Hepatobilier yetmezlikli-transplantasyon adayı neonatal olgular ve anestezi

dc.contributor.author	Tülin ÖZTÜRK;Selçuk BULUT;Verda TOPRAK;Tezcan Gönül KELEŞ
dc.date.accessioned	2020-06-30T10:29:20Z
dc.date.available	2020-06-30T10:29:20Z
dc.date.issued	2008
dc.identifier.citation	0
dc.identifier.uri	https://app.trdizin.gov.tr/publication/paper/detail/T0RVNU1EZzQ=
dc.identifier.uri	http://hdl.handle.net/20.500.12481/2369
dc.description.abstract	Biliary atresia (BA) is the most common and important neonatal hepatobiliary disorder and is seen in 1 in 8.000 to 1 in 18.000. Consequently, 70-80 % of BA patients will eventually require liver transplantation, approximately half in the first 2 y of life. Early diagnosis and therapy is essential especially for the survival of patients with biliary atresia.
dc.language.iso	tur
dc.title	Hepatobilier yetmezlikli-transplantasyon adayı neonatal olgular ve anestezi
dc.title.alternative	Hepatobiliary insufficiency-candidate of transplantation newborns and anesthesia (two cases)
dc.type	FACT_PRESENTATION
dc.contributor.department	CELÂL BAYAR ÜNİVERSİTESİ;CELÂL BAYAR ÜNİVERSİTESİ;CELÂL BAYAR ÜNİVERSİTESİ;CELÂL BAYAR ÜNİVERSİTESİ
dc.identifier.nameOfPublishedMaterial	Göztepe Tıp Dergisi
dc.identifier.volume	23
dc.identifier.issue	3
dc.identifier.startpage	95
dc.identifier.endpage	99
dc.identifier.issn/e-issn	1300-526X;null

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