Efficacy and Safety of Sulfonylurea Use in Permanent Neonatal Diabetes Due to KCNJ11 Gene Mutations: 34-Month Median Follow-Up-Reference-Cited by-同舟云学术

Efficacy and Safety of Sulfonylurea Use in Permanent Neonatal Diabetes Due to KCNJ11 Gene Mutations: 34-Month Median Follow-Up

Published:2010-05 Issue:5 Volume:12 Page:387-391
ISSN:1520-9156
Container-title:Diabetes Technology & Therapeutics
language:en
Short-container-title:Diabetes Technology & Therapeutics

Author:

Klupa Tomasz¹²,Skupien Jan¹²,Mirkiewicz-Sieradzka Barbara¹²,Gach Agnieszka³,Noczynska Anna⁴,Zubkiewicz-Kucharska Agnieszka⁴,Szalecki Mieczyslaw⁵,Kozek Elzbieta¹²,Nazim Joanna⁶,Mlynarski Wojciech³,Malecki Maciej T.¹²

Affiliation:

1. Department of Metabolic Diseases, Jagiellonian University Medical College, Krakow, Poland.

2. Department of University Hospital, Krakow, Poland.

3. Department of Paediatrics, Medical University of Lodz, Lodz, Poland.

4. Department of Endocrinology and Diabetology for Children and Adolescents, Medical University of Wroclaw, Wroclaw, Poland.

5. Pediatric Endocrinology Department, Provincial Hospital in Kielce, Kielce, Poland.

6. Department of Pediatrics, Jagiellonian University Medical College, Krakow, Poland.

Publisher

Mary Ann Liebert Inc

Subject

Medical Laboratory Technology,Endocrinology,Endocrinology, Diabetes and Metabolism

Link

http://www.liebertpub.com/doi/pdf/10.1089/dia.2009.0165

Reference22 articles.

1. Activating Mutations in the Gene Encoding the ATP-Sensitive Potassium-Channel Subunit Kir6.2 and Permanent Neonatal Diabetes

2. ATP-sensitive K+ channels and disease: from molecule to malady

3. ATP and Sulfonylurea Sensitivity of Mutant ATP-Sensitive K+ Channels in Neonatal Diabetes

4. Switching from Insulin to Oral Sulfonylureas in Patients with Diabetes Due to Kir6.2 Mutations

5. The identification of a R201H mutation in KCNJ11, which encodes Kir6.2, and successful transfer to sustained-release sulphonylurea therapy in a subject with neonatal diabetes: evidence for heterogeneity of beta cell function among carriers of the R201H mutation

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