Glyburide ameliorates motor coordination and glucose homeostasis in a child with diabetes associated with theKCNJ11/S225T, del226-232 mutation-Reference-Cited by-同舟云学术

Glyburide ameliorates motor coordination and glucose homeostasis in a child with diabetes associated with theKCNJ11/S225T, del226-232 mutation

Published:2012-06-14 Issue:8 Volume:13 Page:656-660
ISSN:1399-543X
Container-title:Pediatric Diabetes
language:en
Short-container-title:Pediatr Diabetes

Author:

Battaglia Domenica¹,Lin Yu-Wen²,Brogna Claudia¹,Crinò Antonino³,Grasso Valeria⁴,Mozzi Alessia F⁵,Russo Lucia⁴,Spera Sabrina³,Colombo Carlo⁴,Ricci Stefano⁶,Nichols Colin G²,Mercuri Eugenio¹,Barbetti Fabrizio

Affiliation:

1. Child Neurology Unit; Department of Pediatrics; Sacro Cuore Catholic University; 00168; Rome; Italy

2. Department of Cell Biology and Physiology and Center for the Investigation of Membrane Exitability Diseases; Washington University School of Medicine; St Louis; 63110; MO; USA

3. Autoimmune Endocrine Diseases Unit; Endocrinology Department; Bambino Gesù Children's Hospital; Research Institute Palidoro; 00050; Rome; Italy

4. Laboratory of Mendelian Diabetes; Bambino Gesù Children's Hospital; Research Institute; University of Tor Vergata; 00134; Rome; Italy

5. Department of Laboratory Medicine; University of Tor Vergata; 00134; Rome; Italy

6. Department of Neuroscience; Clinical Psychology Unit; Bambino Gesù Children's Hospital Research Institute; 00164; Rome; Italy

Publisher

Wiley

Subject

Endocrinology, Diabetes and Metabolism,Pediatrics, Perinatology and Child Health,Internal Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-5448.2012.00874.x/fullpdf

Reference21 articles.

1. Activating mutations in the gene encoding the ATP-sensitive potassium-channel subunit Kir6.2 and permanent neonatal diabetes;Gloyn;N Engl J Med,2004

2. The C42R mutation in the Kir6.2 (KCNJ11) gene as a cause of transient neonatal diabetes, childhood diabetes or later-onset, apparently type 2 diabetes;Yorifuji;J Clin Endocrinol Metab,2005

3. Activating mutations in Kir6.2 and neonatal diabetes: new clinical syndromes, new scientific insights, and new therapy;Hattersley;Diabetes,2005

4. An ATP-binding mutation (G334D) in KCNJ11 is associated with a sulfonylurea-insensitive form of DEND (Developmental Delay, Epilepsy, and Neonatal Diabetes);Masia;Diabetes,2007

5. KCNJ11 mutations in Italian patients with permanent neonatal diabetes;Massa;Hum Mutat,2005

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