-
1
-
-
0033560942
-
The causes of neonatal hypoglycemic
-
Stanley CA, Baker L. The causes of neonatal hypoglycemic. N Engl J Med 1999;340:1200-1201
-
(1999)
N Engl J Med
, vol.340
, pp. 1200-1201
-
-
Stanley, C.A.1
Baker, L.2
-
3
-
-
2642556203
-
Hyperinsulinemic hypoglycemia of infancy: The challenge continues
-
Dekelbab BH, Sperling MA. Hyperinsulinemic hypoglycemia of infancy: the challenge continues. Diabetes Metab Res Rev 2004;20:189-195
-
(2004)
Diabetes Metab Res Rev
, vol.20
, pp. 189-195
-
-
Dekelbab, B.H.1
Sperling, M.A.2
-
4
-
-
33344464862
-
Clinical features and insulin regulation in infants with a 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 a syndrome of prolonged neonatal hyperinsulinism. J Pediatr 2006;148:207-212
-
(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
-
5
-
-
0025134647
-
Hyperinsulinaemic hypoglycaemia in small for dates babies
-
Collins JE, Leonard JV, Teale D, Marks V, Williams DM, Kennedy CR, Hall MA. Hyperinsulinaemic hypoglycaemia in small for dates babies. Arch Dis Child 1990;65:1118-1120
-
(1990)
Arch Dis Child
, vol.65
, pp. 1118-1120
-
-
Collins, J.E.1
Leonard, J.V.2
Teale, D.3
Marks, V.4
Williams, D.M.5
Kennedy, C.R.6
Hall, M.A.7
-
6
-
-
0021200640
-
Hyperinsulinism in asphyxiated and small-for-dates infants with hypoglycaemia
-
Collins JE, Leonard JV. Hyperinsulinism in asphyxiated and small-for-dates infants with hypoglycaemia. Lancet 1984;2:311-313
-
(1984)
Lancet
, vol.2
, pp. 311-313
-
-
Collins, J.E.1
Leonard, J.V.2
-
7
-
-
0030936881
-
Hyperinsulinism in infants and children
-
Stanley CA. Hyperinsulinism in infants and children. Pediatr Clin North Am 1997;44:363-374
-
(1997)
Pediatr Clin North Am
, vol.44
, pp. 363-374
-
-
Stanley, C.A.1
-
9
-
-
0034099789
-
Controversies regarding definition of neonatal hypoglycemia: Suggested operational thresholds
-
Cornblath M, Hawdon JM, Williams AF, Aynsley-Green A, Ward-Platt MP, Schwartz R, Kalhan SC. Controversies regarding definition of neonatal hypoglycemia: suggested operational thresholds. Pediatrics 2000;105:1141-1145
-
(2000)
Pediatrics
, vol.105
, pp. 1141-1145
-
-
Cornblath, M.1
Hawdon, J.M.2
Williams, A.F.3
Aynsley-Green, A.4
Ward-Platt, M.P.5
Schwartz, R.6
Kalhan, S.C.7
-
10
-
-
0035120388
-
Neurologic outcomes of 90 neonates and infants with persistent hyperinsulinemic hypoglycemia
-
Menni F, de Lonlay P, Sevin C, Touati G, Peigne C, Barbier V, Nihoul-Fekete C, Saudubray JM, Robert JJ. Neurologic outcomes of 90 neonates and infants with persistent hyperinsulinemic hypoglycemia. Pediatrics 2001;107:476-479
-
(2001)
Pediatrics
, vol.107
, pp. 476-479
-
-
Menni, F.1
de Lonlay, P.2
Sevin, C.3
Touati, G.4
Peigne, C.5
Barbier, V.6
Nihoul-Fekete, C.7
Saudubray, J.M.8
Robert, J.J.9
-
11
-
-
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;57:702-711
-
(1976)
Pediatrics
, vol.57
, pp. 702-711
-
-
Stanley, C.A.1
Baker, L.2
-
12
-
-
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;96:257-259
-
