-
1
-
-
84895780170
-
Diabetes in the young: A global view and worldwide estimates of numbers of children with type 1 diabetes
-
1 Patterson, C., Guariguata, L., Dahlquist, G., et al. Diabetes in the young: A global view and worldwide estimates of numbers of children with type 1 diabetes. Diabetes Res Clin Pract 103 (2014), 161–175.
-
(2014)
Diabetes Res Clin Pract
, vol.103
, pp. 161-175
-
-
Patterson, C.1
Guariguata, L.2
Dahlquist, G.3
-
2
-
-
84906839774
-
The diagnosis and management of monogenic diabetes in children and adolescents
-
2 Rubio-Cabezas, O., Hattersley, A.T., Njølstad, P.R., et al. The diagnosis and management of monogenic diabetes in children and adolescents. Pediatr Diabetes 15 (2014), 47–64.
-
(2014)
Pediatr Diabetes
, vol.15
, pp. 47-64
-
-
Rubio-Cabezas, O.1
Hattersley, A.T.2
Njølstad, P.R.3
-
3
-
-
84896495361
-
Many faces of monogenic diabetes
-
3 Schwitzgebel, V.M., Many faces of monogenic diabetes. J Diabetes Investig 5 (2014), 121–133.
-
(2014)
J Diabetes Investig
, vol.5
, pp. 121-133
-
-
Schwitzgebel, V.M.1
-
4
-
-
84890145303
-
Maturity onset diabetes of the young: Identification and diagnosis
-
4 McDonald, T.J., Ellard, S., Maturity onset diabetes of the young: Identification and diagnosis. Ann Clin Biochem 50:Pt 5 (2013), 403–415.
-
(2013)
Ann Clin Biochem
, vol.50
, pp. 403-415
-
-
McDonald, T.J.1
Ellard, S.2
-
5
-
-
78649322855
-
Maturity-onset diabetes of the young (MODY): How many cases are we missing?
-
5 Shields, B.M., Hicks, S., Shepherd, M.H., et al. Maturity-onset diabetes of the young (MODY): How many cases are we missing?. Diabetologia 53 (2010), 2504–2508.
-
(2010)
Diabetologia
, vol.53
, pp. 2504-2508
-
-
Shields, B.M.1
Hicks, S.2
Shepherd, M.H.3
-
6
-
-
84885224469
-
Prevalence, characteristics and clinical diagnosis of maturity onset diabetes of the young due to mutations in HNF1A, HNF4A, and glucokinase: Results from the SEARCH for Diabetes in Youth
-
6 Pihoker, C., Gilliam, L.K., Ellard, S., et al. Prevalence, characteristics and clinical diagnosis of maturity onset diabetes of the young due to mutations in HNF1A, HNF4A, and glucokinase: Results from the SEARCH for Diabetes in Youth. J Clin Endocrinol Metab 98 (2013), 4055–4062.
-
(2013)
J Clin Endocrinol Metab
, vol.98
, pp. 4055-4062
-
-
Pihoker, C.1
Gilliam, L.K.2
Ellard, S.3
-
7
-
-
85006962475
-
Characteristics of maturity onset diabetes of the young in a large diabetes center
-
Epub ahead of print
-
7 Chambers, C., Fouts, A., Dong, F., et al. Characteristics of maturity onset diabetes of the young in a large diabetes center. Pediatr Diabetes, 2015 Epub ahead of print.
-
(2015)
Pediatr Diabetes
-
-
Chambers, C.1
Fouts, A.2
Dong, F.3
-
8
-
-
84926208060
-
Identifying monogenic diabetes in a pediatric cohort with presumed type 1 diabetes
-
8 Gandica, R.G., Chung, W.K., Deng, L., et al. Identifying monogenic diabetes in a pediatric cohort with presumed type 1 diabetes. Pediatr Diabetes 16 (2014), 227–233.
-
(2014)
Pediatr Diabetes
, vol.16
, pp. 227-233
-
-
Gandica, R.G.1
Chung, W.K.2
Deng, L.3
-
9
-
-
77949450581
-
Type 2 diabetes, medication-induced diabetes, and monogenic diabetes in Canadian children: A prospective national surveillance study
-
9 Amed, S., Dean, H.J., Panagiotopoulos, C., et al. Type 2 diabetes, medication-induced diabetes, and monogenic diabetes in Canadian children: A prospective national surveillance study. Diabetes Care 33 (2010), 786–791.
