BPG is committed to discovery and dissemination of knowledge
Cited by in F6Publishing
For: Rajeswaran S, Johnston A, Green J, Riaz A, Thornburg B, Mouli S, Lautz T, Lemoine C, Superina R, Donaldson J. Abernethy Malformations: Evaluation and Management of Congenital Portosystemic Shunts. Journal of Vascular and Interventional Radiology 2020;31:788-94. [DOI: 10.1016/j.jvir.2019.08.007] [Cited by in Crossref: 7] [Cited by in F6Publishing: 11] [Article Influence: 3.5] [Reference Citation Analysis]
Number Citing Articles
1 Donato P, Facas J, Alves FC. Hepatic Vascular Disorders: From Diagnosis to Interventional Radiology. Seminars in Ultrasound, CT and MRI 2022. [DOI: 10.1053/j.sult.2022.06.005] [Reference Citation Analysis]
2 Ghasemi-rad M, Smuclovisky E, Cleveland H, Hernandez JA. Endovascular treatment of a portosystemic shunt presenting with hypoglycemia; case presentation and review of literature. Clinical Imaging 2022;83:131-7. [DOI: 10.1016/j.clinimag.2021.12.020] [Reference Citation Analysis]
3 Leshen MA, Devanagondi R, Saul D, Chaturvedi A. Physiological fetal vascular shunts and failure to regress: what the radiologist needs to know. Pediatr Radiol 2022. [PMID: 35166890 DOI: 10.1007/s00247-022-05302-0] [Reference Citation Analysis]
4 Bombardier B, Alli A, Rohr A, Collins Z, Raval K. A case of two shunts in the endovascular treatment of type II Abernethy syndrome. CVIR Endovasc 2022;5:3. [PMID: 34985620 DOI: 10.1186/s42155-021-00279-7] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
5 Facas J, Cruz M, Costa JF, Agostinho A, Donato P. Multistage closure of a congenital extrahepatic portosystemic shunt. CVIR Endovasc 2021;4:79. [PMID: 34792654 DOI: 10.1186/s42155-021-00267-x] [Reference Citation Analysis]
6 Andrade G, Facas J, Marques P, Mónica AN, Donato P. Congenital extrahepatic portosystemic shunt type II occluded with cardiac closure device. Radiol Case Rep 2021;16:3802-6. [PMID: 34691344 DOI: 10.1016/j.radcr.2021.09.020] [Reference Citation Analysis]
7 Namgoong JM, Hwang S, Park GC, Kwon H, Kim KM, Oh SH. Living donor liver transplantation in a pediatric patient with congenital absence of the portal vein. Ann Hepatobiliary Pancreat Surg 2021;25:401-7. [PMID: 34402443 DOI: 10.14701/ahbps.2021.25.3.401] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
8 Marra P, Dulcetta L, Pellegrinelli C, D'Antiga L, Sironi S. Percutaneous transhepatic treatment of a unique portal vein malformation with portal hypertension in a pediatric patient. CVIR Endovasc 2021;4:47. [PMID: 34097180 DOI: 10.1186/s42155-021-00239-1] [Reference Citation Analysis]
9 Figueras-Coll M, Sabaté-Rotés A, Iglesias-Serrano I, Peñas-Aguilera A, Pérez-Lafuente M. Abernethy Malformation: An Unusual Extrathoracic Cause of Chronic Hypoxemia in Pediatrics. Arch Bronconeumol (Engl Ed) 2021:S0300-2896(21)00062-4. [PMID: 33714659 DOI: 10.1016/j.arbres.2021.02.005] [Reference Citation Analysis]
10 Northup PG, Garcia-Pagan JC, Garcia-Tsao G, Intagliata NM, Superina RA, Roberts LN, Lisman T, Valla DC. Vascular Liver Disorders, Portal Vein Thrombosis, and Procedural Bleeding in Patients With Liver Disease: 2020 Practice Guidance by the American Association for the Study of Liver Diseases. Hepatology 2021;73:366-413. [PMID: 33219529 DOI: 10.1002/hep.31646] [Cited by in Crossref: 100] [Cited by in F6Publishing: 89] [Article Influence: 100.0] [Reference Citation Analysis]
11 Chiang J, Chiu HK, Moriarty JM, McWilliams JP. Hyperandrogenism and malignant degeneration of hepatic adenomas in the setting of Abernethy malformation. Radiol Case Rep 2020;15:2701-5. [PMID: 33117471 DOI: 10.1016/j.radcr.2020.10.026] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 0.5] [Reference Citation Analysis]