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This concise manual provides clinicians and other related health care professionals with an essential reference tool to the background of cystic fibrosis, and the management and treatment of this disease. The latest guidelines are reviewed and current and emerging treatments are discussed in the latter chapters. Cystic fibrosis is an inherited condition where a mutation in the gene coding for the cystic fibrosis transmembrane conductance regulator (CFTR) causes loss of function. The dysfunction of CFTR results in the production of thick mucus in the lungs and digestive tract, causing pulmonary and gastrointestinal manifestations. The incidence of cystic fibrosis in Europe and the US ranges between 1 in 2,000 and 1 in 25,000.


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Recent decades have witnessed strong declines in fish stocks around the globe, amid growing concerns about the impact of fisheries on marine and freshwater biodiversity....


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For any seafarer, splicing rope is an essential skill. But the traditional 3-strand rope is fast disappearing. So how do you splice braided rope? This is the definitive...


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Anti-infection Handbook is a concise A–Z guide to diagnosis and management of most infectious diseases and related conditions found in Australia and worldwide. The handbook...


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This CD-ROM contains the fully updated text and graphics of the "Handbook of Pharmaceutical Excipients". Features include: the complete text of over 210 monographs with...


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The Aviation Instructor’s Handbook is a world-class educational reference tool developed and designed for ground instructors, flight instructors, and aviation maintenance...


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A fully updated, all-in-one guide to synthetic and alternative energy technologiesThoroughly revised to cover today’s essential topics, this practical resource discusses the...


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