-
1
-
-
0035852037
-
Epidemic increase in childhood overweight, 1986-1998
-
Strauss RS, Pollock HA. Epidemic increase in childhood overweight, 1986-1998. JAMA 2001: 286: 2845-2848.
-
(2001)
JAMA
, vol.286
, pp. 2845-2848
-
-
Strauss, R.S.1
Pollock, H.A.2
-
2
-
-
0035689025
-
Type 2 diabetes mellitus in children and adolescents
-
Nesmith JD. Type 2 diabetes mellitus in children and adolescents. Pediatr Rev 2001: 22: 147-152.
-
(2001)
Pediatr Rev
, vol.22
, pp. 147-152
-
-
Nesmith, J.D.1
-
3
-
-
0033429304
-
Worldwide increase in incidence of type 1 diabetes: The analysis of the data on published incidence trends
-
Onkamo P, Vaananen S, Karvonen M, Tuomilehto J. Worldwide increase in incidence of type 1 diabetes: The analysis of the data on published incidence trends. Diabetologia 1999: 42: 1395-1403.
-
(1999)
Diabetologia
, vol.42
, pp. 1395-1403
-
-
Onkamo, P.1
Vaananen, S.2
Karvonen, M.3
Tuomilehto, J.4
-
4
-
-
0141781111
-
Changing prevalence of overweight children and adolescents at onset of insulin-treated diabetes
-
Libman IM, Pietropaolo M, Arslanian SA, Le Porte RE, Becker DJ. Changing prevalence of overweight children and adolescents at onset of insulin-treated diabetes. Diabetes Care 2003: 26: 2871-2875.
-
(2003)
Diabetes Care
, vol.26
, pp. 2871-2875
-
-
Libman, I.M.1
Pietropaolo, M.2
Arslanian, S.A.3
Le Porte, R.E.4
Becker, D.J.5
-
5
-
-
0036236749
-
Maturity-onset diabetes of the young (MODY): Genetic and clinical characteristics
-
Velho G, Robert JJ. Maturity-onset diabetes of the young (MODY): Genetic and clinical characteristics. Horm Res 2002: 57 (Suppl. 1): 29-33.
-
(2002)
Horm Res
, vol.57
, Issue.SUPPL. 1
, pp. 29-33
-
-
Velho, G.1
Robert, J.J.2
-
6
-
-
0028845529
-
Maturity-onset diabetes of the young (MODY) at least ten times more common in Europe than previously assumed
-
Ledermann HM. Maturity-onset diabetes of the young (MODY) at least ten times more common in Europe than previously assumed. Diabetologia 1995: 38: 1482.
-
(1995)
Diabetologia
, vol.38
, pp. 1482
-
-
Ledermann, H.M.1
-
7
-
-
29444440400
-
Mutations in the CEL VNTR cause a syndrome of diabetes and pancreatic exocrine dysfunction
-
Raeder H, Johansson S, Holm PI et al. Mutations in the CEL VNTR cause a syndrome of diabetes and pancreatic exocrine dysfunction. Nat Genet 2005: 38: 54-62.
-
(2005)
Nat Genet
, vol.38
, pp. 54-62
-
-
Raeder, H.1
Johansson, S.2
Holm, P.I.3
-
8
-
-
0002886774
-
Molecular and biochemical analysis of the MODY syndromes
-
Winter WE. Molecular and biochemical analysis of the MODY syndromes. Pediatr Diabetes 2000: 1: 88-118.
-
(2000)
Pediatr Diabetes
, vol.1
, pp. 88-118
-
-
Winter, W.E.1
-
9
-
-
0035960122
-
Molecular mechanism and clinical pathophysiology of maturity-onset diabetes of the young
-
Fajans SS, Bell GI, Polonsky KS. Molecular mechanism and clinical pathophysiology of maturity-onset diabetes of the young. N Engl J Med 2001: 345: 971-980.
-
(2001)
N Engl J Med
, vol.345
, pp. 971-980
-
-
Fajans, S.S.1
Bell, G.I.2
Polonsky, K.S.3
-
10
-
-
0032956493
-
Phenotypic characteristics of early onset autosomal dominant type 2 diabetes unlinked to known maturity onset diabetes of the young (MODY) genes
-
Doria A, Yang Y, Malecki M et al. Phenotypic characteristics of early onset autosomal dominant type 2 diabetes unlinked to known maturity onset diabetes of the young (MODY) genes. Diabetes Care 1999: 22: 253-261.
