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

283 related items for PubMed ID: 22690826

  • 1. 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]

  • 2. Clinical and haematological features in a compound heterozygote (HBB:c.92 + 5G > C/HBB:c.93-2A > C) case of thalassaemia major.
    Agarwal S, Tamhankar PM, Kumar R, Dalal A.
    Int J Lab Hematol; 2010 Jun; 32(3):369-72. PubMed ID: 19486366
    [Abstract] [Full Text] [Related]

  • 3. Haematological and genetic features of deltabeta-thalassaemia in Pakistan.
    Ahmed S, Anwar M.
    J Coll Physicians Surg Pak; 2006 Jan; 16(1):19-22. PubMed ID: 16441982
    [Abstract] [Full Text] [Related]

  • 4. 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]

  • 5. Effects of α-thalassaemia mutations on the haematological parameters of β-thalassaemia carriers.
    Saleh-Gohari N, Khademi Bami M, Nikbakht R, Karimi-Maleh H.
    J Clin Pathol; 2015 Jul; 68(7):562-6. PubMed ID: 25935548
    [Abstract] [Full Text] [Related]

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

  • 7. An interplay of alleviating mutations in the clinical phenotype of beta-thalassaemia intermedia.
    Nadkarni A, Sakaguchi T, Gorakshakar A, Phanasgaonkar S, Kiyama R, Colah R, Mohanty D.
    Clin Lab Haematol; 2004 Dec; 26(6):419-22. PubMed ID: 15596001
    [Abstract] [Full Text] [Related]

  • 8. Haematological and clinical features of beta-thalassaemia associated with Hb Dhofar.
    Daar S, Gravell D, Hussein HM, Pathare AV, Wali Y, Krishnamoorthy R.
    Eur J Haematol; 2008 Jan; 80(1):67-70. PubMed ID: 18173741
    [Abstract] [Full Text] [Related]

  • 9. 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]

  • 10. 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]

  • 11. Impact of beta globin gene mutations on the clinical phenotype of beta thalassemia in India.
    Colah R, Nadkarni A, Gorakshakar A, Phanasgaonkar S, Surve R, Subramaniam PG, Bondge N, Pujari K, Ghosh K, Mohanty D.
    Blood Cells Mol Dis; 2004 Nov; 33(2):153-7. PubMed ID: 15315795
    [Abstract] [Full Text] [Related]

  • 12. Haematological and electrophoretic characterisation of β-thalassaemia in Yunnan province of Southwestern China.
    Zhang J, He J, Mao X, Zeng X, Chen H, Su J, Zhu B.
    BMJ Open; 2017 Jan 31; 7(1):e013367. PubMed ID: 28143837
    [Abstract] [Full Text] [Related]

  • 13. Co-heredity of silent CAP + 1570 T>C (HBB:c*96T>C) defect and severe β-thal mutation: a cause of mild β-thalassemia intermedia.
    Vinciguerra M, Passarello C, Cassarà F, Leto F, Cannata M, Calvaruso G, Di Maggio R, Renda D, Maggio A, Giambona A.
    Int J Lab Hematol; 2016 Feb 31; 38(1):17-26. PubMed ID: 26418075
    [Abstract] [Full Text] [Related]

  • 14. Diverse phenotypes and transfusion requirements due to interaction of β-thalassemias with triplicated α-globin genes.
    Mehta PR, Upadhye DS, Sawant PM, Gorivale MS, Nadkarni AH, Shanmukhaiah C, Ghosh K, Colah RB.
    Ann Hematol; 2015 Dec 31; 94(12):1953-8. PubMed ID: 26319530
    [Abstract] [Full Text] [Related]

  • 15. Mutational spectrum of thalassemias and other hemoglobinopathies in West Bengal, Eastern India.
    Chatterjee T, Chakravarty A, Chakravarty S.
    Hemoglobin; 2014 Dec 31; 38(6):405-8. PubMed ID: 25405918
    [Abstract] [Full Text] [Related]

  • 16. A novel mutation of -73(A-->T) in the CCAAT box of the beta-globin gene identified in a patient with the mild beta-thalassemia intermedia.
    Chen XW, Mo QH, Li Q, Zeng R, Xu XM.
    Ann Hematol; 2007 Sep 31; 86(9):653-7. PubMed ID: 17516066
    [Abstract] [Full Text] [Related]

  • 17. The IVS-II-837 (T>G) appears to be a relatively common 'rare' β-globin gene mutation in β-thalassemia patients in Karnataka State, South India.
    Bashyam MD, Chaudhary AK, Bhat V.
    Hemoglobin; 2012 Sep 31; 36(5):497-503. PubMed ID: 22734501
    [Abstract] [Full Text] [Related]

  • 18. Evaluation of the genetic basis of phenotypic heterogeneity in north Indian patients with thalassemia major.
    Sharma N, Das R, Kaur J, Ahluwalia J, Trehan A, Bansal D, Panigrahi I, Marwaha RK.
    Eur J Haematol; 2010 Jun 31; 84(6):531-7. PubMed ID: 20132300
    [Abstract] [Full Text] [Related]

  • 19. [Molecular characteristics of the thalassemia syndrome and prenatal diagnosis in a high risk family].
    Vujić D, Cvorkov--Drazić M, Pavlović S, Bunjevacki G, Popović Z, Puzigaća Z.
    Srp Arh Celok Lek; 2001 Jun 31; 129 Suppl 1():56-8. PubMed ID: 15637993
    [Abstract] [Full Text] [Related]

  • 20. 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 31; 19(5):428-35. PubMed ID: 10360511
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 15.