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For: Sundaram SS, Mack CL, Feldman AG, Sokol RJ. Biliary atresia: Indications and timing of liver transplantation and optimization of pretransplant care. Liver Transpl. 2017;23:96-109. [PMID: 27650268 DOI: 10.1002/lt.24640] [Cited by in Crossref: 89] [Cited by in F6Publishing: 71] [Article Influence: 17.8] [Reference Citation Analysis]
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4 Mouzaki M, Bronsky J, Gupte G, Hojsak I, Jahnel J, Pai N, Quiros-tejeira RE, Wieman R, Sundaram S. Nutrition Support of Children With Chronic Liver Diseases: A Joint Position Paper of the North American Society for Pediatric Gastroenterology, Hepatology, and Nutrition and the European Society for Pediatric Gastroenterology, Hepatology, and Nutrition. Journal of Pediatric Gastroenterology & Nutrition 2019;69:498-511. [DOI: 10.1097/mpg.0000000000002443] [Cited by in Crossref: 17] [Cited by in F6Publishing: 4] [Article Influence: 5.7] [Reference Citation Analysis]
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8 Liu L, Wei L, Qu W, Liu Y, Zeng Z, Zhang H, Li M, Liu J, Wang HL, Li K, He Y, Jia J, Sun L, Zhao X, Zhu Z. Impact of the Kasai Procedure and the Length of Native Liver Survival Time on Outcomes of Liver Transplantation for Biliary Atresia. Liver Transpl 2021. [PMID: 34482616 DOI: 10.1002/lt.26287] [Reference Citation Analysis]
9 Lupo PJ, Mitchell LE, Jenkins MM. Genome-wide association studies of structural birth defects: A review and commentary. Birth Defects Res 2019;111:1329-42. [PMID: 31654503 DOI: 10.1002/bdr2.1606] [Cited by in Crossref: 14] [Cited by in F6Publishing: 11] [Article Influence: 4.7] [Reference Citation Analysis]
10 Hsiao C, Ho C, Wu Y, Ho M, Hu R, Lee P. Biliary Complication in Pediatric Liver Transplantation: a Single-Center 15-Year Experience. J Gastrointest Surg 2019;23:751-9. [DOI: 10.1007/s11605-018-04076-x] [Cited by in Crossref: 5] [Cited by in F6Publishing: 4] [Article Influence: 1.7] [Reference Citation Analysis]
11 Liu Y, Peng C, Wang K, Wu D, Yan J, Tu W, Chen Y. The utility of shear wave elastography and serum biomarkers for diagnosing biliary atresia and predicting clinical outcomes. Eur J Pediatr 2021. [PMID: 34191129 DOI: 10.1007/s00431-021-04176-y] [Reference Citation Analysis]
12 Karpen SJ, Kelly D, Mack C, Stein P. Ileal bile acid transporter inhibition as an anticholestatic therapeutic target in biliary atresia and other cholestatic disorders. Hepatol Int 2020;14:677-89. [PMID: 32653991 DOI: 10.1007/s12072-020-10070-w] [Cited by in Crossref: 12] [Cited by in F6Publishing: 10] [Article Influence: 6.0] [Reference Citation Analysis]
13 Chung PHY, Chan EKW, Yeung F, Chan ACY, Mou JWC, Lee KH, Hung JWS, Leung MWY, Tam PKH, Wong KKY. Life long follow up and management strategies of patients living with native livers after Kasai portoenterostomy. Sci Rep 2021;11:11207. [PMID: 34045634 DOI: 10.1038/s41598-021-90860-w] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
14 Bezinover D, Nahouraii L, Sviatchenko A, Wang M, Kimatian S, Saner FH, Stine JG. Hyponatremia Is Associated With Increased Mortality in Children on the Waiting List for Liver Transplantation. Transplant Direct 2020;6:e604. [PMID: 33134484 DOI: 10.1097/TXD.0000000000001050] [Cited by in Crossref: 1] [Article Influence: 0.5] [Reference Citation Analysis]