-
(1999)
Diabetes Care
, vol.22
, pp. 253-261
-
-
Doria, A.1
Yang, Y.2
Malecki, M.3
-
11
-
-
0002945752
-
Maturity-onset diabetes of the young: A model for genetic studies of diabetes mellitus
-
In: LeRoith D, Taylor SI, Olefsky JM, eds. 2nd edn. Philadelphia, PA: Lippincott Williams & Wilkins
-
Fajans SS, Bell GI. Maturity-onset diabetes of the young: A model for genetic studies of diabetes mellitus. In: LeRoith D, Taylor SI, Olefsky JM, eds. Diabetes Mellitus: A Fundamental and Clinical Text, 2nd edn. Philadelphia, PA: Lippincott Williams & Wilkins, 2000: 691-705.
-
(2000)
Diabetes Mellitus: A Fundamental and Clinical Text
, pp. 691-705
-
-
Fajans, S.S.1
Bell, G.I.2
-
12
-
-
0028258006
-
A novel radioligand-binding assay to determine diagnostic accuracy of isoform-specific glutamic acid decarboxylase antibodies in childhood IDDM
-
Grubin CE, Daniels T, Toivola B et al. A novel radioligand-binding assay to determine diagnostic accuracy of isoform-specific glutamic acid decarboxylase antibodies in childhood IDDM. Diabetologia 1994: 37: 344-350.
-
(1994)
Diabetologia
, vol.37
, pp. 344-350
-
-
Grubin, C.E.1
Daniels, T.2
Toivola, B.3
-
13
-
-
34249820806
-
Heat shock protein peptide DiaPep277 treatment in children with newly diagnosed type 1 diabetes: A randomized double-blind phase II study
-
Lazar L, Ofan R, Weintrob N et al. Heat shock protein peptide DiaPep277 treatment in children with newly diagnosed type 1 diabetes: A randomized double-blind phase II study. Diabetes Metab Res Rev 2007: 23: 286-291.
-
(2007)
Diabetes Metab Res Rev
, vol.23
, pp. 286-291
-
-
Lazar, L.1
Ofan, R.2
Weintrob, N.3
-
14
-
-
0024284028
-
A simple salting out procedure of extracting DNA from human nucleated cells
-
Miller SA, Dykes DD, Polesky HF. A simple salting out procedure of extracting DNA from human nucleated cells. Nucleic Acids Res 1988: 16: 1215-1219.
-
(1988)
Nucleic Acids Res
, vol.16
, pp. 1215-1219
-
-
Miller, S.A.1
Dykes, D.D.2
Polesky, H.F.3
-
15
-
-
33645577053
-
A novel mutation in the growth hormone releasing hormone receptor gene in Israeli Arab families
-
Haskin O, Lazar L, Phillip M, Salvatori R, Alba M, Gat-Yablonski G. A novel mutation in the growth hormone releasing hormone receptor gene in Israeli Arab families. J Endocrinol Invest 2006: 29: 122-130.
-
(2006)
J Endocrinol Invest
, vol.29
, pp. 122-130
-
-
Haskin, O.1
Lazar, L.2
Phillip, M.3
Salvatori, R.4
Alba, M.5
Gat-Yablonski, G.6
-
16
-
-
10544249874
-
Mutations in the hepatocyte nuclear factor-1-alpha gene in maturity-onset diabetes of the young (MODY3)
-
Yamagata K, Furuta H, Oda N et al. Mutations in the hepatocyte nuclear factor-1-alpha gene in maturity-onset diabetes of the young (MODY3). Nature 1996: 384: 455-457.
-
(1996)
Nature
, vol.384
, pp. 455-457
-
-
Yamagata, K.1
Furuta, H.2
Oda, N.3
-
17
-
-
0013258825
-
The prevalence of the HNF-1 G319S mutation in Canadian Aboriginal youth with type 2 diabetes
-
Sellers EAC, Triggs-Raine B, Rockman-Greenberg C, Dean HJ. The prevalence of the HNF-1 G319S mutation in Canadian Aboriginal youth with type 2 diabetes. Diabetes Care 2002: 25: 2202-2206.
-
(2002)
Diabetes Care
, vol.25
, pp. 2202-2206
-
-
Sellers, E.A.C.1
Triggs-Raine, B.2
Rockman-Greenberg, C.3
Dean, H.J.4
-
18
-
-
0036460039
-
High frequency of mutations in the HNF-1a gene (TCF1) in non-obese patients with diabetes of youth in Japanese and identification of a case of digenic inheritance
-
Tonnoka N, Tomura H, Takahashi Y et al. High frequency of mutations in the HNF-1a gene (TCF1) in non-obese patients with diabetes of youth in Japanese and identification of a case of digenic inheritance. Diabetologia 2002: 45: 1709-1712.
-
(2002)
Diabetologia
, vol.45
, pp. 1709-1712
-
-
Tonnoka, N.1
Tomura, H.2
Takahashi, Y.3
-
19
-
-
0034932098
-
The accelerator hypothesis: Weight gain as the missing link between type 1 and type 2 diabetes
-
Wilkin TJ. The accelerator hypothesis: Weight gain as the missing link between type 1 and type 2 diabetes. Diabetologia 2001: 44: 914-922.
