Identification of Early Clinical and Histological Factors Predictive of Kasai Portoenterostomy Failure
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[1] T. Yanai,et al. Histological significance of hepatitis‐like findings in biliary atresia: An analysis of 34 Japanese cases , 2019, Pediatrics international : official journal of the Japan Pediatric Society.
[2] Shan Zheng,et al. Clinical and pathological features of patients with biliary atresia who survived for more than 5 years with native liver , 2018, Pediatric Surgery International.
[3] Eun Young Chang,et al. Correlation between gamma-glutamyl transpeptidase activity and outcomes after Kasai portoenterostomy for biliary atresia. , 2017, Journal of pediatric surgery.
[4] R. Superina. Biliary atresia and liver transplantation: results and thoughts for primary liver transplantation in select patients , 2017, Pediatric Surgery International.
[5] C. Y. Ooi,et al. Clinical significance of liver histology on outcomes in biliary atresia , 2017, Journal of paediatrics and child health.
[6] N. Hadžić,et al. Guideline for the Evaluation of Cholestatic Jaundice in Infants: Joint Recommendations of the North American Society for Pediatric Gastroenterology, Hepatology, and Nutrition and the European Society for Pediatric Gastroenterology, Hepatology, and Nutrition , 2017, Journal of pediatric gastroenterology and nutrition.
[7] O. Cummings,et al. Key Histopathologic Features of Liver Biopsies That Distinguish Biliary Atresia From Other Causes of Infantile Cholestasis and Their Correlation With Outcome: A Multicenter Study , 2016, The American journal of surgical pathology.
[8] M. Davenport,et al. Biliary atresia: A comprehensive review. , 2016, Journal of autoimmunity.
[9] P. Srinivasan,et al. Diagnostic and Prognostic Significance of Various Histopathological Features in Extrahepatic Biliary Atresia. , 2016, Journal of clinical and diagnostic research : JCDR.
[10] D. El Demellawy,et al. The value of preoperative liver biopsy in the diagnosis of extrahepatic biliary atresia: A systematic review and meta-analysis. , 2016, Journal of pediatric surgery.
[11] W. Cai,et al. Comparison of liver transplantation outcomes in biliary atresia patients with and without prior portoenterostomy: A meta-analysis. , 2016, Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver.
[12] P. Rosenthal,et al. Total Serum Bilirubin within 3 Months of Hepatoportoenterostomy Predicts Short-Term Outcomes in Biliary Atresia. , 2016, The Journal of pediatrics.
[13] D. Kamińska,et al. The limited prognostic value of liver histology in children with biliary atresia. , 2015, Annals of hepatology.
[14] Siddhartha Datta Gupta,et al. Correlation of pre- and post-operative liver function, duct diameter at porta hepatis, and portal fibrosis with surgical outcomes in biliary atresia , 2015, Journal of Indian Association of Pediatric Surgeons.
[15] M. Rela,et al. Impact of ductal plate malformation on survival with native liver in children with biliary atresia , 2015, Pediatric Surgery International.
[16] J. L. Martins,et al. Grade IV fibrosis interferes in biliary drainage after Kasai procedure. , 2014, Transplantation proceedings.
[17] Y. Etani,et al. The most reliable early predictors of outcome in patients with biliary atresia after Kasai's operation. , 2013, Journal of pediatric surgery.
[18] R. Superina. Liver transplantation for biliary atresia: Does the insurance type really make a difference? , 2013, Liver transplantation : official publication of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society.
[19] Xian-min Xiao,et al. Early surgical outcomes and pathological scoring values of older infants (≥ 90 d old) with biliary atresia. , 2012, Journal of pediatric surgery.
[20] K. Iyer,et al. The Anatomic Pattern of Biliary Atresia Identified at Time of Kasai Hepatoportoenterostomy and Early Postoperative Clearance of Jaundice Are Significant Predictors of Transplant-Free Survival , 2011, Annals of surgery.
[21] C. Sempoux,et al. AUTOIMMUNE, CHOLESTATIC AND BILIARY DISEASE A Classification of Ductal Plate Malformations Based on Distinct Pathogenic Mechanisms of Biliary Dysmorphogenesis , 2011 .
[22] T. Raghunathan,et al. Design and validation of the biliary atresia research consortium histologic assessment system for cholestasis in infancy. , 2011, Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association.
[23] H. Hsu,et al. Effects of the infant stool color card screening program on 5‐year outcome of biliary atresia in taiwan , 2011, Hepatology.
[24] A. Yamataka,et al. How valuable is ductal plate malformation as a predictor of clinical course in postoperative biliary atresia patients? , 2011, Pediatric Surgery International.
[25] S. Chatterjee,et al. A histopathological study of liver and biliary remnants with clinical outcome in cases of extrahepatic biliary atresia. , 2010, Indian journal of pathology & microbiology.
[26] J. Sarles,et al. Impact of Age at Kasai Operation on Its Results in Late Childhood and Adolescence: A Rational Basis for Biliary Atresia Screening , 2009, Pediatrics.
[27] S. Ono,et al. Significance of ductal plate malformation in the postoperative clinical course of biliary atresia. , 2008, Journal of pediatric surgery.
[28] Steven R. Martin,et al. Biliary atresia: the Canadian experience. , 2007, The Journal of pediatrics.
[29] M. Davenport,et al. Seamless management of biliary atresia in England and Wales (1999–2002) , 2004, The Lancet.
[30] F. White,et al. Hepatic fibrosis and survival in biliary atresia. , 2004, The Journal of pediatrics.
[31] Y. Low,et al. The prognostic value of ductal plate malformation and other histologic parameters in biliary atresia: an immunohistochemical study. , 2001, The Journal of pediatrics.
[32] K. Azarow,et al. Biliary atresia: should all patients undergo a portoenterostomy? , 1997, Journal of pediatric surgery.
[33] R. Sokol,et al. Long-term results with the Kasai operation for biliary atresia. , 1996, Archives of surgery.
[34] E. Sokal,et al. Sequential treatment of biliary atresia with kasai portoenterostomy and liver transplantation: A review , 1994, Hepatology.
[35] E. Yunis,et al. Syncytial giant-cell hepatitis. , 1992, The New England journal of medicine.
[36] R. Hall,et al. Biliary atresia: early determination of prognosis. , 1989, Journal of pediatric surgery.
[37] B. Nichols,et al. Guide to Early Diagnosis of Biliary Obstruction in Infancy , 1985, Clinical pediatrics.
[38] J. Levy,et al. Biliary atresia. , 1985, Pediatric annals.
[39] R. Williams,et al. Extrahepatic biliary atresia versus neonatal hepatitis. Review of 137 prospectively investigated infants. , 1976, Archives of disease in childhood.