-
1
-
-
2342466734
-
Global Prevalence of Diabetes: Estimates for the year 2000 and projections for 2030
-
DOI 10.2337/diacare.27.5.1047
-
Wild S, Roglic G, Green A, Sicree R, King H. Global prevalence of diabetes: estimates for the year 2000 and projections for 2030. Diabetes Care. 2004;27(5):1047-1053. (Pubitemid 38579764)
-
(2004)
Diabetes Care
, vol.27
, Issue.5
, pp. 1047-1053
-
-
Wild, S.1
Roglic, G.2
Green, A.3
Sicree, R.4
King, H.5
-
2
-
-
80053411257
-
In vitro insulin secretion by pancreatic tissue from infants with diazoxide-resistant congenital hyperinsulinism deviates from model predictions
-
Henquin J-C, et al. In vitro insulin secretion by pancreatic tissue from infants with diazoxide-resistant congenital hyperinsulinism deviates from model predictions. J Clin Invest. 2011;121(10):3932-3942.
-
(2011)
J Clin Invest
, vol.121
, Issue.10
, pp. 3932-3942
-
-
Henquin, J.-C.1
-
4
-
-
0029021696
-
Mutations in the sulfonylurea receptor gene in familial persistent hyperinsulinemic hypoglycemia of infancy
-
Thomas PM, et al. Mutations in the sulfonylurea receptor gene in familial persistent hyperinsulinemic hypoglycemia of infancy. Science. 1995;268(5209):426-429.
-
(1995)
Science
, vol.268
, Issue.5209
, pp. 426-429
-
-
Thomas, P.M.1
-
5
-
-
0024545488
-
Relevance of endocrine pancreas nesidioblastosis to hyperinsulinemic hypogycemia
-
Rahier J. Relevance of endocrine pancreas nesidioblastosis to hyperinsulinemic hypoglycemia. Diabetes Care. 1989;12(2):164-166. (Pubitemid 19064414)
-
(1989)
Diabetes Care
, vol.12
, Issue.2
, pp. 164-166
-
-
Rahier, J.1
-
6
-
-
0017686201
-
Nesidioblastosis: The pathologic basis of persistent hyperinsulinemic hypoglycemia in infants. Morphologic and quantitative analysis of seven cases based on specific immunostaining and electron microscopy
-
Heitz PU, Kloppel G, Hacki WH, Polak JM, Pearse AG. Nesidioblastosis: the pathologic basis of persistent hyperinsulinemic hypoglycemia in infants. Morphologic and quantitative analysis of seven cases based on specific immunostaining and electron microscopy. Diabetes. 1977;26(7):632-642. (Pubitemid 8149650)
-
(1977)
Diabetes
, vol.26
, Issue.7
, pp. 632-642
-
-
Heitz, P.U.1
Kloppel, G.2
Hacki, W.H.3
-
7
-
-
0032447019
-
Loss of imprinted genes and paternal SUR1 mutations lead to hyperinsulinism in focal adenomatous hyperplasia
-
Fournet JC, et al. Loss of imprinted genes and paternal SUR1 mutations lead to hyperinsulinism in focal adenomatous hyperplasia. Ann Endocrinol (Paris). 1998;59(6):485-491.
-
(1998)
Ann Endocrinol (Paris)
, vol.59
, Issue.6
, pp. 485-491
-
-
Fournet, J.C.1
-
8
-
-
0031765251
-
Hyperinsulinism: The molecular aetiology of focal disease
-
Ryan FD, et al. Hyperinsulinism: The molecular aetiology of focal disease. Arch Dis Child. 1998;79(5):445-447.
