-
1
-
-
0001118413
-
Idiopathic spontaneously occurring hypoglycemia in infants: Clinical significance of problem and treatment
-
McQuarrie I. Idiopathic spontaneously occurring hypoglycemia in infants: clinical significance of problem and treatment. AMA Am J Dis Child 1954;87:399-428.
-
(1954)
AMA Am J Dis Child
, vol.87
, pp. 399-428
-
-
McQuarrie, I.1
-
2
-
-
33845725307
-
Mechanisms of disease: Advances in diagnosis and treatment of hyperinsulinism in neonates
-
DeLeón DD, Stanley CA. Mechanisms of disease: advances in diagnosis and treatment of hyperinsulinism in neonates. Nat Clin Pract Endocrinol Metab 2007;3:57-68.
-
(2007)
Nat Clin Pract Endocrinol Metab
, vol.3
, pp. 57-68
-
-
DeLeón, D.D.1
Stanley, C.A.2
-
3
-
-
0015104472
-
β Cell nesidioblastosis in idiopathic hypoglycemia of infancy
-
Yakovac WC, Baker L, Hummeler K. β Cell nesidioblastosis in idiopathic hypoglycemia of infancy. J Pediatr 1971;79:226-31.
-
(1971)
J Pediatr
, vol.79
, pp. 226-231
-
-
Yakovac, W.C.1
Baker, L.2
Hummeler, K.3
-
4
-
-
0034119682
-
Persistent hyperinsulinaemic hypoglycaemia of infancy: A heterogeneous syndrome unrelated to nesidioblastosis
-
Rahier J, Guiot Y, Sempoux C. Persistent hyperinsulinaemic hypoglycaemia of infancy: a heterogeneous syndrome unrelated to nesidioblastosis. Arch Dis Child Fetal Neonatal Ed 2000;82:F108-12.
-
(2000)
Arch Dis Child Fetal Neonatal Ed
, vol.82
-
-
Rahier, J.1
Guiot, Y.2
Sempoux, C.3
-
5
-
-
33748877830
-
Recent advances in hyperinsulinemic hypoglycemia of infancy
-
Dekelbab BH, Sperling MA. Recent advances in hyperinsulinemic hypoglycemia of infancy. Acta Paediatr 2006;95:1157-64.
-
(2006)
Acta Paediatr
, vol.95
, pp. 1157-1164
-
-
Dekelbab, B.H.1
Sperling, M.A.2
-
6
-
-
0029021696
-
Mutations in the sulfonylurea receptor gene in familial persistent hyperinsulinemic hypoglycemia of infancy
-
Thomas PM, Cote GJ, Wohllk N, Haddad B, Mathew PM, Rabl W, et al. Mutations in the sulfonylurea receptor gene in familial persistent hyperinsulinemic hypoglycemia of infancy. Science (Wash DC) 1995;268:426-9.
-
(1995)
Science (Wash DC)
, vol.268
, pp. 426-429
-
-
Thomas, P.M.1
Cote, G.J.2
Wohllk, N.3
Haddad, B.4
Mathew, P.M.5
Rabl, W.6
-
7
-
-
0029836983
-
Mutation of the pancreatic islet inward rectifier Kir6.2 also leads to familial persistent hyperinsulinemic hypoglycemia of infancy
-
Thomas P, Ye Y, Lightner E. Mutation of the pancreatic islet inward rectifier Kir6.2 also leads to familial persistent hyperinsulinemic hypoglycemia of infancy. Hum Mol Genet 1996;5:1809-12.
-
(1996)
Hum Mol Genet
, vol.5
, pp. 1809-1812
-
-
Thomas, P.1
Ye, Y.2
Lightner, E.3
-
8
-
-
0032556969
-
Familial hyperinsulinism caused by an activating glucokinase mutation
-
Glaser B, Kesavan P, Heyman M, Davis E, Cuesta A, Buchs A, et al. Familial hyperinsulinism caused by an activating glucokinase mutation. N Engl J Med 1998;338:226-30.
-
(1998)
N Engl J Med
, vol.338
, pp. 226-230
-
-
Glaser, B.1
Kesavan, P.2
Heyman, M.3
Davis, E.4
Cuesta, A.5
Buchs, A.6
-
9
-
-
0032493123
-
Hyperinsulinism and hyperammonemia in infants with regulatory mutations of the glutamate dehydrogenase gene
-
Stanley CA, Lieu YK, Hsu BY, Burlina AB, Greenberg CR, Hopwood NJ, et al. Hyperinsulinism and hyperammonemia in infants with regulatory mutations of the glutamate dehydrogenase gene. N Engl J Med 1998;338:1352-7.
