dc.contributor.author | AYKUT, AYÇA | |
dc.contributor.author | EVLİYAOĞLU, Saadet Olcay | |
dc.contributor.author | Ozer, Yavuz | |
dc.contributor.author | Durmaz, Asude Alpman | |
dc.contributor.author | ERCAN, Oya | |
dc.contributor.author | Tarcin, Gurkan | |
dc.contributor.author | TURAN, Hande | |
dc.contributor.author | Cakir, Aydilek Dagdeviren | |
dc.date.accessioned | 2021-12-10T13:05:56Z | |
dc.date.available | 2021-12-10T13:05:56Z | |
dc.date.issued | 2021 | |
dc.identifier.citation | Tarcin G., TURAN H., Cakir A. D. , Ozer Y., AYKUT A., Durmaz A. A. , ERCAN O., EVLİYAOĞLU S. O. , "Different clinical entities of the same mutation: a case report of three sisters with Wolfram syndrome and efficacy of dipeptidyl peptidase-4 inhibitor therapy", JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM, cilt.34, sa.8, ss.1049-1053, 2021 | |
dc.identifier.issn | 0334-018X | |
dc.identifier.other | vv_1032021 | |
dc.identifier.other | av_ee0b37c6-7d46-43cd-b3ab-7e954416a498 | |
dc.identifier.uri | http://hdl.handle.net/20.500.12627/175395 | |
dc.identifier.uri | https://doi.org/10.1515/jpem-2020-0699 | |
dc.description.abstract | Objectives: Wolfram syndrome (WS) is a rarely seen autosomal recessive multisystem neurodegenerative disorder caused by mutations in the WFS1 gene. | |
dc.language.iso | eng | |
dc.subject | İç Hastalıkları | |
dc.subject | Endokrinoloji ve Metabolizma Hastalıkları | |
dc.subject | Endocrinology | |
dc.subject | Endocrine and Autonomic Systems | |
dc.subject | Pediatrics | |
dc.subject | Pediatrics, Perinatology and Child Health | |
dc.subject | Endocrinology, Diabetes and Metabolism | |
dc.subject | Life Sciences | |
dc.subject | Health Sciences | |
dc.subject | Sağlık Bilimleri | |
dc.subject | Dahili Tıp Bilimleri | |
dc.subject | Çocuk Sağlığı ve Hastalıkları | |
dc.subject | Tıp | |
dc.subject | PEDİATRİ | |
dc.subject | Klinik Tıp (MED) | |
dc.subject | Klinik Tıp | |
dc.subject | ENDOKRİNOLOJİ VE METABOLİZMA | |
dc.title | Different clinical entities of the same mutation: a case report of three sisters with Wolfram syndrome and efficacy of dipeptidyl peptidase-4 inhibitor therapy | |
dc.type | Makale | |
dc.relation.journal | JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM | |
dc.contributor.department | İstanbul Üniversitesi-Cerrahpaşa , , | |
dc.identifier.volume | 34 | |
dc.identifier.issue | 8 | |
dc.identifier.startpage | 1049 | |
dc.identifier.endpage | 1053 | |
dc.contributor.firstauthorID | 2707250 | |