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Published in partnership with the
European Association for the Study of Diabetes
Research Letter
T. Klupa, E. L. Edghill, J. Nazim, J. Sieradzki, S. Ellard, A. T. Hattersley and M. T. Malecki
Journal Article
Transient neonatal diabetes mellitus is associated with a recurrent (R201H) KCNJ11 (KIR6.2) mutation
C. Colombo, M. Delvecchio, C. Zecchino, M. F. Faienza and L. Cavallo, et al.
Diabetologia, 2005, Volume 48, Number 11, Pages 2439-2441
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
G. Tonini, C. Bizzarri, R. Bonfanti, M. Vanelli and F. Cerutti, et al.
Diabetologia, 2006, Volume 49, Number 9, Pages 2210-2213
Transition from insulin to sulfonylurea in a child with diabetes due to a mutation in KCNJ11 encoding Kir6.2—initial and long-term response to sulfonylurea therapy
Verena M. Wagner, Britta Kremke, Olaf Hiort, Sarah E. Flanagan and Ewan R. Pearson
European Journal of Pediatrics, 2009, Volume 168, Number 3, Pages 359-361
Sulphonylurea action revisited: the post-cloning era
F. M. Gribble and F. Reimann
Diabetologia, 2003, Volume 46, Number 7, Pages 875-891
Human KATP channelopathies: diseases of metabolic homeostasis
Timothy M. Olson and Andre Terzic
Pflügers Archiv European Journal of Physiology, 2010, Volume 460, Number 2, Pages 295-306
Functional analysis of six Kir6.2 ( KCNJ11 ) mutations causing neonatal diabetes
Christophe A. J. Girard, Kenju Shimomura, Peter Proks, Nathan Absalom and Luis Castano, et al.
Pflügers Archiv European Journal of Physiology, 2006, Volume 453, Number 3, Pages 323-332
Book Chapter
ATP-Sensitive Potassium Channels in Health and Disease
Peter Proks and Frances M. Ashcroft
2008, Pancreatic Beta Cell in Health and Disease, V., Pages 431-450
Improved motor development and good long-term glycaemic control with sulfonylurea treatment in a patient with the syndrome of intermediate developmental delay, early-onset generalised epilepsy and neonatal diabetes associated with the V59M mutation in the KCNJ11 gene
A. S. Slingerland, R. Nuboer, M. Hadders-Algra, A. T. Hattersley and G. J. Bruining
Diabetologia, 2006, Volume 49, Number 11, Pages 2559-2563
Mutations in KCNJ11, which encodes Kir6.2, are a common cause of diabetes diagnosed in the first 6 months of life, with the phenotype determined by genotype
S. E. Flanagan, E. L. Edghill, A. L. Gloyn, S. Ellard and A. T. Hattersley
Diabetologia, 2006, Volume 49, Number 6, Pages 1190-1197
KCNJ11 activating mutation in an Indian family with remitting and relapsing diabetes
V. V. Khadilkar, A. V. Khadilkar, R. R. Kapoor, K. Hussain and A. T. Hattersley, et al.
Indian Journal of Pediatrics, 2010, Volume 77, Number 5, Pages 551-554
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