-
1
-
-
54249086716
-
Types of human diabetes
-
Lawrence RD. Types of human diabetes. Br Med J 1951; 1: 373-375.
-
(1951)
Br Med J
, vol.1
, pp. 373-375
-
-
Lawrence, R.D.1
-
2
-
-
84879570186
-
The clinical utility of C-peptide measurement in the care of patients with diabetes
-
Jones AG, Hattersley AT. The clinical utility of C-peptide measurement in the care of patients with diabetes. Diabet Med 2013; 30: 803-817.
-
(2013)
Diabet Med
, vol.30
, pp. 803-817
-
-
Jones, A.G.1
Hattersley, A.T.2
-
3
-
-
9144268894
-
C-peptide is the appropriate outcome measure for type 1 diabetes clinical trials to preserve beta-cell function: report of an ADA workshop, 21-22 October 2001
-
Palmer JP Fleming GA, Greenbaum CJ, Herold KC, Jansa LD, Kolb H et al. C-peptide is the appropriate outcome measure for type 1 diabetes clinical trials to preserve beta-cell function: report of an ADA workshop, 21-22 October 2001. Diabetes 2004; 53: 250-264.
-
(2004)
Diabetes
, vol.53
, pp. 250-264
-
-
Palmer, J.P.1
Fleming, G.A.2
Greenbaum, C.J.3
Herold, K.C.4
Jansa, L.D.5
Kolb, H.6
-
4
-
-
0016641270
-
A difference between the inheritance of classical juvenile-onset and maturity-onset type diabetes of young people
-
Tattersall RB, Fajans SS. A difference between the inheritance of classical juvenile-onset and maturity-onset type diabetes of young people. Diabetes 1975; 24: 44-53.
-
(1975)
Diabetes
, vol.24
, pp. 44-53
-
-
Tattersall, R.B.1
Fajans, S.S.2
-
5
-
-
84874136002
-
Assessing aetiology in diabetes: how C-peptide, CRP and fucosylation came to the party!
-
RD Lawrence lecture 2012.
-
Owen KR. RD Lawrence lecture 2012. Assessing aetiology in diabetes: how C-peptide, CRP and fucosylation came to the party! Diabet Med 2013; 30: 260-266.
-
(2013)
Diabet Med
, vol.30
, pp. 260-266
-
-
Owen, K.R.1
-
6
-
-
0033847575
-
Sensitivity to sulphonylureas in patients with hepatocyte nuclear factor-1alpha gene mutations: evidence for pharmacogenetics in diabetes
-
Pearson ER, Liddell WG, Shepherd M, Corrall RJ, Hattersley AT. Sensitivity to sulphonylureas in patients with hepatocyte nuclear factor-1alpha gene mutations: evidence for pharmacogenetics in diabetes. Diabet Med 2000; 17: 543-545.
-
(2000)
Diabet Med
, vol.17
, pp. 543-545
-
-
Pearson, E.R.1
Liddell, W.G.2
Shepherd, M.3
Corrall, R.J.4
Hattersley, A.T.5
-
7
-
-
0142186278
-
Genetic cause of hyperglycaemia and response to treatment in diabetes
-
Pearson ER, Starkey BJ, Powell RJ, Gribble FM, Clark PM, Hattersley AT. Genetic cause of hyperglycaemia and response to treatment in diabetes. Lancet 2003; 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
-
8
-
-
0242363725
-
No deterioration in glycemic control in HNF-1alpha maturity-onset diabetes of the young following transfer from long-term insulin to sulphonylureas
-
Shepherd M, Pearson ER, Houghton J, Salt G, Ellard S, Hattersley AT. No deterioration in glycemic control in HNF-1alpha maturity-onset diabetes of the young following transfer from long-term insulin to sulphonylureas. Diabetes Care 2003; 26: 3191-3192.
-
(2003)
Diabetes Care
, vol.26
, pp. 3191-3192
-
-
Shepherd, M.1
Pearson, E.R.2
Houghton, J.3
Salt, G.4
Ellard, S.5
Hattersley, A.T.6
-
9
-
-
2342633204
-
Activating mutations in the gene encoding the ATP-sensitive potassium-channel subunit Kir6.2 and permanent neonatal diabetes
-
Gloyn AL, Pearson ER, Antcliff JF, Proks P, Bruining GJ, Slingerland AS et al. Activating mutations in the gene encoding the ATP-sensitive potassium-channel subunit Kir6.2 and permanent neonatal diabetes. N Engl J Med 2004; 350: 1838-1849.
