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Overview Designed as a practical, awareness-raising guide for the clinician Provides key information relevant to the diagnosis and management of each primary immunodeficiency (PID) Comprises a series of case-oriented problems drawn from typical patient scenarios Enables prompt recognition of PIDs, thereby helping to avoid delayed diagnosis and its consequences Includes supplementary material: sn.pub/extras Includes supplementary material: sn.pub/extras Access this book Tax calculation will be finalised at checkout Other ways to access About this book Primary immunodeficiency diseases (PIDs) are a heterogeneous group of inherited disorders characterized by different defects in the development and function of the immune system

And then theres the big question do you need both, or is one enough

Prevalence of the metabolic syndrome in patients with schizophrenia: Baseline results from the Clinical Antipsychotic Trials of Intervention Effectiveness (CATIE) schizophrenia trial and comparison with national estimates from NHANES III

Autophagy in the eye: implications for ocular cell health

Lipopolysaccharide-induced increase in intestinal epithelial tight permeability is mediated by Toll-like receptor 4/myeloid differentiation primary response 88 (Myd88) activation of myosin light chain kinase expression