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Journal Abstract Search


213 related items for PubMed ID: 808940

  • 1. A new Hb variant: Hb F Sardinia gamma75(E19) isoleucine leads to threonine found in a family with Hb G Philadelphia, beta-chain deficiency and a Lepore-like haemoglobin indistinguishable from Hb A2.
    Grifoni V, Kamuzora H, Lehmann H, Charlesworth D.
    Acta Haematol; 1975; 53(6):347-55. PubMed ID: 808940
    [Abstract] [Full Text] [Related]

  • 2. Significance of a new type of human fetal hemoglobin carrying a replacement isoleucine replaced by threonine at position 75 )E 19) of the gamma chain.
    Ricco G, Mazza U, Turi RM, Pich PG, Camaschella C, Saglio G, Bernini LF.
    Hum Genet; 1976 Jun 29; 32(3):305-13. PubMed ID: 939551
    [Abstract] [Full Text] [Related]

  • 3. Detection of the common Hb F Sardinia [A gamma (E19)Ile----Thr] variant by isoelectric focusing in normal newborns and in adults affected by elevated fetal hemoglobin syndromes.
    Masala B, Manca L.
    Clin Chim Acta; 1991 May 15; 198(3):195-202. PubMed ID: 1716185
    [Abstract] [Full Text] [Related]

  • 4. Studies of the proporation and synthesis of haemoblogin C Philadelphia in red cells of heterozygotes, a homozygote, and a heterozygote for both haemoglobin G and alpha thalassaemia.
    Milner PF, Huisman TH.
    Br J Haematol; 1976 Oct 15; 34(2):207-20. PubMed ID: 974034
    [Abstract] [Full Text] [Related]

  • 5. The level of Hb F-Sardinia (alpha 2A gamma 2(75)Ile----Thr) in the fetal hemoglobin of Sardinian beta-thalassemic homozygotes determined by isoelectric focusing.
    Masala B, Manca L, Formato M, Matera A.
    Am J Hematol; 1986 Apr 15; 21(4):367-76. PubMed ID: 2420171
    [Abstract] [Full Text] [Related]

  • 6. Globin chain synthesis in the greek type (A gamma) of hereditary persisitence of fetal haemoglobin.
    Sofroniadou K, Wood WG, Nute PE, Stamatoyannopoulos G.
    Br J Haematol; 1975 Jan 15; 29(1):137-48. PubMed ID: 1201197
    [Abstract] [Full Text] [Related]

  • 7. Hb F-Porto Torres [Agamma75(E19)Ile-->Thr, 136(H14)Ala-->Ser]: a novel variant of the Agamma chain having two substitutions, one being that of Hb F-Sardinia.
    Pirastru M, Manca L, di Suni MP, Speziga SM, Masala B.
    Hemoglobin; 2004 Jan 15; 28(4):297-303. PubMed ID: 15666429
    [Abstract] [Full Text] [Related]

  • 8. beta-Thalassemia present in cis to a new beta-chain structural variant, Hb Vicksburg [beta 75 (E19)Leu leads to 0].
    Adams JG, Steinberg MH, Newman MV, Morrison WT, Benz EJ, Iyer R.
    Proc Natl Acad Sci U S A; 1981 Jan 15; 78(1):469-73. PubMed ID: 6165992
    [Abstract] [Full Text] [Related]

  • 9. Clinical and haematological evaluation of beta thalassaemia intermedia with increased Hb F and Hb A2 in heterozygotes: beta thalassaemia intermedia I.
    Altay C, Gurgey A.
    J Med Genet; 1985 Jun 15; 22(3):205-12. PubMed ID: 2409283
    [Abstract] [Full Text] [Related]

  • 10. An individual with Hb-Lepore-Baltimore- delta beta-thalassaemia in a Yugoslavian family.
    Efremov GD, Rudivić R, Niazi GA, Hunter E, Huisman TH, Schroeder WA.
    Scand J Haematol; 1976 Feb 15; 16(2):81-9. PubMed ID: 1257702
    [Abstract] [Full Text] [Related]

  • 11. The Hb F composition in a Moroccan family with beta zero-thalassaemia and Hb O-Arab.
    Morlé F, Morlé L, Baklouti F, Dorléac E, Baudonnet C, Delaunay J, Godet J.
    Scand J Haematol; 1984 Sep 15; 33(3):281-7. PubMed ID: 6209785
    [Abstract] [Full Text] [Related]

  • 12. The interaction of alpha-thalassaemia and haemoglobin G Philadelphia.
    Rieder RF, Woodbury DH, Rucknagel DL.
    Br J Haematol; 1976 Feb 15; 32(2):159-65. PubMed ID: 1247489
    [Abstract] [Full Text] [Related]

  • 13. Heterozygous beta-thalassaemia with normal haemoglobin pattern. Haematologic, haemoglobin and biosynthesis study of 4 families.
    Silvestroni E, Bianco I, Graziani B, Carboni C.
    Acta Haematol; 1978 Feb 15; 59(6):332-40. PubMed ID: 97891
    [Abstract] [Full Text] [Related]

  • 14. Thalassaemia intermedia in a family with beta 0-thalassaemia and Hb Hasharon.
    Zago MA, Costa FF, Bottura C.
    J Med Genet; 1982 Dec 15; 19(6):437-40. PubMed ID: 7154040
    [Abstract] [Full Text] [Related]

  • 15. Hb Lepore-Hb C and Hb Lepore-beta 0-thalassemia compound heterozygotes in an Algerian family.
    Francina A, Dorleac E, Aubry M, Baklouti F, Elwan S, Roda L, Phillipe N, Delaunay J.
    Hemoglobin; 1985 Dec 15; 9(5):505-8. PubMed ID: 4086305
    [No Abstract] [Full Text] [Related]

  • 16. Unusual combination of genetic defects in a Sicilian family: beta-thalassaemia, haemoglobin Lepore Boston-Washington and heterocellular hereditary persistence of fetal haemoglobin.
    Schilirò G, Musumeci S, Romeo MA, Di Gregorio F, Russo A, Testa R, Russo G.
    Br J Haematol; 1983 Nov 15; 55(3):473-7. PubMed ID: 6196048
    [Abstract] [Full Text] [Related]

  • 17. The Kenya form of hereditary persistence of fetal haemoglobin: structural studies and evidence for homogeneous distribution of haemoglobin F using fluorescent anti-haemoglobin F antibodies.
    Nute PE, Wood WG, Stamatoyannopoulos G, Olweny C, Failkow PJ.
    Br J Haematol; 1976 Jan 15; 32(1):55-63. PubMed ID: 1259926
    [Abstract] [Full Text] [Related]

  • 18. Clinical and haematological evaluation of beta thalassaemia intermedia characterised by unusually low Hb F and increased Hb A2: beta thalassaemia intermedia II.
    Gurgey A, Kayin S, Kansu E, Altay C.
    J Med Genet; 1985 Jun 15; 22(3):213-21. PubMed ID: 2409284
    [Abstract] [Full Text] [Related]

  • 19. [A new case of hemoglobin Lepore-beta-thalassemia disease].
    Ricci G, Scutellari PN, Franceschini F, Gualandi G.
    Minerva Med; 1982 Feb 11; 73(5):191-7. PubMed ID: 7063135
    [Abstract] [Full Text] [Related]

  • 20. Cord blood study on beta-thalassemia and hemoglobin E.
    Pootrakul S, Muang-sup V, Fucharoen S, Wasi P.
    Am J Med Genet; 1988 Jan 11; 29(1):49-57. PubMed ID: 2449818
    [Abstract] [Full Text] [Related]


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