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For: Sanchez-Valle A, Kassira N, Varela VC, Radu SC, Paidas C, Kirby RS. Biliary Atresia: Epidemiology, Genetics, Clinical Update, and Public Health Perspective. Adv Pediatr. 2017;64:285-305. [PMID: 28688594 DOI: 10.1016/j.yapd.2017.03.012] [Cited by in Crossref: 24] [Cited by in F6Publishing: 23] [Article Influence: 6.0] [Reference Citation Analysis]
Number Citing Articles
1 Schreiber RA, Harpavat S, Hulscher JBF, Wildhaber BE. Biliary Atresia in 2021: Epidemiology, Screening and Public Policy. J Clin Med 2022;11:999. [PMID: 35207269 DOI: 10.3390/jcm11040999] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
2 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]
3 Wang Y, Jia LQ, Hu YX, Xin Y, Yang X, Wang XM. Development and Validation of a Nomogram Incorporating Ultrasonic and Elastic Findings for the Preoperative Diagnosis of Biliary Atresia. Acad Radiol 2021;28 Suppl 1:S55-63. [PMID: 32972841 DOI: 10.1016/j.acra.2020.08.035] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 3.0] [Reference Citation Analysis]
4 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]
5 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]
6 Tam PKH, Yiu RS, Lendahl U, Andersson ER. Cholangiopathies - Towards a molecular understanding. EBioMedicine 2018;35:381-93. [PMID: 30236451 DOI: 10.1016/j.ebiom.2018.08.024] [Cited by in Crossref: 11] [Cited by in F6Publishing: 9] [Article Influence: 2.8] [Reference Citation Analysis]
7 Angelico R, Liccardo D, Paoletti M, Pietrobattista A, Basso MS, Mosca A, Safarikia S, Grimaldi C, Saffioti MC, Candusso M, Maggiore G, Spada M. A novel mobile phone application for infant stool color recognition: An easy and effective tool to identify acholic stools in newborns. J Med Screen 2021;28:230-7. [PMID: 33241758 DOI: 10.1177/0969141320974413] [Reference Citation Analysis]
8 Schreiber RA. Newborn Screening for Biliary Atresia. JAMA 2020;323:1137-8. [PMID: 32207779 DOI: 10.1001/jama.2020.2727] [Cited by in Crossref: 5] [Cited by in F6Publishing: 4] [Article Influence: 2.5] [Reference Citation Analysis]
9 Gao E, Hercun J, Heller T, Vilarinho S. Undiagnosed liver diseases. Transl Gastroenterol Hepatol 2021;6:28. [PMID: 33824932 DOI: 10.21037/tgh.2020.04.04] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
10 Zhou Y, Ji H, Xu Q, Zhang X, Cao X, Chen Y, Shao M, Wu Z, Zhang J, Lu C, Yang J, Shi Y, Bu H. Congenital biliary atresia is correlated with disrupted cell junctions and polarity caused by Cdc42 insufficiency in the liver. Theranostics 2021;11:7262-75. [PMID: 34158849 DOI: 10.7150/thno.49116] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
11 Ceza MR, Garcia E, Anselmi CE, Epifanio M, Melere MU, Ferreira CT, Steinhaus C, Coral GP. Prevalence and characteristics of hepatopulmonary syndrome in children with cirrhosis in southern Brazil. European Journal of Gastroenterology & Hepatology 2019;31:10-5. [DOI: 10.1097/meg.0000000000001207] [Cited by in Crossref: 5] [Cited by in F6Publishing: 1] [Article Influence: 1.7] [Reference Citation Analysis]
12 Hinojosa-Gonzalez DE, Bueno LC, Roblesgil-Medrano A, Salgado-Garza G, Hurtado-Arellano S, Farias JS, Torres-Martinez M, Escarcega-Bordagaray JA, Salan-Gomez M, Flores-Villalba E. Laparoscopic vs open portoenterostomy in biliary atresia: a systematic review and meta-analysis. Pediatr Surg Int 2021. [PMID: 34269866 DOI: 10.1007/s00383-021-04964-5] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
