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The New England Journal of Medicine, ISSN 0028-4793, 08/2006, Volume 355, Issue 5, pp. 456 - 466
In this study, mutations in the gene encoding the sulfonylurea receptor, a component of the beta-cell ATP-sensitive potassium channel, are described in infants... 
IMMUNE DYSREGULATION | KIR6.2 MUTATIONS | NUCLEOTIDES | REGULATOR | MEDICINE, GENERAL & INTERNAL | MECHANISM | K-ATP CHANNELS | INSULIN-SECRETION | STOICHIOMETRY | SULFONYLUREA RECEPTOR | TRANSIENT | Tolbutamide - pharmacology | Diabetes Complications | Diabetes Mellitus - genetics | Receptors, Drug - genetics | Humans | Male | Mutation, Missense | Sulfonylurea Receptors | Potassium Channels - metabolism | Insulin-Secreting Cells - metabolism | ATP-Binding Cassette Transporters - genetics | ATP-Binding Cassette Transporters - metabolism | Female | Potassium Channels, Inwardly Rectifying - antagonists & inhibitors | Infant, Newborn | Hypoglycemic Agents - therapeutic use | Sulfonylurea Compounds - therapeutic use | Diabetes Mellitus - drug therapy | Diabetes Mellitus - metabolism | Potassium Channels, Inwardly Rectifying - genetics | Receptors, Drug - metabolism | Potassium Channels - genetics | Birth Weight | Insulin-Secreting Cells - drug effects | Pedigree | Heterozygote | Developmental Disabilities - complications | Potassium Channels, Inwardly Rectifying - metabolism | Receptors, Drug - antagonists & inhibitors | ATP-Binding Cassette Transporters - antagonists & inhibitors | Infants (Newborn) | Genetic aspects | Diabetes | Research | Gene mutations | Diseases | Mutation | Pancreas | Genes | Adenosine triphosphatase | Life Sciences | Genetics | Human genetics
Journal Article
Current Opinion in Endocrinology, Diabetes and Obesity, ISSN 1752-296X, 02/2010, Volume 17, Issue 1, pp. 13 - 19
Journal Article
Padiatrische Praxis, ISSN 0030-9346, 2018, Volume 90, Issue 3, pp. 452 - 460
Journal Article
Indian Pediatrics, ISSN 0019-6061, 1/2017, Volume 54, Issue 1, pp. 33 - 36
Neonatal diabetes mellitusis a rare disorder with an incidence of 1 in 2,60,000 live births.Retrospective analysis of clinical and genetic profile of children... 
Pediatrics | Medicine & Public Health | Permanent | Diabetes mellitus | Maternal and Child Health | Genetics | Transient | Pediatric Surgery | KIR6.2 | KCNJ11 | GENE | PEDIATRICS | MELLITUS | ACTIVATING MUTATIONS | CHILDREN | Infants (Newborn) | Urea | Diabetes | Gene mutations | Analysis | Genes
Journal Article
Scandinavian Journal of Public Health, ISSN 1403-4948, 12/2017, Volume 45, Issue 8, pp. 839 - 845
Aims: The study of imprinting disorders in the context of infertility and its treatment is important, as studies have indicated an increased risk. In this... 
fertility treatment | cohort study | infertility | Epidemiology | transient neonatal diabetes mellitus | ASSISTED REPRODUCTIVE TECHNOLOGY | DEFECTS | METAANALYSIS | CANCER | PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH | BECKWITH-WIEDEMANN-SYNDROME | INCREASE | IVF | IN-VITRO FERTILIZATION | IMPRINTING DISORDERS | ASSOCIATION
Journal Article
American Journal of Physiology - Endocrinology and Metabolism, ISSN 0193-1849, 12/2018, Volume 315, Issue 6, pp. E1121 - E1132
Gain-of-function (GOF) mutations in the ATP-sensitive potassium (KATP) channels cause neonatal diabetes. Despite the well-established genetic root of the... 
Treatment | Permanent | Sulfonylurea | Remission | Inflammation | Mice | Diabetes | K | Transient | Glibenclamide | Insulin | KATP | sulfonylurea | treatment | insulin | inflammation | transient | permanent | remission | diabetes | glibenclamide | mice
Journal Article
Journal Article
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