(1980)
J Pediatr
, vol.96
, pp. 257-259
-
-
Finegold, D.N.1
Stanley, C.A.2
Baker, L.3
-
14
-
-
21444447004
-
Congenital hyperinsulinism
-
Hussain K. Congenital hyperinsulinism. Semin Fetal Neonatal Med 2005;10:369-376
-
(2005)
Semin Fetal Neonatal Med
, vol.10
, pp. 369-376
-
-
Hussain, K.1
-
15
-
-
12344263612
-
-
Hussain K, Aynsley-Green A, Stanley CA. Medications used in the treatment of hypoglycemia due to congenital hyperinsulinism of infancy (HI). Pediatr Endocrinol Rev 2004;2(Suppl 1):163-167
-
Hussain K, Aynsley-Green A, Stanley CA. Medications used in the treatment of hypoglycemia due to congenital hyperinsulinism of infancy (HI). Pediatr Endocrinol Rev 2004;2(Suppl 1):163-167
-
-
-
-
16
-
-
0036833473
-
Advances in diagnosis and treatment of hyperinsulinism in infants and children
-
Stanley CA. Advances in diagnosis and treatment of hyperinsulinism in infants and children. J Clin Endocrinol Metab 2002;87:4857-4859
-
(2002)
J Clin Endocrinol Metab
, vol.87
, pp. 4857-4859
-
-
Stanley, C.A.1
-
17
-
-
15644367096
-
A nonsense mutation in the inward rectifier potassium channel gene, Kir6.2, is associated with familial hyperinsulinism
-
Nestorowicz A, Inagaki N, Gonoi T, Schoor KP, Wilson BA, Glaser B, Landau H, Stanley CA, Thornton PS, Seino S, Permutt MA. A nonsense mutation in the inward rectifier potassium channel gene, Kir6.2, is associated with familial hyperinsulinism. Diabetes 1997;46:1743-1748
-
(1997)
Diabetes
, vol.46
, pp. 1743-1748
-
-
Nestorowicz, A.1
Inagaki, N.2
Gonoi, T.3
Schoor, K.P.4
Wilson, B.A.5
Glaser, B.6
Landau, H.7
Stanley, C.A.8
Thornton, P.S.9
Seino, S.10
Permutt, M.A.11
-
18
-
-
0029658241
-
Mutations in the sulonylurea receptor gene are associated with familial hyperinsulinism in Ashkenazi Jews
-
Nestorowicz A, Wilson BA, Schoor KP, Inoue H, Glaser B, Landau H, Stanley CA, Thornton PS, Clement JPt, Bryan J, Aguilar-Bryan L, Permutt MA. Mutations in the sulonylurea receptor gene are associated with familial hyperinsulinism in Ashkenazi Jews. Hum Mol Genet 1996;5:1813-1822
-
(1996)
Hum Mol Genet
, vol.5
, pp. 1813-1822
-
-
Nestorowicz, A.1
Wilson, B.A.2
Schoor, K.P.3
Inoue, H.4
Glaser, B.5
Landau, H.6
Stanley, C.A.7
Thornton, P.S.8
Clement, J.P.9
Bryan, J.10
Aguilar-Bryan, L.11
Permutt, M.A.12
-
19
-
-
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;5:1809-1812
-
(1996)
Hum Mol Genet
, vol.5
, pp. 1809-1812
-
-
Thomas, P.1
Ye, Y.2
Lightner, E.3
-
20
-
-
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, Aguilar-Bryan L, Gagel RF, Bryan J. Mutations in the sulfonylurea receptor gene in familial persistent hyperinsulinemic hypoglycemia of infancy. Science 1995;268:426-429
-
(1995)
Science
, 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
Aguilar-Bryan, L.7
Gagel, R.F.8
Bryan, J.9
-
21
-
-
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, Perlman K, Rich BH, Zammarchi E, Poncz M. Hyperinsulinism and hyperammonemia in infants with regulatory mutations of the glutamate dehydrogenase gene. N Engl J Med 1998;338:1352-1357