-
(1998)
N Engl J Med
, vol.338
, pp. 1352-1357
-
-
Stanley, C.A.1
Lieu, Y.K.2
Hsu, B.Y.3
Burlina, A.B.4
Greenberg, C.R.5
Hopwood, N.J.6
-
10
-
-
0034902277
-
Hyperinsulinism in short-chain L-3-hydroxyacyl-CoA dehydrogenase deficiency reveals the importance of β-oxidation in insulin secretion
-
Clayton PT, Eaton S, Aynsley-Green A, Edginton M, Hussain K, Krywawych S, et al. Hyperinsulinism in short-chain L-3-hydroxyacyl-CoA dehydrogenase deficiency reveals the importance of β-oxidation in insulin secretion. J Clin Invest 2001;108:457-65.
-
(2001)
J Clin Invest
, vol.108
, pp. 457-465
-
-
Clayton, P.T.1
Eaton, S.2
Aynsley-Green, A.3
Edginton, M.4
Hussain, K.5
Krywawych, S.6
-
11
-
-
34548204386
-
Physical exercise-induced hypoglycemia caused by failed silencing of monocarboxylate transporter 1 in pancreatic β cells
-
Otonkoski T, Jiao H, Kaminen-Ahola N, Tapia-Paez I, Ullah MS, Parton LE, et al. Physical exercise-induced hypoglycemia caused by failed silencing of monocarboxylate transporter 1 in pancreatic β cells. Am J Hum Genet 2007;81:467-74.
-
(2007)
Am J Hum Genet
, vol.81
, 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
-
12
-
-
0347359228
-
Hyperinsulinism in infancy: From basic science to clinical disease
-
Dunne MJ, Cosgrove KE, Shepherd RM, Aynsley-Green A, Lindley KJ. Hyperinsulinism in infancy: from basic science to clinical disease. Physiol Rev 2004;84:239-75.
-
(2004)
Physiol Rev
, vol.84
, pp. 239-275
-
-
Dunne, M.J.1
Cosgrove, K.E.2
Shepherd, R.M.3
Aynsley-Green, A.4
Lindley, K.J.5
-
13
-
-
0037269223
-
The genetics of neonatal hyperinsulinism
-
Fournet JC, Junien C. The genetics of neonatal hyperinsulinism. Horm Res 2003;59(Suppl 1):30-4.
-
(2003)
Horm Res
, vol.59
, Issue.SUPPL. 1
, pp. 30-34
-
-
Fournet, J.C.1
Junien, C.2
-
14
-
-
0033803049
-
Dominantly inherited hyperinsulinism caused by a mutation in the sulfonylurea receptor type 1
-
Huopio H, Reimann F, Ashfield R, Komulainen J, Lenko HL, Rahier J, et al. Dominantly inherited hyperinsulinism caused by a mutation in the sulfonylurea receptor type 1. J Clin Invest 2000;106:897-906.
-
(2000)
J Clin Invest
, vol.106
, pp. 897-906
-
-
Huopio, H.1
Reimann, F.2
Ashfield, R.3
Komulainen, J.4
Lenko, H.L.5
Rahier, J.6
-
15
-
-
0041819997
-
Clinical and molecular characterization of a dominant form of congenital hyperinsulinism caused by a mutation in the high-affinity sulfonylurea receptor
-
Thornton PS, MacMullen C, Ganguly A, Ruchelli E, Steinkrauss L, Crane A, et al. Clinical and molecular characterization of a dominant form of congenital hyperinsulinism caused by a mutation in the high-affinity sulfonylurea receptor. Diabetes 2003;52:2403-10.
-
(2003)
Diabetes
, vol.52
, pp. 2403-2410
-
-
Thornton, P.S.1
MacMullen, C.2
Ganguly, A.3
Ruchelli, E.4
Steinkrauss, L.5
Crane, A.6
-
16
-
-
4544344374
-
Familial leucine-sensitive hypoglycemia of infancy due to a dominant mutation of the β-cell sulfonylurea receptor
-
Magge SN, Shyng SL, MacMullen C, Steinkrauss L, Ganguly A, Katz LE, Stanley CA. Familial leucine-sensitive hypoglycemia of infancy due to a dominant mutation of the β-cell sulfonylurea receptor. J Clin Endocrinol Metab 2004;89:4450-6.