-
(2010)
Diabetes Care
, vol.33
, pp. 786-791
-
-
Amed, S.1
Dean, H.J.2
Panagiotopoulos, C.3
-
10
-
-
84965248555
-
Diabetes mellitus and heredity
-
10 Cammidge, P.J., Diabetes mellitus and heredity. BMJ 2 (1928), 738–741.
-
(1928)
BMJ
, vol.2
, pp. 738-741
-
-
Cammidge, P.J.1
-
11
-
-
0016244025
-
Mild familial diabetes with dominant inheritance
-
11 Tattersall, R.B., Mild familial diabetes with dominant inheritance. Q J Med 43 (1974), 339–357.
-
(1974)
Q J Med
, vol.43
, pp. 339-357
-
-
Tattersall, R.B.1
-
12
-
-
84940998194
-
New insights from monogenic diabetes for “common” type 2 diabetes
-
12 Tallapragada, D.S.P., Bhaskar, S., Chandak, G.R., New insights from monogenic diabetes for “common” type 2 diabetes. Front Genet, 6, 2015, 251.
-
(2015)
Front Genet
, vol.6
, pp. 251
-
-
Tallapragada, D.S.P.1
Bhaskar, S.2
Chandak, G.R.3
-
13
-
-
41149139275
-
Best practice guidelines for the molecular genetic diagnosis of maturity-onset diabetes of the young
-
European Molecular Genetics Quality Network (EMQN) MODY group
-
13 Ellard, S., Bellanné-Chantelot, C., Hattersley, A.T., European Molecular Genetics Quality Network (EMQN) MODY group. Best practice guidelines for the molecular genetic diagnosis of maturity-onset diabetes of the young. Diabetologia 51 (2008), 546–553.
-
(2008)
Diabetologia
, vol.51
, pp. 546-553
-
-
Ellard, S.1
Bellanné-Chantelot, C.2
Hattersley, A.T.3
-
14
-
-
84894515689
-
De novo mutations of GCK, HNF1A and HNF4A may be more frequent in MODY than previously assumed
-
14 Stanik, J., Dusatkova, P., Cinek, O., et al. De novo mutations of GCK, HNF1A and HNF4A may be more frequent in MODY than previously assumed. Diabetologia 57 (2014), 480–484.
-
(2014)
Diabetologia
, vol.57
, pp. 480-484
-
-
Stanik, J.1
Dusatkova, P.2
Cinek, O.3
-
15
-
-
70350741368
-
Update on mutations in glucokinase (GCK), which cause maturity-onset diabetes of the young, permanent neonatal diabetes, and hyperinsulinemic hypoglycemia
-
15 Osbak, K.K., Colclough, K., Saint-Martin, C., et al. Update on mutations in glucokinase (GCK), which cause maturity-onset diabetes of the young, permanent neonatal diabetes, and hyperinsulinemic hypoglycemia. Hum Mutat 30 (2009), 1512–1526.
-
(2009)
Hum Mutat
, vol.30
, pp. 1512-1526
-
-
Osbak, K.K.1
Colclough, K.2
Saint-Martin, C.3
-
16
-
-
84899074567
-
The 0.1% of the population with glucokinase monogenic diabetes can be recognized by clinical characteristics in pregnancy: The Atlantic Diabetes in Pregnancy Cohort
-
16 Chakera, A.J., Spyer, G., Vincent, N., et al. The 0.1% of the population with glucokinase monogenic diabetes can be recognized by clinical characteristics in pregnancy: The Atlantic Diabetes in Pregnancy Cohort. Diabetes Care 37 (2014), 1230–1236.
-
(2014)
Diabetes Care
, vol.37
, pp. 1230-1236
-
-
Chakera, A.J.1
Spyer, G.2
Vincent, N.3
-
17
-
-
0036210337
-
The genetic abnormality in the beta cell determines the response to an oral glucose load
-
17 Stride, A., Vaxillaire, M., Tuomi, T., et al. The genetic abnormality in the beta cell determines the response to an oral glucose load. Diabetologia 45 (2002), 427–435.
-
(2002)
Diabetologia
, vol.45
, pp. 427-435
-
-
Stride, A.1
Vaxillaire, M.2
Tuomi, T.3
-
18
-
-
84892649702
-
Prevalence of vascular complications among patients with glucokinase mutations and prolonged, mild hyperglycemia
-
18 Steele, A.M., Shields, B.M., Wensley, K.J., et al. Prevalence of vascular complications among patients with glucokinase mutations and prolonged, mild hyperglycemia. JAMA 311 (2014), 279–286.