15 Witt M, van Wessel DBE, de Kleine RHJ, Bruggink JLM, Hulscher JBF, Verkade HJ; NeSBAR (Netherlands Study group on Biliary Atresia Registry). Prognosis of Biliary Atresia After 2-year Survival With Native Liver: A Nationwide Cohort Analysis. J Pediatr Gastroenterol Nutr 2018;67:689-94. [PMID: 30095577 DOI: 10.1097/MPG.0000000000002130] [Cited by in Crossref: 11] [Cited by in F6Publishing: 4] [Article Influence: 3.7] [Reference Citation Analysis]
16 Xiao Y, Wang Y, Liu Y, Wang W, Tian X, Chen S, Lu Y, Du J, Cai W. A nonbile acid farnesoid X receptor agonist tropifexor potently inhibits cholestatic liver injury and fibrosis by modulating the gut-liver axis. Liver Int 2021;41:2117-31. [PMID: 33894097 DOI: 10.1111/liv.14906] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
17 Godbole N, Nyholm I, Hukkinen M, Davidson JR, Tyraskis A, Eloranta K, Andersson N, Lohi J, Heikkilä P, Kyrönlahti A, Pihlajoki M, Davenport M, Heikinheimo M, Pakarinen MP. Prognostic and Pathophysiologic Significance of IL-8 (CXCL8) in Biliary Atresia. J Clin Med 2021;10:2705. [PMID: 34207442 DOI: 10.3390/jcm10122705] [Reference Citation Analysis]
18 Zhang Y, Xiang B, Wu Y, Xie X, Wang J, Jin S. Risk factors and associated outcomes of early acute kidney injury in pediatric liver transplant recipients: A retrospective study. J Pediatr Surg 2020;55:446-50. [PMID: 31466815 DOI: 10.1016/j.jpedsurg.2019.07.019] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 0.7] [Reference Citation Analysis]
19 Venkat V, Ng VL, Magee JC, Ye W, Hawthorne K, Harpavat S, Molleston JP, Murray KF, Wang KS, Soufi N, Bass LM, Alonso EM, Bezerra JA, Jensen MK, Kamath BM, Loomes KM, Mack CL, Rosenthal P, Shneider BL, Squires RH, Sokol RJ, Karpen SJ; Childhood Liver Disease Research Network. Modeling Outcomes in Children With Biliary Atresia With Native Liver After 2 Years of Age. Hepatol Commun 2020;4:1824-34. [PMID: 33305153 DOI: 10.1002/hep4.1602] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 0.5] [Reference Citation Analysis]
20 Godfrey E, Desai M, Lam F, Goss J, Rana A, Miloh T. Higher Waitlist Mortality in Pediatric Acute-on-chronic Liver Failure in the UNOS Database. J Pediatr Gastroenterol Nutr 2021;72:80-7. [PMID: 32796428 DOI: 10.1097/MPG.0000000000002891] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
21 Luo Y, Brigham D, Bednarek J, Torres R, Wang D, Ahmad S, Mack CL. Unique Cholangiocyte-Targeted IgM Autoantibodies Correlate With Poor Outcome in Biliary Atresia. Hepatology 2021;73:1855-67. [PMID: 32767570 DOI: 10.1002/hep.31504] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
22 Yang L, Mizuochi T, Shivakumar P, Mourya R, Luo Z, Gutta S, Bezerra JA. Regulation of epithelial injury and bile duct obstruction by NLRP3, IL-1R1 in experimental biliary atresia. J Hepatol 2018;69:1136-44. [PMID: 29886157 DOI: 10.1016/j.jhep.2018.05.038] [Cited by in Crossref: 11] [Cited by in F6Publishing: 11] [Article Influence: 2.8] [Reference Citation Analysis]
23 Makhmudi A, Supanji R, Putra BP, Gunadi. The effect of APTR, Fn14 and CD133 expressions on liver fibrosis in biliary atresia patients. Pediatr Surg Int 2020;36:75-9. [PMID: 31549181 DOI: 10.1007/s00383-019-04582-2] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
