{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"omics_type":["Unknown"],"volume":["67(5)"],"submitter":["Rajesh GN"],"pubmed_abstract":["Pulmonary arteriovenous malformations (AVM) are very rare and carry the risk of cerebral thrombo-embolism, brain abscess or pulmonary hemorrhage. The Amplatzer vascular plug II (AVP II) is a new device, used for embolization of the pulmonary AVMs. We report a case of pulmonary AVM successfully managed by using AVP II in a patient with hereditary hemorrhagic telangiectasia (HHT)."],"journal":["Indian heart journal"],"pagination":["455-8"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC4593798"],"repository":["biostudies-literature"],"pubmed_title":["Device closure of pulmonary arteriovenous malformation using Amplatzer vascular plug II in hereditary hemorrhagic telangiectasia."],"pmcid":["PMC4593798"],"pubmed_authors":["Rajesh GN","Haridasan V","Krishnan MN","Sajeer K","Nair A","Sajeev CG"],"additional_accession":[]},"is_claimable":false,"name":"Device closure of pulmonary arteriovenous malformation using Amplatzer vascular plug II in hereditary hemorrhagic telangiectasia.","description":"Pulmonary arteriovenous malformations (AVM) are very rare and carry the risk of cerebral thrombo-embolism, brain abscess or pulmonary hemorrhage. The Amplatzer vascular plug II (AVP II) is a new device, used for embolization of the pulmonary AVMs. We report a case of pulmonary AVM successfully managed by using AVP II in a patient with hereditary hemorrhagic telangiectasia (HHT).","dates":{"release":"2015-01-01T00:00:00Z","publication":"2015 Sep-Oct","modification":"2025-04-04T13:25:09.734Z","creation":"2019-03-27T01:59:32Z"},"accession":"S-EPMC4593798","cross_references":{"pubmed":["26432734"],"doi":["10.1016/j.ihj.2015.05.024"]}}