-
(2004)
N Engl J Med
, vol.350
, pp. 1838-1849
-
-
Gloyn, A.L.1
Pearson, E.R.2
Antcliff, J.F.3
Proks, P.4
Bruining, G.J.5
Slingerland, A.S.6
-
10
-
-
33746778878
-
Activating mutations in ABCC8 cause neonatal diabetes mellitus
-
Babenko AP, Polak M, Cave H, Busiah K, Czernichow P, Scharfmann R et al. Activating mutations in ABCC8 cause neonatal diabetes mellitus. N Engl J Med 2006; 355: 456-466.
-
(2006)
N Engl J Med
, vol.355
, pp. 456-466
-
-
Babenko, A.P.1
Polak, M.2
Cave, H.3
Busiah, K.4
Czernichow, P.5
Scharfmann, R.6
-
11
-
-
33746686369
-
Switching from insulin to oral sulfonylureas in patients with diabetes due to Kir6.2 mutations
-
Pearson ER, Flechtner I, Njolstad PR, Malecki MT, Flanagan SE, Larkin B et al. Switching from insulin to oral sulfonylureas in patients with diabetes due to Kir6.2 mutations. N Engl J Med 2006; 355: 467-477.
-
(2006)
N Engl J Med
, vol.355
, pp. 467-477
-
-
Pearson, E.R.1
Flechtner, I.2
Njolstad, P.R.3
Malecki, M.T.4
Flanagan, S.E.5
Larkin, B.6
-
12
-
-
10544236911
-
Mutations in the hepatocyte nuclear factor-4alpha gene in maturity-onset diabetes of the young (MODY1)
-
Yamagata K, Furuta H, Oda N, Kaisaki PJ, Menzel S, Cox NJ et al. Mutations in the hepatocyte nuclear factor-4alpha gene in maturity-onset diabetes of the young (MODY1). Nature 1996; 384: 458-460.
-
(1996)
Nature
, vol.384
, pp. 458-460
-
-
Yamagata, K.1
Furuta, H.2
Oda, N.3
Kaisaki, P.J.4
Menzel, S.5
Cox, N.J.6
-
13
-
-
84885750551
-
Diabetes mellitus in neonates and infants: genetic heterogeneity, clinical approach to diagnosis, and therapeutic options
-
Rubio-Cabezas O, Ellard S. Diabetes mellitus in neonates and infants: genetic heterogeneity, clinical approach to diagnosis, and therapeutic options. Horm Res Paediatr 2013; 80: 137-146.
-
(2013)
Horm Res Paediatr
, vol.80
, pp. 137-146
-
-
Rubio-Cabezas, O.1
Ellard, S.2
-
14
-
-
72849111539
-
Loss-of-function CYP2C9 variants improve therapeutic response to sulfonylureas in Type 2 diabetes: a Go-DARTS Study
-
Zhou K, Donnelly L, Burch L, Tavendale R, Doney AS, Leese G et al. Loss-of-function CYP2C9 variants improve therapeutic response to sulfonylureas in Type 2 diabetes: a Go-DARTS Study. Clin Pharmacol Ther 2010; 87: 52-56.
-
(2010)
Clin Pharmacol Ther
, vol.87
, pp. 52-56
-
-
Zhou, K.1
Donnelly, L.2
Burch, L.3
Tavendale, R.4
Doney, A.S.5
Leese, G.6
-
15
-
-
34248156160
-
Effect of genetic variation in the organic cation transporter 1 (OCT1) on metformin action
-
Shu Y, Sheardown SA, Brown C, Owen RP, Zhang S, Castro RA et al. Effect of genetic variation in the organic cation transporter 1 (OCT1) on metformin action. J Clin Invest 2007; 117: 1422-1431.
-
(2007)
J Clin Invest
, vol.117
, pp. 1422-1431
-
-
Shu, Y.1
Sheardown, S.A.2
Brown, C.3
Owen, R.P.4
Zhang, S.5
Castro, R.A.6
-
16
-
-
29144523534
-
A human transporter protein that mediates the final excretion step for toxic organic cations
-
Otsuka M, Matsumoto T, Morimoto R, Arioka S, Omote H, Moriyama Y. A human transporter protein that mediates the final excretion step for toxic organic cations. Proc Natl Acad Sci U S A 2005; 102: 17923-17928.
-
(2005)
Proc Natl Acad Sci U S A
, vol.102
, pp. 17923-17928
-
-
Otsuka, M.1
Matsumoto, T.2
Morimoto, R.3
Arioka, S.4
Omote, H.5
Moriyama, Y.6
-
17
-
-
33644664085
-
Metformin is a superior substrate for renal organic cation transporter OCT2 rather than hepatic OCT1
-
Kimura N, Masuda S, Tanihara Y, Ueo H, Okuda M, Katsura T et al. Metformin is a superior substrate for renal organic cation transporter OCT2 rather than hepatic OCT1. Drug Metab Pharmacokinet 2005; 20: 379-386.
