Living-donor liver transplantation for congenital biliary atresia with porto-pulmonary hypertension and moderate or severe pulmonary arterial hypertension: Kyoto University experience-Reference-Cited by-同舟云学术

Living-donor liver transplantation for congenital biliary atresia with porto-pulmonary hypertension and moderate or severe pulmonary arterial hypertension: Kyoto University experience

Published:2014-07-28 Issue:9 Volume:28 Page:1031-1040
ISSN:0902-0063
Container-title:Clinical Transplantation
language:en
Short-container-title:Clin Transplant

Author:

Ogawa Eri¹,Hori Tomohide²,Doi Hiraku³,Segawa Hajime⁴,Uemoto Shinji¹²

Affiliation:

1. Department of Pediatric Surgery; Kyoto University Hospital; Kyoto Japan

2. Department of Hepato-Pancreato-Biliary and Transplant Surgery; Kyoto University Hospital; Kyoto Japan

3. Department of Pediatric Cardiology and Department of Pediatrics; Kyoto University Hospital; Kyoto Japan

4. Department of Critical Care Medicine and Anesthesia; Kyoto University Hospital; Kyoto Japan

Publisher

Wiley

Subject

Transplantation

Reference52 articles.

1. Long-term results of biliary atresia in the era of liver transplantation;Lee;Pediatr Surg Int,2013

2. Current options for management of biliary atresia;Gallo;Pediatr Transplant,2013

3. Portopulmonary hypertension;Wells;Hepatology,2008

4. Portopulmonary hypertension: results from a 10-year screening algorithm;Krowka;Hepatology,2006

5. Living-donor liver transplantation for moderate or severe porto-pulmonary hypertension accompanied by pulmonary arterial hypertension: a single-centre experience over 2 decades in Japan;Ogawa;J Hepatobiliary Pancreat Sci,2012

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3. Long-Term Complications: Portopulmonary Hypertension;Introduction to Biliary Atresia;2021

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