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Titlebook: Immunodeficiency and Disease; A. D. B. Webster (Consultant Physician and Senior Book 1988 Springer Science+Business Media New York 1988 A

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C. Cunningham-Rundlessh, complement Greiner’s textsonquantumphysics,mostofwhichhavebeenavailabletoEnglish-speakingaudiences for some time. The complete set of books will thus provide a coherent view of physics that978-0-387-95586-5978-0-387-21851-9Series ISSN 1431-083X
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B. J. M. Zegers,J. W. Stoopsh, complement Greiner’s textsonquantumphysics,mostofwhichhavebeenavailabletoEnglish-speakingaudiences for some time. The complete set of books will thus provide a coherent view of physics that978-0-387-95586-5978-0-387-21851-9Series ISSN 1431-083X
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Hypogammaglobulinaemia: Recent Advances,ded by a more descriptive classification (see Table 2.1). Selective deficiencies of IgG subclasses and of IgA are discussed in Chapter 5. Some patients with selective deficiencies of both IgA and IgG. may be included under the broad classification of ‘primary’ hypogammaglobulinaemia if the total ser
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Immunoglobulin Replacement Therapy,clarified.. Other mechanisms of microbial destruction by serum factors were then elucidated — for example, the bacteriolysis of cholera vibrios and Gram negative organisms was shown to be dependent upon interactions between specific antibodies and bacterial cell wall structures.. Bordet then showed
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Metabolic Causes of Immune Deficiency: Mechanisms and Treatment,ng the Nezelof syndrome.. The discovery of more PNP deficient patients showed that this was also an autosomal recessive disease.. Nowadays ADA and PNP deficiency are recognized as the primary cause of the associated immune deficiency.
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