Prognosis of Biliary Atresia After 2-year Survival With Native Liver: A Nationwide Cohort Analysis.

Autor: Witt, Mauri, van Wessel, Daan B.E., de Kleine, Ruben H.J., Bruggink, Janneke L.M., Hulscher, Jan B.F., Verkade, Henkjan J., NeSBAR (Netherlands Study group on Biliary Atresia Registry)

Publikováno v: Journal of Pediatric Gastroenterology & Nutrition; Dec2018, Vol. 67 Issue 6, p689-694, 6p

담도폐쇄증의 개요.

Autor: 전태연¹ hathor97.jeon@samsung.com

Publikováno v: Journal of the Korean Society of Radiology (2951-0805). Sep2022, Vol. 83 Issue 5, p979-990. 12p.

Normal Gamma Glutamyl Transferase Levels at Presentation Predict Poor Outcome in Biliary Atresia.

Autor: Shankar, Sahana, Bolia, Rishi, Hee Wei Foo, D’Arcy, Colleen E., Hardikar, Natasha, Wensing, Martin, Hardikar, Winita, Foo, Hee Wei, D'Arcy, Colleen E

Publikováno v: Journal of Pediatric Gastroenterology & Nutrition; Mar2020, Vol. 70 Issue 3, p350-355, 6p

Revisiting long-term prognostic factors of biliary atresia: A 20-year experience with 81 patients from a single center.

Autor: Hanalioğlu, Damla, Özen, Hasan, Karhan, Asuman, Gümüş, Ersin, Demir, Hülya, Saltık-Temizel, İnci N., Ekinci, Saniye, Karnak, İbrahim, Çiftçi, Arbay O., Tanyel, Feridun C., Yüce, Aysel

Publikováno v: Turkish Journal of Gastroenterology; May2019, Vol. 30 Issue 5, p467-474, 8p

Overall Quality of Life in Adult Biliary Atresia Survivors with or without Liver Transplantation: Results from a National Cohort

Autor: Robert J. Porte, Yuk-Kueng Sze, Robert C. Lind, Jan B F Hulscher, Alida F. W. van der Steeg, Willemien de Vries, Josephine Hoekstra-Weebers, Henkjan J. Verkade, Egbert Sieders

Publikováno v: European Journal of Pediatric Surgery, 26(4), 349-356. GEORG THIEME VERLAG KG
European journal of pediatric surgery, 26(4). Thieme Medical Publishers
European journal of pediatric surgery, 26(4), 349-356. Thieme Medical Publishers
de Vries, W, Lind, R C, Sze, Y K, van der Steeg, A F W, Sieders, E, Porte, R J, Verkade, H J, Hulscher, J B F & Hoekstra-Weeber, J E H M 2016, ' Overall Quality of Life in Adult Biliary Atresia Survivors with or without Liver Transplantation : Results from a National Cohort ', European Journal of Pediatric Surgery, vol. 26, no. 4, pp. 349-356 . https://doi.org/10.1055/s-0035-1554913
European Journal of Pediatric Surgery, 26(4), 349-356. Thieme Medical Publishers

Background Biliary atresia (BA) is a rare cholestatic disease of infancy. Kasai portoenterostomy and liver transplantation (LT) are the two sequential treatment options. An increasing number of patients survive into adulthood. Little is known about t

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9da30995d5568c575152d74a62728143
https://doi.org/10.1055/s-0035-1554913