Purtilo DT; Dept. Pathology, Univ. Massachusetts Medical Center, Worcester,; MA, 01605
Immunopathologic studies of affected individuals and carrier females from 25 kindreds exhibiting the X-linked lymphoproliferative syndrome (XLP) were carried out. XLP is a combined, variable immune deficiency with four phenotypes, all apparently triggered by Epstein-Barr virus (EBV) infection: (1) fatal infectious mon
Med Clin North Am. 1981 Sep;65(5):959-76. Unique Identifier : AIDSLINE MED/82034710
Bardana EJ Jr
Immunodeficiency represents a congenital or acquired aberration of immune function which is commonly associated with autoimmunity and neoplasia as a potential triad of biologic sequelae. Irrespective of the initial focal point in the triad, the natural evolution of the condition is frequently associated with the other
Med Cutan Ibero Lat Am. 1981;9(3):179-82. Unique Identifier : AIDSLINE MED/82034733
Honeyman J; Saavedra T; Villagra R; Cabezas AM; Awad P
The cell mediated immunity is studied in 1,500 patients with a superficial fungal infections or a cutaneous vitral infection (warts, condylomata and recurrent herpes simplex). None of the patients have another cutaneous or systemic disease. Delayed cutaneous or systemic disease. Delayed cutaneous hypersensitivity test
Chan EW; Lee CK; Dale PJ; Nortridge KR; Hom SS; Seed TM
Polyinosinic acids containing methyl and sulphur substitutions are potent inhibitors of reverse transcriptase. Substitution of sulphur for oxygen at the 6 position produces significant effects on the properties of polyinosinic acid: the kinetics of inhibition change from competitive to mixed-type and the inhibition co
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