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

556 related items for PubMed ID: 17654068

  • 1. Hb St. Jozef, A Val-->Leu N-terminal mutation leading to retention of the methionine, and partial acetylation found in the globin gene in Cis with a -alpha3.7 thalassemia deletion.
    Harteveld CL, Versteegh FG, van Leer EH, Starreveld JS, Kok PJ, van Rooijen-Nijdam I, van Delft P, Zanella-Cleon I, Becchi M, Wajcman H, Giordano PC.
    Hemoglobin; 2007; 31(3):313-23. PubMed ID: 17654068
    [Abstract] [Full Text] [Related]

  • 2. Hb Bleuland [alpha108(G15)Thr-->Asn, ACC-->AAC (alpha2)]: a new abnormal hemoglobin associated with a mild alpha-thalassemia phenotype.
    Harteveld CL, Versteegh FG, Kok PJ, van Rooijen-Nijdam IH, van Delft P, Giordano PC.
    Hemoglobin; 2006; 30(3):349-54. PubMed ID: 16840225
    [Abstract] [Full Text] [Related]

  • 3. Hb Zoetermeer: a new mutation on the alpha2 gene inducing an Ala-->Ser substitution at codon 21 is possibly associated with a mild thalassemic phenotype.
    Harteveld CL, van Helden WC, Boxma GL, van Delft P, Bakker-Verweij M, Wajcman H, Zanella-Cleon I, Becchi M, Giordano PC.
    Hemoglobin; 2007; 31(3):325-32. PubMed ID: 17654069
    [Abstract] [Full Text] [Related]

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

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

  • 6. Alpha-thalassemia phenotype induced by the new IVS-II-2 (T --> A) splice donor site mutation on the alpha2-globin gene.
    Harteveld CL, Jebbink MC, van der Lely N, van Delft P, Akkermans N, Arkesteyn S, Giordano PC.
    Hemoglobin; 2006; 30(1):3-7. PubMed ID: 16540408
    [Abstract] [Full Text] [Related]

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

  • 8. Hb L'Aquila [beta106(G8)Leu-->Val, CTG-->GTG]: a novel thalassemic hemoglobin variant.
    Amato A, Cappabianca MP, Ponzini D, Rinaldi S, Biagio PD, Foglietta E, Grisanti P, Mastropietro F.
    Hemoglobin; 2007; 31(3):375-8. PubMed ID: 17654075
    [Abstract] [Full Text] [Related]

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

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13. Complex interaction of Hb E [beta26(B8)Glu-->Lys], Hb Korle-Bu [beta73(E17)Asp-->Asn] and a deletional alpha-thalassemia-1 in pregnancy.
    Siriratmanawong N, Chansri W, Singsanan S, Fucharoen G, Fucharoen S.
    Hemoglobin; 2009; 33(6):507-14. PubMed ID: 19958198
    [Abstract] [Full Text] [Related]

  • 14. Hb Charlieu [alpha106(G13)Leu-->Pro (alpha1)]: a new phenotypically silent hemoglobin variant associated with a mild alpha-thalassemia phenotype.
    Joly P, Szymanowicz A, Neyron MJ, Zine A, Wajcman H, Francina A.
    Hemoglobin; 2010; 34(4):366-73. PubMed ID: 20642334
    [Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16. Hb Florida: a novel elongated C-terminal beta-globin variant causing dominant beta-thalassemia phenotype.
    Weinstein BI, Erramouspe B, Albuquerque DM, Oliveira DM, Kimura EM, Costa FF, Sonati MF.
    Am J Hematol; 2006 May; 81(5):358-60. PubMed ID: 16628732
    [Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18. Strategy for identification by mass spectrometry of a new human hemoglobin variant with two mutations in Cis in the beta-globin chain: Hb S-Clichy [beta6(A3)Glu-->Val; beta8(A5)Lys-->Thr].
    Zanella-Cleon I, Préhu C, Joly P, Riou J, Becchi M, Wajcman H, Francina A.
    Hemoglobin; 2009 May; 33(3):177-87. PubMed ID: 19657831
    [Abstract] [Full Text] [Related]

  • 19. A new alpha chain hemoglobin variant: Hb Al-Hammadi Riyadh [alpha75(EF4)Asp-->Val (alpha2)].
    Burnichon N, Lacan P, Becchi M, Zanella-Cleon I, Aubry M, Mowafy M, Couprie N, Francina A.
    Hemoglobin; 2006 May; 30(2):155-64. PubMed ID: 16798639
    [Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 28.