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Titlebook: Life with Epidermolysis Bullosa (EB); Etiology, Diagnosis, Jo-David Fine,Helmut Hintner Book 2009 Springer-Verlag Vienna 2009 Butterfly Chi

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書目名稱Life with Epidermolysis Bullosa (EB)
副標題Etiology, Diagnosis,
編輯Jo-David Fine,Helmut Hintner
視頻videohttp://file.papertrans.cn/586/585903/585903.mp4
概述First comprehensive presentation of a multidisciplinary approach to the treatment of Epidermolysis Bullosa.Update on the therapy of this inherited disease.Practical reference for day-to-day care and i
圖書封面Titlebook: Life with Epidermolysis Bullosa (EB); Etiology, Diagnosis, Jo-David Fine,Helmut Hintner Book 2009 Springer-Verlag Vienna 2009 Butterfly Chi
描述.Epidermolysis bullosa (EB) is a heterogenous group of genodermatoses characterized by the formation of blisters and erosions on skin and mucous membrans from birth on. The cause are mutations in the genes of structural proteins of the junction between epidermis and dermis. This book deals with the treatment of this skin disease itself and its many extracutaneous complications. There is no previous book which has been focused on the therapy and it will be based on evidence-based data derived from the world′s largest cohort of inherited EB-patients, the American EB Registry. An important chapter will discuss gene therapy in hereditary EB which has been recently successfully performed within a localized skin site on a single EB patient as a proof-of-principle test. Given its unique collective contents, the monograph will provide the primary source for clinical informations of this oftentimes severe multiorgan disease..
出版日期Book 2009
關(guān)鍵詞Butterfly Children; Chronic Skin Disease; Epidermolysis; Epidermolysis Bullosa; Genetic Disease; Internal
版次1
doihttps://doi.org/10.1007/978-3-211-79271-1
isbn_softcover978-3-211-99934-9
isbn_ebook978-3-211-79271-1
copyrightSpringer-Verlag Vienna 2009
The information of publication is updating

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Jo-David Fine,Helmut HintnerFirst comprehensive presentation of a multidisciplinary approach to the treatment of Epidermolysis Bullosa.Update on the therapy of this inherited disease.Practical reference for day-to-day care and i
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Book 2009ans from birth on. The cause are mutations in the genes of structural proteins of the junction between epidermis and dermis. This book deals with the treatment of this skin disease itself and its many extracutaneous complications. There is no previous book which has been focused on the therapy and i
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Book 2009r will discuss gene therapy in hereditary EB which has been recently successfully performed within a localized skin site on a single EB patient as a proof-of-principle test. Given its unique collective contents, the monograph will provide the primary source for clinical informations of this oftentimes severe multiorgan disease..
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