24 Ventura F, Barranco R, Buffelli F, Fulcheri E, Palmieri A. Unexpected Infant Death Due to Undiagnosed Biliary Atresia: A Case of Fatal Neglect. Am J Forensic Med Pathol 2019;40:399-402. [PMID: 31634153 DOI: 10.1097/PAF.0000000000000511] [Cited by in Crossref: 1] [Article Influence: 0.3] [Reference Citation Analysis]
25 Lin Z, Xie X, Lin H, Fu M, Su L, Tong Y, Chen H, Wang H, Zhao J, Xia H, Zhang Y, Zhang R. Epistatic Association of CD14 and NOTCH2 Genetic Polymorphisms with Biliary Atresia in a Southern Chinese Population. Mol Ther Nucleic Acids 2018;13:590-5. [PMID: 30439647 DOI: 10.1016/j.omtn.2018.10.006] [Cited by in Crossref: 1] [Article Influence: 0.3] [Reference Citation Analysis]
26 Song W, Sun LY, Zhu ZJ. Effects of Previous Kasai Surgery on Gut Microbiota and Bile Acid in Biliary Atresia With End-Stage Liver Disease. Front Med (Lausanne) 2021;8:704328. [PMID: 34646837 DOI: 10.3389/fmed.2021.704328] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
27 Ziogas IA, Ye F, Zhao Z, Cao S, Rauf MA, Izzy M, Matsuoka LK, Gillis LA, Alexopoulos SP. Mortality Determinants in Children with Biliary Atresia Awaiting Liver Transplantation. J Pediatr 2021;228:177-82. [PMID: 32950533 DOI: 10.1016/j.jpeds.2020.09.005] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
28 Taylor SA, Venkat V, Arnon R, Gopalareddy VV, Rosenthal P, Erinjeri J, Anand R, Daniel JF. Improved Outcomes for Liver Transplantation in Patients with Biliary Atresia Since Pediatric End-Stage Liver Disease Implementation: Analysis of the Society of Pediatric Liver Transplantation Registry. The Journal of Pediatrics 2020;219:89-97. [DOI: 10.1016/j.jpeds.2019.12.023] [Cited by in Crossref: 6] [Cited by in F6Publishing: 2] [Article Influence: 3.0] [Reference Citation Analysis]
29 Petersen C. Biliary atresia: unity in diversity. Pediatr Surg Int 2017;33:1255-61. [PMID: 28983682 DOI: 10.1007/s00383-017-4156-6] [Cited by in Crossref: 6] [Cited by in F6Publishing: 3] [Article Influence: 1.2] [Reference Citation Analysis]
30 Tambucci R, de Magnée C, Szabo M, Channaoui A, Pire A, de Meester de Betzenbroeck V, Scheers I, Stephenne X, Smets F, Sokal EM, Reding R. Sequential Treatment of Biliary Atresia With Kasai Hepatoportoenterostomy and Liver Transplantation: Benefits, Risks, and Outcome in 393 Children. Front Pediatr 2021;9:697581. [PMID: 34307260 DOI: 10.3389/fped.2021.697581] [Reference Citation Analysis]
31 Malik A, Thanekar U, Mourya R, Shivakumar P. Recent developments in etiology and disease modeling of biliary atresia: a narrative review. Dig Med Res 2020;3:59. [PMID: 33615212 DOI: 10.21037/dmr-20-97] [Reference Citation Analysis]
32 Parolini F, Boroni G, Betalli P, Cheli M, Pinelli D, Colledan M, Alberti D. Extended Adhesion-Sparing Liver Eversion during Kasai Portoenterostomy for Infants with Biliary Atresia. Children (Basel) 2021;8:820. [PMID: 34572252 DOI: 10.3390/children8090820] [Reference Citation Analysis]
33 Azeltine MW, Chavez EJ, Nemec KM, Bednarek JM, Asokan R, Balasubramaniyan N, Zgheib C, Mack CL, Roach JP. Inflammation Drives MicroRNAs to Limit Hepatocyte Bile Acid Transport in Murine Biliary Atresia. J Surg Res 2020;256:663-72. [PMID: 32818799 DOI: 10.1016/j.jss.2020.07.003] [Reference Citation Analysis]
34 Lendahl U, Lui VCH, Chung PHY, Tam PKH. Biliary Atresia - emerging diagnostic and therapy opportunities. EBioMedicine 2021;74:103689. [PMID: 34781099 DOI: 10.1016/j.ebiom.2021.103689] [Reference Citation Analysis]
