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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
6
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pubmed:dateCreated |
2004-6-7
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pubmed:abstractText |
With the improved survival of patients with cystic fibrosis (CF), gastrointestinal complications become more evident in adults with this condition. The aims of this study were to determine the prevalence and clinical features of distal intestinal obstruction syndrome (DIOS) and its relationship with the cystic fibrosis transmembrane conductance regulator (CFTR) genotype in an adult CF population.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Jun
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pubmed:issn |
1542-3565
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:volume |
2
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
498-503
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pubmed:dateRevised |
2006-9-18
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pubmed:meshHeading |
pubmed-meshheading:15181619-Adolescent,
pubmed-meshheading:15181619-Adult,
pubmed-meshheading:15181619-Cecal Diseases,
pubmed-meshheading:15181619-Cystic Fibrosis,
pubmed-meshheading:15181619-Cystic Fibrosis Transmembrane Conductance Regulator,
pubmed-meshheading:15181619-Female,
pubmed-meshheading:15181619-Follow-Up Studies,
pubmed-meshheading:15181619-Genotype,
pubmed-meshheading:15181619-Humans,
pubmed-meshheading:15181619-Ileal Diseases,
pubmed-meshheading:15181619-Intestinal Obstruction,
pubmed-meshheading:15181619-Male,
pubmed-meshheading:15181619-Middle Aged,
pubmed-meshheading:15181619-Mutation,
pubmed-meshheading:15181619-Retrospective Studies,
pubmed-meshheading:15181619-Syndrome
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pubmed:year |
2004
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pubmed:articleTitle |
Distal intestinal obstruction syndrome in adults with cystic fibrosis.
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pubmed:affiliation |
Service d'Hépati-gastroentérologie, Hôpital Européen Georges Pompidou, Paris, France.
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pubmed:publicationType |
Journal Article
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