-
1
-
-
0038487619
-
Long-term follow-up of 114 with congenital hyperinsulinism
-
Meissner T, Wendel U, Burgard P, Schaetzle S, Mayatepek E. Long-term follow-up of 114 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
-
2
-
-
0036136040
-
Clinical and genetic heterogeneity in congenital hyperinsulinism
-
Meissner T, Mayatepek E. Clinical and genetic heterogeneity in congenital hyperinsulinism. Eur J Pediatr. 2002;161:6-20.
-
(2002)
Eur J Pediatr
, vol.161
, pp. 6-20
-
-
Meissner, T.1
Mayatepek, E.2
-
3
-
-
0019416744
-
Nesidioblastosis of the pancreas: Definition of the syndrome and the management of the severe neonatal hyperinsulinaemic hypoglycaemia
-
Aynsley-Green A, Polak JM, Bloom SR, Gough MH, Keeling J, Ashcroft SH. Nesidioblastosis of the pancreas: Definition of the syndrome and the management of the severe neonatal hyperinsulinaemic hypoglycaemia. Arch Dis Child. 1982;56:546-98.
-
(1982)
Arch Dis Child
, vol.56
, pp. 546-598
-
-
Aynsley-Green, A.1
Polak, J.M.2
Bloom, S.R.3
Gough, M.H.4
Keeling, J.5
Ashcroft, S.H.6
-
5
-
-
0034067782
-
Practical management of hyperinsulinism in infancy
-
Aynsley-Green A, Hussain K, Hall J, Saudubray JM, Nihoul- Fékété, De Lounlay-Debeney P, et al. Practical management of hyperinsulinism in infancy. Arch Dis Child Fetal Neonatal. 2000;82:98-107.
-
(2000)
Arch Dis Child Fetal Neonatal
, vol.82
, pp. 98-107
-
-
Aynsley-Green, A.1
Hussain, K.2
Hall, J.3
Saudubray, J.M.4
Nihoul- Fékété5
De Lounlay-Debeney, P.6
-
6
-
-
0023837804
-
Persistent neonatal hyperinsulinism
-
Mathew PM, Young YM, Abu-Osba YK, Mulhern BD, Hammoudi S, Hamdan JA, et al. Persistent neonatal hyperinsulinism. Clin Pediatr. 1988;27:148-51.
-
(1988)
Clin Pediatr
, vol.27
, pp. 148-151
-
-
Mathew, P.M.1
Young, Y.M.2
Abu-Osba, Y.K.3
Mulhern, B.D.4
Hammoudi, S.5
Hamdan, J.A.6
-
7
-
-
24344463035
-
Severe congenital hyperinsulinism due to a mutation in the KIR6.2 subunit of the K-ATP channel impairing trafficking and function
-
Marthinet E, Bloc A, Oka Y, Tanizawa Y, Wherle-Haller B, Bancila V, et al. Severe congenital hyperinsulinism due to a mutation in the KIR6.2 subunit of the K-ATP channel impairing trafficking and function. J Clin Endocrinol Metab. 2005;90:5401-6.
-
(2005)
J Clin Endocrinol Metab
, vol.90
, pp. 5401-5406
-
-
Marthinet, E.1
Bloc, A.2
Oka, Y.3
Tanizawa, Y.4
Wherle-Haller, B.5
Bancila, V.6
-
8
-
-
21444435680
-
From congenital hyperinsulinism to diabetes mellitus: The role of pancreatic beta-cell K channels
-
Hussain K, Cosgrove KE. From congenital hyperinsulinism to diabetes mellitus: The role of pancreatic beta-cell K channels. Pediatr Diabetes. 2005;6:103-12.
-
(2005)
Pediatr Diabetes
, vol.6
, pp. 103-112
-
-
Hussain, K.1
Cosgrove, K.E.2
-
9
-
-
0036135191
-
Heterogeneity of Persistent Hyperinsulinaemic hypoglycaemia a series of 175 cases
-
De Lonlay P, Fournet JC, Touati G, Groos M, Martin D, Sevin C, et al. Heterogeneity of Persistent Hyperinsulinaemic hypoglycaemia a series of 175 cases. Eur J Pediatr. 2002;161:37-48.
