Mannose binding protein gene mutations associated with unusual and severe infections in adults
- 1 April 1995
- journal article
- case report
- Published by Elsevier in The Lancet
- Vol. 345 (8954) , 886-889
- https://doi.org/10.1016/s0140-6736(95)90009-8
Abstract
No abstract availableKeywords
This publication has 21 references indexed in Scilit:
- Bacteraemia due to recurrent reinfection with Staphylococcus epidermidis associated with defective opsonisation and procidin function in serum.Journal of Clinical Pathology, 1993
- Human mannose-binding protein functions as an opsonin for influenza A viruses.Journal of Clinical Investigation, 1993
- Role of the Collagen-like Domain of the Human Serum Mannan-Binding Protein in the Activation of Complement and the Secretion of This LectinBiochemical and Biophysical Research Communications, 1993
- Retrospective analysis of the incidence of pulmonary disease in hypogammaglobulinemiaJournal of Allergy and Clinical Immunology, 1991
- Molecular basis of a common opsonic defectClinical and Experimental Allergy, 1991
- Defective Candida Opsonin and Procidin Function in Patients with Recurrent Pyogenic Infection: A Common ImmunodeficiencyScandinavian Journal of Immunology, 1991
- Protracted enteric cryptosporidial infection in selective immunoglobulin A and saccharomyces opsonin deficiencies.Gut, 1990
- The human mannose-binding protein functions as an opsonin.The Journal of Experimental Medicine, 1989
- CONCURRENT HEPATITIS B AND DISSEMINATED GONOCOCCAL INFECTION ASSOCIATED WITH DEFECTIVE OPSONISATIONThe Lancet, 1988
- A common congenital immunodeficiency predisposing to infection and atopy in infancy.Archives of Disease in Childhood, 1983