-
(2004)
J Clin Endocrinol Metab
, vol.89
, pp. 4450-4456
-
-
Magge, S.N.1
Shyng, S.L.2
MacMullen, C.3
Steinkrauss, L.4
Ganguly, A.5
Katz, L.E.6
Stanley, C.A.7
-
17
-
-
33646357267
-
A novel KCNJ11 mutation associated with congenital hyperinsulinism reduces the intrinsic open probability of β-cell ATP-sensitive potassium channels
-
Lin YW, MacMullen C, Ganguly A, Stanley CA, Shyng SL. A novel KCNJ11 mutation associated with congenital hyperinsulinism reduces the intrinsic open probability of β-cell ATP-sensitive potassium channels. J Biol Chem 2006;281:3006-12.
-
(2006)
J Biol Chem
, vol.281
, pp. 3006-3012
-
-
Lin, Y.W.1
MacMullen, C.2
Ganguly, A.3
Stanley, C.A.4
Shyng, S.L.5
-
18
-
-
0032190017
-
Paternal mutation of the sulfonylurea receptor (SUR1) gene and maternal loss of 11p15 imprinted genes lead to persistent hyperinsulinism in focal adenomatous hyperplasia
-
Verkarre V, Fournet JC, de Lonlay P, Gross-Morand MS, Devillers M, Rahier J, et al. Paternal mutation of the sulfonylurea receptor (SUR1) gene and maternal loss of 11p15 imprinted genes lead to persistent hyperinsulinism in focal adenomatous hyperplasia. J Clin Invest 1998;102:1286-91.
-
(1998)
J Clin Invest
, vol.102
, pp. 1286-1291
-
-
Verkarre, V.1
Fournet, J.C.2
de Lonlay, P.3
Gross-Morand, M.S.4
Devillers, M.5
Rahier, J.6
-
19
-
-
0037341243
-
The focal form of persistent hyperinsulinemic hypoglycemia of infancy: Morphological and molecular studies show structural and functional differences with insulinoma
-
Sempoux C, Guiot Y, Dahan K, Moulin P, Stevens M, Lambot V, et al. The focal form of persistent hyperinsulinemic hypoglycemia of infancy: morphological and molecular studies show structural and functional differences with insulinoma. Diabetes 2003;52:784-94.
-
(2003)
Diabetes
, vol.52
, pp. 784-794
-
-
Sempoux, C.1
Guiot, Y.2
Dahan, K.3
Moulin, P.4
Stevens, M.5
Lambot, V.6
-
20
-
-
1642465556
-
Hyperinsulinism/hyperammonemia syndrome: Insights into the regulatory role of glutamate dehydrogenase in ammonia metabolism
-
Stanley CA. Hyperinsulinism/hyperammonemia syndrome: insights into the regulatory role of glutamate dehydrogenase in ammonia metabolism. Mol Genet Metab 2004;81(Suppl 1):S45-51.
-
(2004)
Mol Genet Metab
, vol.81
, Issue.SUPPL. 1
-
-
Stanley, C.A.1
-
21
-
-
33748316536
-
SIRT4 inhibits glutamate dehydrogenase and opposes the effects of calorie restriction in pancreatic β cells
-
Haigis MC, Mostoslavsky R, Haigis KM, Fahie K, Christodoulou DC, Murphy AJ, et al. SIRT4 inhibits glutamate dehydrogenase and opposes the effects of calorie restriction in pancreatic β cells. Cell 2006;126:941-54.
-
(2006)
Cell
, vol.126
, pp. 941-954
-
-
Haigis, M.C.1
Mostoslavsky, R.2
Haigis, K.M.3
Fahie, K.4
Christodoulou, D.C.5
Murphy, A.J.6
-
22
-
-
0036894314
-
Glutaminolysis and insulin secretion: From bedside to bench and back
-
Kelly A, Li C, Gao Z, Stanley CA, Matschinsky FM. Glutaminolysis and insulin secretion: from bedside to bench and back. Diabetes 2002;51(Suppl 3):S421-26.
-
(2002)
Diabetes
, vol.51
, Issue.SUPPL. 3
-
-
Kelly, A.1
Li, C.2
Gao, Z.3
Stanley, C.A.4
Matschinsky, F.M.5
-
23
-
-
0035091975
-
Protein-sensitive and fasting hypoglycemia in children with the hyperinsulinism/hyperammonemia syndrome
-
Hsu BY, Kelly A, Thornton PS, Greenberg CR, Dilling LA, Stanley CA. Protein-sensitive and fasting hypoglycemia in children with the hyperinsulinism/hyperammonemia syndrome. J Pediatr 2001;138:383-9.
