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     Treatment of Metabolic Bone Disease: Management Strategy and Drug Therapy
Publisher: Informa Healthcare
Author(s): David J Hosking, Johann D Ringe

A comprehensive review of pharmacologic treatments for metabolic bone disease. The authors discuss the clinical pharmacology and practical aspects, including dose, frequency and route of administration, side effects and monitoring of a variety of drug treatments as they are applied to conditions such as hypoparathyroidism, Paget's disease and osteoporosis. Cost and advantages and disadvantages of the various preparations are also discussed in full, and an indication of the drug of first choice is given.

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     Duchenne Muscular Dystrophy: Advances in Therapeutics (Neurological Disease and Therapy)
Publisher: Informa Healthcare
Author(s):

Duchenne Muscular Dystrophy (DMD) is one of the most prevalent genetic disorders of childhood for which there is no cure. This authoritative guide provides a clear overview of the clinical, genetic, and pathophysiological aspects of the disease in the context of emerging therapeutic modalities. The only available source on the subject, this reference emphasizes the importance of accurate diagnosis, carrier detection, and genetic counseling, and supplies state-of-the-art information on pharmacological interventions, regenerative medicine, and gene therapy.



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     Duchenne Muscular Dystrophy: Webster's Timeline History, 1806 - 2007
Publisher: ICON Group International, Inc.
Author(s): Icon Group International

Webster's bibliographic and event-based timelines are comprehensive in scope, covering virtually all topics, geographic locations and people. They do so from a linguistic point of view, and in the case of this book, the focus is on "Duchenne Muscular Dystrophy," including when used in literature (e.g. all authors that might have Duchenne Muscular Dystrophy in their name). As such, this book represents the largest compilation of timeline events associated with Duchenne Muscular Dystrophy when it is used in proper noun form. Webster's timelines cover bibliographic citations, patented inventions, as well as non-conventional and alternative meanings which capture ambiguities in usage. These furthermore cover all parts of speech (possessive, institutional usage, geographic usage) and contexts, including pop culture, the arts, social sciences (linguistics, history, geography, economics, sociology, political science), business, computer science, literature, law, medicine, psychology, mathematics, chemistry, physics, biology and other physical sciences. This "data dump" results in a comprehensive set of entries for a bibliographic and/or event-based timeline on the proper name Duchenne Muscular Dystrophy, since editorial decisions to include or exclude events is purely a linguistic process. The resulting entries are used under license or with permission, used under "fair use" conditions, used in agreement with the original authors, or are in the public domain.

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     The Muscular Dystrophies
Publisher: Oxford University Press, USA
Author(s):

The muscular dystrophies are an important group of inherited disorders. They are characterized by muscle wasting and weakness, but vary considerably in their clinical manifestations and severity.
This text reviews our understanding of the most important of these disorders. In many instances, the genes and protein products responsible for the dystrophies have been identified and it is now possible to establish a precise diagnosis, detect preclinical cases, identify carriers and offer prenatal dianostic testing. The book goes on to describe the opportunities for management of the symptoms through respiratory care, physiotherapy and surgical correction of contracture, and examines the potential, in the future, for effective treatment utilizing the new techniques of gene and cell therapy.
Professor Emery has invited chapters from the leading international experts in the field providing a unique insight into the current situation and the hopes for the future.


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