| pubmed-article:7678788 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:7678788 | lifeskim:mentions | umls-concept:C0231330 | lld:lifeskim |
| pubmed-article:7678788 | lifeskim:mentions | umls-concept:C0243002 | lld:lifeskim |
| pubmed-article:7678788 | lifeskim:mentions | umls-concept:C0038952 | lld:lifeskim |
| pubmed-article:7678788 | lifeskim:mentions | umls-concept:C0190010 | lld:lifeskim |
| pubmed-article:7678788 | lifeskim:mentions | umls-concept:C0449450 | lld:lifeskim |
| pubmed-article:7678788 | pubmed:issue | 2 | lld:pubmed |
| pubmed-article:7678788 | pubmed:dateCreated | 1993-3-3 | lld:pubmed |
| pubmed-article:7678788 | pubmed:abstractText | The Fontan operation is the usual goal of therapy for children with tricuspid atresia. The influences of morphology and different management strategies on survival and subsequent suitability for this procedure are crucial but unstudied in an unselected population during the Fontan era. | lld:pubmed |
| pubmed-article:7678788 | pubmed:language | eng | lld:pubmed |
| pubmed-article:7678788 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:7678788 | pubmed:citationSubset | AIM | lld:pubmed |
| pubmed-article:7678788 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:7678788 | pubmed:month | Feb | lld:pubmed |
| pubmed-article:7678788 | pubmed:issn | 0009-7322 | lld:pubmed |
| pubmed-article:7678788 | pubmed:author | pubmed-author:FranklinR CRC | lld:pubmed |
| pubmed-article:7678788 | pubmed:author | pubmed-author:AndersonR HRH | lld:pubmed |
| pubmed-article:7678788 | pubmed:author | pubmed-author:ShinebourneE... | lld:pubmed |
| pubmed-article:7678788 | pubmed:author | pubmed-author:Spiegelhalter... | lld:pubmed |
| pubmed-article:7678788 | pubmed:author | pubmed-author:DeanfieldJ... | lld:pubmed |
| pubmed-article:7678788 | pubmed:author | pubmed-author:SullivanI DID | lld:pubmed |
| pubmed-article:7678788 | pubmed:author | pubmed-author:ThoeleD GDG | lld:pubmed |
| pubmed-article:7678788 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:7678788 | pubmed:volume | 87 | lld:pubmed |
| pubmed-article:7678788 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:7678788 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:7678788 | pubmed:pagination | 427-39 | lld:pubmed |
| pubmed-article:7678788 | pubmed:dateRevised | 2010-3-24 | lld:pubmed |
| pubmed-article:7678788 | pubmed:meshHeading | pubmed-meshheading:7678788-... | lld:pubmed |
| pubmed-article:7678788 | pubmed:meshHeading | pubmed-meshheading:7678788-... | lld:pubmed |
| pubmed-article:7678788 | pubmed:meshHeading | pubmed-meshheading:7678788-... | lld:pubmed |
| pubmed-article:7678788 | pubmed:meshHeading | pubmed-meshheading:7678788-... | lld:pubmed |
| pubmed-article:7678788 | pubmed:meshHeading | pubmed-meshheading:7678788-... | lld:pubmed |
| pubmed-article:7678788 | pubmed:meshHeading | pubmed-meshheading:7678788-... | lld:pubmed |
| pubmed-article:7678788 | pubmed:meshHeading | pubmed-meshheading:7678788-... | lld:pubmed |
| pubmed-article:7678788 | pubmed:meshHeading | pubmed-meshheading:7678788-... | lld:pubmed |
| pubmed-article:7678788 | pubmed:meshHeading | pubmed-meshheading:7678788-... | lld:pubmed |
| pubmed-article:7678788 | pubmed:meshHeading | pubmed-meshheading:7678788-... | lld:pubmed |
| pubmed-article:7678788 | pubmed:meshHeading | pubmed-meshheading:7678788-... | lld:pubmed |
| pubmed-article:7678788 | pubmed:meshHeading | pubmed-meshheading:7678788-... | lld:pubmed |
| pubmed-article:7678788 | pubmed:year | 1993 | lld:pubmed |
| pubmed-article:7678788 | pubmed:articleTitle | Tricuspid atresia presenting in infancy. Survival and suitability for the Fontan operation. | lld:pubmed |
| pubmed-article:7678788 | pubmed:affiliation | Thoracic Unit, Hospital for Sick Children, London, England. | lld:pubmed |
| pubmed-article:7678788 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:7678788 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
