9607272

Source:http://linkedlifedata.com/resource/pubmed/id/9607272

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0007320, umls-concept:C0085973, umls-concept:C1608393
pubmed:issue	1
pubmed:dateCreated	1998-6-11
pubmed:abstractText	Megacystis-microcolon-intestinal hypoperistalsis syndrome (MMIHS) is a rare congenital disorder characterized by a massively enlarged urinary bladder without mechanical outlet obstruction and microcolon, as well as a hypoperistaltic bowel with normal ganglion cell distribution. We report one such case to discuss the findings of antenatal ultrasound and the radiologic and pathologic features of this condition.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/9809559
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:month	Mar
pubmed:author	pubmed-author:ChenLL, pubmed-author:ChuangJ HJH, pubmed-author:ChungM YMY, pubmed-author:HuangC BCB, pubmed-author:OOITT
pubmed:volume	21
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	92-6
pubmed:dateRevised	2006-11-15
pubmed:meshHeading	pubmed-meshheading:9607272-Abnormalities, Multiple, pubmed-meshheading:9607272-Colon, pubmed-meshheading:9607272-Female, pubmed-meshheading:9607272-Humans, pubmed-meshheading:9607272-Infant, Newborn, pubmed-meshheading:9607272-Peristalsis, pubmed-meshheading:9607272-Syndrome, pubmed-meshheading:9607272-Urinary Bladder
pubmed:year	1998
pubmed:articleTitle	Megacystis-microcolon-intestinal hypoperistalsis syndrome (MMIHS): a case report.
pubmed:affiliation	Department of Pediatrics, Chang Gung Children's Hospital, Kaohsiung, Taiwan, R.O.C.
pubmed:publicationType	Journal Article, Case Reports