-
(2001)
J Pediatr
, vol.138
, pp. 383-389
-
-
Hsu, B.Y.1
Kelly, A.2
Thornton, P.S.3
Greenberg, C.R.4
Dilling, L.A.5
Stanley, C.A.6
-
24
-
-
14844302859
-
Central nervous system hyperexcitability associated with glutamate dehydrogenase gain of function mutations
-
Raizen DM, Brooks-Kayal A, Steinkrauss L, Tennekoon GI, Stanley CA, Kelly A. Central nervous system hyperexcitability associated with glutamate dehydrogenase gain of function mutations. J Pediatr 2005;146:388-94.
-
(2005)
J Pediatr
, vol.146
, pp. 388-394
-
-
Raizen, D.M.1
Brooks-Kayal, A.2
Steinkrauss, L.3
Tennekoon, G.I.4
Stanley, C.A.5
Kelly, A.6
-
25
-
-
0036896635
-
Regulation of pancreatic β-cell glucokinase: From basics to therapeutics
-
Matschinsky FM. Regulation of pancreatic β-cell glucokinase: from basics to therapeutics. Diabetes 2002;51(Suppl 3):S394-404.
-
(2002)
Diabetes
, vol.51
, Issue.SUPPL. 3
-
-
Matschinsky, F.M.1
-
26
-
-
21144435356
-
Dominantly inherited hyperinsulinaemic hypoglycaemia
-
de Lonlay P, Giurgea I, Sempoux C, Touati G, Jaubert F, Rahier J, et al. Dominantly inherited hyperinsulinaemic hypoglycaemia. J Inherit Metab Dis 2005;28:267-76.
-
(2005)
J Inherit Metab Dis
, vol.28
, pp. 267-276
-
-
de Lonlay, P.1
Giurgea, I.2
Sempoux, C.3
Touati, G.4
Jaubert, F.5
Rahier, J.6
-
27
-
-
0036227541
-
The second activating glucokinase mutation (A456V): Implications for glucose homeostasis and diabetes therapy
-
Christesen HB, Jacobsen BB, Odili S, Buettger C, Cuesta-Munoz A, Hansen T, et al. The second activating glucokinase mutation (A456V): implications for glucose homeostasis and diabetes therapy. Diabetes 2002;51:1240-6.
-
(2002)
Diabetes
, vol.51
, pp. 1240-1246
-
-
Christesen, H.B.1
Jacobsen, B.B.2
Odili, S.3
Buettger, C.4
Cuesta-Munoz, A.5
Hansen, T.6
-
28
-
-
0041319267
-
Insights into the biochemical and genetic basis of glucokinase activation from naturally occurring hypoglycemia mutations
-
Gloyn AL, Noordam K, Willemsen MA, Ellard S, Lam WW, Campbell IW, et al. Insights into the biochemical and genetic basis of glucokinase activation from naturally occurring hypoglycemia mutations. Diabetes 2003;52:2433-40.
-
(2003)
Diabetes
, vol.52
, pp. 2433-2440
-
-
Gloyn, A.L.1
Noordam, K.2
Willemsen, M.A.3
Ellard, S.4
Lam, W.W.5
Campbell, I.W.6
-
29
-
-
3242770556
-
Severe persistent hyperinsulinemic hypoglycemia due to a de novo glucokinase mutation
-
Cuesta-Munoz AL, Huopio H, Otonkoski T, Gomez-Zumaquero JM, Nanto-Salonen K, Rahier J, et al. Severe persistent hyperinsulinemic hypoglycemia due to a de novo glucokinase mutation. Diabetes 2004;53:2164-8.
-
(2004)
Diabetes
, vol.53
, pp. 2164-2168
-
-
Cuesta-Munoz, A.L.1
Huopio, H.2
Otonkoski, T.3
Gomez-Zumaquero, J.M.4
Nanto-Salonen, K.5
Rahier, J.6
-
30
-
-
0347990591
-
Familial hyperinsulinemic hypoglycemia caused by a defect in the SCHAD enzyme of mitochondrial fatty acid oxidation
-
Molven A, Matre GE, Duran M, Wanders RJ, Rishaug U, Njølstad PR, et al. Familial hyperinsulinemic hypoglycemia caused by a defect in the SCHAD enzyme of mitochondrial fatty acid oxidation. Diabetes 2004;53:221-7.
