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An adolescent with idiopathic pleuroparenchymal fibroelastosis. Case report

dc.contributor.authorKIYAN, GÜRSU
dc.contributor.authorYilmazbayhan, Dilek
dc.contributor.authorGÖKDEMİR, YASEMİN
dc.contributor.authorERDEM ERALP, ELA
dc.contributor.authorKaradag, Bulent
dc.contributor.authorAtag, Emine
dc.contributor.authorIkizoglu, Nilay Bas
dc.date.accessioned2021-03-04T17:56:01Z
dc.date.available2021-03-04T17:56:01Z
dc.date.issued2018
dc.identifier.citationAtag E., Ikizoglu N. B. , GÖKDEMİR Y., ERDEM ERALP E., KIYAN G., Yilmazbayhan D., Karadag B., "An adolescent with idiopathic pleuroparenchymal fibroelastosis. Case report", ARCHIVOS ARGENTINOS DE PEDIATRIA, cilt.116, 2018
dc.identifier.issn0325-0075
dc.identifier.otherav_880d45b5-6b9c-4b29-be44-bf802308d029
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/92357
dc.identifier.urihttps://doi.org/10.5546/aap.2018.eng.e147
dc.description.abstractIdiopathic pleuroparenchymal fibroelastosis (IPPFE) is a rare disorder recently included in rare idiopathic interstitial pneumonias according to the updated American Thoracic Society/European Respiratory Society classification. IPPFE is characterized by pleural and subpleural parenchymal fibrosis causing volume loss predominantly in the upper lung lobes. Age of onset is variable, IPPFE mainly occurs in third and fourth decades.
dc.language.isoeng
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectÇocuk Sağlığı ve Hastalıkları
dc.subjectTıp
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectPEDİATRİ
dc.titleAn adolescent with idiopathic pleuroparenchymal fibroelastosis. Case report
dc.typeMakale
dc.relation.journalARCHIVOS ARGENTINOS DE PEDIATRIA
dc.contributor.departmentMarmara Üniversitesi , ,
dc.identifier.volume116
dc.identifier.issue1
dc.contributor.firstauthorID251243


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