-
(2002)
Eur J Pediatr
, vol.161
, pp. 37-48
-
-
De Lonlay, P.1
Fournet, J.C.2
Touati, G.3
Groos, M.4
Martin, D.5
Sevin, C.6
-
10
-
-
12844269202
-
Genetics of congenital hyperinsulinism
-
Fournet JC, Junien C. Genetics of congenital hyperinsulinism. Endocrinol Pathol. 2004;15:233-40.
-
(2004)
Endocrinol Pathol
, vol.15
, pp. 233-240
-
-
Fournet, J.C.1
Junien, C.2
-
11
-
-
10344259091
-
Hyperinsulinism of infancy: Novel ABCC8 and KCNJ11 mutations and evidence for additional locus heterogeneity
-
Tornovsky S, Crane A, Cosgrove KE, Hussain K, Lavie J, Heyman M, et al. Hyperinsulinism of infancy: novel ABCC8 and KCNJ11 mutations and evidence for additional locus heterogeneity. J Clin Endocrinol Metab. 2004;89:6224-34.
-
(2004)
J Clin Endocrinol Metab
, vol.89
, pp. 6224-6234
-
-
Tornovsky, S.1
Crane, A.2
Cosgrove, K.E.3
Hussain, K.4
Lavie, J.5
Heyman, M.6
-
12
-
-
20944434799
-
Hyperinsulinism of infancy associated with a novel splice site mutation in the SHAD 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 SHAD 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
-
13
-
-
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, 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
Njolstad, P.R.6
-
14
-
-
0032992651
-
Intragenic single nucleotide polymorphism haplotype analisys of SUR1 mutations in familial hyperinsulinism
-
Glaser B, Furth J, Stanley CA, Baker L, Thornton PS, Landau H, et al. Intragenic single nucleotide polymorphism haplotype analisys of SUR1 mutations in familial hyperinsulinism. Hum Mutat. 1999;14:23-9.
-
(1999)
Hum Mutat
, vol.14
, pp. 23-29
-
-
Glaser, B.1
Furth, J.2
Stanley, C.A.3
Baker, L.4
Thornton, P.S.5
Landau, H.6
-
15
-
-
0035142144
-
Dysregulation of insulin secretion in children with congenital hyperinsulinism due to sulfonylurea receptor mutations
-
Grimberg A, Ferry RJ, 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, R.J.2
Kelly, A.3
Koo-McCoy, S.4
Polonsky, K.5
Glaser, B.6
-
16
-
-
0001334566
-
Nesidioblastoma, the islet tumor of the pancreas
-
Laidlaw GF. Nesidioblastoma, the islet tumor of the pancreas. Am J Pathol. 1938;14:125-34.
-
(1938)
Am J Pathol
, vol.14
, pp. 125-134
-
-
Laidlaw, G.F.1
-
17
-
-
0015104472
-
Beta cell nesidioblastosis in idiopathic hypoglucemia of infancy
-
Yakovac WC, Baker L, Hummeler K. Beta cell nesidioblastosis in idiopathic hypoglucemia 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
-
18
-
-
0018851716
-
Pancreatic pathology in hyperinsulinemic hypoglucemia of infancy
-
Jaffe R, Hashida Y, Yunis EJ. Pancreatic pathology in hyperinsulinemic hypoglucemia of infancy. Lab Invest. 1980;42:356-65.
-
(1980)
Lab Invest
, vol.42
, pp. 356-365
-
-
Jaffe, R.1
Hashida, Y.2
Yunis, E.J.3
-
19
-
-
12844251849
-
Focal and diffuse forms of congenital hyperinsulinism: The keys for diferential diagnosis
-
Sempoux C, Guiot Y, Jaubert F, Rahier J. Focal and diffuse forms of congenital hyperinsulinism: the keys for diferential diagnosis. Endocrinol Pathol. 2004;15:241-6.
-
(2004)
Endocrinol Pathol
, vol.15
, pp. 241-246
-
-
Sempoux, C.1
Guiot, Y.2
Jaubert, F.3
Rahier, J.4
-
20
-
-
0021320297
-
The basic structural lesion of persistent neonatal hypoglycaemia with hyperinsulinism: Deficiency of pancreatic D cells or hyperactivity of B cells?