-
(1998)
Arch Dis Child
, vol.79
, Issue.5
, pp. 445-447
-
-
Ryan, F.D.1
-
9
-
-
0035145905
-
ATP channel-independent pathways
-
Straub SG, et al. Hyperinsulinism of infancy: the regulated release of insulin by KATP channel-independent pathways. Diabetes. 2001;50(2):329-339. (Pubitemid 32127290)
-
(2001)
Diabetes
, vol.50
, Issue.2
, pp. 329-339
-
-
Straub, S.G.1
Cosgrove, K.E.2
Ammala, C.3
Shepherd, R.M.4
O'Brien, R.E.5
Barnes, P.D.6
Kuchinski, N.7
Chapman, J.C.8
Schaeppi, M.9
Glaser, B.10
Lindley, K.J.11
Sharp, G.W.G.12
Aynsley-Green, A.13
Dunne, M.J.14
-
10
-
-
0029658788
-
Loss of functional K(ATP) channels in pancreatic β-cells causes persistent hyperinsulinemic hypoglycemia of infancy
-
DOI 10.1038/nm1296-1344
-
Kane C, et al. Loss of functional KATP channels in pancreatic β-cells causes persistent hyperinsulinemic hypoglycemia of infancy. Nat Med. 1996;2(12):1344-1347. (Pubitemid 26401737)
-
(1996)
Nature Medicine
, vol.2
, Issue.12
, pp. 1344-1347
-
-
Kane, C.1
Shepherd, R.M.2
Squires, P.E.3
Johnson, P.R.V.4
James, R.F.L.5
Milla, P.J.6
Aynsley-Green, A.7
Lindley, K.J.8
Dunne, M.J.9
-
12
-
-
0024995560
-
Regulation of insulin release in persistent hyperinsulinaemic hypoglycaemia of infancy studied in long-term culture of pancreatic tissue
-
DOI 10.1007/BF00405110
-
Kaiser N, et al. Regulation of insulin release in persistent hyperinsulinaemic hypoglycaemia of infancy studied in long-term culture of pancreatic tissue. Diabetologia. 1990;33(8):482-488. (Pubitemid 20254871)
-
(1990)
Diabetologia
, vol.33
, Issue.8
, pp. 482-488
-
-
Kaiser, N.1
Corcos, A.P.2
Tur-Sinai, A.3
Ariav, Y.4
Glaser, B.5
Landau, H.6
Cerasi, E.7
-
13
-
-
0027460026
-
Somatostatin regulation of β-cell function in the normal human fetuses and in neonates with persistent hyperinsulinemic hypoglycemia
-
DOI 10.1210/jc.76.1.184
-
Otonkoski T, Andersson S, Simell O. Somatostatin regulation of β-cell function in the normal human fetuses and in neonates with persistent hyperinsulinemic hypoglycemia. J Clin Endocrinol Metab. 1993;76(1):184-188. (Pubitemid 23027577)
-
(1993)
Journal of Clinical Endocrinology and Metabolism
, vol.76
, Issue.1
, pp. 184-188
-
-
Otonkoski, T.1
Andersson, S.2
Simell, O.3
-
14
-
-
0033853921
-
β-Cell proliferation and apoptosis in the developing normal human pancreas and in hyperinsulinism of infancy
-
Kassem SA, Ariel I, Thornton PS, Scheimberg I, Glaser B. β-cell proliferation and apoptosis in the developing normal human pancreas and in hyperinsulinism of infancy. Diabetes. 2000;49(8):1325-1333. (Pubitemid 30624233)
-
(2000)
Diabetes
, vol.49
, Issue.8
, pp. 1325-1333
-
-
Kassem, S.A.1
Ariel, I.2
Thornton, P.S.3
Scheimberg, I.4
Glaser, B.5
-
15
-
-
0036135191
-
Heterogeneity of persistent hyperinsulinaemic hypoglycaemia. A series of 175 cases
-
De Lonlay P, et al. Heterogeneity of persistent hyperinsulinaemic hypoglycaemia. A series of 175 cases. Eur J Pediatr. 2002;161(1):37-48. (Pubitemid 34031274)
-
(2002)
European Journal of Pediatrics
, vol.161
, Issue.1
, pp. 37-48
-
-
De Lonlay, P.1
Fournet, J.-C.2
Touati, G.3
Groos, M.-S.4
Martin, D.5
Sevin, C.6
Delagne, V.7
Mayaud, C.8
Chigot, V.9
Sempoux, C.10
Brusset, M.-C.11
Laborde, K.12
Bellane-Chantelot, C.13
Vassault, A.14
Rahier, J.15
Junien, C.16
Brunelle, F.17
Nihoul-Fekete, C.18
Saudubray, J.-M.19
Robert, J.-J.20
more..
