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dc.contributor.authorSukasom Attanawanichen_US
dc.contributor.authorMontein Ngodngarmtaweesuken_US
dc.contributor.authorPongsak Kowsatiten_US
dc.contributor.authorPiya Samankatiwaten_US
dc.contributor.authorSuthep Wanitkulen_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2018-09-07T08:57:01Z-
dc.date.available2018-09-07T08:57:01Z-
dc.date.issued1999-06-01en_US
dc.identifier.citationJournal of the Medical Association of Thailand. Vol.82, No.6 (1999), 610-614en_US
dc.identifier.issn01252208en_US
dc.identifier.other2-s2.0-0033142431en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0033142431&origin=inwarden_US
dc.identifier.urihttp://repository.li.mahidol.ac.th/dspace/handle/123456789/25636-
dc.description.abstractAortopulmonary window (A-P window) is a rare congenital heart disease. The majority of patients come to the hospital with congestive heart failure. If they are left untreated, irreversible pulmonary vascular hypertension inevitably occurs. Although the hemodynamic of this disease resembles large persistent ductus arteriosus, the treatment is quite different. We report one patient of A-P window, a 4 month-old girl, who presented with fever and dyspnea. On investigations, she had A-P window. We successfully treated her by closure the defect under cardiopulmonary bypass. We describe the technique we used.en_US
dc.rightsMahidol Universityen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0033142431&origin=inwarden_US
dc.subjectMedicineen_US
dc.titleAortopulmonary window : A case reporten_US
dc.typeArticleen_US
dc.rights.holderSCOPUSen_US
Appears in Collections:Scopus 1991-2000

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