-
Rahier J, Fait K, Muntefering H, Becker K, Gepts W, Falkmer S. The basic structural lesion of persistent neonatal hypoglycaemia with hyperinsulinism: deficiency of pancreatic D cells or hyperactivity of B cells? Diabetologia. 1984;26:282-9.
-
(1984)
Diabetologia
, vol.26
, pp. 282-289
-
-
Rahier, J.1
Fait, K.2
Muntefering, H.3
Becker, K.4
Gepts, W.5
Falkmer, S.6
-
21
-
-
0024545488
-
Relevance of endocrine pancreas nesiodioblastosis to hyperinsulinemic hypoglycaemia
-
Rahier J. Relevance of endocrine pancreas nesiodioblastosis to hyperinsulinemic hypoglycaemia. Diabetes Care. 1989;12:164-6.
-
(1989)
Diabetes Care
, vol.12
, pp. 164-166
-
-
Rahier, J.1
-
22
-
-
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
-
23
-
-
0031765251
-
Hyperinsulinism: Molecular aetiology of focal disease
-
Ryan F, Devaney D, Joyce C, Nestorowicz MA, Thornton PS, Permutt MA, et al. Hyperinsulinism: molecular aetiology of focal disease. Arch Dis Child. 1998;79:445-7.
-
(1998)
Arch Dis Child
, vol.79
, pp. 445-447
-
-
Ryan, F.1
Devaney, D.2
Joyce, C.3
Nestorowicz, M.A.4
Thornton, P.S.5
Permutt, M.A.6
-
24
-
-
0031799545
-
Functional analyses of novel mutations in the sulfonylurea receptor 1 associated with persistent hyperinsulinemic hypoglycemia of infancy
-
Shyng SL, Ferrigni T, Shepard JB, Nestorowicz A, Glaser B, Permutt MA, et al. Functional analyses of novel mutations in the sulfonylurea receptor 1 associated with persistent hyperinsulinemic hypoglycemia of infancy. Diabetes. 1998;47:1145-51.
-
(1998)
Diabetes
, vol.47
, pp. 1145-1151
-
-
Shyng, S.L.1
Ferrigni, T.2
Shepard, J.B.3
Nestorowicz, A.4
Glaser, B.5
Permutt, M.A.6
-
25
-
-
0033909936
-
Loss of imprinted genes and paternal SUR1 mutations lead to focal form of congenital hyperinsulinism
-
Fournet JC, Mayaud C, De Lonlay P, Verkarre V, Rahier J, Brunelle F, et al. Loss of imprinted genes and paternal SUR1 mutations lead to focal form of congenital hyperinsulinism. Horm Res. 2000;53 (Suppl 1):2-6.
-
(2000)
Horm Res
, vol.53
, Issue.SUPPL. 1
, pp. 2-6
-
-
Fournet, J.C.1
Mayaud, C.2
De Lonlay, P.3
Verkarre, V.4
Rahier, J.5
Brunelle, F.6
-
26
-
-
0742304100
-
Severe transient hyperinsulinaemic hypoglycaemia: Two neonates without predisposing factors and a review of the literature
-
Yap F, Hogler W, Vora A, Halliday R, Ambler G. Severe transient hyperinsulinaemic hypoglycaemia: two neonates without predisposing factors and a review of the literature. Eur J Pediatr. 2004;163:38-41.
-
(2004)
Eur J Pediatr
, vol.163
, pp. 38-41
-
-
Yap, F.1
Hogler, W.2
Vora, A.3
Halliday, R.4
Ambler, G.5
-
27
-
-
1542618112
-
A multidisciplinary approach to the focal form of congenital hyperinsulinism leads to successful treatment by partial pancreatectomy
-
Adzick NS, Thorntorn 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;39:270-5.
-
(2004)
J Pediatr Surg
, vol.39
, pp. 270-275
-
-
Adzick, N.S.1
Thorntorn, P.S.2
Stanley, C.A.3
Kaye, R.D.4
Ruchelli, E.5
-
28
-
-
14044265775
-
Genotype-phenotype correlations in children with congenital hyperinsulinism due to recesive mutations of the adenosine triphospahte- sensitive potassium channel genes
-
Henwood MJ, Nelly A, Macmullen C, Bathia P, Ganguly A, Thorntorn PS, et al. Genotype-phenotype correlations in children with congenital hyperinsulinism due to recesive mutations of the adenosine triphospahte-sensitive potassium channel genes. J Clin Endocrinol Metab. 2005;90:789-94.