-
(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
Perlman, K.7
Rich, B.H.8
Zammarchi, E.9
Poncz, M.10
-
22
-
-
0032556969
-
Familial hyperinsulinism caused by an activating glucokinase mutation
-
Glaser B, Kesavan P, Heyman M, Davis E, Cuesta A, Buchs A, Stanley CA, Thornton PS, Permutt MA, Matschinsky FM, Herold KC. Familial hyperinsulinism caused by an activating glucokinase mutation. N Engl J Med 1998;338:226-230
-
(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
Stanley, C.A.7
Thornton, P.S.8
Permutt, M.A.9
Matschinsky, F.M.10
Herold, K.C.11
-
23
-
-
0034902277
-
Hyperinsulinism in short-chain L-3-hydroxyacyl-CoA dehydrogenase deficiency reveals the importance of beta-oxidation in insulin secretion
-
Clayton PT, Eaton S, Aynsley-Green A, Edginton M, Hussein K, Krywawych S, Datta V, Malingre HE, Berger R, van den Berg IE. Hyperinsulinism in short-chain L-3-hydroxyacyl-CoA dehydrogenase deficiency reveals the importance of beta-oxidation in insulin secretion. J Clin Invest 2001;108:457-465
-
(2001)
J Clin Invest
, vol.108
, pp. 457-465
-
-
Clayton, P.T.1
Eaton, S.2
Aynsley-Green, A.3
Edginton, M.4
Hussein, K.5
Krywawych, S.6
Datta, V.7
Malingre, H.E.8
Berger, R.9
van den Berg, I.E.10
-
24
-
-
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, Njolstad PR, Jellum E, Sovik O. Familial hyperinsulinemic hypoglycemia caused by a defect in the SCHAD enzyme of mitochondrial fatty acid oxidation. Diabetes 2004;53:221-227
-
(2004)
Diabetes
, vol.53
, pp. 221-227
-
-
Molven, A.1
Matre, G.E.2
Duran, M.3
Wanders, R.J.4
Rishaug, U.5
Njolstad, P.R.6
Jellum, E.7
Sovik, O.8
-
25
-
-
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, Aguilar-Bryan L, Stanley CA. Clinical and molecular characterization of a dominant form of congenital hyperinsulinism caused by a mutation in the high-affinity sulfonylurea receptor. Diabetes 2003;52:2403-2410
-
(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
Aguilar-Bryan, L.7
Stanley, C.A.8
-
26
-
-
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-F112
-
(2000)
Arch Dis Child Fetal Neonatal Ed
, vol.82
-
-
Rahier, J.1
Guiot, Y.2
Sempoux, C.3
-
27
-
-
0028972501
-
Reconstitution of IKATP: An inward rectifier subunit plus the sulfonylurea receptor
-
Inagaki N, Gonoi T, Clement JPt, Namba N, Inazawa J, Gonzalez G, Aguilar-Bryan L, Seino S, Bryan J. Reconstitution of IKATP: an inward rectifier subunit plus the sulfonylurea receptor. Science 1995;270:1166-1170
-
(1995)
Science
, vol.270
, pp. 1166-1170
-
-
Inagaki, N.1
Gonoi, T.2
Clement, J.P.3
Namba, N.4
Inazawa, J.5
Gonzalez, G.6
Aguilar-Bryan, L.7
Seino, S.8
Bryan, J.9
-
28
-
-
0030880778
-
Somatic deletion of the imprinted 11p15 region in sporadic persistent hyperinsulinemic hypoglycemia of infancy is specific of focal adenomatous hyperplasia and endorses partial pancreatectomy
-