35 Tessier MEM, Shneider BL, Brandt ML, Cerminara DN, Harpavat S. A phase 2 trial of N-Acetylcysteine in Biliary atresia after Kasai portoenterostomy. Contemp Clin Trials Commun 2019;15:100370. [PMID: 31193715 DOI: 10.1016/j.conctc.2019.100370] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 0.7] [Reference Citation Analysis]
36 Machhua S, Kumar Y, Prakash Kanojia R, Bhatia A, Thapa BR, Walker Minz R, Kumar Ram A, Dhawan V. An improved and easy protocol for primary epithelial cell culture from atretic tissue in biliary atresia. Tissue Cell 2019;56:83-9. [PMID: 30736909 DOI: 10.1016/j.tice.2019.01.001] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
37 Kelley-Quon LI, Shue E, Burke RV, Smith C, Kling K, Mahdi E, Ourshalimian S, Fenlon M, Dellinger M, Shew SB, Lee J, Padilla B, Inge T, Roach J, Marwan AI, Russell KW, Ignacio R, Fialkowski E, Nijagal A, Im C, Azarow KS, Ostlie DJ, Wang K. The need for early Kasai portoenterostomy: a Western Pediatric Surgery Research Consortium study. Pediatr Surg Int 2021. [PMID: 34854975 DOI: 10.1007/s00383-021-05047-1] [Reference Citation Analysis]
38 Duan X, Peng Y, Liu W, Yang L, Zhang J. Does Supersonic Shear Wave Elastography Help Differentiate Biliary Atresia from Other Causes of Cholestatic Hepatitis in Infants Less than 90 Days Old? Compared with Grey-Scale US. Biomed Res Int 2019;2019:9036362. [PMID: 31275991 DOI: 10.1155/2019/9036362] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
39 Squires JE, Ng VL, Hawthorne K, Henn LL, Sorensen LG, Fredericks EM, Alonso EM, Murray KF, Loomes KM, Karpen SJ, Cavallo LA, Molleston JP, Bezerra JA, Rosenthal P, Squires RH, Wang KS, Schwarz KB, Arnon R, Magee JC, Sokol RJ; Childhood Liver Disease Research Network (ChiLDReN). Neurodevelopmental Outcomes in Preschool and School Aged Children With Biliary Atresia and Their Native Liver. J Pediatr Gastroenterol Nutr 2020;70:79-86. [PMID: 31503218 DOI: 10.1097/MPG.0000000000002489] [Cited by in Crossref: 3] [Article Influence: 3.0] [Reference Citation Analysis]
40 Covarrubias K, Luo X, Massie A, Schwarz KB, Garonzik-Wang J, Segev DL, Mogul DB. Determinants of length of stay after pediatric liver transplantation. Pediatr Transplant 2020;24:e13702. [PMID: 32212292 DOI: 10.1111/petr.13702] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.5] [Reference Citation Analysis]
41 Chung PHY, Chok KSH, Wong KKY, Tam PKH, Lo CM. Determining the optimal timing of liver transplant for pediatric patients after Kasai portoenterostomy based on disease severity scores. J Pediatr Surg 2020;55:1892-6. [PMID: 31759650 DOI: 10.1016/j.jpedsurg.2019.10.016] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.7] [Reference Citation Analysis]
42 Feldman AG, Sokol RJ. Neonatal Cholestasis: Updates on Diagnostics, Therapeutics, and Prevention. Neoreviews 2021;22:e819-36. [PMID: 34850148 DOI: 10.1542/neo.22-12-e819] [Reference Citation Analysis]
43 Li Y, Gan J, Wang C, Xu Z, Zhao Y, Ji Y. Comparison of laparoscopic portoenterostomy and open portoenterostomy for the treatment of biliary atresia. Surg Endosc 2019;33:3143-52. [PMID: 31190228 DOI: 10.1007/s00464-019-06905-9] [Cited by in Crossref: 7] [Cited by in F6Publishing: 4] [Article Influence: 2.3] [Reference Citation Analysis]
44 Sun Y, Jia L, Yu H, Zhu M, Sheng M, Yu W. The Effect of Pediatric Living Donor Liver Transplantation on Neurocognitive Outcomes in Children. Ann Transplant 2019;24:446-53. [PMID: 31371696 DOI: 10.12659/AOT.914164] [Cited by in Crossref: 2] [Article Influence: 0.7] [Reference Citation Analysis]