-
(2014)
JAMA
, vol.311
, pp. 279-286
-
-
Steele, A.M.1
Shields, B.M.2
Wensley, K.J.3
-
19
-
-
58149216624
-
Pregnancy outcome in patients with raised blood glucose due to a heterozygous glucokinase gene mutation
-
19 Spyer, G., Macleod, K.M., Shepherd, M., et al. Pregnancy outcome in patients with raised blood glucose due to a heterozygous glucokinase gene mutation. Diabet Med 26 (2009), 14–18.
-
(2009)
Diabet Med
, vol.26
, pp. 14-18
-
-
Spyer, G.1
Macleod, K.M.2
Shepherd, M.3
-
20
-
-
0031859976
-
Mutations in the glucokinase gene of the fetus result in reduced birth weight
-
20 Hattersley, A.T., Beards, F., Ballantyne, E., et al. Mutations in the glucokinase gene of the fetus result in reduced birth weight. Nat Genet 19 (1998), 268–270.
-
(1998)
Nat Genet
, vol.19
, pp. 268-270
-
-
Hattersley, A.T.1
Beards, F.2
Ballantyne, E.3
-
21
-
-
33846826605
-
The long-term impact on offspring of exposure to hyperglycaemia in utero due to maternal glucokinase gene mutations
-
21 Singh, R., Pearson, E.R., Clark, P.M., Hattersley, A.T., The long-term impact on offspring of exposure to hyperglycaemia in utero due to maternal glucokinase gene mutations. Diabetologia 50 (2007), 620–624.
-
(2007)
Diabetologia
, vol.50
, pp. 620-624
-
-
Singh, R.1
Pearson, E.R.2
Clark, P.M.3
Hattersley, A.T.4
-
22
-
-
20044396943
-
Molecular genetics and phenotypic characteristics of MODY caused by hepatocyte nuclear factor 4alpha mutations in a large European collection
-
22 Pearson, E.R., Pruhova, S., Tack, C.J., et al. Molecular genetics and phenotypic characteristics of MODY caused by hepatocyte nuclear factor 4alpha mutations in a large European collection. Diabetologia 48 (2005), 878–885.
-
(2005)
Diabetologia
, vol.48
, pp. 878-885
-
-
Pearson, E.R.1
Pruhova, S.2
Tack, C.J.3
-
23
-
-
41149084500
-
Clinical implications of a molecular genetic classification of monogenic β-cell diabetes
-
23 Murphy, R., Ellard, S., Hattersley, A.T., Clinical implications of a molecular genetic classification of monogenic β-cell diabetes. Nat Clin Pract Endocrinol Metab 4 (2008), 200–213.
-
(2008)
Nat Clin Pract Endocrinol Metab
, vol.4
, pp. 200-213
-
-
Murphy, R.1
Ellard, S.2
Hattersley, A.T.3
-
24
-
-
40749151157
-
The type and the position of HNF1A mutation modulate age at diagnosis of diabetes in patients with maturity-onset diabetes of the young (MODY)-3
-
24 Bellanné-Chantelot, C., Carette, C., Riveline, J.-P., et al. The type and the position of HNF1A mutation modulate age at diagnosis of diabetes in patients with maturity-onset diabetes of the young (MODY)-3. Diabetes 57 (2008), 503–508.
-
(2008)
Diabetes
, vol.57
, pp. 503-508
-
-
Bellanné-Chantelot, C.1
Carette, C.2
Riveline, J.-P.3
-
25
-
-
0034304925
-
HNF1alpha controls renal glucose reabsorption in mouse and man
-
25 Pontoglio, M., Prié, D., Cheret, C., et al. HNF1alpha controls renal glucose reabsorption in mouse and man. EMBO Rep 1 (2000), 359–365.
-
(2000)
EMBO Rep
, vol.1
, pp. 359-365
-
-
Pontoglio, M.1
Prié, D.2
Cheret, C.3
-
26
-
-
84858622767
-
Lipoprotein composition in HNF1A-MODY: Differentiating between HNF1A-MODY and type 2 diabetes
-
26 McDonald, T.J., McEneny, J., Pearson, E.R., et al. Lipoprotein composition in HNF1A-MODY: Differentiating between HNF1A-MODY and type 2 diabetes. Clin Chim Acta 413 (2012), 927–932.
-
(2012)
Clin Chim Acta
, vol.413
, pp. 927-932
-
-
McDonald, T.J.1
McEneny, J.2
Pearson, E.R.3
-
27
-
-
76249111249
-
Increased all-cause and cardiovascular mortality in monogenic diabetes as a result of mutations in the HNF1A gene
-
27 Steele, A.M., Shields, B.M., Shepherd, M., et al. Increased all-cause and cardiovascular mortality in monogenic diabetes as a result of mutations in the HNF1A gene. Diabet Med 27 (2010), 157–161.
