Skip to main content
NCBI home page
British Medical Journal logoLink to British Medical Journal
. 1980 Nov 22;281(6252):1376–1378. doi: 10.1136/bmj.281.6252.1376

Immunodeficiency and general medicine.

A M Denman
PMCID: PMC1714993  PMID: 6777017

Full text

PDF
1376

Selected References

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

  1. Agnello V. Complement deficiency states. Medicine (Baltimore) 1978 Jan;57(1):1–23. doi: 10.1097/00005792-197801000-00001. [DOI] [PubMed] [Google Scholar]
  2. Buckley R. H., Sidbury J. B., Jr Hereditary alterations in the immune response: coexistence of "agammaglobulinemia", acquired hypogammaglobulinemia and selective immunoglobulin deficiency in a sibship. Pediatr Res. 1968 Mar;2(2):72–84. doi: 10.1203/00006450-196803000-00002. [DOI] [PubMed] [Google Scholar]
  3. Cruchaud A., Robert M., Girard J. P., Laperrouza C., Rivat L., Ropartz C. Primary antibody deficiency syndrome of adult onset. Evidence for genetic transmission. Am J Med. 1970 Apr;48(4):515–523. doi: 10.1016/0002-9343(70)90053-7. [DOI] [PubMed] [Google Scholar]
  4. Fontan D., Micheau M., Guillard J. M., Verger P. Encéphalopathie dégénérative survenue dans un cas de maladie de Bruton. Arch Fr Pediatr. 1975 Jun-Jul;32(6):581–581. [PubMed] [Google Scholar]
  5. Friedman J. M., Fialkow P. J., Davis S. D., Ochs H. D., Wedgwood R. J. Autoimmunity in the relatives of patients with immunodeficiency diseases. Clin Exp Immunol. 1977 Jun;28(3):375–388. [PMC free article] [PubMed] [Google Scholar]
  6. Giblett E. R., Ammann A. J., Wara D. W., Sandman R., Diamond L. K. Nucleoside-phosphorylase deficiency in a child with severely defective T-cell immunity and normal B-cell immunity. Lancet. 1975 May 3;1(7914):1010–1013. doi: 10.1016/s0140-6736(75)91950-9. [DOI] [PubMed] [Google Scholar]
  7. Giblett E. R., Anderson J. E., Cohen F., Pollara B., Meuwissen H. J. Adenosine-deaminase deficiency in two patients with severely impaired cellular immunity. Lancet. 1972 Nov 18;2(7786):1067–1069. doi: 10.1016/s0140-6736(72)92345-8. [DOI] [PubMed] [Google Scholar]
  8. Goldblum R. M., Lord R. A., Cooper M. D., Gathings W. E., Goldman A. S. X-linked B lymphocyte deficiency. I. Panhypo-gamma-globulinemia and dys-gamma-globulinemia in siblings. J Pediatr. 1974 Aug;85(2):188–191. doi: 10.1016/s0022-3476(74)80390-2. [DOI] [PubMed] [Google Scholar]
  9. Hayward A. R. Hypoimmunoglobulinaemia with deficiency of pre-B cells. Lancet. 1978 May 13;1(8072):1014–1015. doi: 10.1016/s0140-6736(78)90739-0. [DOI] [PubMed] [Google Scholar]
  10. Hoffman T., Winchester R., Schulkind M., Frias J. L., Ayoub E. M., Good R. A. Hypoimmunoglobulinemia with normal T cell function in female siblings. Clin Immunol Immunopathol. 1977 May;7(3):364–371. doi: 10.1016/0090-1229(77)90070-8. [DOI] [PubMed] [Google Scholar]
  11. Lehman A. R., Stevens S. The production and repair of double strand breaks in cells from normal humans and from patients with ataxia telangiectasia. Biochim Biophys Acta. 1977 Jan 3;474(1):49–60. doi: 10.1016/0005-2787(77)90213-1. [DOI] [PubMed] [Google Scholar]
  12. Medici M. A., Kagan B. M., Gatti R. A. Chronic progressive panencephalitis in hypogammaglobulinemia. J Pediatr. 1978 Jul;93(1):73–75. doi: 10.1016/s0022-3476(78)80605-2. [DOI] [PubMed] [Google Scholar]
  13. Pearl E. R., Vogler L. B., Okos A. J., Crist W. M., Lawton A. R., 3rd, Cooper M. D. B lymphocyte precursors in human bone marrow: an analysis of normal individuals and patients with antibody-deficiency states. J Immunol. 1978 Apr;120(4):1169–1175. [PubMed] [Google Scholar]
  14. Polmar S. H., Stern R. C., Schwartz A. L., Wetzler E. M., Chase P. A., Hirschhorn R. Enzyme replacement therapy for adenosine deaminase deficiency and severe combined immunodeficiency. N Engl J Med. 1976 Dec 9;295(24):1337–1343. doi: 10.1056/NEJM197612092952402. [DOI] [PubMed] [Google Scholar]
  15. Segal A. W., Peters T. J. Analytical subcellular fractionation of neutrophils from patients with chronic granulomatous disease. Demonstration of the enzyme defect in four cases. Q J Med. 1978 Apr;47(186):213–220. [PubMed] [Google Scholar]
  16. Sharma O. P., James D. G. Hypogammaglobulinemia, depression of delayed-type hypersensitivity, and granuloma formation. Am Rev Respir Dis. 1971 Aug;104(2):228–231. doi: 10.1164/arrd.1971.104.2.228. [DOI] [PubMed] [Google Scholar]
  17. Taylor-Robinson D., Gumpel J. M., Hill A., Swannell A. J. Isolation of Mycoplasma pneumoniae from the synovial fluid of a hypogrammaglobulinaemic patient in a survey of patients with inflammatory polyarthritis. Ann Rheum Dis. 1978 Apr;37(2):180–182. doi: 10.1136/ard.37.2.180. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Valdimarsson H., Higgs J. M., Wells R. S., Yamamura M., Hobbs J. R., Holt P. J. Immune abnormalities associated with chronic mucocutaneous candidiasis. Cell Immunol. 1973 Mar;6(3):348–361. doi: 10.1016/0008-8749(73)90035-x. [DOI] [PubMed] [Google Scholar]
  19. Waldmann T. A., Durm M., Broder S., Blackman M., Blaese R. M., Strober W. Role of suppressor T cells in pathogenesis of common variable hypogammaglobulinaemia. Lancet. 1974 Sep 14;2(7881):609–613. doi: 10.1016/s0140-6736(74)91940-0. [DOI] [PubMed] [Google Scholar]
  20. Webster A. D., Loewi G., Dourmashkin R. D., Golding D. N., Ward D. J., Asherson G. L. Polyarthritis in adults with hypogammaglobulinaemia and its rapid response to immunoglobulin treatment. Br Med J. 1976 May 29;1(6021):1314–1316. doi: 10.1136/bmj.1.6021.1314. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Webster A. D. Thymoma, polyarthropathy and hypogammaglobulinaemia. Proc R Soc Med. 1976 Jan;69(1):58–59. doi: 10.1177/003591577606900127. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from British Medical Journal are provided here courtesy of BMJ Publishing Group

RESOURCES