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Journal Abstract Search

354 related items for PubMed ID: 17365011

  • 1. High oxygen affinity hemoglobin variant in a Canadian family: Hb Bunbury [beta94(FG1)Asp-->Asn, GAC-->AAC].
    Walker L, Eng B, McFarlane A, Waye JS.
    Hemoglobin; 2007; 31(1):101-3. PubMed ID: 17365011
    [Abstract] [Full Text] [Related]

  • 2. Characterization of a new hemoglobin variant: Hb Badalona (beta31[B13]Leu-->Val).
    Junca J, Villegas A, Ropero P, González FA, Motos A, Valverde F.
    Ann Hematol; 2002 Apr; 81(4):179-81. PubMed ID: 11976817
    [Abstract] [Full Text] [Related]

  • 3. Hb Geldrop St. Anna [beta94(FG1)Asp --> Tyr]: a new hemoglobin variant observed in a diabetic patient.
    Harteveld CL, Thelen MH, Rutten JJ, Leuverman J, Akkermans N, van Delft P, Arkesteijn S, Giordano PC.
    Hemoglobin; 2005 Apr; 29(2):107-12. PubMed ID: 15921162
    [Abstract] [Full Text] [Related]

  • 4. Hb La Coruña [beta38(C4)Thr-->Ile]: a new hemoglobin variant leading to familial polycythemia.
    Ropero P, Fernández-Lago C, Villegas A, Polo M, Mateo M, Mora A, González FA.
    Hemoglobin; 2006 Apr; 30(3):379-83. PubMed ID: 16840229
    [Abstract] [Full Text] [Related]

  • 5. Molecular characterization and functional studies on Hb Kempsey, beta 99 (G-1) Asp----Asn, a high-oxygen affinity variant.
    Ricco G, Scaroina F, Amprimo MC, Gottardi E, Parziale A, Alfarano A, Camaschella C.
    Haematologica; 1992 Apr; 77(3):215-20. PubMed ID: 1427427
    [Abstract] [Full Text] [Related]

  • 6. Hb Montfermeil [beta 130(H8) Tyr-->Cys]: suggests a key role for the interaction between helix A and H in oxygen affinity of the hemoglobin molecule.
    Kister J, Baudin-Creuza V, Kiger L, Préhu C, Papassotiriou I, Riou J, Galactéros F, Wajcman H.
    Blood Cells Mol Dis; 2005 Apr; 34(2):166-73. PubMed ID: 15727901
    [Abstract] [Full Text] [Related]

  • 7. Low affinity and unstable hemoglobin variant caused by AAC-->ATC (Asn-->Ile) mutation at codon 108 of the beta-globin gene.
    Ma ES, Chow EY, Chan AY, Chu CM, Lin SY, Chan LC.
    Haematologica; 2002 May; 87(5):553-4. PubMed ID: 12010673
    [No Abstract] [Full Text] [Related]

  • 8. A new hemoglobin with high oxygen affinity--hemoglobin bunbury: alpha 2 beta 2 [94 (FG1) Asp replaced by Asn].
    Como PF, Kennett D, Wilkinson T, Kronenberg H.
    Hemoglobin; 1983 May; 7(5):413-21. PubMed ID: 6629823
    [Abstract] [Full Text] [Related]

  • 9. Hemoglobin Titusville, a low oxygen affinity variant hemoglobin, in a family of Northern European background.
    Luo HY, Irving I, Prior J, Lim E, Eung SH, Skelton TP, Erber WN, Steinberg MH, Chui DH.
    Am J Hematol; 2004 Dec; 77(4):384-6. PubMed ID: 15551405
    [Abstract] [Full Text] [Related]

  • 10. 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 Dec; 30(2):155-64. PubMed ID: 16798639
    [Abstract] [Full Text] [Related]

  • 11. Hb Marineo [beta70(E14)Ala-->Val]: a silent hemoglobin variant with a mutation within the heme pocket.
    Giambona A, Vinciguerra M, Cassarà F, Li Muli R, Leto F, Passarello C, Wajcman H, Maggio A.
    Hemoglobin; 2006 Dec; 30(2):139-48. PubMed ID: 16798637
    [Abstract] [Full Text] [Related]

  • 12. Hb Trollhättan [beta 20(B2)Val-->Glu]--a new haemoglobin variant with increased oxygen affinity causing erythrocytosis.
    Landin B, Berglund S, Lindoff B.
    Eur J Haematol; 1994 Jul; 53(1):21-5. PubMed ID: 7914875
    [Abstract] [Full Text] [Related]

  • 13. Erythrocytosis due to a combination of the high oxygen affinity hemoglobin variant, Hb Olympia [beta20(B2)Val-->Met] with beta- and alpha-thalassemia mutations: first case in the literature.
    Kalotychou V, Tzanetea R, Konstantopoulos K, Papassotiriou I, Rombos I.
    Hemoglobin; 2010 Jul; 34(4):383-8. PubMed ID: 20642336
    [Abstract] [Full Text] [Related]

  • 14. Hb Nebraska [β86(F2)Ala→Ile (HBB:c.259G>A;260C>T)]: a unique high oxygen affinity hemoglobin variant with a double nucleotide substitution within the same codon.
    Hoyer JD, Wendt PC, Hogan WJ, Oliveira JL.
    Hemoglobin; 2011 Jul; 35(1):22-7. PubMed ID: 21250878
    [Abstract] [Full Text] [Related]

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  • 17. Compound heterozygous Hb Tak/Hb E causes secondary erythrocytosis in a Thai family.
    Teawtrakul N, Sirijirachai C, Chansung G, Fucharoen G.
    Hemoglobin; 2010 Jan; 34(2):165-8. PubMed ID: 20353353
    [Abstract] [Full Text] [Related]

  • 18. Hb A2-Pasteur-Tunis [delta59(E3)Lys-->Asn, AAG-->AAC]: a new delta chain variant detected by DNA sequencing in a Tunisian carrier of the codon 39 (C-->T) beta0-Thalassemia mutation.
    Moumni I, Zorai A, Daoued BB, Mosbahi I, Omar S, Kaabachi N, Dellagi K, Abbes S.
    Hemoglobin; 2007 Jan; 31(1):23-9. PubMed ID: 17365002
    [Abstract] [Full Text] [Related]

  • 19. Hb Calais [beta76(E20)Ala --> Pro]: a family study of a variant with decreased oxygen affinity.
    Bardet V, Adam M, Yvart J, Wajcman H, Galacteros F, Favier R.
    Hemoglobin; 2006 Jan; 30(1):35-8. PubMed ID: 16540413
    [Abstract] [Full Text] [Related]

  • 20. Hemoglobin Ypsilanti: a high-oxygen-affinity hemoglobin demonstrated by two automated high-pressure liquid chromatography systems.
    Mais DD, Boxer LA, Gulbranson RD, Keren DF.
    Am J Clin Pathol; 2007 Nov; 128(5):850-3. PubMed ID: 17951209
    [Abstract] [Full Text] [Related]

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