Ten years of DNA diagnostics of epidermolysis bullosa in the Czech Republic

Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00159816%3A_____%2F16%3A00066237" target="_blank" >RIV/00159816:_____/16:00066237 - isvavai.cz</a>
Alternative codes found
RIV/65269705:_____/16:00066237 RIV/00216224:14740/16:00087620
Result on the web
<a href="http://onlinelibrary.wiley.com/doi/10.1111/bjd.14370/abstract" target="_blank" >http://onlinelibrary.wiley.com/doi/10.1111/bjd.14370/abstract</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1111/bjd.14370" target="_blank" >10.1111/bjd.14370</a>

Result language
angličtina
Original language name
Ten years of DNA diagnostics of epidermolysis bullosa in the Czech Republic
Original language description
Epidermolysis bullosa (EB) is a heterogeneous group of inherited skin disorders characterized by blister formation. Classification of patients with EB begins with their separation into one of the four major EB groups, based on the level to which blisters develop: EB simplex (EBS), junctional EB (JEB), dystrophic EB (DEB) and Kindler syndrome. The next level of subclassification takes into account the clinical features present in a given patient, most notably the distribution and severity of cutaneous and extracutaneous disease involvement.
Czech name
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Czech description
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Type
J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)
CEP classification
FO - Dermatology and venereology
OECD FORD branch
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Project
Result was created during the realization of more than one project. More information in the Projects tab.
Continuities
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Publication year
2016
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

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