-
(2004)
Diabetes
, vol.53
, pp. 221-227
-
-
Molven, A.1
Matre, G.E.2
Duran, M.3
Wanders, R.J.4
Rishaug, U.5
Njølstad, P.R.6
-
31
-
-
20944434799
-
Hyperinsulinism of infancy associated with a novel splice site mutation in the SCHAD gene
-
Hussain K, Clayton PT, Krywawych S, Chatziandreou I, Mills P, Ginbey DW, et al. Hyperinsulinism of infancy associated with a novel splice site mutation in the SCHAD gene. J Pediatr 2005;146:706-8.
-
(2005)
J Pediatr
, vol.146
, pp. 706-708
-
-
Hussain, K.1
Clayton, P.T.2
Krywawych, S.3
Chatziandreou, I.4
Mills, P.5
Ginbey, D.W.6
-
32
-
-
33747006635
-
Reye-like syndrome resulting from novel missense mutations in mitochondrial medium- and short-chain L-3-hydroxyacyl-CoA dehydrogenase
-
Bennett MJ, Russell LK, Tokunaga C, Narayan SB, Tan L, Seegmiller A, et al. Reye-like syndrome resulting from novel missense mutations in mitochondrial medium- and short-chain L-3-hydroxyacyl-CoA dehydrogenase. Mol Genet Metab 2006;89:74-9.
-
(2006)
Mol Genet Metab
, vol.89
, pp. 74-79
-
-
Bennett, M.J.1
Russell, L.K.2
Tokunaga, C.3
Narayan, S.B.4
Tan, L.5
Seegmiller, A.6
-
33
-
-
0346788907
-
Short-chain 3-hydroxyacyl-CoA dehydrogenase deficiency associated with hyperinsulinism: A novel glucose-fatty acid cycle?
-
Eaton S, Chatziandreou I, Krywawych S, Pen S, Clayton PT, Hussain K. Short-chain 3-hydroxyacyl-CoA dehydrogenase deficiency associated with hyperinsulinism: a novel glucose-fatty acid cycle? Biochem Soc Trans 2003;31:1137-9.
-
(2003)
Biochem Soc Trans
, vol.31
, pp. 1137-1139
-
-
Eaton, S.1
Chatziandreou, I.2
Krywawych, S.3
Pen, S.4
Clayton, P.T.5
Hussain, K.6
-
34
-
-
29144504358
-
Massive insulin secretion in response to anaerobic exercise in exercise-induced hyperinsulinism
-
Meissner T, Friedmann B, Okun JG, Schwab MA, Otonkoski T, Bauer T, et al. Massive insulin secretion in response to anaerobic exercise in exercise-induced hyperinsulinism. Horm Metab Res 2005;37:690-4.
-
(2005)
Horm Metab Res
, vol.37
, pp. 690-694
-
-
Meissner, T.1
Friedmann, B.2
Okun, J.G.3
Schwab, M.A.4
Otonkoski, T.5
Bauer, T.6
-
35
-
-
0037221769
-
Physical exercise-induced hyperinsulinemic hypoglycemia is an autosomal dominant trait characterized by abnormal pyruvate-induced insulin release
-
Otonkoski T, Kaminen N, Ustinov J, Lapatto R, Meissner T, Mayatepek E, et al. Physical exercise-induced hyperinsulinemic hypoglycemia is an autosomal dominant trait characterized by abnormal pyruvate-induced insulin release. Diabetes 2003;52:199-204.
-
(2003)
Diabetes
, vol.52
, pp. 199-204
-
-
Otonkoski, T.1
Kaminen, N.2
Ustinov, J.3
Lapatto, R.4
Meissner, T.5
Mayatepek, E.6
-
36
-
-
33344464862
-
Clinical features and insulin regulation in infants with syndrome of prolonged neonatal hyperinsulinism
-
Hoe FM, Thornton PS, Wanner LA, Steinkrauss L, Simmons RA, Stanley CA. Clinical features and insulin regulation in infants with syndrome of prolonged neonatal hyperinsulinism. J Pediatr 2006;148:207-12.
