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Search Results to Graeme Bell

This is a "connection" page, showing the details of why an item matched the keywords from your search.


One or more keywords matched the following items that are connected to Bell, Graeme

Item TypeName
Concept Animals, Newborn
Concept Infant, Newborn
Concept Infant, Newborn, Diseases
Academic Article Searching for NIDDM susceptibility genes: studies of genes with triplet repeats expressed in skeletal muscle.
Academic Article Abnormal nephron development associated with a frameshift mutation in the transcription factor hepatocyte nuclear factor-1 beta.
Academic Article Neonatal diabetes mellitus due to complete glucokinase deficiency.
Academic Article Treatment of hyperglycemia in a 7-year-old child diagnosed with neonatal diabetes.
Academic Article Permanent neonatal diabetes due to mutations in KCNJ11 encoding Kir6.2: patient characteristics and initial response to sulfonylurea therapy.
Academic Article Insulin gene mutations as a cause of permanent neonatal diabetes.
Academic Article Macrosomia and neonatal hypoglycaemia in RW pedigree subjects with a mutation (Q268X) in the gene encoding hepatocyte nuclear factor 4alpha (HNF4A).
Academic Article Diagnosis and treatment of neonatal diabetes: a United States experience.
Academic Article Insulin mutation screening in 1,044 patients with diabetes: mutations in the INS gene are a common cause of neonatal diabetes but a rare cause of diabetes diagnosed in childhood or adulthood.
Academic Article Update in neonatal diabetes.
Academic Article Obesity and hyperinsulinemia in a family with pancreatic agenesis and MODY caused by the IPF1 mutation Pro63fsX60.
Academic Article Mutant proinsulin proteins associated with neonatal diabetes are retained in the endoplasmic reticulum and not efficiently secreted.
Academic Article Neonatal diabetes mellitus: a model for personalized medicine.
Academic Article The cost-effectiveness of personalized genetic medicine: the case of genetic testing in neonatal diabetes.
Academic Article Neonatal diabetes: an expanding list of genes allows for improved diagnosis and treatment.
Academic Article In vitro processing and secretion of mutant insulin proteins that cause permanent neonatal diabetes.
Academic Article Clinical and molecular genetics of neonatal diabetes due to mutations in the insulin gene.
Academic Article Identification of 14 new glucokinase mutations and description of the clinical profile of 42 MODY-2 families.
Academic Article Mutations in the insulin gene can cause MODY and autoantibody-negative type 1 diabetes.
Academic Article Microcephaly, epilepsy, and neonatal diabetes due to compound heterozygous mutations in IER3IP1: insights into the natural history of a rare disorder.
Academic Article A One Health investigation of Salmonella enterica serovar Wangata in north-eastern New South Wales, Australia, 2016-2017.
Academic Article In celebration of a century with insulin - Update of insulin gene mutations in diabetes.

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  • Infant Newborn