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Hyperexcitability to sulphonylurea in MODY3.
Søvik O, Njølstad P, Følling I, Sagen J, Cockburn BN, Bell GI. Søvik O, et al. Among authors: cockburn bn. Diabetologia. 1998 May;41(5):607-8. doi: 10.1007/s001250050956. Diabetologia. 1998. PMID: 9628283 No abstract available.
Molecular genetics of MODY in Germany.
Lindner TH, Cockburn BN, Bell GI. Lindner TH, et al. Among authors: cockburn bn. Diabetologia. 1999 Jan;42(1):121-3. doi: 10.1007/s001250051128. Diabetologia. 1999. PMID: 10027594 No abstract available.
[Non-insulin dependent diabetes in children and adolescents].
Njølstad PR, Søvik O, Bell GI, Cockburn BN, Følling I, Sagen J. Njølstad PR, et al. Among authors: cockburn bn. Tidsskr Nor Laegeforen. 1998 Mar 10;118(7):1054-7. Tidsskr Nor Laegeforen. 1998. PMID: 9531829 Norwegian.
Mutation in hepatocyte nuclear factor-1 beta gene (TCF2) associated with MODY.
Horikawa Y, Iwasaki N, Hara M, Furuta H, Hinokio Y, Cockburn BN, Lindner T, Yamagata K, Ogata M, Tomonaga O, Kuroki H, Kasahara T, Iwamoto Y, Bell GI. Horikawa Y, et al. Among authors: cockburn bn. Nat Genet. 1997 Dec;17(4):384-5. doi: 10.1038/ng1297-384. Nat Genet. 1997. PMID: 9398836 No abstract available.
Molecular genetics of diabetes mellitus in Chinese subjects: identification of mutations in glucokinase and hepatocyte nuclear factor-1alpha genes in patients with early-onset type 2 diabetes mellitus/MODY.
Ng MC, Cockburn BN, Lindner TH, Yeung VT, Chow CC, So WY, Li JK, Lo YM, Lee ZS, Cockram CS, Critchley JA, Bell GI, Chan JC. Ng MC, et al. Among authors: cockburn bn. Diabet Med. 1999 Nov;16(11):956-63. doi: 10.1046/j.1464-5491.1999.00188.x. Diabet Med. 1999. PMID: 10588527
25 results