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Published in: Diabetologia 9/2006

01-09-2006 | Letter

Sulfonylurea treatment outweighs insulin therapy in short-term metabolic control of patients with permanent neonatal diabetes mellitus due to activating mutations of the KCNJ11 (KIR6.2) gene

Authors: G. Tonini, C. Bizzarri, R. Bonfanti, M. Vanelli, F. Cerutti, E. Faleschini, F. Meschi, F. Prisco, E. Ciacco, M. Cappa, C. Torelli, V. Cauvin, S. Tumini, D. Iafusco, F. Barbetti, Early-Onset Diabetes Study Group of the Italian Society of Paediatric Endocrinology and Diabetology

Published in: Diabetologia | Issue 9/2006

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Excerpt

To the Editor, …
Literature
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go back to reference Gloyn AL, Pearson ER, Antcliff JF et al (2004) Activating mutations in the ATP-sensitive potassium channel subunit Kir6.2 gene are associated with permanent neonatal diabetes. N Engl J Med 350:1838–1849PubMedCrossRef Gloyn AL, Pearson ER, Antcliff JF et al (2004) Activating mutations in the ATP-sensitive potassium channel subunit Kir6.2 gene are associated with permanent neonatal diabetes. N Engl J Med 350:1838–1849PubMedCrossRef
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go back to reference Gloyn AL, Reimann F, Girard C et al (2005) Relapsing diabetes can result from moderately activating mutations in KCNJ11. Hum Mol Genet 14:925–934PubMedCrossRef Gloyn AL, Reimann F, Girard C et al (2005) Relapsing diabetes can result from moderately activating mutations in KCNJ11. Hum Mol Genet 14:925–934PubMedCrossRef
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go back to reference Colombo C, Del Vecchio M, Zecchino C, Faienza MF, Cavallo L, Barbetti F (2005) Transient neonatal diabetes mellitus is associated with a recurrent (R201H) KCNJ11 (KIR6.2) mutation. Diabetologia 48:2439–2441PubMedCrossRef Colombo C, Del Vecchio M, Zecchino C, Faienza MF, Cavallo L, Barbetti F (2005) Transient neonatal diabetes mellitus is associated with a recurrent (R201H) KCNJ11 (KIR6.2) mutation. Diabetologia 48:2439–2441PubMedCrossRef
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go back to reference Sagen J, Raeder H, Hathout E et al (2004) Permanent neonatal diabetes due to mutations in KCNJ11 encoding Kir6.2. Patient characteristics and initial response to sulfonylurea therapy. Diabetes 53:2713–2718PubMedCrossRef Sagen J, Raeder H, Hathout E et al (2004) Permanent neonatal diabetes due to mutations in KCNJ11 encoding Kir6.2. Patient characteristics and initial response to sulfonylurea therapy. Diabetes 53:2713–2718PubMedCrossRef
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go back to reference Zung A, Glaser B, Nimri R, Zadik Z (2004) Glibenclamide treatment in permanent neonatal diabetes mellitus due to an activating mutation in Kir6.2. J Clin Endocrinol Metab 89:5504–5507PubMedCrossRef Zung A, Glaser B, Nimri R, Zadik Z (2004) Glibenclamide treatment in permanent neonatal diabetes mellitus due to an activating mutation in Kir6.2. J Clin Endocrinol Metab 89:5504–5507PubMedCrossRef
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go back to reference Codner E, Flanagan S, Ellard S, Hernan G, Hattersley AT (2005) High dose glibenclamide can replace insulin therapy despite transitory diarrhea in early-onset diabetes caused by a novel R201L Kir6.2 mutation. Diabetes Care 28:758–759PubMedCrossRef Codner E, Flanagan S, Ellard S, Hernan G, Hattersley AT (2005) High dose glibenclamide can replace insulin therapy despite transitory diarrhea in early-onset diabetes caused by a novel R201L Kir6.2 mutation. Diabetes Care 28:758–759PubMedCrossRef
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Metadata
Title
Sulfonylurea treatment outweighs insulin therapy in short-term metabolic control of patients with permanent neonatal diabetes mellitus due to activating mutations of the KCNJ11 (KIR6.2) gene
Authors
G. Tonini
C. Bizzarri
R. Bonfanti
M. Vanelli
F. Cerutti
E. Faleschini
F. Meschi
F. Prisco
E. Ciacco
M. Cappa
C. Torelli
V. Cauvin
S. Tumini
D. Iafusco
F. Barbetti
Early-Onset Diabetes Study Group of the Italian Society of Paediatric Endocrinology and Diabetology
Publication date
01-09-2006
Publisher
Springer-Verlag
Published in
Diabetologia / Issue 9/2006
Print ISSN: 0012-186X
Electronic ISSN: 1432-0428
DOI
https://doi.org/10.1007/s00125-006-0329-x

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