-
16
-
-
0035142144
-
Dysregulation of insulin secretion in children with congenital hyperinsulinism due to sulfonylurea receptor mutations
-
Grimberg A, et al. Dysregulation of insulin secretion in children with congenital hyperinsulinism due to sulfonylurea receptor mutations. Diabetes. 2001;50(2):322-328. (Pubitemid 32127289)
-
(2001)
Diabetes
, vol.50
, Issue.2
, pp. 322-328
-
-
Grimberg, A.1
Ferry Jr., R.J.2
Kelly, A.3
Koo-McCoy, S.4
Polonsky, K.5
Glaser, B.6
Permutt, M.A.7
Aguilar-Bryan, L.8
Stafford, D.9
Thornton, P.S.10
Baker, L.11
Stanley, C.A.12
-
17
-
-
0033214491
-
Identification of the potassium channel opener site on sulfonylurea receptors
-
Uhde I, Toman A, Gross I, Schwanstecher C, Schwanstecher M. Identification of the potassium channel opener site on sulfonylurea receptors. J Biol Chem. 1999;274(40):28079-28082.
-
(1999)
J Biol Chem
, vol.274
, Issue.40
, pp. 28079-28082
-
-
Uhde, I.1
Toman, A.2
Gross, I.3
Schwanstecher, C.4
Schwanstecher, M.5
-
18
-
-
0032556969
-
Familial hyperinsulinism caused by an activating glucokinase mutation
-
DOI 10.1056/NEJM199801223380404
-
Glaser B, et al. Familial hyperinsulinism caused by an activating glucokinase mutation. N Engl J Med. 1998;338(4):226-230. (Pubitemid 28047576)
-
(1998)
New England Journal of Medicine
, vol.338
, Issue.4
, pp. 226-230
-
-
Glaser, B.1
Kesavan, P.2
Heyman, M.3
Davis, E.4
Cuesta, A.5
Buchs, A.6
Stanley, C.A.7
Thornton, P.S.8
Permutt, M.A.9
Matschinsky, F.M.10
Herold, K.C.11
-
19
-
-
0032493123
-
Hyperinsulinism and hyperammonemia in infants with regulatory mutations of the glutamate dehydrogenase gene
-
DOI 10.1056/NEJM199805073381904
-
Stanley CA, et al. Hyperinsulinism and hyperammonemia in infants with regulatory mutations of the glutamate dehydrogenase gene. N Engl J Med. 1998;338(19):1352-1357. (Pubitemid 28216664)
-
(1998)
New England Journal of Medicine
, vol.338
, Issue.19
, pp. 1352-1357
-
-
Stanley, C.A.1
Lieu, Y.K.2
Hsu, B.Y.L.3
Burlina, A.B.4
Greenberg, C.R.5
Hopwood, N.J.6
Perlman, K.7
Rich, B.H.8
Zammarchi, E.9
Poncz, M.10
-
20
-
-
34548204386
-
Physical exercise-induced hypoglycemia caused by failed silencing of monocarboxylate transporter 1 in pancreatic β cells
-
DOI 10.1086/520960
-
Otonkoski T, et al. Physical exercise-induced hypoglycemia caused by failed silencing of monocarboxylate transporter 1 in pancreatic β cells. Am J Hum Genet. 2007;81(3):467-474. (Pubitemid 47330206)
-
(2007)
American Journal of Human Genetics
, vol.81
, Issue.3
, pp. 467-474
-
-
Otonkoski, T.1
Jiao, H.2
Kaminen-Ahola, N.3
Tapia-Paez, I.4
Ullah, M.S.5
Parton, L.E.6
Schuit, F.7
Quintens, R.8
Sipila, I.9
Mayatepek, E.10
Meissner, T.11
Halestrap, A.P.12
Rutter, G.A.13
Kere, J.14
-
21
-
-
33847196062
-
Functional genomics of the β-cell: Short-chain 3-hydroxyacyl- coenzyme A dehydrogenase regulates insulin secretion independent of K+ currents
-
Hardy OT, et al. Functional genomics of the β-cell: short-chain 3-hydroxyacyl-coenzyme A dehydrogenase regulates insulin secretion independent of K+ currents. Mol Endocrinol. 2007;21(3):765-773.
-
(2007)
Mol Endocrinol
, vol.21
, Issue.3
, pp. 765-773
-
-
Hardy, O.T.1
-
22
-
-
77957760755
-
Mechanism of hyperinsulinism in short-chain 3-hydroxyacyl-CoA dehydrogenase deficiency involves activation of glutamate dehydrogenase
-
Li C, et al. Mechanism of hyperinsulinism in short-chain 3-hydroxyacyl-CoA dehydrogenase deficiency involves activation of glutamate dehydrogenase. J Biol Chem. 2010;285(41):31806-31818.
-
(2010)
J Biol Chem
, vol.285
, Issue.41
, pp. 31806-31818
-
-
Li, C.1
|