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Volumn 4, Issue 9, 2013, Pages 1078-1081

Changing the treatment of permanent neonatal diabetes mellitus from insulin to glibenclamide in a 4-month-old infant with KCNJ11 activating mutation

Author keywords

KCNJ11; Permanent neonatal diabetes mellitus; Sulfonylurea

Indexed keywords

BICARBONATE; GLIBENCLAMIDE; GLUCOSE; INWARDLY RECTIFYING POTASSIUM CHANNEL SUBUNIT KIR6.2; ISOPHANE INSULIN; POTASSIUM; SODIUM;

EID: 84883867056     PISSN: 20087802     EISSN: 20088213     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (4)

References (17)
  • 1
    • 79957954692 scopus 로고    scopus 로고
    • Neonatal diabetes mellitus: Description of two Puerto Rican children with KCNJ11 activating gene mutation
    • Nieves-Rivera F, González-Pijem L. Neonatal diabetes mellitus: Description of two Puerto Rican children with KCNJ11 activating gene mutation. PR Health Sci J 2011;30:87-9.
    • (2011) PR Health Sci J , vol.30 , pp. 87-89
    • Nieves-Rivera, F.1    González-Pijem, L.2
  • 2
    • 79956111232 scopus 로고    scopus 로고
    • The cost-effectiveness of personalized genetic medicine: The case of genetic testing in neonatal diabetes
    • Greeley SA, John PM, Winn AN, Ornelas J, Lipton RB, Philipson LH, et al. The cost-effectiveness of personalized genetic medicine: The case of genetic testing in neonatal diabetes. Diabetes Care 2011;34:622-7.
    • (2011) Diabetes Care , vol.34 , pp. 622-627
    • Greeley, S.A.1    John, P.M.2    Winn, A.N.3    Ornelas, J.4    Lipton, R.B.5    Philipson, L.H.6
  • 3
    • 4043088022 scopus 로고    scopus 로고
    • Permanent neonatal diabetes due to paternal germline mosaicism for an activating mutation of the KCNJ11 Gene encoding the Kir6.2 subunit of the beta-cell potassium adenosine triphosphate channel
    • Gloyn AL, Cummings EA, Edghill EL, Harries LW, Scott R, Costa T, et al. Permanent neonatal diabetes due to paternal germline mosaicism for an activating mutation of the KCNJ11 Gene encoding the Kir6.2 subunit of the beta-cell potassium adenosine triphosphate channel. J Clin Endocrinol Metab 2004;89:3932-5.
    • (2004) J Clin Endocrinol Metab , vol.89 , pp. 3932-3935
    • Gloyn, A.L.1    Cummings, E.A.2    Edghill, E.L.3    Harries, L.W.4    Scott, R.5    Costa, T.6
  • 4
    • 77249133116 scopus 로고    scopus 로고
    • New uses for old drugs: Neonatal diabetes and sulphonylureas
    • Ashcroft FM. New uses for old drugs: Neonatal diabetes and sulphonylureas. Cell Metab 2010;11:179-81.
    • (2010) Cell Metab , vol.11 , pp. 179-181
    • Ashcroft, F.M.1
  • 6
    • 84861618060 scopus 로고    scopus 로고
    • Permanent neonatal diabetes mellitus due to KCNJ11 mutation in a Portuguese family: Transition from insulin to oral sulfonylureas
    • Dupont J, Pereira C, Medeira A, Duarte R, Ellard S, Sampaio L. Permanent neonatal diabetes mellitus due to KCNJ11 mutation in a Portuguese family: Transition from insulin to oral sulfonylureas. J Pediatr Endocrinol Metab 2012;25:367-70.
    • (2012) J Pediatr Endocrinol Metab , vol.25 , pp. 367-370
    • Dupont, J.1    Pereira, C.2    Medeira, A.3    Duarte, R.4    Ellard, S.5    Sampaio, L.6
  • 7
    • 83655172910 scopus 로고    scopus 로고
    • Transient neonatal diabetes with two novel mutations in the KCNJ11 gene and response to sulfonylurea treatment in a preterm infant
    • Siklar Z, Ellard S, Okulu E, Berberoǧlu M, Young E, Savaş Erdeve S, et al. Transient neonatal diabetes with two novel mutations in the KCNJ11 gene and response to sulfonylurea treatment in a preterm infant. J Pediatr Endocrinol Metab 2011;24:1077-80.
    • (2011) J Pediatr Endocrinol Metab , vol.24 , pp. 1077-1080
    • Siklar, Z.1    Ellard, S.2    Okulu, E.3    Berberoǧlu, M.4    Young, E.5    Savaş erdeve, S.6
  • 8
    • 77953039833 scopus 로고    scopus 로고
    • Successful transfer from insulin to oral sulfonylurea in a 3-year-old girl with a mutation in the KCNJ11 gene
