A familial defect in cellular chemotaxis associated with redheadedness and recurrent infection
- 1 July 1976
- journal article
- research article
- Published by Elsevier in The Journal of Pediatrics
- Vol. 89 (1) , 33-37
- https://doi.org/10.1016/s0022-3476(76)80922-5
Abstract
No abstract availableThis publication has 14 references indexed in Scilit:
- The phagocytic cell in host resistanceFEBS Letters, 1975
- DEFECT IN NEUTROPHIL GRANULOCYTE CHEMOTAXIS IN JOB'S SYNDROME OF RECURRENT "COLD" STAPHYLOCOCCAL ABSCESSESThe Lancet, 1974
- RAISED SERUM-IgE LEVELS AND DEFECTIVE NEUTROPHIL CHEMOTAXIS IN THREE CHILDREN WITH ECZEMA AND RECURRENT BACTERIAL INFECTIONSThe Lancet, 1974
- Defect of neutrophil motility in a child with recurrent bacterial infections and disseminated cytomegalovirus infectionThe Journal of Pediatrics, 1973
- Properdin and C3 Proactivator: Alternate Pathway Components in Human GlomerulonephritisJournal of Clinical Investigation, 1973
- Defective granulocyte chemotaxis in the Chediak-Higashi syndromeJournal of Clinical Investigation, 1971
- TUBERCULIN‐INDUCED MIGRATION INHIBITION OF HUMAN PERIPHERAL LEUCOCYTES IN AGAROSE MEDIUMAllergy, 1971
- DEFICIENCY OF C1r IN HUMAN SERUMThe Journal of Experimental Medicine, 1970
- IMPAIRED LEUCOTACTIC RESPONSIVENESS IN A CHILD WITH RECURRENT INFECTIONSThe Lancet, 1969
- JOB'S SYNDROMEThe Lancet, 1966