Immunoregulatory defects in a family with selective IgA deficiency
- 1 January 1981
- journal article
- research article
- Published by Elsevier in The Journal of Pediatrics
- Vol. 98 (1), 52-58
- https://doi.org/10.1016/s0022-3476(81)80532-x
Abstract
No abstract availableThis publication has 23 references indexed in Scilit:
- Role of Helper, Suppressor and B-Cell Defects in the Pathogenesis of the HypogammaglobulinemiasNew England Journal of Medicine, 1978
- Suppressor cells and IgA deficiencyClinical Immunology and Immunopathology, 1978
- Selective IgA Deficiency in Blood DonorsVox Sanguinis, 1975
- Expression of a receptor for IgM by human T cells in vitroEuropean Journal of Immunology, 1975
- Enhancement of sheep red blood cell human lymphocyte rosette formation by the sulfhydryl compound 2-amino ethylisothiouronium bromideClinical Immunology and Immunopathology, 1975
- ROLE OF SUPPRESSOR T CELLS IN PATHOGENESIS OF COMMON VARIABLE HYPOGAMMAGLOBULINÆMIAThe Lancet, 1974
- Differentiation Capacity of Cultured B Lymphocytes from Immunodeficient PatientsJCI Insight, 1973
- SELECTIVE IgA DEFICIENCYMedicine, 1971
- Selective gamma-A-globulin deficiency, with dominant autosomal inheritance in a Swiss family.Archives of Disease in Childhood, 1968
- Studies on the Serum γA-Globulin Level III. The Frequency of A-γA-GlobulinemiaScandinavian Journal of Clinical and Laboratory Investigation, 1965