-
(2005)
J Clin Endocrinol Metab
, vol.90
, pp. 789-794
-
-
Henwood, M.J.1
Nelly, A.2
Macmullen, C.3
Bathia, P.4
Ganguly, A.5
Thorntorn, P.S.6
-
29
-
-
0034029974
-
Molecular basis and characterization of the hyperinsulinism/ hyperamoniemia syndrome: Predominance of mutations in exons 11 and 12 of the glutamate deshydrogenase gene
-
HI/HA Contributing Investigators
-
Stanley CA, Fang J, Kutyna K, Hsu BY, Ming JE, Glaser B, et al. Molecular basis and characterization of the hyperinsulinism/hyperamoniemia syndrome: Predominance of mutations in exons 11 and 12 of the glutamate deshydrogenase gene. HI/HA Contributing Investigators. Diabetes. 2000;49;667-73.
-
(2000)
Diabetes
, vol.49
, pp. 667-673
-
-
Stanley, C.A.1
Fang, J.2
Kutyna, K.3
Hsu, B.Y.4
Ming, J.E.5
Glaser, B.6
-
30
-
-
9744256201
-
Síndrome de hiperinsulinismo-hiperamoniemia por mutación de novo en el exón 7 (G979A) del gen GLUD-1, con excelente respuesta a diazóxido
-
Montero Luis C, Pozo Román J, Muǹoz Calvo MT, Martos Moreno G, Donoso MA, Rubio Cabezas O, et al. Síndrome de hiperinsulinismo- hiperamoniemia por mutación de novo en el exón 7 (G979A) del gen GLUD-1, con excelente respuesta a diazóxido. An Pediatr (Barc). 2004;61:433-7.
-
(2004)
An Pediatr (Barc)
, vol.61
, pp. 433-437
-
-
Montero Luis, C.1
Pozo Román, J.2
Muǹoz Calvo, M.T.3
Martos Moreno, G.4
Donoso, M.A.5
Rubio Cabezas, O.6
-
31
-
-
0034772757
-
Ten years'experience of persistent hyperinsulinaemic hypoglycaemia of infancy
-
Tyrrell VJ, Ambler GR, Yeow WH, Cowell CT, Silink M. Ten years'experience of persistent hyperinsulinaemic hypoglycaemia of infancy. J Paediatr Child Health. 2001;37:483-8.
-
(2001)
J Paediatr Child Health
, vol.37
, pp. 483-488
-
-
Tyrrell, V.J.1
Ambler, G.R.2
Yeow, W.H.3
Cowell, C.T.4
Silink, M.5
-
32
-
-
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. Hyperinsulinism in children: Diagnostic value of pancreatic venous sampling correlated with clinical, pathological and surgical outcome in 25 cases. Pediatric Radiol. 1995;25:512-6.
-
(1995)
Pediatric Radiol
, vol.25
, pp. 512-516
-
-
Dubois, J.1
Brunelle, F.2
Touati, G.3
Sebag, G.4
Nuttin, C.5
Thach, T.6
-
33
-
-
0031891277
-
Intraarterial calcium stimulation test in the investigation of hyperinsulinaemic hypoglycaemia
-
Abernethy LJ, Davidson DC, Lamont GL, Shepherd RM, Dunne MJ. Intraarterial calcium stimulation test in the investigation of hyperinsulinaemic hypoglycaemia. Arch Dis Child. 1998;78:359-63.
