| P50 | author | Takako Yonemoto | Q96205874 |
| P2093 | author name string | Chika Kyo | |
| | Kae Morishita | |
| | Rieko Kosugi | |
| | Tatsuhide Inoue | |
| | Tatsuo Ogawa | |
| P2860 | cites work | Mutation of the pancreatic islet inward rectifier Kir6.2 also leads to familial persistent hyperinsulinemic hypoglycemia of infancy | Q24321513 |
| | Physical exercise-induced hypoglycemia caused by failed silencing of monocarboxylate transporter 1 in pancreatic beta cells | Q28241044 |
| | A novel syndrome of autosomal-dominant hyperinsulinemic hypoglycemia linked to a mutation in the human insulin receptor gene | Q28263279 |
| | Hyperinsulinism and hyperammonemia in infants with regulatory mutations of the glutamate dehydrogenase gene | Q28269681 |
| | Macrosomia and hyperinsulinaemic hypoglycaemia in patients with heterozygous mutations in the HNF4A gene | Q28469173 |
| | Mutations in the sulfonylurea receptor gene in familial persistent hyperinsulinemic hypoglycemia of infancy | Q34308497 |
| | Glucokinase inhibitor glucosamine stimulates feeding and activates hypothalamic neuropeptide Y and orexin neurons | Q35097342 |
| | Reversible Adrenal Insufficiency in Three Patients With Post-Roux-en-Y Gastric Bypass Noninsulinoma Pancreatogenous Hypoglycemia Syndrome | Q35927608 |
| | Management of adrenal insufficiency in different clinical settings | Q36301569 |
| | Perspective on the Genetics and Diagnosis of Congenital Hyperinsulinism Disorders | Q36716020 |
| | Extremes of clinical and enzymatic phenotypes in children with hyperinsulinism caused by glucokinase activating mutations | Q37193748 |
| | Update on mutations in glucokinase (GCK), which cause maturity-onset diabetes of the young, permanent neonatal diabetes, and hyperinsulinemic hypoglycemia | Q37605708 |
| | Rare forms of congenital hyperinsulinism | Q37824091 |
| | Mechanisms of hypoglycemia-associated autonomic failure in diabetes | Q38123894 |
| | Short-term food restriction and refeeding alter expression of genes likely involved in brain glucosensing. | Q44580861 |
| | Severe persistent hyperinsulinemic hypoglycemia due to a de novo glucokinase mutation | Q44995571 |
| | Diagnostic difficulties in glucokinase hyperinsulinism. | Q46215511 |
| | Congenital hyperinsulinism: global and Japanese perspectives. | Q51261501 |
| | Familial hyperinsulinism caused by an activating glucokinase mutation | Q55670538 |
| P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
| P6216 | copyright status | copyrighted | Q50423863 |
| P921 | main subject | congenital disorder | Q727096 |
| | adrenal insufficiency | Q2507454 |
| P304 | page(s) | 4709262 | |
| P577 | publication date | 2017-01-09 | |
| P1433 | published in | Case reports in endocrinology | Q27724372 |
| P1476 | title | Asymptomatic Congenital Hyperinsulinism due to a Glucokinase-Activating Mutation, Treated as Adrenal Insufficiency for Twelve Years | |
| P478 | volume | 2017 | |