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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
6 Pt 1
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pubmed:dateCreated |
2003-6-2
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pubmed:abstractText |
Transplantation of isolated hepatocytes in animal models has been shown to correct inborn errors of metabolism. Based on these studies and our experience with hepatocyte transplantation in a child with Crigler-Najjar syndrome, isolated hepatocyte transplantation was performed to attempt metabolic reconstitution in a male infant with severe ornithine transcarbamylase (OTC) deficiency.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
AIM
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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 |
1098-4275
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pubmed:author |
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pubmed:issnType |
Electronic
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pubmed:volume |
111
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1262-7
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pubmed:dateRevised |
2004-11-17
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pubmed:meshHeading |
pubmed-meshheading:12777539-Adult,
pubmed-meshheading:12777539-Crigler-Najjar Syndrome,
pubmed-meshheading:12777539-Female,
pubmed-meshheading:12777539-Hepatocytes,
pubmed-meshheading:12777539-Heterozygote Detection,
pubmed-meshheading:12777539-Humans,
pubmed-meshheading:12777539-Hyperammonemia,
pubmed-meshheading:12777539-Infant,
pubmed-meshheading:12777539-Liver Transplantation,
pubmed-meshheading:12777539-Male,
pubmed-meshheading:12777539-Ornithine Carbamoyltransferase Deficiency Disease,
pubmed-meshheading:12777539-Prenatal Diagnosis,
pubmed-meshheading:12777539-Urea
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pubmed:year |
2003
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pubmed:articleTitle |
Isolated hepatocyte transplantation in an infant with a severe urea cycle disorder.
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pubmed:affiliation |
Section of Pediatric Gastroenterology, University of Nebraska Medical Center, Omaha, Nebraska 68198-3285, USA. shorslen@surgery.unmc.edu
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pubmed:publicationType |
Journal Article,
Case Reports
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