Clinical and genetic characteristics, management and long-term follow-Up of Turkish Patients with Congenital Hyperinsulinism.

2.50
Hdl Handle:
http://hdl.handle.net/11287/618141
Title:
Clinical and genetic characteristics, management and long-term follow-Up of Turkish Patients with Congenital Hyperinsulinism.
Authors:
Güven, A.; Cebeci, A. N.; Ellard, Sian ( 0000-0002-7620-5526 ) ; Flanagan, Sarah
Abstract:
Mutations 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.
Citation:
Clinical and Genetic Characteristics, Management and Long-Term Follow-Up of Turkish Patients with Congenital Hyperinsulinism. 2016, 8 (2):197-204 J Clin Res Pediatr Endocrinol
Publisher:
Galenos
Journal:
Journal of clinical research in pediatric endocrinology
Issue Date:
5-Jun-2016
URI:
http://hdl.handle.net/11287/618141
DOI:
10.4274/jcrpe.2408
PubMed ID:
26758964
Additional Links:
http://dx.doi.org/10.4274/jcrpe.2408
Note:
This article is freely available online, click on the 'Additional Link' above to access the full text.
Type:
Journal Article
Language:
en
ISSN:
1308-5735
Appears in Collections:
Molecular Genetics; 2016 RD&E publications

Full metadata record

DC FieldValue Language
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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