A rare cause of congenital portosystemic shunt: Type 2 Abernethy malformation

ArticleAçık Erişim

Özet

patient and to discuss the imaging findings of Abernethy malformation. Copyright © 2020 Via Medica

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RDL Kalıcı Bağlantı (PID)
https://rdlopen.rawdatalibrary.net/r/ebyu/13944Resmi atıflarda kullanılan kalıcı adres
DOI
https://doi.org/10.5603/fm.a2019.0063Yayıncı resmi DOI adresi
Tam Kayıt
AlanDeğerDil
dc.contributor.authorTaydas, O.
dc.contributor.authorDanisan, G.
dc.contributor.authorOgul, H.
dc.contributor.authorKantarci, M.
dc.date.accessioned2026-10-18T20:28:44.736288975Z
dc.date.available2026-10-18T20:28:44.736288975Z
dc.date.issued2020
dc.description.abstractpatient and to discuss the imaging findings of Abernethy malformation. Copyright © 2020 Via Medica
dc.identifier.doi10.5603/fm.a2019.0063
dc.identifier.eissn1644-3284
dc.identifier.endpage175
dc.identifier.issn0015-5659
dc.identifier.issue1
dc.identifier.pmid31282554
dc.identifier.scopus2-s2.0-85081941121
dc.identifier.startpage172
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/ebyu/13944
dc.identifier.volume79
dc.identifier.wosWOS:000518814400025
dc.language.isoen
dc.publisherVia Medica
dc.relation.ispartofFolia Morphologica (Poland)
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectAbernethy malformation
dc.subjectMagnetic resonance imaging
dc.subjectRadiology
dc.subjectAdolescent
dc.subjectHumans
dc.subjectMale
dc.subjectPortal Vein
dc.subjectVascular Malformations
dc.subjectcase report
dc.subjectcongenital blood vessel malformation
dc.subjectdiagnostic imaging
dc.subjecthepatic portal vein
dc.subjecthuman
dc.subjectnuclear magnetic resonance imaging
dc.subjectpathology
dc.titleA rare cause of congenital portosystemic shunt: Type 2 Abernethy malformation
dc.typeArticle
dspace.entity.typePublication
rdl.citation.scopus3
rdl.citation.wos2
rdl.oa.statusgold
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.wos.indexScience Citation Index Expanded (SCI-EXPANDED)