A rare cause of recurrent abdominal pain: Three familial cases with hereditary angioedema

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dc.contributor.authorDertlioglu, Selma B.
dc.contributor.authorCicek, Demet
dc.contributor.authorYesilova, Yavuz
dc.date.accessioned2026-08-12T17:46:50Z
dc.date.issued2013
dc.departmentFırat Üniversitesi
dc.description.abstract[Abstract Not Available]
dc.identifier.doi10.4103/0378-6323.104681
dc.identifier.issn0378-6323
dc.identifier.issue1
dc.identifier.pmid23254741
dc.identifier.scopus2-s2.0-84878778271
dc.identifier.scopusqualityQ2
dc.identifier.urihttps://doi.org/10.4103/0378-6323.104681
dc.identifier.urihttps://hdl.handle.net/11508/61245
dc.identifier.volume79
dc.identifier.wosWOS:000313292900020
dc.identifier.wosqualityQ1
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherMedknow Publications & Media Pvt Ltd
dc.relation.ispartofIndian Journal of Dermatology Venereology & Leprology
dc.relation.publicationcategoryDiğer
dc.rightsinfo:eu-repo/semantics/openAccess
dc.snmzKA_WoS_20260511
dc.subjectC1 Inhibitor Deficiency
dc.subjectManagement
dc.subjectConsensus
dc.titleA rare cause of recurrent abdominal pain: Three familial cases with hereditary angioedema
dc.typeLetter

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