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 *

134 related articles for article (PubMed ID: 6180586)

  • 1. Lasting Hb F reactivation and Hb A2 reduction induced by the treatment of Hodgkin's disease in a woman heterozygous for beta-thalassemia and the Swiss type of the heterocellular hereditary persistence of Hb F.
    Cech P; Testa U; Dubart A; Schneider P; Bachmann F; Guerrasio A; Beuzard Y; Schmidt PM; Clément F; Rosa J
    Acta Haematol; 1982; 67(4):275-84. PubMed ID: 6180586
    [TBL] [Abstract][Full Text] [Related]  

  • 2. beta Thalassemia associated with increased HB F production. Evidence for the existence of a heterocellular hereditary persistence of fetal hemoglobin (HPFH) determinant linked to beta thalassemia in a southern Italian population.
    Marinucci M; Mavilio F; Giuliani A; Gabbianelli M; Tentori L; Tentori L; Zorini CO; Lamberti E; Palazzolo A; Lanzo D
    Hemoglobin; 1981; 5(1):1-17. PubMed ID: 6162827
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Elevated Hb F associated with beta-thalassaemia trait: haemoglobin synthesis in reticulocytes and in blood BFU-E.
    Dubart A; Testa U; Musumeci S; Vainchenker W; Beuzard Y; Henri A; Schirilo G; Romeo MA; Russo G; Rochant H; Rosa J
    Scand J Haematol; 1980 Oct; 25(4):339-46. PubMed ID: 6163196
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Prospective study of red blood cell indices, hemoglobin A2, and hemoglobin F in infants heterozygous for Beta-thalassemia.
    Galanello R; Melis MA; Ruggeri R; Cao A
    J Pediatr; 1981 Jul; 99(1):105-8. PubMed ID: 6166735
    [No Abstract]   [Full Text] [Related]  

  • 5. 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; 22(3):205-12. PubMed ID: 2409283
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Adult and fetal hemoglobin production in erythroid colonies from subjects with beta-thalassemia or with hereditary persistance of fetal hemoglobin (HPFH).
    Huisman TH; Reese AL; Gravely ME; Wilson JB; Webber B; Felice AE
    Hemoglobin; 1980; 4(3-4):449-67. PubMed ID: 6158501
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Globin chain synthesis in beta-thalassemia with normal hemoglobins A2 and F.
    Aksoy M; Almiş G; Bermek E
    Hemoglobin; 1979; 3(4):263-70. PubMed ID: 500371
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Compound heterozygosity of non-deletional hereditary persistence of fetal hemoglobin and deltabeta-thalassemia.
    Kalamaras A; Chassanidis C; Samara M; Papadakis MN; Vagena A; Aleporou-Marinou V; Patrinos GP; Kollia P
    Am J Hematol; 2008 Sep; 83(9):760. PubMed ID: 18615450
    [No Abstract]   [Full Text] [Related]  

  • 9. beta-Thalassemia intermedia homozygous for normal hemoglobin A2 beta-thalassemia. Study in four families.
    Aksoy M; Bermek E; Almiş G; Kutlar A
    Acta Haematol; 1982; 67(1):57-61. PubMed ID: 6174012
    [TBL] [Abstract][Full Text] [Related]  

  • 10. beta+ -Thalassemia intermedia. Genetic and biochemical study of a family including 3 cases.
    Philip T; Souillet G; Philippe N; Freycon F; Bektas S; Morlé L; Trabuchet G; Godet J
    Hum Hered; 1980; 30(5):324-30. PubMed ID: 6156119
    [TBL] [Abstract][Full Text] [Related]  

  • 11. In vitro synthesis of hemoglobin and hemoglobin chains in the BFUe-derived colonies form person with alpha- or beta-thalassemia.
    Huisman TH; Reese AL; Webber B; Okonjo K; Altay C; Felice AE
    Am J Hematol; 1981; 10(3):227-37. PubMed ID: 6166190
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Intrinsic potential for high fetal hemoglobin production in a Druz family with beta-thalassemia is due to an unlinked genetic determinant.
    Oppenheim A; Yaari A; Rund D; Rachmilewitz EA; Nathan D; Wong C; Kazazian HH; Miller B
    Hum Genet; 1990 Dec; 86(2):175-80. PubMed ID: 1702403
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The quiet carrier of beta-thalassemia.
    Kelleher JF; Schwartz E
    Am J Pediatr Hematol Oncol; 1979; 1(1):15-7. PubMed ID: 543507
    [TBL] [Abstract][Full Text] [Related]  

  • 14. %Hb A2, %Hb F, %G gamma values and the haplotypes in the beta-globin gene cluster in Japanese adults with elevated Hb F.
    Shimizu K; Keino H
    Hum Hered; 1992; 42(4):222-30. PubMed ID: 1380945
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Hematological and hemoglobin synthesis studies in a family with deltabeta-thalassemia trait.
    Pagnier J; Amegnizin KP; Labie D; Hayat M
    Acta Haematol; 1979; 61(1):27-32. PubMed ID: 105537
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Genetic regulation of gamma gene expression: study of the interaction of beta-thalassemia with heterocellular HPFH.
    Soummer AM; Testa U; Dujardin P; Guerrasio A; Henri A; Gazaix M; Riou J; Rochant H; Beuzard Y; Rosa J
    Hum Genet; 1981; 57(4):371-5. PubMed ID: 6169619
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Sickle cell traits in Canada. Trimodal distribution of Hb S as a result of interaction with alpha-thalassaemia gene.
    Wong SC; Ali MA; Boyadjian SE
    Acta Haematol; 1981; 65(3):157-63. PubMed ID: 6165216
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Regulation of the beta- and delta-hemoglobin genes. A family with hereditary persistent fetal hemoglobin and beta-thalassemia.
    Rothschild H; Bickers J; Marcus R
    Acta Haematol; 1976; 56(5):285-91. PubMed ID: 826085
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Clinical, haematological, and genetic studies of type 2 normal Hb A2 beta thalassaemia.
    Metaxotou-Mavromati A; Kattamis C; Matathia L; Tzetis M; Kanavakis E
    J Med Genet; 1988 Mar; 25(3):195-9. PubMed ID: 3351907
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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; 55(3):473-7. PubMed ID: 6196048
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.