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Volumn 92, Issue 10, 2007, Pages 3774-3776

Neonatal diabetes mellitus: Insights for more common forms of diabetes

Author keywords

[No Author keywords available]

Indexed keywords

GLIBENCLAMIDE; GLIPIZIDE; GLUCOSE DEHYDROGENASE; INSULIN; SULFONYLUREA; TOLBUTAMIDE;

EID: 35349005196     PISSN: 0021972X     EISSN: 0021972X     Source Type: Journal    
DOI: 10.1210/jc.2007-1710     Document Type: Editorial
Times cited : (11)

References (19)
  • 1
    • 34247880183 scopus 로고    scopus 로고
    • Neonatal diabetes mellitus: A disease linked to multiple mechanisms
    • Polak M, Cavé H2007 Neonatal diabetes mellitus: a disease linked to multiple mechanisms. Orphanet J Rare Dis Mar 9;2:12
    • (2007) Orphanet J Rare Dis Mar 9;2 , vol.12
    • Polak, M.1    Cavé, H.2
  • 3
    • 0036797965 scopus 로고    scopus 로고
    • Metz C, Cave H, Bertrand AM, Deffert C, Gueguen-Giroux B, Czernichow P, Polak M; NDM French Study Group. Neonatal diabetes mellitus 2002 Neonatal diabetes mellitus: chromosomal analysis in transient and permanent cases. J Pediatr 141:483-489
    • Metz C, Cave H, Bertrand AM, Deffert C, Gueguen-Giroux B, Czernichow P, Polak M; NDM French Study Group. Neonatal diabetes mellitus 2002 Neonatal diabetes mellitus: chromosomal analysis in transient and permanent cases. J Pediatr 141:483-489
  • 5
    • 0028888383 scopus 로고
    • Transient neonatal diabetes and later onset diabetes: A case of inherited insulin resistance
    • Shield JP, Baum JD 1995 Transient neonatal diabetes and later onset diabetes: a case of inherited insulin resistance. Arch Dis Child 72:56-57
    • (1995) Arch Dis Child , vol.72 , pp. 56-57
    • Shield, J.P.1    Baum, J.D.2
  • 7
    • 3042637568 scopus 로고    scopus 로고
    • Iafusco D, Stazi MA, Cotichini R, Cotellessa M, Martinucci ME, Mazzella M, Cherubini V, Barbetti F, Martinetti M, Cerutti F, Prisco F; Early Onset Diabetes Study Group of the Italian Society of Paediatric Endocrinology and Diabetology 2002 Permanent diabetes mellitus in the first year of life. Diabetologia 45:798-804
    • Iafusco D, Stazi MA, Cotichini R, Cotellessa M, Martinucci ME, Mazzella M, Cherubini V, Barbetti F, Martinetti M, Cerutti F, Prisco F; Early Onset Diabetes Study Group of the Italian Society of Paediatric Endocrinology and Diabetology 2002 Permanent diabetes mellitus in the first year of life. Diabetologia 45:798-804
  • 10
    • 19944427182 scopus 로고    scopus 로고
    • Massa O, Iafusco D, D'Amato E, Gloyn AL, Hattersley AT, Pasquino B, Tonini G, Dammacco F, Zanette G, Meschi F, Porzio O, Bottazzo G, Crino' A, Lorini R, Cerutti F, Vanelli M, Barbetti F; Early Onset Diabetes Study Group of the Italian Society of Pediatric Endocrinology and Diabetology 2005 KCNJ11 activating mutations in Italian patients with permanent neonatal diabetes. Hum Mutat 25:22-27
    • Massa O, Iafusco D, D'Amato E, Gloyn AL, Hattersley AT, Pasquino B, Tonini G, Dammacco F, Zanette G, Meschi F, Porzio O, Bottazzo G, Crino' A, Lorini R, Cerutti F, Vanelli M, Barbetti F; Early Onset Diabetes Study Group of the Italian Society of Pediatric Endocrinology and Diabetology 2005 KCNJ11 activating mutations in Italian patients with permanent neonatal diabetes. Hum Mutat 25:22-27
  • 12
    • 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 β-cell potassium adenosine triphosphate channel
    • Gloyn AL, Cummings EA, Edghill EL, Harries LW, Scott R, Costa T, Temple IK, Hattersley AT, Ellard S 2004 Permanent neonatal diabetes due to paternal germline mosaicism for an activating mutation of the KCNJ11 gene encoding the Kir6.2 subunit of the β-cell potassium adenosine triphosphate channel. J Clin Endocrinol Metab 89:3932-3935
    • (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    Temple, I.K.7    Hattersley, A.T.8    Ellard, S.9
  • 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 2004 Molecular basis of Kir6.2 mutations associated with neonatal diabetes or neonatal diabetes plus neurological features. Proc Natl Acad Sci USA 101:17539-17544
    • (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
  • 19
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    • Pearson ER, Flechtner I, Njølstad PR, Malecki MT, Flanagan SE, Larkin B, Ashcroft FM, Klimes I, Codner E, Iotova V, Slingerland AS, Shield J, Robert JJ, Holst JJ, Clark PM, Ellard S, Søvik O, Polak M, Hattersley AT; Neonatal Diabetes International Collaborative Group 2006 Switching from insulin to oral sulfonylureas in patients with diabetes due to Kir6.2 mutations. N Engl J Med 355:467-477
    • Pearson ER, Flechtner I, Njølstad PR, Malecki MT, Flanagan SE, Larkin B, Ashcroft FM, Klimes I, Codner E, Iotova V, Slingerland AS, Shield J, Robert JJ, Holst JJ, Clark PM, Ellard S, Søvik O, Polak M, Hattersley AT; Neonatal Diabetes International Collaborative Group 2006 Switching from insulin to oral sulfonylureas in patients with diabetes due to Kir6.2 mutations. N Engl J Med 355:467-477


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.