45 Udomsinprasert W, Angkathunyakul N, Jittikoon J, Chaikledkaew U, Vejchapipat P, Poovorawan Y, Honsawek S. Cartilage oligomeric matrix protein as a marker of progressive liver fibrosis in biliary atresia. Sci Rep 2021;11:16695. [PMID: 34404836 DOI: 10.1038/s41598-021-95805-x] [Reference Citation Analysis]
46 Pang WB, Zhang TC, Chen YJ, Peng CH, Wang ZM, Wu DY, Wang K. Ten-Year Experience in the Prevention of Post-Kasai Cholangitis. Surg Infect (Larchmt) 2019;20:231-5. [PMID: 30657432 DOI: 10.1089/sur.2018.047] [Cited by in Crossref: 3] [Article Influence: 1.0] [Reference Citation Analysis]
47 Pu S, Jin S, Xiang B, Yang J, Li K, Xie X, Huang B, Lai W, Yan L, Zhang M, Dong C. The current status and outcomes of pediatric liver transplantation in western China: A multi-center retrospective study. Pediatr Transplant 2020;24:e13810. [PMID: 32845541 DOI: 10.1111/petr.13810] [Reference Citation Analysis]
48 Hukkinen M, Kerola A, Lohi J, Heikkilä P, Merras-Salmio L, Jahnukainen T, Koivusalo A, Jalanko H, Pakarinen MP. Treatment Policy and Liver Histopathology Predict Biliary Atresia Outcomes: Results after National Centralization and Protocol Biopsies. J Am Coll Surg 2018;226:46-57.e1. [PMID: 28958913 DOI: 10.1016/j.jamcollsurg.2017.09.009] [Cited by in Crossref: 22] [Cited by in F6Publishing: 19] [Article Influence: 4.4] [Reference Citation Analysis]
49 Bednarek J, Traxinger B, Brigham D, Roach J, Orlicky D, Wang D, Pelanda R, Mack CL. Cytokine-Producing B Cells Promote Immune-Mediated Bile Duct Injury in Murine Biliary Atresia. Hepatology 2018;68:1890-904. [PMID: 29679373 DOI: 10.1002/hep.30051] [Cited by in Crossref: 10] [Cited by in F6Publishing: 11] [Article Influence: 2.5] [Reference Citation Analysis]
50 Boo YA, Chang MH, Jeng YM, Peng SF, Hsu WM, Lin WH, Chen HL, Ni YH, Hsu HY, Wu JF. Diagnostic Performance of Transient Elastography in Biliary Atresia Among Infants With Cholestasis. Hepatol Commun 2021;5:882-90. [PMID: 34027275 DOI: 10.1002/hep4.1672] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
51 Kang Y, Park S, Kim S, Han SJ, Koh H. Validating the BAVENO VI criteria to identify low risk biliary atresia patients without endoscopy for esophageal varix. Clin Res Hepatol Gastroenterol 2021;45:101437. [PMID: 32417223 DOI: 10.1016/j.clinre.2020.04.007] [Reference Citation Analysis]
52 Feldman AG, Sokol RJ. Neonatal cholestasis: emerging molecular diagnostics and potential novel therapeutics. Nat Rev Gastroenterol Hepatol 2019;16:346-60. [PMID: 30903105 DOI: 10.1038/s41575-019-0132-z] [Cited by in Crossref: 32] [Cited by in F6Publishing: 26] [Article Influence: 10.7] [Reference Citation Analysis]
53 Pakarinen MP, Johansen LS, Svensson JF, Bjørnland K, Gatzinsky V, Stenström P, Koivusalo A, Kvist N, Almström M, Emblem R, Björnsson S, Backman T, Almaas R, Jalanko H, Fischler B, Thorup J; Nordic Pediatric Surgery Study Consortium. Outcomes of biliary atresia in the Nordic countries - a multicenter study of 158 patients during 2005-2016. J Pediatr Surg 2018;53:1509-15. [PMID: 28947328 DOI: 10.1016/j.jpedsurg.2017.08.048] [Cited by in Crossref: 19] [Cited by in F6Publishing: 16] [Article Influence: 3.8] [Reference Citation Analysis]