-
(2005)
Drug Metab Pharmacokinet
, vol.20
, pp. 379-386
-
-
Kimura, N.1
Masuda, S.2
Tanihara, Y.3
Ueo, H.4
Okuda, M.5
Katsura, T.6
-
18
-
-
34250005960
-
Substrate specificity of MATE1 and MATE2-K, human multidrug and toxin extrusions/H(+)-organic cation antiporters
-
Tanihara Y, Masuda S, Sato T, Katsura T, Ogawa O, Inui K. Substrate specificity of MATE1 and MATE2-K, human multidrug and toxin extrusions/H(+)-organic cation antiporters. Biochem Pharmacol 2007; 74: 359-371.
-
(2007)
Biochem Pharmacol
, vol.74
, pp. 359-371
-
-
Tanihara, Y.1
Masuda, S.2
Sato, T.3
Katsura, T.4
Ogawa, O.5
Inui, K.6
-
19
-
-
81055140250
-
The pharmacogenetics of metformin and its impact on plasma metformin steady-state levels and glycosylated hemoglobin A1c
-
Christensen MM, Brasch-Andersen C, Green H, Nielsen F, Damkier P, Beck-Nielsen H et al. The pharmacogenetics of metformin and its impact on plasma metformin steady-state levels and glycosylated hemoglobin A1c. Pharmacogenet Genomics 2011 21: 837-850.
-
(2011)
Pharmacogenet Genomics
, vol.21
, pp. 837-850
-
-
Christensen, M.M.1
Brasch-Andersen, C.2
Green, H.3
Nielsen, F.4
Damkier, P.5
Beck-Nielsen, H.6
-
20
-
-
79251612707
-
Common variants near ATM are associated with glycemic response to metformin in type 2 diabetes
-
Zhou K, Bellenguez C, Spencer CC, Bennett AJ, Coleman RL, Tavendale R et al. Common variants near ATM are associated with glycemic response to metformin in type 2 diabetes. Nat Genet 2011; 43: 117-120.
-
(2011)
Nat Genet
, vol.43
, pp. 117-120
-
-
Zhou, K.1
Bellenguez, C.2
Spencer, C.C.3
Bennett, A.J.4
Coleman, R.L.5
Tavendale, R.6
-
21
-
-
84866319096
-
A gene variant near ATM is significantly associated with metformin treatment response in type 2 diabetes: a replication and meta-analysis of five cohorts
-
Van Leeuwen N, Nijpels G, Becker M, Deshmukh H, Zhou K, Stricker B et al. A gene variant near ATM is significantly associated with metformin treatment response in type 2 diabetes: a replication and meta-analysis of five cohorts. Diabetologia. 2012; 55: 1971-1977.
-
(2012)
Diabetologia
, vol.55
, pp. 1971-1977
-
-
Van, L.N.1
Nijpels, G.2
Becker, M.3
Deshmukh, H.4
Zhou, K.5
Stricker, B.6
-
23
-
-
0014954015
-
An unusual form of diabetes mellitus in ataxia telangiectasia
-
Schalch DS, McFarlin DE, Barlow MH. An unusual form of diabetes mellitus in ataxia telangiectasia. N Engl J Med 1970; 282: 1396-1402.
-
(1970)
N Engl J Med
, vol.282
, pp. 1396-1402
-
-
Schalch, D.S.1
McFarlin, D.E.2
Barlow, M.H.3
-
24
-
-
48749096999
-
-
National Institute for Health and Clinical Excellence. Clinical guideline 87. London: NICE
-
National Institute for Health and Clinical Excellence. Clinical guideline 87. Type 2 Diabetes: The Management of Type 2 Diabetes. London: NICE, 2009.
-
(2009)
Type 2 Diabetes: The Management of Type 2 Diabetes
-
-
-
25
-
-
77956860381
-
-
Network Scottish Intercollegiate Guidelines. A national clinical guideline. Edinburgh, UK: SIGN
-
Network Scottish Intercollegiate Guidelines. SIGN 116: Management of Diabetes. A national clinical guideline. Edinburgh, UK: SIGN, 2010.
-
(2010)
SIGN 116: Management of Diabetes
-
-
-
26
-
-
84866065910
-
ADA/EASD position statement of the treatment of type 2 diabetes: Reply to Rodbard HW and Jellinger PS (letter), Scheen AJ (letter) and Ceriello A, Gallo M, Gentile S (letter)
-
Matthews DR, Inzucchi SE. ADA/EASD position statement of the treatment of type 2 diabetes: Reply to Rodbard HW and Jellinger PS (letter), Scheen AJ (letter) and Ceriello A, Gallo M, Gentile S et al. (letter). Diabetologia 2012; 55: 2856-2857.
-
(2012)
Diabetologia
, vol.55
, pp. 2856-2857
-
-
Matthews, D.R.1
Inzucchi, S.E.2
|