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For: Timpanaro T, Passanisi S, Sauna A, Trombatore C, Pennisi M, Petrillo G, Smilari P, Greco F. Congenital portosystemic shunt: our experience. Case Rep Pediatr 2015;2015:691618. [PMID: 25709849 DOI: 10.1155/2015/691618] [Cited by in Crossref: 8] [Cited by in F6Publishing: 6] [Article Influence: 1.1] [Reference Citation Analysis]
Number Citing Articles
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5 Jaklitsch M, Sobral M, Carvalho AM, Marques HP. Abernethy malformation and hepatocellular carcinoma: a serious consequence of a rare disease. BMJ Case Rep 2020;13:e231843. [PMID: 31911408 DOI: 10.1136/bcr-2019-231843] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 1.5] [Reference Citation Analysis]
6 Majid Z, Haque MMU, Ashraf MD, Luck NH, Lalwani AK. Intrahepatic Portosystemic Shunt in a Young Female: Views from a Developing Country. J Transl Int Med 2019;7:118-20. [PMID: 31637183 DOI: 10.2478/jtim-2019-0017] [Reference Citation Analysis]
7 Mreish S, Hamdan MA. Pre and postnatal diagnosis of congenital portosystemic shunt: Impact of interventional therapy. Int J Pediatr Adolesc Med 2020;7:127-31. [PMID: 33094141 DOI: 10.1016/j.ijpam.2019.02.009] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
8 Yangın-Ergon E, Ermis N, Colak R, Polat B, Alkan-Ozdemir S, Yıldız M, Kulalı F, Omur-Ecevit C, Ergun O, Calkavur S. Abernethy Malformation Type 2 and Biliary Atresia Coexistence: A Rare Cause of Infantile Liver Transplant. Euroasian J Hepatogastroenterol 2018;8:163-6. [PMID: 30828559 DOI: 10.5005/jp-journals-10018-1283] [Cited by in Crossref: 4] [Cited by in F6Publishing: 2] [Article Influence: 1.3] [Reference Citation Analysis]
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