassemia screening.
    Panyasai S, Fucharoen G, Fucharoen S.
    Clin Chim Acta; 2015 Jan 01; 438():226-30. PubMed ID: 25218786
    [Abstract] [Full Text] [Related]

  • 13. 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 01; 89(2):160-4. PubMed ID: 22690826
    [Abstract] [Full Text] [Related]

  • 14. A novel β-globin gene mutation HBB.c.22 G>C produces a hemoglobin variant (Hb Vellore) mimicking HbS in HPLC.
    Edison ES, Sathya M, Rajkumar SV, Nair SC, Srivastava A, Shaji RV.
    Int J Lab Hematol; 2012 Oct 01; 34(5):556-8. PubMed ID: 22471768
    [Abstract] [Full Text] [Related]

  • 15. 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 Oct 01; 29(2):119-32. PubMed ID: 15921164
    [Abstract] [Full Text] [Related]

  • 16. Analyzing 5'HS3 and 5'HS4 LCR core regions and NF-E2 in Iranian thalassemia intermedia patients with normal or carrier status for beta-globin mutations.
    Neishabury M, Azarkeivan A, Oberkanins C, Abedini SS, Zamani S, Najmabadi H.
    Blood Cells Mol Dis; 2011 Mar 15; 46(3):201-5. PubMed ID: 21232998
    [Abstract] [Full Text] [Related]

  • 17. Hemoglobin D/beta-thalassemia and beta-thalassemia major in a Saudi family.
    Owaidah TM, Al-Saleh MM, Al-Hellani AM.
    Saudi Med J; 2005 Apr 15; 26(4):674-7. PubMed ID: 15900384
    [Abstract] [Full Text] [Related]

  • 18. [A study on gene mutation spectrums of α- and β-thalassemias in populations of Yunnan Province and the prenatal gene diagnosis].
    Zhu BS, He J, Zhang J, Zeng XH, Su J, Xu XH, Li SY, Chen H, Zhang YH.
    Zhonghua Fu Chan Ke Za Zhi; 2012 Feb 15; 47(2):85-9. PubMed ID: 22455737
    [Abstract] [Full Text] [Related]

  • 19. Distinct phenotypic expression associated with a new hyperunstable alpha globin variant (Hb heraklion, alpha1cd37(C2)Pro>0): comparison to other alpha-thalassemic hemoglobinopathies.
    Traeger-Synodinos J, Papassotiriou I, Metaxotou-Mavrommati A, Vrettou C, Stamoulakatou A, Kanavakis E.
    Blood Cells Mol Dis; 2000 Aug 15; 26(4):276-84. PubMed ID: 11042028
    [Abstract] [Full Text] [Related]

  • 20. First observation of homozygous hemoglobin hamadan (B 56 (D7) GLY-ARG) and beta thalassemia (-29 G>A)- hemoglobin Hamadan combination in a Turkish family.
    Akar E, Ozdemir S, Hakki Timur I, Akar N.
    Am J Hematol; 2003 Dec 15; 74(4):280-2. PubMed ID: 14635211
    [Abstract] [Full Text] [Related]

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