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Volumn 22, Issue 4, 2007, Pages 616-620

Sulfonylurea therapy in two Korean patients with insulin-treated neonatal diabetes due to heterozygous mutations of the KCNJ11 gene encoding Kir6.2

Author keywords

Kir6.2 channel; Korean; Mutation; Neonatal diabetes; Permanent; Sulfonylurea

Indexed keywords


EID: 34548561525     PISSN: 10118934     EISSN: 15986357     Source Type: Journal    
DOI: 10.3346/jkms.2007.22.4.616     Document Type: Article
Times cited : (18)

References (18)
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    • Activating Mutations in Kir6.2 and neonatal diabetes: New clinical syndromes, new scientific insights and new therapy
    • Hattersley AT, Ashcroft FM. Activating Mutations in Kir6.2 and neonatal diabetes: New clinical syndromes, new scientific insights and new therapy. Diabetes 2005; 54: 2503-13.
    • (2005) Diabetes , vol.54 , pp. 2503-2513
    • Hattersley, A.T.1    Ashcroft, F.M.2
  • 9
    • 33646513278 scopus 로고    scopus 로고
    • Mutation in KCNJ11, which encodes Kir6.2, are a common cause of diabetes diagnosed in the first 6 months of life, with the phenotype determined by genotype
    • Flanagan SE, Edghill EL, Gloyn AL, Ellard S, Hattersley AT. Mutation in KCNJ11, which encodes Kir6.2, are a common cause of diabetes diagnosed in the first 6 months of life, with the phenotype determined by genotype. Diabetologia 2006; 49: 1190-7.
    • (2006) Diabetologia , vol.49 , pp. 1190-1197
    • Flanagan, S.E.1    Edghill, E.L.2    Gloyn, A.L.3    Ellard, S.4    Hattersley, A.T.5
  • 10
    • 34548594723 scopus 로고    scopus 로고
    • KCNJ11 gene activating mutations in Japanese patients with neonatal diabetes mellitus
    • Suzuki S, Mukai T, Matsuo K, Ueda O, Ito Y, Makita Y, Fujieda K. KCNJ11 gene activating mutations in Japanese patients with neonatal diabetes mellitus. Horm Research 2005; 64 (Suppl 1): 136.
    • (2005) Horm Research , vol.64 , Issue.SUPPL. 1 , pp. 136
    • Suzuki, S.1    Mukai, T.2    Matsuo, K.3    Ueda, O.4    Ito, Y.5    Makita, Y.6    Fujieda, K.7
  • 13
    • 10644233000 scopus 로고    scopus 로고
    • Molecular basis of Kir6.2 mutations associated with neonatal diabetes or neonatal diabetes plus neurological features
    • Proks P, Antcliff JF, Lippiat J, Gloyn AL, Hattersley AT, Ashcroft FM. Molecular basis of Kir6.2 mutations associated with neonatal diabetes or neonatal diabetes plus neurological features. Proc Natl Acad Sci USA 2004; 101: 17539-44.
    • (2004) Proc Natl Acad Sci USA , vol.101 , pp. 17539-17544
    • Proks, P.1    Antcliff, J.F.2    Lippiat, J.3    Gloyn, A.L.4    Hattersley, A.T.5    Ashcroft, F.M.6
  • 15
    • 8744262895 scopus 로고    scopus 로고
    • Glibenclamide treatment in permanent neonatal diabetes mellitus due to an activating mutation in Kir6.2
    • Zung A, Glaser B, Nimri R, Zadik Z. Glibenclamide treatment in permanent neonatal diabetes mellitus due to an activating mutation in Kir6.2. J Clin Endocrinol Metab 2004; 89: 5504-7.
    • (2004) J Clin Endocrinol Metab , vol.89 , pp. 5504-5507
    • Zung, A.1    Glaser, B.2    Nimri, R.3    Zadik, Z.4
  • 16
    • 14644408737 scopus 로고    scopus 로고
    • High-dose glibenclamide can replace insulin therapy despite transitory diarrhea in early-onset diabetes caused by a novel R201L Kir6.2 mutation
    • Codner E, Flanagan S, Ellard S, Garcia H, Hattersley A. High-dose glibenclamide can replace insulin therapy despite transitory diarrhea in early-onset diabetes caused by a novel R201L Kir6.2 mutation. Diabetes Care 2005; 28: 758-9.
    • (2005) Diabetes Care , vol.28 , pp. 758-759
    • Codner, E.1    Flanagan, S.2    Ellard, S.3    Garcia, H.4    Hattersley, A.5
  • 17
    • 20044387060 scopus 로고    scopus 로고
    • The identification of a R201H mutation in KCNJ11, which encodes Kir6.2, and successful transfer to sustained-release sulphonylurea therapy in a subject with neonatal diabetes: Evidence for heterogeneity of beta cell function among carriers of the R201H mutation
    • Klupa T, Edghill EL, Nazim J, Sieradzki J, Ellard S, Hattersley AT, Malecki MT. The identification of a R201H mutation in KCNJ11, which encodes Kir6.2, and successful transfer to sustained-release sulphonylurea therapy in a subject with neonatal diabetes: evidence for heterogeneity of beta cell function among carriers of the R201H mutation. Diabetologia 2005; 48: 1029-31.
    • (2005) Diabetologia , vol.48 , pp. 1029-1031
    • Klupa, T.1    Edghill, E.L.2    Nazim, J.3    Sieradzki, J.4    Ellard, S.5    Hattersley, A.T.6    Malecki, M.T.7


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.