    • Al-Mahdi M, Al Mutair A, Al Balwi M, Hussain K. Successful transfer from insulin to oral sulfonylurea in a 3-year-old girl with a mutation in the KCNJ11 gene. Ann Saudi Med 2010;30:162-4.
    • (2010) Ann Saudi Med , vol.30 , pp. 162-164
    • Al-Mahdi, M.1    Al Mutair, A.2    Al Balwi, M.3    Hussain, K.4
  • 9
    • 77954491071 scopus 로고    scopus 로고
    • Successful sulfonylurea treatment of an insulin-naïve neonate with diabetes mellitus due to a KCNJ11 mutation
    • Wambach JA, Marshall BA, Koster JC, White NH, Nichols CG. Successful sulfonylurea treatment of an insulin-naïve neonate with diabetes mellitus due to a KCNJ11 mutation. Pediatr Diabetes 2010;11:286-8.
    • (2010) Pediatr Diabetes , vol.11 , pp. 286-288
    • Wambach, J.A.1    Marshall, B.A.2    Koster, J.C.3    White, N.H.4    Nichols, C.G.5
  • 10
    • 69949118026 scopus 로고    scopus 로고
    • Improved diabetic control during oral sulfonylurea treatment in two children with permanent neonatal diabetes mellitus
    • Ting WH, Huang CY, Lo FS, Lee HC, Lin CL, Guo WL, et al. Improved diabetic control during oral sulfonylurea treatment in two children with permanent neonatal diabetes mellitus. J Pediatr Endocrinol Metab 2009;22:661-7.
    • (2009) J Pediatr Endocrinol Metab , vol.22 , pp. 661-667
    • Ting, W.H.1    Huang, C.Y.2    Lo, F.S.3    Lee, H.C.4    Lin, C.L.5    Guo, W.L.6
  • 11
    • 34548561525 scopus 로고    scopus 로고
    • Sulfonylurea therapy in two Korean patients with insulin-treated neonatal diabetes due to heterozygous mutations of the KCNJ11 gene encoding Kir6.2
    • Kim MS, Kim SY, Kim GH, Yoo HW, Lee DW, Lee DY. Sulfonylurea therapy in two Korean patients with insulin-treated neonatal diabetes due to heterozygous mutations of the KCNJ11 gene encoding Kir6.2. J Korean Med Sci 2007;22:616-20.
    • (2007) J Korean Med Sci , vol.22 , pp. 616-620
    • Kim, M.S.1    Kim, S.Y.2    Kim, G.H.3    Yoo, H.W.4    Lee, D.W.5    Lee, D.Y.6
  • 12
    • 34547124328 scopus 로고    scopus 로고
    • Transition from insulin to glyburide in a 4-month-old girl with neonatal diabetes mellitus caused by a mutation in KCNJ11
    • Chan YM, Laffel LM. Transition from insulin to glyburide in a 4-month-old girl with neonatal diabetes mellitus caused by a mutation in KCNJ11. Pediatr Diabetes 2007;8:235-8.
    • (2007) Pediatr Diabetes , vol.8 , pp. 235-238
    • Chan, Y.M.1    Laffel, L.M.2
  • 14
    • 4644309915 scopus 로고    scopus 로고
    • Kir6.2 mutations are a common cause of permanent neonatal diabetes in a large cohort of French patients
    • Vaxillaire M, Populaire C, Busiah K, Cavé H, Gloyn AL, Hattersley AT, et al. Kir6.2 mutations are a common cause of permanent neonatal diabetes in a large cohort of French patients. Diabetes 2004;53:2719-22.
    • (2004) Diabetes , vol.53 , pp. 2719-2722
    • Vaxillaire, M.1    Populaire, C.2    Busiah, K.3    Cavé, H.4    Gloyn, A.L.5    Hattersley, A.T.6
  • 15
    • 4644260056 scopus 로고    scopus 로고
    • Permanent neonatal diabetes due to mutations in KCNJ11 encoding Kir6.2: Patient characteristics and initial response to sulfonylurea therapy
    • Sagen JV, Raeder H, Hathout E, Shehadeh N, Gudmundsson K, Baevre H, et al. Permanent neonatal diabetes due to mutations in KCNJ11 encoding Kir6.2: Patient characteristics and initial response to sulfonylurea therapy. Diabetes 2004;53:2713-8.
    • (2004) Diabetes , vol.53 , pp. 2713-2718
    • Sagen, J.V.1    Raeder, H.2    Hathout, E.3    Shehadeh, N.4    Gudmundsson, K.5    Baevre, H.6
  • 17
    • 79951998572 scopus 로고    scopus 로고
    • Long-term response to sulfonylurea in a patient with diabetes due to mutation in the KCNJ11 gene
    • Vendramini MF, Gurgel LC, Moisés RS. Long-term response to sulfonylurea in a patient with diabetes due to mutation in the KCNJ11 gene. Arq Bras Endocrinol Metabol 2010;54:682-4.
    • (2010) Arq Bras Endocrinol Metabol , vol.54 , pp. 682-684
    • Vendramini, M.F.1    Gurgel, L.C.2    Moisés, R.S.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.