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dc.contributor.authorGüven, A.en
dc.contributor.authorCebeci, A. N.en
dc.contributor.authorEllard, Sianen
dc.contributor.authorFlanagan, Sarahen
dc.date.accessioned2016-08-10T09:13:11Z
dc.date.available2016-08-10T09:13:11Z
dc.date.issued2016-06-05
dc.identifier.citationClinical and Genetic Characteristics, Management and Long-Term Follow-Up of Turkish Patients with Congenital Hyperinsulinism. 2016, 8 (2):197-204 J Clin Res Pediatr Endocrinolen
dc.identifier.issn1308-5735
dc.identifier.pmid26758964
dc.identifier.doi10.4274/jcrpe.2408
dc.identifier.urihttp://hdl.handle.net/11287/618141
dc.description.abstractMutations in the KATP channel genes is the most common cause of congenital hyperinsulinism (CHI) of infancy. Our aim was to report the clinical and genetic characteristics, treatment modalities, and long-term prognosis of patients with CHI.en
dc.language.isoenen
dc.publisherGalenosen
dc.relation.urlhttp://dx.doi.org/10.4274/jcrpe.2408en
dc.rightsArchived with thanks to Journal of clinical research in pediatric endocrinologyen
dc.subjectWessex Classification Subject Headings::Oncology. Pathology.::Geneticsen
dc.titleClinical and genetic characteristics, management and long-term follow-Up of Turkish Patients with Congenital Hyperinsulinism.en
dc.typeJournal Articleen
dc.identifier.journalJournal of clinical research in pediatric endocrinologyen
dc.description.noteThis article is freely available online, click on the 'Additional Link' above to access the full text.en
dc.type.versionPublisheden


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