54 Feldman AG, Sokol RJ. Recent developments in diagnostics and treatment of neonatal cholestasis. Semin Pediatr Surg 2020;29:150945. [PMID: 32861449 DOI: 10.1016/j.sempedsurg.2020.150945] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
55 Sonoda S, Yoshimaru K, Yamaza H, Yuniartha R, Matsuura T, Yamauchi-Tomoda E, Murata S, Nishida K, Oda Y, Ohga S, Tajiri T, Taguchi T, Yamaza T. Biliary atresia-specific deciduous pulp stem cells feature biliary deficiency. Stem Cell Res Ther 2021;12:582. [PMID: 34809720 DOI: 10.1186/s13287-021-02652-8] [Reference Citation Analysis]
56 Wang Z, Chen Y, Peng C, Pang W, Zhang T, Wu D, Shen Q, Li M. Five-year native liver survival analysis in biliary atresia from a single large Chinese center: The death/liver transplantation hazard change and the importance of rapid early clearance of jaundice.J Pediatr Surg. 2019;54:1680-1685. [PMID: 30518490 DOI: 10.1016/j.jpedsurg.2018.09.025] [Cited by in Crossref: 6] [Cited by in F6Publishing: 5] [Article Influence: 1.5] [Reference Citation Analysis]
57 Catzola A, Vajro P. Management options for cholestatic liver disease in children. Expert Review of Gastroenterology & Hepatology 2017;11:1019-30. [DOI: 10.1080/17474124.2017.1359538] [Cited by in Crossref: 12] [Cited by in F6Publishing: 8] [Article Influence: 2.4] [Reference Citation Analysis]
58 Ochi T, Nakamura H, Wada M, Tamura T, Koga H, Okazaki T, Urao M, Ishizaki Y, Kawasaki S, Kasahara M, Mizuta K, Lane GJ, Yamataka A. Liver transplantation for deterioration in native liver function after portoenterostomy for biliary atresia in Japan: Short- versus long-term survivors. Journal of Pediatric Surgery 2018;53:277-80. [DOI: 10.1016/j.jpedsurg.2017.11.016] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 0.8] [Reference Citation Analysis]
59 Di Dato F, Ranucci G, de Ville de Goyet J, Alberti D, Iorio R. Unusual Clinical Course for Untreated Malformative Biliary Atresia Infant: Is Portal Hypertension an Important Driver of Liver Fibrosis? J Pediatr Gastroenterol Nutr 2021;72:216-9. [PMID: 32925558 DOI: 10.1097/MPG.0000000000002932] [Reference Citation Analysis]
60 Du M, Wang J, Tang Y, Jiang J, Chen G, Huang Y, Shen Z, Dong R, Zheng S. Evaluation of Perioperative Complications in the Management of Biliary Atresia. Front Pediatr 2020;8:460. [PMID: 33014917 DOI: 10.3389/fped.2020.00460] [Cited by in Crossref: 1] [Article Influence: 0.5] [Reference Citation Analysis]
61 Nakamura H, Ara M, Koga H, Miyano G, Okawada M, Doi T, Lane GJ, Okazaki T, Urao M, Yamataka A. Duration from the first pale stool to portoenterostomy is prognostic in biliary atresia. Comparison with age at portoenterostomy. Clin Res Hepatol Gastroenterol 2021;45:101584. [PMID: 33744827 DOI: 10.1016/j.clinre.2020.11.014] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
62 Bezerra JA, Wells RG, Mack CL, Karpen SJ, Hoofnagle JH, Doo E, Sokol RJ. Biliary Atresia: Clinical and Research Challenges for the Twenty-First Century. Hepatology 2018;68:1163-73. [PMID: 29604222 DOI: 10.1002/hep.29905] [Cited by in Crossref: 64] [Cited by in F6Publishing: 62] [Article Influence: 21.3] [Reference Citation Analysis]
63 Mazzoni BP, Lessa BV, Zamberlan P. METABOLIC AND NUTRITIONAL REPERCUSSIONS OF LIVER DISEASE ON CHILDREN: HOW TO MINIMIZE THEM? Rev Paul Pediatr 2021;40:e2020149. [PMID: 34076201 DOI: 10.1590/1984-0462/2022/40/2020149] [Reference Citation Analysis]
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