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Neonatal Diabetes Caused by Activating Mutations in the Sulphonylurea Receptor
Peter Proks
Diabetes Metab J. 2013;37(3):157-164.   Published online June 14, 2013
DOI: https://doi.org/10.4093/dmj.2013.37.3.157

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Neonatal Diabetes Caused by Activating Mutations in the Sulphonylurea Receptor
Diabetes & Metabolism Journal. 2013;37(3):157   Crossref logo
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Molecular Mechanism of Sulphonylurea Block of KATP Channels Carrying Mutations That Impair ATP Inhibition and Cause Neonatal Diabetes
Diabetes. 2013;62(11):3909-3919   Crossref logo
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KCNJ11 activating mutations cause both transient and permanent neonatal diabetes mellitus in Cypriot patients
Pediatric Diabetes. 2011;12(2):133-137   Crossref logo
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Empirical sulphonylurea in neonatal diabetes: results from a tertiary care center
International Journal of Diabetes in Developing Countries. 2021;   Crossref logo
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Functional characterization of activating mutations in the sulfonylurea receptor 1 ( ABCC8 ) causing neonatal diabetes mellitus in Asian Indian children
Pediatric Diabetes. 2019;20(4):397-407   Crossref logo
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Sulphonylurea/Insulin Combination in Diabetes Mellitus Following Secondary Failure to Tablets
Insulin / Sulphonylurea. ;51-67   Crossref logo
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Four novel cases of permanent neonatal diabetes mellitus caused by homozygous mutations in the glucokinase gene
Pediatric Diabetes. 2010;12(3pt1):192-196   Crossref logo
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Insulin Treatment in Type-II Diabetes in Presence of Secondary Failure to Sulphonylurea Therapy
Insulin / Sulphonylurea. ;78-84   Crossref logo
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Permanent Neonatal Diabetes Mellitus Caused by a Novel Homozygous (T168A) Glucokinase (GCK) Mutation: Initial Response to Oral Sulphonylurea Therapy
The Journal of Pediatrics. 2008;153(1):122-126   Crossref logo
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Activating and Inactivating Receptor Mutations
Encyclopedia of Hormones. 2003;10-17   Crossref logo
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