rdf:type |
|
lifeskim:mentions |
|
pubmed:issue |
1-2
|
pubmed:dateCreated |
1995-10-12
|
pubmed:abstractText |
Hereditary angio-oedema is a poorly understood disease. In more than 70 p. 100 of the cases, diagnosis is made 5 to 10 years after the first manifestations despite their typical nature.
|
pubmed:language |
fre
|
pubmed:journal |
|
pubmed:citationSubset |
IM
|
pubmed:chemical |
|
pubmed:status |
MEDLINE
|
pubmed:issn |
0151-9638
|
pubmed:author |
|
pubmed:issnType |
Print
|
pubmed:volume |
122
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
11-5
|
pubmed:dateRevised |
2010-3-24
|
pubmed:meshHeading |
pubmed-meshheading:7668774-Adolescent,
pubmed-meshheading:7668774-Adult,
pubmed-meshheading:7668774-Angioedema,
pubmed-meshheading:7668774-Complement C1 Inactivator Proteins,
pubmed-meshheading:7668774-Danazol,
pubmed-meshheading:7668774-Emergencies,
pubmed-meshheading:7668774-Female,
pubmed-meshheading:7668774-Humans,
pubmed-meshheading:7668774-Laryngeal Edema,
pubmed-meshheading:7668774-Male,
pubmed-meshheading:7668774-Retrospective Studies
|
pubmed:year |
1995
|
pubmed:articleTitle |
[Hereditary angioneurotic edema: an underestimated medical emergency. Apropos of 33 cases].
|
pubmed:affiliation |
Service de Médecine interne et Immunologie clinique, Centre Hospitalier Universitaire, Besançon.
|
pubmed:publicationType |
Journal Article,
English Abstract
|