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dc.contributor.editorFeng, Dali
dc.date.accessioned2021-04-20T15:46:41Z
dc.date.available2021-04-20T15:46:41Z
dc.date.issued2013
dc.identifierONIX_20210420_9789535111009_1914
dc.identifier.urihttps://directory.doabooks.org/handle/20.500.12854/66555
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.languageEnglish
dc.subject.classificationthema EDItEUR::M Medicine and Nursing::MJ Clinical and internal medicine::MJC Diseases and disorders::MJCJ Infectious and contagious diseasesen_US
dc.subject.otherInfectious & contagious diseases
dc.titleAmyloidosis
dc.typebook
oapen.identifier.doi10.5772/46140
oapen.relation.isPublishedBy78a36484-2c0c-47cb-ad67-2b9f5cd4a8f6
oapen.relation.isbn9789535111009
oapen.relation.isbn9789535171607
oapen.imprintIntechOpen
oapen.pages250


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