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Journal of Clinical Pathology logoLink to Journal of Clinical Pathology
. 1990 Oct;43(10):789–791. doi: 10.1136/jcp.43.10.789

Current concerns in haematology. 1. Is the painful crisis of sickle cell disease a "steal" syndrome?

G R Serjeant 1, R M Chalmers 1
PMCID: PMC502823  PMID: 1699977

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Selected References

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

  1. Addae S. Effect of acute temperature change in some renal functions in sickle cell disease. Afr J Med Sci. 1971 Oct;2(4):335–348. [PubMed] [Google Scholar]
  2. Addae S. Mechanism for the high incidence of sickle-cell crisis in the tropical cool season. Lancet. 1971 Dec 4;2(7736):1256–1256. doi: 10.1016/s0140-6736(71)90564-2. [DOI] [PubMed] [Google Scholar]
  3. Alavi A., Bond J. P., Kuhl D., Creech R. H. Scan detection of bone marrow infarcts in sickle cell disorders. J Nucl Med. 1974 Nov;15(11):1003–1007. [PubMed] [Google Scholar]
  4. Alavi A., Schumacher H. R., Dorwart B., Kuhl D. E. Bone marrow scan evaluation of arthropathy in sickle cell disorders. Arch Intern Med. 1976 Apr;136(4):436–440. [PubMed] [Google Scholar]
  5. Amjad H., Bannerman R. M., Judisch J. M. Letter: Sickling pain and season. Br Med J. 1974 Apr 6;2(5909):54–54. doi: 10.1136/bmj.2.5909.54. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Bainbridge R., Higgs D. R., Maude G. H., Serjeant G. R. Clinical presentation of homozygous sickle cell disease. J Pediatr. 1985 Jun;106(6):881–885. doi: 10.1016/s0022-3476(85)80230-4. [DOI] [PubMed] [Google Scholar]
  7. Baum K. F., Dunn D. T., Maude G. H., Serjeant G. R. The painful crisis of homozygous sickle cell disease. A study of the risk factors. Arch Intern Med. 1987 Jul;147(7):1231–1234. [PubMed] [Google Scholar]
  8. Charache S., Page D. L. Infarction of bone marrow in the sickle cell disorders. Ann Intern Med. 1967 Dec;67(6):1195–1200. doi: 10.7326/0003-4819-67-6-1195. [DOI] [PubMed] [Google Scholar]
  9. Hammel C. F., DeNardo S. J., DeNardo G. L., Lewis J. P. Bone marrow and bone mineral scintigraphic studies in sickle cell disease. Br J Haematol. 1973 Nov;25(5):593–598. doi: 10.1111/j.1365-2141.1973.tb01771.x. [DOI] [PubMed] [Google Scholar]
  10. Harkness D. R., Roth S. Clinical evaluation of cyanate in sickle cell anemia. Prog Hematol. 1975;9:157–184. [PubMed] [Google Scholar]
  11. Hatch F. E., Crowe L. R., Miles D. E., Young J. P., Portner M. E. Altered vascular reactivity in sickle hemoglobinopathy. A possible protective factor from hypertension. Am J Hypertens. 1989 Jan;2(1):2–8. doi: 10.1093/ajh/2.1.2. [DOI] [PubMed] [Google Scholar]
  12. Higgs D. R., Aldridge B. E., Lamb J., Clegg J. B., Weatherall D. J., Hayes R. J., Grandison Y., Lowrie Y., Mason K. P., Serjeant B. E. The interaction of alpha-thalassemia and homozygous sickle-cell disease. N Engl J Med. 1982 Jun 17;306(24):1441–1446. doi: 10.1056/NEJM198206173062402. [DOI] [PubMed] [Google Scholar]
  13. Hutchinson R. M., Merrick M. V., White J. M. Fat embolism in sickle cell disease. J Clin Pathol. 1973 Aug;26(8):620–622. doi: 10.1136/jcp.26.8.620. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Kar B. C., Satapathy R. K., Kulozik A. E., Kulozik M., Sirr S., Serjeant B. E., Serjeant G. R. Sickle cell disease in Orissa State, India. Lancet. 1986 Nov 22;2(8517):1198–1201. doi: 10.1016/s0140-6736(86)92205-1. [DOI] [PubMed] [Google Scholar]
  15. MANFREDI F., SPOTO A. P., SALTZMAN H. A., SIEKER H. O. Studies of peripheral circulation during sickle-cell crisis. Circulation. 1960 Oct;22:602–607. doi: 10.1161/01.cir.22.4.602. [DOI] [PubMed] [Google Scholar]
  16. MARSDEN P. D., SHAH K. K. ARTIFICIALLY INDUCED OEDEMA IN SICKLE CELL ANAEMIA. J Trop Med Hyg. 1964 Feb;67:31–34. [PubMed] [Google Scholar]
  17. Majd M., Frankel R. S. Radionclide imaging in skeletal inflammatory and ischemic disease in children. AJR Am J Roentgenol. 1976 Apr;126(4):832–841. doi: 10.2214/ajr.126.4.832. [DOI] [PubMed] [Google Scholar]
  18. Perrine R. P., Pembrey M. E., John P., Perrine S., Shoup F. Natural history of sickle cell anemia in Saudi Arabs. A study of 270 subjects. Ann Intern Med. 1978 Jan;88(1):1–6. doi: 10.7326/0003-4819-88-1-1. [DOI] [PubMed] [Google Scholar]
  19. Powars D. R., Schroeder W. A., Weiss J. N., Chan L. S., Azen S. P. Lack of influence of fetal hemoglobin levels or erythrocyte indices on the severity of sickle cell anemia. J Clin Invest. 1980 Mar;65(3):732–740. doi: 10.1172/JCI109720. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Redwood A. M., Williams E. M., Desal P., Serjeant G. R. Climate and painful crisis of sickle-cell disease in Jamaica. Br Med J. 1976 Jan 10;1(6001):66–68. doi: 10.1136/bmj.1.6001.66. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Serjeant G. R. Irreversibly sickled cells and splenomegaly in sickle-cell anaemia. Br J Haematol. 1970 Nov;19(5):635–641. doi: 10.1111/j.1365-2141.1970.tb01647.x. [DOI] [PubMed] [Google Scholar]
  22. Serjeant G. R., Sommereux A. M., Stevenson M., Mason K., Serjeant B. E. Comparison of sickle cell-beta0 thalassaemia with homozygous sickle cell disease. Br J Haematol. 1979 Jan;41(1):83–93. doi: 10.1111/j.1365-2141.1979.tb03684.x. [DOI] [PubMed] [Google Scholar]
  23. Stevens M. C., Hayes R. J., Vaidya S., Serjeant G. R. Fetal hemoglobin and clinical severity of homozygous sickle cell disease in early childhood. J Pediatr. 1981 Jan;98(1):37–41. doi: 10.1016/s0022-3476(81)80529-x. [DOI] [PubMed] [Google Scholar]
  24. de Ceulaer K., Higgs D. R., Weatherall D. J., Hayes R. J., Serjeant B. E., Serjeant G. R. alpha-Thalassemia reduces the hemolytic rate in homozygous sickle-cell disease. N Engl J Med. 1983 Jul 21;309(3):189–190. doi: 10.1056/NEJM198307213090320. [DOI] [PubMed] [Google Scholar]

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