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Search Results (18)

Update of variants identified in the pancreatic ß-cell KATP channel genes KCNJ11 and ABCC8 in individuals with congenital hyperinsulinism and diabetes.Academic Article Why?
Congenital Diabetes: Comprehensive Genetic Testing Allows for Improved Diagnosis and Treatment of Diabetes and Other Associated Features.Academic Article Why?
Congenital forms of diabetes: the beta-cell and beyond.Academic Article Why?
Type 2 diabetes and congenital hyperinsulinism cause DNA double-strand breaks and p53 activity in ß cells.Academic Article Why?
Diabetes insipidus associated with symptomatic congenital cytomegalovirus infection.Academic Article Why?
Periconception glycemic control and congenital anomalies in women with pregestational diabetes.Academic Article Why?
Utilization of extracorporeal membrane oxygenation in congenital hypertrophic cardiomyopathy caused by maternal diabetes.Academic Article Why?
A loss-of-function mutation in KCNJ11 causing sulfonylurea-sensitive diabetes in early adult life.Academic Article Why?
Diagnosis, Treatment, and Outcomes in Children With Congenital Nephrogenic Diabetes Insipidus: A Pediatric Nephrology Research Consortium Study.Academic Article Why?
Geobiology of CataractsGrant Why?
Molecular and Cellular Mechanisms of Calcific Aortic StenosisGrant Why?
Dysregulation of insulin secretion in children with congenital hyperinsulinism due to sulfonylurea receptor mutations.Academic Article Why?
New recessive syndrome of microcephaly, cerebellar hypoplasia, and congenital heart conduction defect.Academic Article Why?
Clinical and molecular genetics of neonatal diabetes due to mutations in the insulin gene.Academic Article Why?
Neonatal diabetes, gallbladder agenesis, duodenal atresia, and intestinal malrotation caused by a novel homozygous mutation in RFX6.Academic Article Why?
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