Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
3
pubmed:dateCreated
2008-3-31
pubmed:abstractText
Dystrophic epidermolysis bullosa is a hereditary heterogeneous blistering disease. Clinical examination and additional tests are not always sufficient to identify the subtype or mode of transmission. We describe a case of de novo dominant inherited dystrophic epidermolysis bullosa localised strictly to the knees.
pubmed:language
fre
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Mar
pubmed:issn
0151-9638
pubmed:author
pubmed:issnType
Print
pubmed:volume
135
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
195-9
pubmed:meshHeading
pubmed:year
2008
pubmed:articleTitle
[Localised de novo dominant dystrophic epidermolysis bullosa].
pubmed:affiliation
Service dermatologie, CHR de Metz-Thionville, hôpital Beauregard, 21, rue des Frères, 57 100 Thionville, France.
pubmed:publicationType
Journal Article, English Abstract, Case Reports