13 Babu RO, Lui VCH, Chen Y, Yiu RSW, Ye Y, Niu B, Wu Z, Zhang R, Yu MON, Chung PHY, Wong KKY, Xia H, Zhang MQ, Wang B, Lendahl U, Tam PKH. Beta-amyloid deposition around hepatic bile ducts is a novel pathobiological and diagnostic feature of biliary atresia. J Hepatol 2020;73:1391-403. [PMID: 32553668 DOI: 10.1016/j.jhep.2020.06.012] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 2.5] [Reference Citation Analysis]
14 Gad EH, Kamel Y, Salem TA, Ali MA, Sallam AN. Short- and long-term outcomes after Kasai operation for type III biliary atresia: Twenty years of experience in a single tertiary Egyptian center-A retrospective cohort study. Ann Med Surg (Lond) 2021;62:302-14. [PMID: 33552489 DOI: 10.1016/j.amsu.2021.01.052] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
15 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]
16 Vij M, Rela M. Biliary atresia: pathology, etiology and pathogenesis. Future Sci OA 2020;6:FSO466. [PMID: 32518681 DOI: 10.2144/fsoa-2019-0153] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 3.0] [Reference Citation Analysis]
17 Ohyama K, Fujikawa A, Okamura T, Furuta S, Nagae H, Tanaka K, Kawaguchi T, Nishiya Y, Kudo K, Kawase H, Kitagawa H. The triangular cord ratio and the presence of a cystic lesion in the triangular cord. Suggested new ultrasound findings in the early diagnosis of Biliary Atresia. Pediatr Surg Int 2021;37:1693-7. [PMID: 34524521 DOI: 10.1007/s00383-021-04997-w] [Reference Citation Analysis]
18 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]
19 Blachman-Braun R, Lopez-Verdugo F, Alonso D, Book L, Feola GP, Rodriguez-Davalos MI. Revision of meso-Rex bypass utilizing a collateral vein in a patient with portal steal phenomenon after liver transplant: A case report. Int J Surg Case Rep 2019;60:230-3. [PMID: 31252380 DOI: 10.1016/j.ijscr.2019.05.051] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
20 Shin HJ, Yoon H, Kim MJ, Han SJ, Koh H, Kim S, Lee MJ. Liver intravoxel incoherent motion diffusion-weighted imaging for the assessment of hepatic steatosis and fibrosis in children. World J Gastroenterol 2018; 24(27): 3013-3020 [PMID: 30038468 DOI: 10.3748/wjg.v24.i27.3013] [Cited by in CrossRef: 9] [Cited by in F6Publishing: 9] [Article Influence: 2.3] [Reference Citation Analysis]
21 Xu X, Zhan J. Biliary atresia in twins: a systematic review and meta-analysis. Pediatr Surg Int 2020;36:953-8. [PMID: 32504124 DOI: 10.1007/s00383-020-04690-4] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 1.5] [Reference Citation Analysis]
22 Cheung Y, Wu Z, Garcia-Barcelo MM, Tam PKH, Ma ACH, Lui VCH. Deletion of interleukin enhancer binding factor 2 (ILF2) resulted in defective biliary development and bile flow blockage. J Pediatr Surg 2021;56:352-9. [PMID: 32709532 DOI: 10.1016/j.jpedsurg.2020.06.032] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
