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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

153 related articles for article (PubMed ID: 10554822)

  • 1. Severe inclusion body beta-thalassaemia with haemolysis in a patient double heterozygous for beta(0)-thalassaemia and quadruplicated alpha-globin gene arrangement of the anti-4.2 type.
    Beris P; Solenthaler M; Deutsch S; Darbellay R; Tobler A; Bochaton-Pialat ML; Gabbiani G
    Br J Haematol; 1999 Jun; 105(4):1074-80. PubMed ID: 10554822
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Observations on the relationship between gamma-globin chain content and globin chain precipitation in thalassaemic erythroblasts and on the composition of erythroblastic inclusions in HbE/beta-thalassaemia.
    Wickramasinghe SN; Lee MJ
    Eur J Haematol; 1997 Nov; 59(5):305-9. PubMed ID: 9414642
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Composition of the intra-erythroblastic precipitates in thalassaemia and congenital dyserythropoietic anaemia (CDA): identification of a new type of CDA with intra-erythroblastic precipitates not reacting with monoclonal antibodies to alpha- and beta-globin chains.
    Wickramasinghe SN; Lee MJ; Furukawa T; Eguchi M; Reid CD
    Br J Haematol; 1996 Jun; 93(3):576-85. PubMed ID: 8652376
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Severe thalassaemia intermedia caused by interaction of homozygosity for alpha-globin gene triplication with heterozygosity for beta zero-thalassaemia.
    Oron V; Filon D; Oppenheim A; Rund D
    Br J Haematol; 1994 Feb; 86(2):377-9. PubMed ID: 8199028
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The triplicated alpha-globin gene locus in beta-thalassaemia heterozygotes: clinical, haematological, biosynthetic and molecular studies.
    Traeger-Synodinos J; Kanavakis E; Vrettou C; Maragoudaki E; Michael T; Metaxotou-Mavromati A; Kattamis C
    Br J Haematol; 1996 Dec; 95(3):467-71. PubMed ID: 8943886
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Chronic and severe haemolytic anaemia caused by co-inheritance of beta-thalassaemia and triplicated alpha-globin genes.
    Wang C; Amato D
    Br J Haematol; 2007 Jun; 137(6):489. PubMed ID: 17408397
    [No Abstract]   [Full Text] [Related]  

  • 7. A beta-thalassaemia phenotype not linked to the beta-globin cluster in an Italian family.
    Murru S; Loudianos G; Porcu S; Sciarratta GV; Agosti S; Parodi MI; Cao A; Pirastu M
    Br J Haematol; 1992 Jun; 81(2):283-7. PubMed ID: 1643026
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Association of alpha and beta thalassemia with alpha gene triplication in one family].
    Villegas A; Muñoz JA; Risueño CF; Castro JM; Sánchez J; Ropero P; González FA
    Med Clin (Barc); 1997 May; 108(20):781-3. PubMed ID: 9265084
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The molecular basis for the thalassaemias in Sri Lanka.
    Fisher CA; Premawardhena A; de Silva S; Perera G; Rajapaksa S; Olivieri NA; Old JM; Weatherall DJ;
    Br J Haematol; 2003 May; 121(4):662-71. PubMed ID: 12752111
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Thalassaemia intermedia: interaction of the triple alpha-globin gene arrangement and heterozygous beta-thalassaemia.
    Kulozik AE; Thein SL; Wainscoat JS; Gale R; Kay LA; Wood JK; Weatherall DJ; Huehns ER
    Br J Haematol; 1987 May; 66(1):109-12. PubMed ID: 3593645
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Co-inheritance of alpha- and beta-thalassaemia in mice ameliorates thalassaemic phenotype.
    Voon HP; Wardan H; Vadolas J
    Blood Cells Mol Dis; 2007; 39(2):184-8. PubMed ID: 17493845
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Somatic deletion of the normal beta-globin gene leading to thalassaemia intermedia in heterozygous beta-thalassaemic patients.
    Galanello R; Perseu L; Perra C; Maccioni L; Barella S; Longinotti M; Cao A; Cazzola M
    Br J Haematol; 2004 Dec; 127(5):604-6. PubMed ID: 15566365
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The C-T substitution in the distal CACCC box of the beta-globin gene promoter is a common cause of silent beta thalassaemia in the Italian population.
    Ristaldi MS; Murru S; Loudianos G; Casula L; Porcu S; Pigheddu D; Fanni B; Sciarratta GV; Agosti S; Parodi MI
    Br J Haematol; 1990 Apr; 74(4):480-6. PubMed ID: 2346726
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A case of non-beta-globin gene linked beta thalassaemia in a Dutch family with two additional alpha-gene defects: the common -alpha3.7 deletion and the rare IVS1-116 (A-->G) acceptor splice site mutation.
    Giordano PC; Harteveld CL; Haak HL; Batelaan D; van Delft P; Plug RJ; Emonts M; Zanardini R; Bernini LF
    Br J Haematol; 1998 Nov; 103(2):370-6. PubMed ID: 9827907
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Heterozygous beta thalassaemia of unusual severity.
    Friedman S; Ozsoylu S; Luddy R; Schwartz E
    Br J Haematol; 1976 Jan; 32(1):65-77. PubMed ID: 1259927
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Silent carrier beta-thalassaemia due to a severe beta-globin mutation interacting with other genetic elements.
    Rund D; Filon D; Oppenheim A; Abramov A
    Eur J Pediatr; 1993 Jul; 152(7):574-6. PubMed ID: 8354316
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Molecular, haematological and clinical studies of the -101 C --> T substitution of the beta-globin gene promoter in 25 beta-thalassaemia intermedia patients and 45 heterozygotes.
    Maragoudaki E; Kanavakis E; Traeger-Synodinos J; Vrettou C; Tzetis M; Metaxotou-Mavrommati A; Kattamis C
    Br J Haematol; 1999 Dec; 107(4):699-706. PubMed ID: 10606872
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Different hematological phenotypes caused by the interaction of triplicated alpha-globin genes and heterozygous beta-thalassemia.
    Camaschella C; Kattamis AC; Petroni D; Roetto A; Sivera P; Sbaiz L; Cohen A; Ohene-Frempong K; Trifillis P; Surrey S; Fortina P
    Am J Hematol; 1997 Jun; 55(2):83-8. PubMed ID: 9209003
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Segmental duplications involving the alpha-globin gene cluster are causing beta-thalassemia intermedia phenotypes in beta-thalassemia heterozygous patients.
    Harteveld CL; Refaldi C; Cassinerio E; Cappellini MD; Giordano PC
    Blood Cells Mol Dis; 2008; 40(3):312-6. PubMed ID: 18249014
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Co-inheritance of alpha-and beta-thalassemia in Khuzestan Province, Iran.
    Rahim F; Kaikhaei B; Zandian K; Hoseini A
    Hematology; 2008 Feb; 13(1):59-64. PubMed ID: 18534068
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.