Please use this identifier to cite or link to this item: http://localhost:8080/xmlui/handle/123456789/131735
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dc.contributor.authorDali Feng
dc.date.accessioned2017-04-30T13:33:23Z-
dc.date.available2017-04-30T13:33:23Z-
dc.date.issued2013
dc.identifier.isbn978-953-51-1100-9
dc.identifier.urihttp://hdl.handle.net/123456789/131735-
dc.description.abstractAmyloidosis is an uncommon disorder characterized by the deposition of extracellular amyloid proteins in tissues. Significant advancement has been made recently, which not only provides insight in to the pathophysiology of the disease but also helps to discover new therapies to fight the deadly disease. If accurate diagnosis and typing are made early, effective or even curative therapies are available. Unfortunately, because of the rarity of the disease and its protean clinical manifestations, patients may be misdiagnosed, especially at early stage of the disease, and this could lead to missed opportunities to effective therapy. The aim of the book is to help readers become familiar with the clinical presentation of amyloidosis and to review the latest diagnostic and therapeutic development.
dc.language.isoeng
dc.publisherInTech
dc.relation.isbasedon10.5772/46140
dc.relation.urihttp://www.intechopen.com/books/amyloidosis
dc.rights.uriCC by (姓名標示)
dc.sourceInTech
dc.subject.classificationMedicine
dc.subject.classification Endocrinology and Metabolism
dc.titleAmyloidosis
dc.type電子教課書
dc.classification醫學類
Theme:教科書-醫學類

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