Skip to main content
Archives of Disease in Childhood logoLink to Archives of Disease in Childhood
. 1983 Dec;58(12):1026–1030. doi: 10.1136/adc.58.12.1026

Management of thalassaemia major.

B Modell, M Petrou
PMCID: PMC1628578  PMID: 6660889

Full text

PDF
1029

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Angastiniotis M. A., Hadjiminas M. G. Prevention of thalassaemia in Cyprus. Lancet. 1981 Feb 14;1(8216):369–371. doi: 10.1016/s0140-6736(81)91682-2. [DOI] [PubMed] [Google Scholar]
  2. Barry M., Flynn D. M., Letsky E. A., Risdon R. A. Long-term chelation therapy in thalassaemia major: effect on liver iron concentration, liver histology, and clinical progress. Br Med J. 1974 Apr 6;2(5909):16–20. doi: 10.1136/bmj.2.5909.16. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Blendis L. M., Modell C. B., Bowdler A. J., Williams R. Some effects of splenectomy in thalassaemia major. Br J Haematol. 1974 Sep;28(1):77–87. doi: 10.1111/j.1365-2141.1974.tb06641.x. [DOI] [PubMed] [Google Scholar]
  4. Gabutti V., Piga A., Nicola P., Vullo C., Capra L., Di Palma A., Masera G., Terzoli S., Mauri R. Haemoglobin levels and blood requirement in thalassaemia. Arch Dis Child. 1982 Feb;57(2):156–158. doi: 10.1136/adc.57.2.156. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Masera G., Jean G., Gazzola G., Novakova M. Role of chronic hepatitis in development of thalassaemic liver disease. Arch Dis Child. 1976 Sep;51(9):680–685. doi: 10.1136/adc.51.9.680. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Masera G., Terzoli S., Avanzini A., Fontanelli G., Mauri R. A., Piacentini G., Ferrari M. Evaluation of the supertransfusion regimen in homozygous beta-thalassaemia children. Br J Haematol. 1982 Sep;52(1):111–113. doi: 10.1111/j.1365-2141.1982.tb03867.x. [DOI] [PubMed] [Google Scholar]
  7. Modell B., Letsky E. A., Flynn D. M., Peto R., Weatherall D. J. Survival and desferrioxamine in thalassaemia major. Br Med J (Clin Res Ed) 1982 Apr 10;284(6322):1081–1084. doi: 10.1136/bmj.284.6322.1081. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Modell B. Total management of thalassaemia major. Arch Dis Child. 1977 Jun;52(6):489–500. doi: 10.1136/adc.52.6.489. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Modell B., Ward R. H., Fairweather D. V. Effect of introducing antenatal diagnosis on reproductive behaviour of families at risk for thalassaemia major. Br Med J. 1980 Jun 7;280(6228):1347–1350. doi: 10.1136/bmj.280.6228.1347. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Old J. M., Ward R. H., Petrou M., Karagözlu F., Modell B., Weatherall D. J. First-trimester fetal diagnosis for haemoglobinopathies: three cases. Lancet. 1982 Dec 25;2(8313):1413–1416. doi: 10.1016/s0140-6736(82)91324-1. [DOI] [PubMed] [Google Scholar]
  11. Pippard M. J., Callender S. T., Finch C. A. Ferrioxamine excretion in iron-loaded man. Blood. 1982 Aug;60(2):288–294. [PubMed] [Google Scholar]
  12. Propper R. D., Button L. N., Nathan D. G. New approaches to the transfusion management of thalassemia. Blood. 1980 Jan;55(1):55–60. [PubMed] [Google Scholar]
  13. Propper R. D., Cooper B., Rufo R. R., Nienhuis A. W., Anderson W. F., Bunn H. F., Rosenthal A., Nathan D. G. Continuous subcutaenous administration of deferoxamine in patients with iron overload. N Engl J Med. 1977 Aug 25;297(8):418–423. doi: 10.1056/NEJM197708252970804. [DOI] [PubMed] [Google Scholar]
  14. SMITH C. H., ERLANDSON M. E., STERN G., HILGARTNER M. W. POSTSPLENECTOMY INFECTION IN COOLEY'S ANEMIA. Ann N Y Acad Sci. 1964 Oct 7;119:748–757. doi: 10.1111/j.1749-6632.1965.tb54076.x. [DOI] [PubMed] [Google Scholar]
  15. SMITH R. S. CHELATING AGENTS IN THE DIAGNOSIS AND TREATMENT OF IRON OVERLOAD IN THALASSEMIA. Ann N Y Acad Sci. 1964 Oct 7;119:776–788. doi: 10.1111/j.1749-6632.1965.tb54079.x. [DOI] [PubMed] [Google Scholar]
  16. Thomas E. D., Buckner C. D., Sanders J. E., Papayannopoulou T., Borgna-Pignatti C., De Stefano P., Sullivan K. M., Clift R. A., Storb R. Marrow transplantation for thalassaemia. Lancet. 1982 Jul 31;2(8292):227–229. doi: 10.1016/s0140-6736(82)90319-1. [DOI] [PubMed] [Google Scholar]
  17. Wasi P., Fucharoen S., Youngchaiyud P., Sonakul D. Hypoxemia in thalassemia. Birth Defects Orig Artic Ser. 1982;18(7):213–217. [PubMed] [Google Scholar]
  18. de Alarcon P. A., Donovan M. E., Forbes G. B., Landaw S. A., Stockman J. A., 3rd Iron absorption in the thalassemia syndromes and its inhibition by tea. N Engl J Med. 1979 Jan 4;300(1):5–8. doi: 10.1056/NEJM197901043000102. [DOI] [PubMed] [Google Scholar]

Articles from Archives of Disease in Childhood are provided here courtesy of BMJ Publishing Group

RESOURCES