-
(1998)
Arch Dis Child
, vol.78
, pp. 359-363
-
-
Abernethy, L.J.1
Davidson, D.C.2
Lamont, G.L.3
Shepherd, R.M.4
Dunne, M.J.5
-
35
-
-
10744222224
-
Acute insulin responses to calcium and tolbutamide do not differenciate focal from diffuse congenital hyperinsulinism
-
Giurgea I, Laborde K, Touati G, Bellanne-Chantelot C, Nassogne MC, Sempoux C, et al. Acute insulin responses to calcium and tolbutamide do not differenciate 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
Bellanne-Chantelot, C.4
Nassogne, M.C.5
Sempoux, C.6
-
36
-
-
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, Thorntorn 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
Thorntorn, P.S.2
Ganguly, A.3
MacMullen, C.4
Underwood, P.5
Bhatia, P.6
-
37
-
-
0031782335
-
Neonatal hyperinsulinemic hypoglycemia: Heterogeneity of the syndrome and keys for differential diagnosis
-
Sempoux Y, Guiot A, Lefevre C, Fekete CN, Jaubert JM, Saudubray JM, et al. Neonatal hyperinsulinemic hypoglycemia: Heterogeneity of the syndrome and keys for differential diagnosis. J Clin Endocrinol Metab. 1998;83:1455-61.
-
(1998)
J Clin Endocrinol Metab
, vol.83
, pp. 1455-1461
-
-
Sempoux, Y.1
Guiot, A.2
Lefevre, C.3
Fekete, C.N.4
Jaubert, J.M.5
Saudubray, J.M.6
-
38
-
-
13544271859
-
Contemporary strategies in the diagnosis and management of neonatal hyperinsulinaemic hypoglicaemia
-
Lindley KJ, Dune MJ. Contemporary strategies in the diagnosis and management of neonatal hyperinsulinaemic hypoglicaemia. Early Hum Dev. 2005;81:61-72.
-
(2005)
Early Hum Dev
, vol.81
, pp. 61-72
-
-
Lindley, K.J.1
Dune, M.J.2
-
39
-
-
16244375889
-
Effects of hypoglycaemia on developmental outcome in children with congenital hyperinsulinism
-
Steinkrauss L, Lipman TH, Hendell CD, Gerdes M, Thornton PS, Stanley CA. Effects of hypoglycaemia 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
-
40
-
-
0027375645
-
Persistent hyperinsulinemic hypoglycemia of infancy: Long-term octreotide treatment without pancreatectomy
-
Glaser B, Hirsch HJ, Landau H. Persistent hyperinsulinemic hypoglycemia of infancy: Long-term octreotide treatment without pancreatectomy. J Pediatr. 1993;123:644-50.
-
(1993)
J Pediatr
, vol.123
, pp. 644-650
-
-
Glaser, B.1
Hirsch, H.J.2
Landau, H.3
-
41
-
-
0027374336
-
Short-and long-term use octreotide in the treatment of congenital hyperinsulinism
-
Thornton P, Alter CA, Levitt LE, Baker L, Stanley CA. Short-and long-term use octreotide in the treatment of congenital hyperinsulinism. J Pediatr. 1993;123:637-43.
-
(1993)
J Pediatr
, vol.123
, pp. 637-643
-
-
Thornton, P.1
Alter, C.A.2
Levitt, L.E.3
Baker, L.4
Stanley, C.A.5
-
42
-
-
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 Chile Fetal Neonatol Ed. 2000;82:F108-F12.
-
(2000)
Arch Dis Chile Fetal Neonatol Ed
, vol.82
-
-
Rahier, J.1
Guiot, Y.2
Sempoux, C.3
-
43
-
-
14844333161
-
Congenital hyperinsulinism of infancy: Surgical treatment in 60 cases of focal form
-
Cretolle C, De Lonlay P, Sauvat F, Brunelle F, Rahier J, Saudubray JM, et al. Congenital hyperinsulinism of infancy: Surgical treatment in 60 cases of focal form. Arch Pediatr. 2005;12:258-63.
-
(2005)
Arch Pediatr
, vol.12
, pp. 258-263
-
-
Cretolle, C.1
De Lonlay, P.2
Sauvat, F.3
Brunelle, F.4
Rahier, J.5
Saudubray, J.M.6
-
44
-
-
12144291344
-
The surgical manegement of congenital hyperinsulinemic hypoglycemia in infancy
-
Fekete CN, De Lonlay P, Jaubert F, Rahier J, Brunelle F, Saudubray JM. The surgical manegement of congenital hyperinsulinemic hypoglycemia in infancy. J Pediatr Surg. 2004;39:267-9.
