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Emergence of insulin resistance following empirical glibenclamide therapy: a case report of neonatal diabetes with a recessive INS gene mutation

dc.contributor.authorOnal, Hasan
dc.contributor.authorAkcay, Teoman
dc.contributor.authorYildiz, Melek
dc.contributor.authorAydin, Banu
dc.contributor.authorAkgun, Abdurrahman
dc.contributor.authorDogan, Beyza Belde
dc.contributor.authorDe Franco, Elisa
dc.contributor.authorEllard, Sian
dc.date.accessioned2021-03-06T09:13:34Z
dc.date.available2021-03-06T09:13:34Z
dc.date.issued2018
dc.identifier.citationYildiz M., Akcay T., Aydin B., Akgun A., Dogan B. B. , De Franco E., Ellard S., Onal H., "Emergence of insulin resistance following empirical glibenclamide therapy: a case report of neonatal diabetes with a recessive INS gene mutation", JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM, cilt.31, ss.345-348, 2018
dc.identifier.issn0334-018X
dc.identifier.otherav_e4a89a72-6c59-4c39-a01c-0fa7acbf25ec
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/150457
dc.identifier.urihttps://doi.org/10.1515/jpem-2017-0325
dc.description.abstractBackground: As K-ATP channel mutations are the most common cause of neonatal diabetes mellitus (NDM) and patients with these mutations can be treated with oral sulfonyl-ureas, empiric therapy is a common practice for NDM patients.
dc.language.isoeng
dc.subjectEndocrinology, Diabetes and Metabolism
dc.subjectEndokrinoloji ve Metabolizma Hastalıkları
dc.subjectEndocrinology
dc.subjectEndocrine and Autonomic Systems
dc.subjectPediatrics
dc.subjectPediatrics, Perinatology and Child Health
dc.subjectLife Sciences
dc.subjectHealth Sciences
dc.subjectENDOKRİNOLOJİ VE METABOLİZMA
dc.subjectKlinik Tıp
dc.subjectKlinik Tıp (MED)
dc.subjectPEDİATRİ
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectÇocuk Sağlığı ve Hastalıkları
dc.subjectİç Hastalıkları
dc.titleEmergence of insulin resistance following empirical glibenclamide therapy: a case report of neonatal diabetes with a recessive INS gene mutation
dc.typeMakale
dc.relation.journalJOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM
dc.contributor.departmentİstanbul Üniversitesi , İstanbul Tıp Fakültesi , Dahili Tıp Bilimleri Bölümü
dc.identifier.volume31
dc.identifier.issue3
dc.identifier.startpage345
dc.identifier.endpage348
dc.contributor.firstauthorID2507700


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