메뉴 건너뛰기




Volumn 57, Issue 1, 2014, Pages 54-56

Cross-sectional and longitudinal studies suggest pharmacological treatment used in patients with glucokinase mutations does not alter glycaemia

Author keywords

GCK mutation; Glucokinase; MODY; Pharmacogenetics; Treatment

Indexed keywords

GLIBENCLAMIDE; GLUCOKINASE; GLUCOSE; HEMOGLOBIN A1C; INSULIN; METFORMIN; ORAL ANTIDIABETIC AGENT;

EID: 84890900649     PISSN: 0012186X     EISSN: 14320428     Source Type: Journal    
DOI: 10.1007/s00125-013-3075-x     Document Type: Article
Times cited : (169)

References (9)
  • 1
    • 0026583193 scopus 로고
    • Linkage of type 2 diabetes to the glucokinase gene
    • 1349989 10.1016/0140-6736(92)91958-B 1:STN:280:DyaK383mtFWqsQ%3D%3D
    • Hattersley AT, Turner RC, Permutt MA et al (1992) Linkage of type 2 diabetes to the glucokinase gene. Lancet 339:1307-1310
    • (1992) Lancet , vol.339 , pp. 1307-1310
    • Hattersley, A.T.1    Turner, R.C.2    Permutt, M.A.3
  • 2
    • 0036210337 scopus 로고    scopus 로고
    • The genetic abnormality in the beta cell determines the response to an oral glucose load
    • 11914749 10.1007/s00125-001-0770-9 1:CAS:528:DC%2BD38XitVeisr8%3D
    • Stride A, Vaxillaire M, Tuomi T et al (2002) The genetic abnormality in the beta cell determines the response to an oral glucose load. Diabetologia 45:427-435
    • (2002) Diabetologia , vol.45 , pp. 427-435
    • Stride, A.1    Vaxillaire, M.2    Tuomi, T.3
  • 3
    • 0028353674 scopus 로고
    • Insulin secretory abnormalities in subjects with hyperglycemia due to glucokinase mutations
    • 8132752 10.1172/JCI117064 1:STN:280:DyaK2c7nvFCmug%3D%3D
    • Byrne MM, Sturis J, Clement K et al (1994) Insulin secretory abnormalities in subjects with hyperglycemia due to glucokinase mutations. J Clin Invest 93:1120-1130
    • (1994) J Clin Invest , vol.93 , pp. 1120-1130
    • Byrne, M.M.1    Sturis, J.2    Clement, K.3
  • 4
    • 33744466577 scopus 로고    scopus 로고
    • Aetiological heterogeneity of asymptomatic hyperglycaemia in children and adolescents
    • 16602010 10.1007/s00431-006-0106-3 1:STN:280:DC%2BD283oslaksw%3D%3D
    • Feigerlova E, Pruhova S, Dittertova L et al (2006) Aetiological heterogeneity of asymptomatic hyperglycaemia in children and adolescents. Eur J Pediatr 165:446-452
    • (2006) Eur J Pediatr , vol.165 , pp. 446-452
    • Feigerlova, E.1    Pruhova, S.2    Dittertova, L.3
  • 5
    • 84879055014 scopus 로고    scopus 로고
    • 1c in the identification of patients with hyperglycaemia caused by a glucokinase mutation: Observational case control studies
    • 23799006 10.1371/journal.pone.0065326 1:CAS:528:DC%2BC3sXhtVCms7bM
    • 1c in the identification of patients with hyperglycaemia caused by a glucokinase mutation: observational case control studies. PLoS One 8:e65326
    • (2013) PLoS One , vol.8 , pp. 65326
    • Steele, A.M.1    Wensley, K.J.2    Ellard, S.3
  • 6
    • 0029762068 scopus 로고    scopus 로고
    • Diabetes complications in NIDDM kindreds linked to the MODY3 locus on chromosome 12q
    • 8875082 10.2337/diacare.19.9.915 1:STN:280:DyaK2s%2FivFSksg%3D%3D
    • Velho G, Vaxillaire M, Boccio V, Charpentier G, Froguel P (1996) Diabetes complications in NIDDM kindreds linked to the MODY3 locus on chromosome 12q. Diabetes Care 19:915-919
    • (1996) Diabetes Care , vol.19 , pp. 915-919
    • Velho, G.1    Vaxillaire, M.2    Boccio, V.3    Charpentier, G.4    Froguel, P.5
  • 7
    • 58149216624 scopus 로고    scopus 로고
    • Pregnancy outcome in patients with raised blood glucose due to a heterozygous glucokinase gene mutation
    • 19125755 10.1111/j.1464-5491.2008.02622.x 1:STN:280: DC%2BD1M%2FlsFehsA%3D%3D
    • Spyer G, Macleod KM, Shepherd M, Ellard S, Hattersley AT (2009) Pregnancy outcome in patients with raised blood glucose due to a heterozygous glucokinase gene mutation. Diabet Med 26:14-18
    • (2009) Diabet Med , vol.26 , pp. 14-18
    • Spyer, G.1    Macleod, K.M.2    Shepherd, M.3    Ellard, S.4    Hattersley, A.T.5
  • 8
    • 33746686369 scopus 로고    scopus 로고
    • Switching from insulin to oral sulfonylureas in patients with diabetes due to Kir6.2 mutations
    • 16885550 10.1056/NEJMoa061759 1:CAS:528:DC%2BD28XnslyktrY%3D
    • Pearson ER, Flechtner I, Njolstad PR et al (2006) Switching from insulin to oral sulfonylureas in patients with diabetes due to Kir6.2 mutations. N Engl J Med 355:467-477
    • (2006) N Engl J Med , vol.355 , pp. 467-477
    • Pearson, E.R.1    Flechtner, I.2    Njolstad, P.R.3
  • 9
    • 0142186278 scopus 로고    scopus 로고
    • Genetic cause of hyperglycaemia and response to treatment in diabetes
    • 14575972 10.1016/S0140-6736(03)14571-0 1:CAS:528:DC%2BD3sXot1Cjt7s%3D
    • Pearson ER, Starkey BJ, Powell RJ, Gribble FM, Clark PM, Hattersley AT (2003) Genetic cause of hyperglycaemia and response to treatment in diabetes. Lancet 362:1275-1281
    • (2003) Lancet , vol.362 , pp. 1275-1281
    • Pearson, E.R.1    Starkey, B.J.2    Powell, R.J.3    Gribble, F.M.4    Clark, P.M.5    Hattersley, A.T.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.