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Hereditary tyrosinemia type 1 in Turkey: Twenty year single-center experience

dc.contributor.authorZeybek, A. Cigdem Aktuglu
dc.contributor.authorCansever, Serif
dc.contributor.authorAltay, Suheyla
dc.contributor.authorZubarioglu, Tanyel
dc.contributor.authorAydin, Ahmet
dc.contributor.authorErkan, Tulay
dc.contributor.authorKiykim, Ertugrul
dc.contributor.authorSOYUÇEN, ERDOĞAN
dc.date.accessioned2021-03-06T08:11:11Z
dc.date.available2021-03-06T08:11:11Z
dc.date.issued2015
dc.identifier.citationZeybek A. C. A. , Kiykim E., SOYUÇEN E., Cansever S., Altay S., Zubarioglu T., Erkan T., Aydin A., "Hereditary tyrosinemia type 1 in Turkey: Twenty year single-center experience", PEDIATRICS INTERNATIONAL, cilt.57, ss.281-289, 2015
dc.identifier.issn1328-8067
dc.identifier.otherav_dfb26658-637c-4725-871d-e80a10e43a92
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/147372
dc.identifier.urihttps://doi.org/10.1111/ped.12503
dc.description.abstractBackgroundHereditary tyrosinemia type 1(HT1) is a chronic disorder leading to severe hepatic, renal and peripheral nerve damage if left untreated. Despite nitisinone treatment HT1 still carries the risks of hepatocellular carcinoma (HCC) and neuropsychological outcome.
dc.language.isoeng
dc.subjectDahili Tıp Bilimleri
dc.subjectPEDİATRİ
dc.subjectKlinik Tıp
dc.subjectKlinik Tıp (MED)
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectÇocuk Sağlığı ve Hastalıkları
dc.titleHereditary tyrosinemia type 1 in Turkey: Twenty year single-center experience
dc.typeMakale
dc.relation.journalPEDIATRICS INTERNATIONAL
dc.contributor.departmentAkdeniz Üniversitesi , Tıp Fakültesi , Dahili Tıp Bilimleri Bölümü
dc.identifier.volume57
dc.identifier.issue2
dc.identifier.startpage281
dc.identifier.endpage289
dc.contributor.firstauthorID30714


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