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dc.contributor.authorBuyukozturk, Suna
dc.contributor.authorOnay-Ucar, Evren
dc.contributor.authorArda, Nazli
dc.contributor.authorDeniz, Gunnur
dc.contributor.authorCinar, Suzan
dc.contributor.authorDemirturk, Mustafa
dc.contributor.authorGelincik, Ash
dc.contributor.authorKILERCIK, Meltem
dc.contributor.authorColakoglu, Bahattin
dc.date.accessioned2021-03-03T19:42:46Z
dc.date.available2021-03-03T19:42:46Z
dc.date.issued2014
dc.identifier.citationDemirturk M., Gelincik A., Cinar S., KILERCIK M., Onay-Ucar E., Colakoglu B., Arda N., Buyukozturk S., Deniz G., "Increased eNOS levels in hereditary angioedema", INTERNATIONAL IMMUNOPHARMACOLOGY, cilt.20, sa.1, ss.264-268, 2014
dc.identifier.issn1567-5769
dc.identifier.otherav_56099678-c224-49a6-92cf-7c8840a94277
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/60761
dc.identifier.urihttps://doi.org/10.1016/j.intimp.2014.03.007
dc.description.abstractBackground: Hereditary angio-edema (HAE), characterized by recurrent episodes of angioedema involving the skin and the mucosa of the upper respiratory or the gastrointestinal tracts, results from heterozygosity for deficiency of the serine proteinase inhibitor (serpin), C1 inhibitor (C1-INH).
dc.language.isoeng
dc.subjectTemel Bilimler
dc.subjectSağlık Bilimleri
dc.subjectYaşam Bilimleri
dc.subjectEczacılık
dc.subjectTemel Eczacılık Bilimleri
dc.subjectFarmakoloji ve Toksikoloji
dc.subjectFARMAKOLOJİ VE ECZACILIK
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectİmmünoloji
dc.titleIncreased eNOS levels in hereditary angioedema
dc.typeMakale
dc.relation.journalINTERNATIONAL IMMUNOPHARMACOLOGY
dc.contributor.departmentİstanbul Üniversitesi , ,
dc.identifier.volume20
dc.identifier.issue1
dc.identifier.startpage264
dc.identifier.endpage268
dc.contributor.firstauthorID45659


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