1Metz C, Cave H, Bertrand AM, et al. Neonatal diabetes mellitus: chramosomal analysis in transient and permanent cases[ J]. Pediatr, 2002,141 (45) :483 -489.
2Rariq M, Flanagan SE, Patch AM, et al. Effective treatment with oral sulfonylureas in patients with diabetes due to sulfonylurea receptor I ( SURI ) mutation [ J ]. Diabetes Care,2008,31 ( 2 ) :204 - 209.
6Pearson ER, Flechtner I, Njolstad PR, et al. Neonatal Diabetes Inter- national Collaborative Group. Switching from insulin to oral sulfony- lureas in patients with diabetes due to Kit6.2 mutations[ J]. N Engl J Med ,2006,355 (5) :467 -477.
7Suzuki S,Makita Y,Mukai T,ct al. Molecular basis of neonatal dia- betes in Japanese patients [ J ]. J Clin Endocrinol Metab, 2007,92 (10) :3979 -3985.
9Hattersley AT, Ashcroft FM. Activating mutations in Kit6.2 and neo- natal dlabetes:new clinical syndromes, new seientire insights, and new therapy [ J ]. Diabetes, 2005,54 ( 9 ) : 2503 - 2513.
10Stoy J, Greeley SA. Paz VP, et al. Diagnosis and treatment of neo- natal diabetes : a United States experience [ J ]. Pediatr Diabetes, 2008,9 (5) :450 - 459.
3Gloyn AL, Pearson ER, Antcliff JF, et al. Activating mutations in the gene encoding the ATP-sensltive potassium-channel subunit Kit6.2 and permanent neonatal diabetes. N Engl J Med,2004, 350 : 1838-1849.
5Babenko AP, Polak M, CaveH, et al. Activating mutations in the ABCC8 gene in neonatal diabetes mellltus. N Engl J Med,2006, 355:456-466.
6Polak M, Cave H. Neonatal diabetes mellitus:a disease linked to multiple mechanisms. Orphanet J Rare Dis,2007,9:2-12.
7Suzuki S, Makita Y, Mukai T, et al. Molecular basis of neonatal diabetes in Japanese patients. J Clin Endocrinol Metab ,2007,92 : 3979-1985.
8Rubio-abezas O, Diaz Gonzalez F, Arayones A, et al. Permanent neonatal diabetes caused by a homozygous nonsense mutation in the glucokinase gene. Pediatr Diabetes, 2008, [ Epub ahead of print].
9Edghill EL,Flanagan SE,Patch AM ,et al. Insulin mutation screening in 1044 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. Diabetes,2008, [ Epub ahead of print].
10Senee V, Chelala C, Duchatelet S,et al. Mutations in GLIS3 are responsible for a rare syndrome with neonatal diabetes mellitus and congenital hypothyroidism. Nat Genet,2006,38:682-687.