de Lonlay P, Fournet JC, Rahier J, Gross-Morand MS, Poggi-Travert F, Foussier V, Bonnefont JP, Brusset MC, Brunelle F, Robert JJ, Nihoul Fekete C, Saudubray JM, Junien C. Somatic deletion of the imprinted 11p15 region in sporadic persistent hyperinsulinemic hypoglycemia of infancy is specific of focal adenomatous hyperplasia and endorses partial pancreatectomy. J Clin Invest 1997;100:802-807
-
(1997)
J Clin Invest
, vol.100
, pp. 802-807
-
-
de Lonlay, P.1
Fournet, J.C.2
Rahier, J.3
Gross-Morand, M.S.4
Poggi-Travert, F.5
Foussier, V.6
Bonnefont, J.P.7
Brusset, M.C.8
Brunelle, F.9
Robert, J.J.10
Nihoul Fekete, C.11
Saudubray, J.M.12
Junien, C.13
-
29
-
-
32844459139
-
Molecular and immunohistochemical analyses of the focal form of congenital hyperinsulinism
-
Suchi M, MacMullen CM, Thornton PS, Adzick NS, Ganguly A, Ruchelli ED, Stanley CA. Molecular and immunohistochemical analyses of the focal form of congenital hyperinsulinism. Mod Pathol 2006;19:122-129
-
(2006)
Mod Pathol
, vol.19
, pp. 122-129
-
-
Suchi, M.1
MacMullen, C.M.2
Thornton, P.S.3
Adzick, N.S.4
Ganguly, A.5
Ruchelli, E.D.6
Stanley, C.A.7
-
30
-
-
1542618112
-
A multidisciplinary approach to the focal form of congenital hyperinsulinism leads to successful treatment by partial pancreatectomy
-
Adzick NS, Thornton PS, Stanley CA, Kaye RD, Ruchelli E. A multidisciplinary approach to the focal form of congenital hyperinsulinism leads to successful treatment by partial pancreatectomy. J Pediatr Surg 2004;39:270-275
-
(2004)
J Pediatr Surg
, vol.39
, pp. 270-275
-
-
Adzick, N.S.1
Thornton, P.S.2
Stanley, C.A.3
Kaye, R.D.4
Ruchelli, E.5
-
31
-
-
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;28:1326-1335
-
(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
-
32
-
-
33644782807
-
Noninvasive diagnosis of focal hyperinsulinism of infancy with (18F)-DOPA positron emission tomography
-
Otonkoski T, Nanto-Salonen K, Seppanen M, Veijola R, Huopio H, Hussain K, Tapanainen P, Eskola O, Parkkola R, Ekstrom K, Guiot Y, Rahier J, Laakso M, Rintala R, Nuutila P, Minn H. Noninvasive diagnosis of focal hyperinsulinism of infancy with (18F)-DOPA positron emission tomography. Diabetes 2006;55:13-18
-
(2006)
Diabetes
, vol.55
, pp. 13-18
-
-
Otonkoski, T.1
Nanto-Salonen, K.2
Seppanen, M.3
Veijola, R.4
Huopio, H.5
Hussain, K.6
Tapanainen, P.7
Eskola, O.8
Parkkola, R.9
Ekstrom, K.10
Guiot, Y.11
Rahier, J.12
Laakso, M.13
Rintala, R.14
Nuutila, P.15
Minn, H.16
-
33
-
-
19644398630
-
Characterization of hyperinsulinism in infancy assessed with PET and 18F-fluoro-L-DOPA
-
Ribeiro MJ, De Lonlay P, Delzescaux T, Boddaert N, Jaubert F, Bourgeois S, Dolle F, Nihoul-Fekete C, Syrota A, Brunelle F. Characterization of hyperinsulinism in infancy assessed with PET and 18F-fluoro-L-DOPA. J Nucl Med 2005;46:560-566
-
(2005)
J Nucl Med
, vol.46
, pp. 560-566
-
-
Ribeiro, M.J.1
De Lonlay, P.2
Delzescaux, T.3
Boddaert, N.4
Jaubert, F.5
Bourgeois, S.6
Dolle, F.7
Nihoul-Fekete, C.8
Syrota, A.9
Brunelle, F.10
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