-
(2010)
Diabet Med
, vol.27
, pp. 157-161
-
-
Steele, A.M.1
Shields, B.M.2
Shepherd, M.3
-
28
-
-
34247500820
-
Macrosomia and hyperinsulinaemic hypoglycaemia in patients with heterozygous mutations in the HNF4A gene
-
28 Pearson, E.R., Boj, S.F., Steele, A.M., et al. Macrosomia and hyperinsulinaemic hypoglycaemia in patients with heterozygous mutations in the HNF4A gene. PLoS Med, 4, 2007, e118.
-
(2007)
PLoS Med
, vol.4
, pp. e118
-
-
Pearson, E.R.1
Boj, S.F.2
Steele, A.M.3
-
29
-
-
77951662347
-
Diazoxide-responsive hyperinsulinemic hypoglycemia caused by HNF4A gene mutations
-
29 Flanagan, S.E., Kapoor, R.R., Mali, G., et al. Diazoxide-responsive hyperinsulinemic hypoglycemia caused by HNF4A gene mutations. Eur J Endocrinol 162 (2010), 987–992.
-
(2010)
Eur J Endocrinol
, vol.162
, pp. 987-992
-
-
Flanagan, S.E.1
Kapoor, R.R.2
Mali, G.3
-
30
-
-
48249154650
-
Persistent hyperinsulinemic hypoglycemia and maturity-onset diabetes of the young due to heterozygous HNF4A mutations
-
30 Kapoor, R.R., Locke, J., Colclough, K., et al. Persistent hyperinsulinemic hypoglycemia and maturity-onset diabetes of the young due to heterozygous HNF4A mutations. Diabetes 57 (2008), 1659–1663.
-
(2008)
Diabetes
, vol.57
, pp. 1659-1663
-
-
Kapoor, R.R.1
Locke, J.2
Colclough, K.3
-
31
-
-
84876809846
-
Home urine C-peptide creatinine ratio testing can identify type 2 and MODY in pediatric diabetes
-
31 Besser, R.E., Shields, B.M., Hammersley, S.E., et al. Home urine C-peptide creatinine ratio testing can identify type 2 and MODY in pediatric diabetes. Pediatr Diabetes 14 (2013), 181–188.
-
(2013)
Pediatr Diabetes
, vol.14
, pp. 181-188
-
-
Besser, R.E.1
Shields, B.M.2
Hammersley, S.E.3
-
32
-
-
80051653635
-
Islet autoantibodies can discriminate maturity-onset diabetes of the young (MODY) from type 1 diabetes
-
32 McDonald, T.J., Colclough, K., Brown, R., et al. Islet autoantibodies can discriminate maturity-onset diabetes of the young (MODY) from type 1 diabetes. Diabet Med 28 (2011), 1028–1033.
-
(2011)
Diabet Med
, vol.28
, pp. 1028-1033
-
-
McDonald, T.J.1
Colclough, K.2
Brown, R.3
-
33
-
-
48249145862
-
Diabetes susceptibility in the Canadian Oji-Cree population is moderated by abnormal mRNA processing of HNF1A G319S transcripts
-
33 Harries, L.W., Sloman, M.J., Sellers, E.A.C., et al. Diabetes susceptibility in the Canadian Oji-Cree population is moderated by abnormal mRNA processing of HNF1A G319S transcripts. Diabetes 57 (2008), 1978–1982.
-
(2008)
Diabetes
, vol.57
, pp. 1978-1982
-
-
Harries, L.W.1
Sloman, M.J.2
Sellers, E.A.C.3
-
34
-
-
0013258825
-
The prevalence of the HNF-1alpha G319S mutation in Canadian aboriginal youth with type 2 diabetes
-
34 Sellers, E.A.C., Triggs-Raine, B., Rockman-Greenberg, C., Dean, H.J., The prevalence of the HNF-1alpha G319S mutation in Canadian aboriginal youth with type 2 diabetes. Diabetes Care 25 (2002), 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
-
35
-
-
75149163252
-
Clinical applications of diabetes antibody testing
-
35 Bingley, P.J., Clinical applications of diabetes antibody testing. J Clin Endocrinol Metab 95 (2010), 25–33.
-
(2010)
J Clin Endocrinol Metab
, vol.95
, pp. 25-33
-
-
Bingley, P.J.1
-
36
-
-
79956067719
-
Urine C-peptide creatinine ratio is a noninvasive alternative to the mixed-meal tolerance test in children and adults with type 1 diabetes
-
36 Besser, R.E.J., Ludvigsson, J., Jones, A.G., et al. Urine C-peptide creatinine ratio is a noninvasive alternative to the mixed-meal tolerance test in children and adults with type 1 diabetes. Diabetes Care 34 (2011), 607–609.
