-
1
-
-
0026583193
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
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