-
(2006)
J Pediatr
, vol.148
, pp. 207-212
-
-
Hoe, F.M.1
Thornton, P.S.2
Wanner, L.A.3
Steinkrauss, L.4
Simmons, R.A.5
Stanley, C.A.6
-
38
-
-
0035721309
-
Hyperinsulinaemic hypoglycaemia: Leading symptom in a patient with congenital disorder of glycosylation Ia (phosphomannomutase deficiency)
-
Böhles H, Sewell AA, Gebhardt B, Reinecke-Lüthge A, Klöppel G, Marquardt T. Hyperinsulinaemic hypoglycaemia: leading symptom in a patient with congenital disorder of glycosylation Ia (phosphomannomutase deficiency). J Inherit Metab Dis 2001;24:858-62.
-
(2001)
J Inherit Metab Dis
, vol.24
, pp. 858-862
-
-
Böhles, H.1
Sewell, A.A.2
Gebhardt, B.3
Reinecke-Lüthge, A.4
Klöppel, G.5
Marquardt, T.6
-
39
-
-
0033510652
-
Hyperinsulinemic hypoglycemia as a presenting sign in phosphomannose isomerase deficiency: A new manifestation of carbohydrate-deficient glycoprotein syndrome treatable with mannose
-
de Lonlay P, Cuer M, Vuillaumier-Barrot S, Beaune G, Castelnau P, Kretz M, et al. Hyperinsulinemic hypoglycemia as a presenting sign in phosphomannose isomerase deficiency: a new manifestation of carbohydrate-deficient glycoprotein syndrome treatable with mannose. J Pediatr 1999;135:379-83.
-
(1999)
J Pediatr
, vol.135
, pp. 379-383
-
-
de Lonlay, P.1
Cuer, M.2
Vuillaumier-Barrot, S.3
Beaune, G.4
Castelnau, P.5
Kretz, M.6
-
40
-
-
0033505855
-
Severe hypoglycemia as a presenting symptom of carbohydrate-deficient glycoprotein syndrome
-
Babovic-Vuksanovic D, Patterson MC, Schwenk WF, O'Brien JF, Vockley J, Freeze HH, et al. Severe hypoglycemia as a presenting symptom of carbohydrate-deficient glycoprotein syndrome. J Pediatr 1999;135:775-81.
-
(1999)
J Pediatr
, vol.135
, pp. 775-781
-
-
Babovic-Vuksanovic, D.1
Patterson, M.C.2
Schwenk, W.F.3
O'Brien, J.F.4
Vockley, J.5
Freeze, H.H.6
-
41
-
-
23044496263
-
Congenital disorder of glycosylation id presenting with hyperinsulinemic hypoglycemia and islet cell hyperplasia
-
Sun L, Eklund EA, Chung WK, Wang C, Cohen J, Freeze HH. Congenital disorder of glycosylation id presenting with hyperinsulinemic hypoglycemia and islet cell hyperplasia. J Clin Endocrinol Metab 2005;90:4371-5.
-
(2005)
J Clin Endocrinol Metab
, vol.90
, pp. 4371-4375
-
-
Sun, L.1
Eklund, E.A.2
Chung, W.K.3
Wang, C.4
Cohen, J.5
Freeze, H.H.6
-
42
-
-
0033846802
-
Calcium-stimulated insulin secretion in diffuse and focal forms of congenital hyperinsulinism
-
Ferry RJ Jr., Kelly A, Grimberg A, Koo-McCoy S, Shapiro MJ, Fellows KE, et al. Calcium-stimulated insulin secretion in diffuse and focal forms of congenital hyperinsulinism. J Pediatr 2000;137:239-46.
-
(2000)
J Pediatr
, vol.137
, pp. 239-246
-
-
Ferry Jr., R.J.1
Kelly, A.2
Grimberg, A.3
Koo-McCoy, S.4
Shapiro, M.J.5
Fellows, K.E.6
-
43
-
-
0035142144
-
Dysregulation of insulin secretion in children with congenital hyperinsulinism due to sulfonylurea receptor mutations
-
Grimberg A, Ferry RJ Jr, Kelly A, Koo-McCoy S, Polonsky K, Glaser B, et al. Dysregulation of insulin secretion in children with congenital hyperinsulinism due to sulfonylurea receptor mutations. Diabetes 2001;50:322-8.
