Results 291 to 300 of about 1,195,963 (357)
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Postgraduate Medicine, 1973
In the past few decades, bedside observation and laboratory investigation have yielded important information concerning the modus operandi of the immune system. This article examines newer basic immunologic information, clinical features of the main immune deficiencies, and tests for investigation of these defects.
P E, Hermans, R E, Ritts, G J, Gleich
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In the past few decades, bedside observation and laboratory investigation have yielded important information concerning the modus operandi of the immune system. This article examines newer basic immunologic information, clinical features of the main immune deficiencies, and tests for investigation of these defects.
P E, Hermans, R E, Ritts, G J, Gleich
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Trypsinogen Deficiency Disease
Archives of Pediatrics & Adolescent Medicine, 1967TOWNES,1in 1965, reported a 6-week-old white male infant with chronic diarrhea, failure to gain weight, hypoproteinemia, and edema. The infant was unable to hydrolyze dietary protein due to a singular deficiency of pancreatic trypsinogen. The present report describes a second instance of this interesting defect.
M D, Morris, D A, Fisher
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Trypsinogen deficiency disease
The Journal of Pediatrics, 1964An infant with severe growth failure, hypoproteinemia, and edema is described. Clinical and laboratory studies indicate that this disorder results from an impaired capacity to hydrolyze ingested protein. By means of specific pancreatic proteolytic enzyme assays, it was established that the primary defect is a complete absence of trypsinogen. Absence of
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Complement deficiency and disease
Immunology Today, 1991Complement deficiency is associated with an increased prevalence of pyogenic infections and immune complex disease. The spectrum of disease in deficient individuals depends on the stage in the complement system at which the block in activation occurs. Here, Paul Morgan and Mark Walport review current knowledge of hereditary complement deficiencies in ...
B P, Morgan, M J, Walport
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Steroid sulphatase deficiency disease
Clinical Genetics, 1985Seventy‐six ichthyotic male patients with a biochemically confirmed diagnosis of steroid sulphatase deficiency are reported. Ascertainment was based on either a previous diagnosis of placental steroid sulphatase deficiency (21 probands and 15 secondary cases), or ichthyosis with steroid sulphatase deficiency (29 probands and 11 secondary cases).
G, Lykkesfeldt +3 more
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Complement Deficiency and Disease
Australian and New Zealand Journal of Medicine, 1982: The complement system consists of a series of serum proteins which interact to facilitate the action of certain classes of antibody and antigen/antibody complexes. Complement may be disturbed by pathological utilisation of one or both of its pathways or by a primary deficiency of an individual component.
J A, Charlesworth, B A, Pussell
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Complement deficiency and disease
Journal of Clinical Pathology, 2008There are approximately 30 serum complement proteins (15% of the globulin fraction), excluding cell surface receptors, and regulatory proteins. Many are manufactured in the liver, and reduced complement is a feature of severe liver failure. Complement proteins contribute to the acute phase response, and high levels are seen in chronic untreated ...
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