logo

EbookBell.com

Most ebook files are in PDF format, so you can easily read them using various software such as Foxit Reader or directly on the Google Chrome browser.
Some ebook files are released by publishers in other formats such as .awz, .mobi, .epub, .fb2, etc. You may need to install specific software to read these formats on mobile/PC, such as Calibre.

Please read the tutorial at this link:  https://ebookbell.com/faq 


We offer FREE conversion to the popular formats you request; however, this may take some time. Therefore, right after payment, please email us, and we will try to provide the service as quickly as possible.


For some exceptional file formats or broken links (if any), please refrain from opening any disputes. Instead, email us first, and we will try to assist within a maximum of 6 hours.

EbookBell Team

Life With Epidermolysis Bullosa Eb Etiology Diagnosis Multidisciplinary Care And Therapy 1st Edition Dr Christoph M Lanschuetzer

  • SKU: BELL-4396598
Life With Epidermolysis Bullosa Eb Etiology Diagnosis Multidisciplinary Care And Therapy 1st Edition Dr Christoph M Lanschuetzer
$ 31.00 $ 45.00 (-31%)

5.0

110 reviews

Life With Epidermolysis Bullosa Eb Etiology Diagnosis Multidisciplinary Care And Therapy 1st Edition Dr Christoph M Lanschuetzer instant download after payment.

Publisher: Springer-Verlag Wien
File Extension: PDF
File size: 5.78 MB
Pages: 338
Author: Dr. Christoph M. Lanschuetzer, Prof. Jo-David Fine (auth.), Professor Dr. Jo-David Fine, Universitäts-Professor Prim. Dr. Helmut Hintner (eds.)
ISBN: 9783211792704, 9783211792711, 3211792708, 3211792716
Language: English
Year: 2009
Edition: 1

Product desciption

Life With Epidermolysis Bullosa Eb Etiology Diagnosis Multidisciplinary Care And Therapy 1st Edition Dr Christoph M Lanschuetzer by Dr. Christoph M. Lanschuetzer, Prof. Jo-david Fine (auth.), Professor Dr. Jo-david Fine, Universitäts-professor Prim. Dr. Helmut Hintner (eds.) 9783211792704, 9783211792711, 3211792708, 3211792716 instant download after payment.

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.

Related Products