-
(2001)
Diabetes
, vol.50
, pp. 322-328
-
-
Grimberg, A.1
Ferry Jr, R.J.2
Kelly, A.3
Koo-McCoy, S.4
Polonsky, K.5
Glaser, B.6
-
44
-
-
10744221944
-
Preoperative evaluation of infants with focal or diffuse congenital hyperinsulinism by intravenous acute insulin response tests and selective pancreatic arterial calcium stimulation
-
Stanley CA, Thornton PS, Ganguly A, MacMullen C, Underwood P, Bhatia P, et al. Preoperative evaluation of infants with focal or diffuse congenital hyperinsulinism by intravenous acute insulin response tests and selective pancreatic arterial calcium stimulation. J Clin Endocrinol Metab 2004;89:288-96.
-
(2004)
J Clin Endocrinol Metab
, vol.89
, pp. 288-296
-
-
Stanley, C.A.1
Thornton, P.S.2
Ganguly, A.3
MacMullen, C.4
Underwood, P.5
Bhatia, P.6
-
45
-
-
10744222224
-
Acute insulin responses to calcium and tolbutamide do not differentiate focal from diffuse congenital hyperinsulinism
-
Giurgea I, Laborde K, Touati G, Bellanné-Chantelot C, Nassogne MC, Sempoux C, et al. Acute insulin responses to calcium and tolbutamide do not differentiate focal from diffuse congenital hyperinsulinism. J Clin Endocrinol Metab 2004;89:925-9.
-
(2004)
J Clin Endocrinol Metab
, vol.89
, pp. 925-929
-
-
Giurgea, I.1
Laborde, K.2
Touati, G.3
Bellanné-Chantelot, C.4
Nassogne, M.C.5
Sempoux, C.6
-
46
-
-
0034886416
-
Acute insulin responses to leucine in children with the hyperinsulinism/hyperammonemia syndrome
-
Kelly A, Ng D, Ferry RJ Jr., Grimberg A, Koo-McCoy S, Thornton PS, Stanley CA. Acute insulin responses to leucine in children with the hyperinsulinism/hyperammonemia syndrome. J Clin Endocrinol Metab 2001;86:3724-8.
-
(2001)
J Clin Endocrinol Metab
, vol.86
, pp. 3724-3728
-
-
Kelly, A.1
Ng, D.2
Ferry Jr., R.J.3
Grimberg, A.4
Koo-McCoy, S.5
Thornton, P.S.6
Stanley, C.A.7
-
47
-
-
0029098644
-
Hyperinsulinism in children: Diagnostic value of pancreatic venous sampling correlated with clinical, pathological and surgical outcome in 25 cases
-
Dubois J, Brunelle F, Touati G, Sebag G, Nuttin C, Thach T, et al. (1995) Hyperinsulinism in children: diagnostic value of pancreatic venous sampling correlated with clinical, pathological and surgical outcome in 25 cases. Pediatr Radiol 1995;25:512-6.
-
(1995)
Pediatr Radiol 1995
, vol.25
, pp. 512-516
-
-
Dubois, J.1
Brunelle, F.2
Touati, G.3
Sebag, G.4
Nuttin, C.5
Thach, T.6
-
52
-
-
0017578837
-
Accumulation of dopamine in mouse pancreatic β-cells following injection of L-DOPA: Localization to secretory granules and inhibition of insulin secretion
-
Ericson LE, Hakanson R, Lundquist I. Accumulation of dopamine in mouse pancreatic β-cells following injection of L-DOPA: localization to secretory granules and inhibition of insulin secretion. Diabetologia 1977;13:117-24.
-
(1977)
Diabetologia
, vol.13
, pp. 117-124
-
-
Ericson, L.E.1
Hakanson, R.2
Lundquist, I.3
-
53
-
-
0030937436
-
Presence of DOPA decarboxylase and its localization in adult rat pancreatic islet cells
-
Borelli MI, Villar MJ, Orezzoli A, Gagliardino JJ. Presence of DOPA decarboxylase and its localization in adult rat pancreatic islet cells. Diabetes Metab 1977;23:161-3.
-
(1977)
Diabetes Metab
, vol.23
, pp. 161-163
-
-
Borelli, M.I.1
Villar, M.J.2
Orezzoli, A.3
Gagliardino, J.J.4
-
55
-
-
5044232961
-
Congenital hyperinsulinism: Intraoperative biopsy interpretation can direct the extent of pancreatectomy
-
Suchi M, Thornton PS, Adzick NS, MacMullen C, Ganguly A, Stanley CA, Ruchelli ED. Congenital hyperinsulinism: intraoperative biopsy interpretation can direct the extent of pancreatectomy. Am J Surg Pathol 2004;28:1326-35.
