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Cited by in F6Publishing
For: 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]
Number Citing Articles
1 Liu JQ, Chen WJ, Zhou MJ, Li WF, Tang J, Zhou QC. A Nomogram Predicting the Prognosis of Children With Biliary Atresia After Hepatoportoenterostomy. Front Pediatr 2021;9:641318. [PMID: 33718307 DOI: 10.3389/fped.2021.641318] [Reference Citation Analysis]
2 Zhang Y, Wang Q, Pu S, Wang J, Xiang B, Liu J, Jin S. A Novel Model for Predicting the Clearance of Jaundice in Patients With Biliary Atresia After Kasai Procedure. Front Pediatr 2022;10:837247. [DOI: 10.3389/fped.2022.837247] [Reference Citation Analysis]
3 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]
4 Hukkinen M, Ruuska S, Pihlajoki M, Kyrönlahti A, Pakarinen MP. Long-term outcomes of biliary atresia patients surviving with their native livers. Best Pract Res Clin Gastroenterol 2022;56-57:101764. [PMID: 35331404 DOI: 10.1016/j.bpg.2021.101764] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
5 Hanalioğlu D, Özen H, Karhan A, Gümüş E, Demir H, Saltık-Temizel İN, Ekinci S, Karnak İ, Çiftçi AO, Tanyel FC, Yüce A. Revisiting long-term prognostic factors of biliary atresia: A 20-year experience with 81 patients from a single center. Turk J Gastroenterol 2019;30:467-74. [PMID: 31061002 DOI: 10.5152/tjg.2019.18590] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
6 Sergi CM, Gilmour S. Biliary Atresia: A Complex Hepatobiliary Disease with Variable Gene Involvement, Diagnostic Procedures, and Prognosis. Diagnostics 2022;12:330. [DOI: 10.3390/diagnostics12020330] [Reference Citation Analysis]
7 Nomden M, Beljaars L, Verkade HJ, Hulscher JBF, Olinga P. Current Concepts of Biliary Atresia and Matrix Metalloproteinase-7: A Review of Literature. Front Med (Lausanne) 2020;7:617261. [PMID: 33409288 DOI: 10.3389/fmed.2020.617261] [Reference Citation Analysis]