-
(2004)
J Pediatr Surg
, vol.39
, pp. 267-269
-
-
Fekete, C.N.1
De Lonlay, P.2
Jaubert, F.3
Rahier, J.4
Brunelle, F.5
Saudubray, J.M.6
-
45
-
-
0025759231
-
Pancreatic growth and function following surgical treatment of nesidioblastosis in infancy
-
Schhönau E, Deeg KH, Huemmer HP, Akcetin YZ, Böhles HJ. Pancreatic growth and function following surgical treatment of nesidioblastosis in infancy. Eur J Pediatr. 1991;150:550-3.
-
(1991)
Eur J Pediatr
, vol.150
, pp. 550-553
-
-
Schhönau, E.1
Deeg, K.H.2
Huemmer, H.P.3
Akcetin, Y.Z.4
Böhles, H.J.5
-
46
-
-
0021338774
-
The surgical treatment of hyperinsulinism in infancy and childhood
-
Gough MH. The surgical treatment of hyperinsulinism in infancy and childhood. Br J Surg. 1984;71:75-8.
-
(1984)
Br J Surg
, vol.71
, pp. 75-78
-
-
Gough, M.H.1
-
47
-
-
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
-
48
-
-
0031732166
-
Pancreatic exocrine and endocrine function after pancreatectomy for persistent hyperinsulinaemic hypoglycaemia of infancy
-
Cade A, Walters M, Puntis JWL, Arthur RJ, Stringer MD. Pancreatic exocrine and endocrine function after pancreatectomy for persistent hyperinsulinaemic hypoglycaemia of infancy. Arch Dis Child. 1998;79:435-9.
-
(1998)
Arch Dis Child
, vol.79
, pp. 435-439
-
-
Cade, A.1
Walters, M.2
Puntis, J.W.L.3
Arthur, R.J.4
Stringer, M.D.5
-
49
-
-
0030026603
-
Growth and endocrine function after near total pancreatectomy for hyperinsulinaemic hypoglycaemia
-
Soliman AT, Alsalmi I, Darwish A, Asfour MG. Growth and endocrine function after near total pancreatectomy for hyperinsulinaemic hypoglycaemia. Arch Dis Child. 1996;74:379-85.
-
(1996)
Arch Dis Child
, vol.74
, pp. 379-385
-
-
Soliman, A.T.1
Alsalmi, I.2
Darwish, A.3
Asfour, M.G.4
-
50
-
-
0032937898
-
Congenital hyperinsulinism and the surgeon: Lessons learned over 35 years
-
Lovvorn HN, Nance ML, Ferry RJ Jr, Stolte L, O'Neill JA, Schnaufer L, et al. Congenital hyperinsulinism and the surgeon: Lessons learned over 35 years. J Pediatr Surg. 1999;34:786-92.
-
(1999)
J Pediatr Surg
, vol.34
, pp. 786-792
-
-
Lovvorn, H.N.1
Nance, M.L.2
Ferry Jr., R.J.3
Stolte, L.4
O'Neill, J.A.5
Schnaufer, L.6
-
52
-
-
0035120388
-
Neurologic outcomes of 90 neonates and infants with persistent hyperinsulinemic hypoglycemia
-
Menni F, 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
Lonlay, P.2
Sevin, C.3
Touati, G.4
Peigné, C.5
Barbier, V.6
-
53
-
-
0034902794
-
Sub-total pancreatectomy for hypoglycaemia due to congenital hyperinsulinism: Long-term follow-up of neurodevelopmental and pancreatic function
-
Rother KI, Matsumoto JM, Rasmussen NH, Schwenk WF. Sub-total pancreatectomy for hypoglycaemia due to congenital hyperinsulinism: Long-term follow-up of neurodevelopmental and pancreatic function. Pediatr Diabetes. 2001;2:115-22.
-
(2001)
Pediatr Diabetes
, vol.2
, pp. 115-122
-
-
Rother, K.I.1
Matsumoto, J.M.2
Rasmussen, N.H.3
Schwenk, W.F.4
-
54
-
-
0033853921
-
Beta-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. Beta-cell proliferation and apoptosis in the developing normal human pancreas and in hyperinsulinism of infancy. Diabetes. 2000;49:1325-33.
-
(2000)
Diabetes
, vol.49
, pp. 1325-1333
-
-
Kassem, S.A.1
Ariel, I.2
Thornton, P.S.3
Scheimberg, I.4
Glaser, B.5
-
55
-
-
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
|