-
(2011)
Diabetes Care
, vol.34
, pp. 607-609
-
-
Besser, R.E.J.1
Ludvigsson, J.2
Jones, A.G.3
-
37
-
-
79951709597
-
Urinary C-peptide creatinine ratio is a practical outpatient tool for identifying hepatocyte nuclear factor 1-{alpha}/hepatocyte nuclear factor 4-{alpha} maturity-onset diabetes of the young from long-duration type 1 diabetes
-
37 Besser, R.E.J., Shepherd, M.H., McDonald, T.J., et al. Urinary C-peptide creatinine ratio is a practical outpatient tool for identifying hepatocyte nuclear factor 1-{alpha}/hepatocyte nuclear factor 4-{alpha} maturity-onset diabetes of the young from long-duration type 1 diabetes. Diabetes Care 34 (2011), 286–291.
-
(2011)
Diabetes Care
, vol.34
, pp. 286-291
-
-
Besser, R.E.J.1
Shepherd, M.H.2
McDonald, T.J.3
-
38
-
-
84861333315
-
Systematic assessment of etiology in adults with a clinical diagnosis of young-onset type 2 diabetes is a successful strategy for identifying maturity-onset diabetes of the young
-
38 Thanabalasingham, G., Pal, A., Selwood, M.P., et al. Systematic assessment of etiology in adults with a clinical diagnosis of young-onset type 2 diabetes is a successful strategy for identifying maturity-onset diabetes of the young. Diabetes Care 35 (2012), 1206–1212.
-
(2012)
Diabetes Care
, vol.35
, pp. 1206-1212
-
-
Thanabalasingham, G.1
Pal, A.2
Selwood, M.P.3
-
39
-
-
84879570186
-
The clinical utility of C-peptide measurement in the care of patients with diabetes
-
39 Jones, A.G., Hattersley, A.T., The clinical utility of C-peptide measurement in the care of patients with diabetes. Diabet Med 30 (2013), 803–817.
-
(2013)
Diabet Med
, vol.30
, pp. 803-817
-
-
Jones, A.G.1
Hattersley, A.T.2
-
40
-
-
78649810544
-
Assessment of high-sensitivity C-reactive protein levels as diagnostic discriminator of maturity-onset diabetes of the young due to HNF1A mutations
-
40 Owen, K.R., Thanabalasingham, G., James, T.J., et al. Assessment of high-sensitivity C-reactive protein levels as diagnostic discriminator of maturity-onset diabetes of the young due to HNF1A mutations. Diabetes Care 33 (2010), 1919–1924.
-
(2010)
Diabetes Care
, vol.33
, pp. 1919-1924
-
-
Owen, K.R.1
Thanabalasingham, G.2
James, T.J.3
-
41
-
-
84862526033
-
The development and validation of a clinical prediction model to determine the probability of MODY in patients with young-onset diabetes
-
41 Shields, B.M., McDonald, T.J., Ellard, S., et al. The development and validation of a clinical prediction model to determine the probability of MODY in patients with young-onset diabetes. Diabetologia 55 (2012), 1265–1272.
-
(2012)
Diabetologia
, vol.55
, pp. 1265-1272
-
-
Shields, B.M.1
McDonald, T.J.2
Ellard, S.3
-
42
-
-
0242363725
-
No deterioration in glycemic control in HNF-1alpha maturity-onset diabetes of the young following transfer from long-term insulin to sulphonylureas
-
42 Shepherd, M., Pearson, E.R., Houghton, J., et al. No deterioration in glycemic control in HNF-1alpha maturity-onset diabetes of the young following transfer from long-term insulin to sulphonylureas. Diabetes Care 26 (2003), 3191–3192.
-
(2003)
Diabetes Care
, vol.26
, pp. 3191-3192
-
-
Shepherd, M.1
Pearson, E.R.2
Houghton, J.3
-
43
-
-
84924674598
-
Treatment of young patients with HNF1A mutations (HNF1A-MODY)
-
43 Raile, K., Schober, E., Konrad, K., et al. Treatment of young patients with HNF1A mutations (HNF1A-MODY). Diabet Med 32 (2015), 526–530.
-
(2015)
Diabet Med
, vol.32
, pp. 526-530
-
-
Raile, K.1
Schober, E.2
Konrad, K.3
|