-
1
-
-
0029021696
-
Mutations in the sulfo- nylurea receptor gene in familial hyperin- sulinemic 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 sulfo- nylurea receptor gene in familial hyperin- sulinemic hypoglycemia of infancy. Science 268:426-429, 1995
-
(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
-
2
-
-
33645221787
-
ATP channel subunits Kir6.2 (KCNJ11) and SUR1 (ABCC8) in diabetes and hyperinsulinism
-
ATP channel subunits Kir6.2 (KCNJ11) and SUR1 (ABCC8) in diabetes and hyperinsulinism. Hum Mutat 27: 220-231, 2006
-
(2006)
Hum Mutat
, vol.27
, pp. 220-231
-
-
Gloyn, A.L.1
Siddiqui, J.2
Ellard, S.3
-
3
-
-
0036135191
-
Heterogeneity of persistent hyperinsu- linemic hypoglycemia
-
De Lonlay P, Fournet JCh, Touati G, Groos MS, Martin D, Sevin C, Delagne V, Mayaud C, Chigot V, Sempoux C, Brusset MC, Laborde K, Bellane-Chantelot C, Vessault A, Rahier J, Junien C, Brunelle F, Nihoul-Fekete C, Saudubray JM, Robert JJ: Heterogeneity of persistent hyperinsu- linemic hypoglycemia. Eur J Pediatr 161: 37-48, 2002
-
(2002)
Eur J Pediatr
, vol.161
, 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
Vessault, A.14
Rahier, J.15
Junien, C.16
Brunelle, F.17
Nihoul-Fekete, C.18
Saudubray, J.M.19
Robert, J.J.20
more..
-
4
-
-
33745952809
-
Mutation spectra of ABCC8 gene in Spanish patients with hyperinsu- linism of infancy
-
Fernández-Marmiesse A, Salas A, Vega A, Fernandez-Lorenzo JR, Barreiro J, Car- racedo A: Mutation spectra of ABCC8 gene in Spanish patients with hyperinsu- linism of infancy. Hum Mutat 27:214, 2006.
-
(2006)
Hum Mutat
, vol.27
, pp. 214
-
-
Fernández-Marmiesse, A.1
Salas, A.2
Vega, A.3
Fernandez-Lorenzo, J.R.4
Barreiro, J.5
Car- racedo, A.6
-
5
-
-
11844299586
-
Diagnosis and classification of diabetes mellitus (Position Statement)
-
American Diabetes Association
-
American Diabetes Association: Diagnosis and classification of diabetes mellitus (Position Statement). Diabetes Care 28:S37-S42, 2005
-
(2005)
Diabetes Care
, vol.28
-
-
-
6
-
-
34447131400
-
Inter- leukin-6 in obese children with and without glucose intolerance
-
Yeste D, Vendrell J, Tomasini R, Broch M, Gussinye M, Megia A, Carrascosa A: Inter- leukin-6 in obese children with and without glucose intolerance. Diabetes Care 30: 1892-1894, 2007
-
(2007)
Diabetes Care
, vol.30
, pp. 1892-1894
-
-
Yeste, D.1
Vendrell, J.2
Tomasini, R.3
Broch, M.4
Gussinye, M.5
Megia, A.6
Carrascosa, A.7
-
7
-
-
8644261515
-
Patrones de crecimiento en ninos normales tras el nacimiento y hasta la edad adulta.
-
in Spanish
-
Carrascosa A, Copil A, Yeste D, Gussinye M: Patrones de crecimiento en ninos normales tras el nacimiento y hasta la edad adulta. Med Clin (Bare) 123:445-451, 2004 [in Spanish]
-
(2004)
Med Clin (Bare)
, vol.123
, pp. 445-451
-
-
Carrascosa, A.1
Copil, A.2
Yeste, D.3
Gussinye, M.4
-
8
-
-
0842289921
-
Diabetes in anonpancreatectomized child withnesid- ioblastosis
-
Bin-Abbas BS, Al-Ashwal AA: Diabetes in anonpancreatectomized child withnesid- ioblastosis. Diabetes Care 27:626-627, 2004
-
(2004)
Diabetes Care
, vol.27
, pp. 626-627
-
-
Bin-Abbas, B.S.1
Al-Ashwal, A.A.2
-
9
-
-
0037464795
-
A new subtype of autosomal dominant diabetes attributable to a mutation in the gene for sulfonylurea receptor type 1
-
Huopio H, Otonkoski T, Vauhkonen I, Reimann F, Ashcroft FM, Laakso M: A new subtype of autosomal dominant diabetes attributable to a mutation in the gene for sulfonylurea receptor type 1. Lancet 361:301-307, 2003
-
(2003)
Lancet
, vol.361
, pp. 301-307
-
-
Huopio, H.1
Otonkoski, T.2
Vauhkonen, I.3
Reimann, F.4
Ashcroft, F.M.5
Laakso, M.6
-
10
-
-
34247500820
-
Hat- tersley: Macrosomia and hyperinsulinaemic hypoglycaemia in patients with heterozygous mutations in the HNF4A gene
-
Pearson RE, Boj SF, Steele AM, Barrett T, Stals K, Shield Jp, Ellard S, Ferrer J, Hat- tersley: Macrosomia and hyperinsulinaemic hypoglycaemia in patients with heterozygous mutations in the HNF4A gene. PLoS Med 4:e118, 2004
-
(2004)
PLoS Med
, vol.4
-
-
Pearson, R.E.1
Boj, S.F.2
Steele, A.M.3
Barrett, T.4
Stals, K.5
Shield, J.6
Ellard, S.7
Ferrer, J.8
-
11
-
-
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 49:1325-1333, 2000
-
(2000)
Diabetes
, vol.49
, pp. 1325-1333
-
-
Kassem, S.A.1
Ariel, I.2
Thornton, P.S.3
Scheimberg, I.4
Glaser, B.5
-
12
-
-
0035142144
-
Dysregulation of insulin secretion in children with congenital hyperinsulinism due to sulfonylurea receptor mutations
-
Grimberg A, Ferry RJ, Kelly A, Koo-Mc- Coy S, Polonsky K, Glaser B, Permutt MA, Aguilar-Bryan L, Stafford D, Thornton PS, Baker L, Stanley CA: Dysregulation of insulin secretion in children with congenital hyperinsulinism due to sulfonylurea receptor mutations. Diabetes 50:322-328, 2001
-
(2001)
Diabetes
, vol.50
, pp. 322-328
-
-
Grimberg, A.1
Ferry, R.J.2
Kelly, A.3
Koo-Mc- Coy, 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
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