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rdf:type |
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lifeskim:mentions |
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pubmed:dateCreated |
1998-6-3
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pubmed:abstractText |
In a prospective study 106 children with intestinal neuronal malformations underwent intestinal transit-time studies. In only 50% of the children with intestinal neuronal dysplasia type B or immature ganglia was the transit time prolonged. On the contrary, hypoganglionosis and heterotopia of the submucous plexus led to severe transport disorders with subsequent bowel resection.
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pubmed:language |
ger
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:status |
MEDLINE
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pubmed:issn |
0942-2854
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:volume |
114
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1337-9
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pubmed:dateRevised |
2008-2-20
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pubmed:meshHeading |
pubmed-meshheading:9574421-Adolescent,
pubmed-meshheading:9574421-Child,
pubmed-meshheading:9574421-Child, Preschool,
pubmed-meshheading:9574421-Diagnosis, Differential,
pubmed-meshheading:9574421-Female,
pubmed-meshheading:9574421-Gastrointestinal Transit,
pubmed-meshheading:9574421-Hirschsprung Disease,
pubmed-meshheading:9574421-Humans,
pubmed-meshheading:9574421-Infant,
pubmed-meshheading:9574421-Infant, Newborn,
pubmed-meshheading:9574421-Male,
pubmed-meshheading:9574421-Prognosis,
pubmed-meshheading:9574421-Prospective Studies,
pubmed-meshheading:9574421-Reference Values,
pubmed-meshheading:9574421-Submucous Plexus
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pubmed:year |
1997
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pubmed:articleTitle |
[Prospective study of the transit time in intestinal neuronal abnormalities].
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pubmed:affiliation |
Kinderchirurgische Klinik, Kinderkrankenhaus, Köln.
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pubmed:publicationType |
Journal Article,
English Abstract
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