-
(2004)
Am J Surg Pathol
, vol.28
, pp. 1326-1335
-
-
Suchi, M.1
Thornton, P.S.2
Adzick, N.S.3
MacMullen, C.4
Ganguly, A.5
Stanley, C.A.6
Ruchelli, E.D.7
-
56
-
-
0035120388
-
Neurologic outcomes of 90 neonates and infants with persistent hyperinsulinemic hypoglycemia
-
Menni F, de Lonlay P, Sevin C, Touati G, Peigné C, Barbier V, et al. Neurologic outcomes of 90 neonates and infants with persistent hyperinsulinemic hypoglycemia. Pediatrics 2001;107:476-9.
-
(2001)
Pediatrics
, vol.107
, pp. 476-479
-
-
Menni, F.1
de Lonlay, P.2
Sevin, C.3
Touati, G.4
Peigné, C.5
Barbier, V.6
-
57
-
-
16244375889
-
Effects of hypoglycemia on developmental outcome in children with congenital hyperinsulinism
-
Steinkrauss L, Lipman TH, Hendell CD, Gerdes M, Thornton PS, Stanley CA. Effects of hypoglycemia on developmental outcome in children with congenital hyperinsulinism. J Pediatr Nurs 2005;20:109-18.
-
(2005)
J Pediatr Nurs
, vol.20
, pp. 109-118
-
-
Steinkrauss, L.1
Lipman, T.H.2
Hendell, C.D.3
Gerdes, M.4
Thornton, P.S.5
Stanley, C.A.6
-
58
-
-
0028813928
-
Hyperinsulinemic hypoglycemia of infancy (nesidioblastosis) in clinical remission: High incidence of diabetes mellitus and persistent β-cell dysfunction at long term follow up
-
Leibowitz G, Glaser B, Higazi AA, Salameh M, Cerasi E, Landau H. Hyperinsulinemic hypoglycemia of infancy (nesidioblastosis) in clinical remission: high incidence of diabetes mellitus and persistent β-cell dysfunction at long term follow up. J Clin Endocrinol Metab 1995;80:386-92.
-
(1995)
J Clin Endocrinol Metab
, vol.80
, pp. 386-392
-
-
Leibowitz, G.1
Glaser, B.2
Higazi, A.A.3
Salameh, M.4
Cerasi, E.5
Landau, H.6
-
59
-
-
0038487619
-
Long-term follow-up of 114 patients with congenital hyperinsulinism
-
Meissner T, Wendel U, Burgard P, Schaetzle S, Mayatepek E. Long-term follow-up of 114 patients with congenital hyperinsulinism. Eur J Endocrinol 2003;149:43-51.
-
(2003)
Eur J Endocrinol
, vol.149
, pp. 43-51
-
-
Meissner, T.1
Wendel, U.2
Burgard, P.3
Schaetzle, S.4
Mayatepek, E.5
-
60
-
-
0018906219
-
Glycemic response to glucagon during fasting hypoglycemia: An aid in the diagnosis of hyperinsulinism
-
Finegold DN, Stanley CA, Baker L. Glycemic response to glucagon during fasting hypoglycemia: an aid in the diagnosis of hyperinsulinism. J Pediatr 1980;96:257-9.
-
(1980)
J Pediatr
, vol.96
, pp. 257-259
-
-
Finegold, D.N.1
Stanley, C.A.2
Baker, L.3
-
61
-
-
0036080347
-
Hypopituitarism in childhood
-
Geffner ME. Hypopituitarism in childhood. Cancer Control 2002;9:212-22.
-
(2002)
Cancer Control
, vol.9
, pp. 212-222
-
-
Geffner, M.E.1
-
64
-
-
0024586640
-
Drug-induced hypoglycemia: A review of 1418 cases
-
Seltzer HS. Drug-induced hypoglycemia: a review of 1418 cases. Endocrinol Metab Clin North Am 1989;18:163-83.
-
(1989)
Endocrinol Metab Clin North Am
, vol.18
, pp. 163-183
-
-
Seltzer, H.S.1
-
65
-
-
0017062640
-
Hyperinsulinism in infancy: Diagnosis by demonstration of abnormal response to fasting hypoglycemia
-
Stanley CA, Baker L. Hyperinsulinism in infancy: diagnosis by demonstration of abnormal response to fasting hypoglycemia. Pediatrics 1976;57:702-11.
-
(1976)
Pediatrics
, vol.57
, pp. 702-711
-
-
Stanley, C.A.1
Baker, L.2
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