23 Ranucci G, Della Corte C, Alberti D, Bondioni MP, Boroni G, Calvo PL, Cananzi M, Candusso M, Clemente MG, D'Antiga L, Degrassi I, De Ville De Goyet J, Di Dato F, Di Giorgio A, Vici CD, Ferrari F, Francalanci P, Fuoti M, Fusaro F, Gaio P, Grimaldi C, Iascone M, Indolfi G, Iorio R, Maggiore G, Mandato C, Matarazzo L, Monti L, Mosca F, Nebbia G, Nuti F, Paolella G, Pinon M, Roggero P, Sciveres M, Serranti D, Spada M, Vajro P, Nicastro E. Diagnostic approach to neonatal and infantile cholestasis: A position paper by the SIGENP liver disease working group. Dig Liver Dis 2021:S1590-8658(21)00780-5. [PMID: 34688573 DOI: 10.1016/j.dld.2021.09.011] [Reference Citation Analysis]
24 Gad EH, Kamel Y, Salem TA, Ali MA, Sallam AN. Short- and long-term outcomes after Kasai operation for type III biliary atresia: Twenty years of experience in a single tertiary Egyptian center-A retrospective cohort study. Ann Med Surg (Lond) 2021;62:302-14. [PMID: 33552489 DOI: 10.1016/j.amsu.2021.01.052] [Reference Citation Analysis]
25 Virani S, Akers A, Stephenson K, Smith S, Kennedy L, Alpini G, Francis H. Comprehensive Review of Molecular Mechanisms during Cholestatic Liver Injury and Cholangiocarcinoma. J Liver 2018;7:231. [PMID: 30613437 DOI: 10.4172/2167-0889.1000231] [Cited by in Crossref: 2] [Cited by in F6Publishing: 4] [Article Influence: 0.5] [Reference Citation Analysis]
26 Lupo PJ, Isenburg JL, Salemi JL, Mai CT, Liberman RF, Canfield MA, Copeland G, Haight S, Harpavat S, Hoyt AT, Moore CA, Nembhard WN, Nguyen HN, Rutkowski RE, Steele A, Alverson CJ, Stallings EB, Kirby RS; and The National Birth Defects Prevention Network. Population-based birth defects data in the United States, 2010-2014: A focus on gastrointestinal defects. Birth Defects Res 2017;109:1504-14. [PMID: 29152924 DOI: 10.1002/bdr2.1145] [Cited by in Crossref: 33] [Cited by in F6Publishing: 25] [Article Influence: 8.3] [Reference Citation Analysis]
27 Jiao C, Yu K, Li D, Fu K, Wang P, He Y, Feng J. A retrospective study of the ideal operation time for preterm biliary atresia patients. Pediatr Surg Int 2019;35:679-84. [DOI: 10.1007/s00383-019-04464-7] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
28 Sangkhathat S, Laochareonsuk W, Maneechay W, Kayasut K, Chiengkriwate P. Variants Associated with Infantile Cholestatic Syndromes Detected in Extrahepatic Biliary Atresia by Whole Exome Studies: A 20-Case Series from Thailand. J Pediatr Genet 2018;7:67-73. [PMID: 29707407 DOI: 10.1055/s-0038-1632395] [Cited by in Crossref: 8] [Cited by in F6Publishing: 5] [Article Influence: 2.0] [Reference Citation Analysis]
29 He L, Ip DKM, Tam G, Lui VCH, Tam PKH, Chung PHY. Biomarkers for the diagnosis and post-Kasai portoenterostomy prognosis of biliary atresia: a systematic review and meta-analysis. Sci Rep 2021;11:11692. [PMID: 34083585 DOI: 10.1038/s41598-021-91072-y] [Reference Citation Analysis]
30 Ho A, Sacks MA, Sapra A, Khan FA. The Utility of Gallbladder Absence on Ultrasound for Children With Biliary Atresia. Front Pediatr 2021;9:685268. [PMID: 34268279 DOI: 10.3389/fped.2021.685268] [Reference Citation Analysis]
31 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]
32 Apostu RC, Fagarasan V, Ciuce CC, Drasovean R, Gheban D, Scurtu RR, Grama A, Stefanescu AC, Ciuce C, Pop TL. Biological and Histological Assessment of the Hepatoportoenterostomy Role in Biliary Atresia as a Stand-Alone Procedure or as a Bridge toward Liver Transplantation. Medicina (Kaunas) 2020;57:16. [PMID: 33379246 DOI: 10.3390/medicina57010016] [Reference Citation Analysis]