Clinical and molecular genetics of neonatal diabetes due to mutations in the insulin gene

By Støy Julie  

Reviews in Endocrine and Metabolic Disorders, Vol. 11, Iss. 3, 2010-09 ,pp. : 205-215

Springer Publishing Company

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Improved motor development and good long-term glycaemic control with sulfonylurea treatment in a patient with the syndrome of intermediate developmental delay, early-onset generalised epilepsy and neonatal diabetes associated with the V59M mutation in the KCNJ11 gene

By Slingerland A.   Nuboer R.   Hadders-Algra M.   Hattersley A.   Bruining G.  

Diabetologia, Vol. 49, Iss. 11, 2006-11 ,pp. : 2559-2563

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Mutations in pancreatic ß-cell Glucokinase as a cause of hyperinsulinaemic hypoglycaemia and neonatal diabetes mellitus

By Hussain Khalid  

Reviews in Endocrine and Metabolic Disorders, Vol. 11, Iss. 3, 2010-09 ,pp. : 179-183

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Mutations in the SLC30A8 gene are not a major cause of MODY or other forms of early-onset, autosomal dominant type 2 diabetes

By Borowiec M.   Thompson R.   Powers C.   Xu R.   Dickey T.   Doria A.  

Diabetologia, Vol. 50, Iss. 10, 2007-10 ,pp. : 2224-2226

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Congenital hyperinsulinism and neonatal diabetes mellitus

By Hussain Khalid  

Reviews in Endocrine and Metabolic Disorders, Vol. 11, Iss. 3, 2010-09 ,pp. : 155-156

Springer Publishing Company

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