-
(2001)
Diabetologia
, vol.44
, pp. 914-922
-
-
Wilkin, T.J.1
-
20
-
-
0035122282
-
Beta-cell genes and diabetes molecular and clinical characterization of mutations in transcription factors
-
Frayling TM, Evans JC, Badman MP et al. Beta-cell genes and diabetes molecular and clinical characterization of mutations in transcription factors. Diabetes 2001: 50: S94-S100.
-
(2001)
Diabetes
, vol.50
-
-
Frayling, T.M.1
Evans, J.C.2
Badman, M.P.3
-
21
-
-
13444271883
-
Clinical characteristics, beta-cell function, HLA class II and mutations in MODY genes in non-paediatric subjects with type 1 diabetes without pancreatic autoantibodies
-
Aguilera E, Casamitjana R, Ercilla G et al. Clinical characteristics, beta-cell function, HLA class II and mutations in MODY genes in non-paediatric subjects with type 1 diabetes without pancreatic autoantibodies. Diabet Med 2004: 22: 137-143.
-
(2004)
Diabet Med
, vol.22
, pp. 137-143
-
-
Aguilera, E.1
Casamitjana, R.2
Ercilla, G.3
-
22
-
-
9644257222
-
Acquired non-type 1 diabetes in childhood: Subtypes, diagnosis, and management
-
Porter JR, Barrett TG. Acquired non-type 1 diabetes in childhood: subtypes, diagnosis, and management. Arch Dis Child 2004: 89: 1138-1144.
-
(2004)
Arch Dis Child
, vol.89
, pp. 1138-1144
-
-
Porter, J.R.1
Barrett, T.G.2
-
23
-
-
0038054448
-
Effect of a diabetic environment in utero on predisposition to type 2 diabetes
-
Sobngwi E, Boudou P, Mauvais-Jarvis F et al. Effect of a diabetic environment in utero on predisposition to type 2 diabetes. Lancet 2003: 361: 1861-1865.
-
(2003)
Lancet
, vol.361
, pp. 1861-1865
-
-
Sobngwi, E.1
Boudou, P.2
Mauvais-Jarvis, F.3
-
24
-
-
33750172941
-
Mother to child transmission of diabetes mellitus: Does gestational diabetes program type 2 diabetes in the next generation?
-
McLean M, Chipps D, Cheung NW. Mother to child transmission of diabetes mellitus: Does gestational diabetes program type 2 diabetes in the next generation? Diabet Med 2006: 23: 1213-1215.
-
(2006)
Diabet Med
, vol.23
, pp. 1213-1215
-
-
McLean, M.1
Chipps, D.2
Cheung, N.W.3
-
25
-
-
0026928723
-
HNF1, a homeoprotein member of the hepatic transcription regulatory network
-
Tronche F, Yaniv M. HNF1, a homeoprotein member of the hepatic transcription regulatory network. Bioessays 1992: 14: 579-587.
-
(1992)
Bioessays
, vol.14
, pp. 579-587
-
-
Tronche, F.1
Yaniv, M.2
-
26
-
-
0034663750
-
Molecular targets of a human HNF1 alpha mutation responsible for pancreatic beta-cell dysfunction
-
Wang H, Antinozzi PA, Hagenfeldt KA, Maechler P, Wollheim CB. Molecular targets of a human HNF1 alpha mutation responsible for pancreatic beta-cell dysfunction. EMBO J 2000: 19: 4257-4264.
-
(2000)
EMBO J
, vol.19
, pp. 4257-4264
-
-
Wang, H.1
Antinozzi, P.A.2
Hagenfeldt, K.A.3
Maechler, P.4
Wollheim, C.B.5
-
27
-
-
0031848797
-
Mutation P291fsinsC in the transcription factor hepatocyte nuclear factor-alpha is dominant negative
-
Yamagata K, Yank Q, Yamamoto K et al. Mutation P291fsinsC in the transcription factor hepatocyte nuclear factor-alpha is dominant negative. Diabetes 1998: 47: 1231-1235.
-
(1998)
Diabetes
, vol.47
, pp. 1231-1235
-
-
Yamagata, K.1
Yank, Q.2
Yamamoto, K.3
-
28
-
-
0036290741
-
Type 2 diabetes mellitus in children and youth: A new epidemic
-
Kaufman F. Type 2 diabetes mellitus in children and youth: A new epidemic. J Pediatr Endocrinol Metab 2002: 15 (Suppl. 2): 737-744.
-
(2002)
J Pediatr Endocrinol Metab
, vol.15
, Issue.SUPPL. 2
, pp. 737-744
-
-
Kaufman, F.1
-
29
-
-
0033847575
-
Sensitivity to sulphonylureas in patients with hepatocyte nuclear factor-1 alpha 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-1 alpha 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
|