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Results: 1-9 |
Results: 9
Blue balls
Authors: Weinzimer, SA Thornton, PS
Citation: Sa. Weinzimer et Ps. Thornton, Blue balls, PEDIATRICS, 108(5), 2001, pp. 1233-1233
Protein-sensitive and fasting hypoglycemia in children with the hyperinsulinism/hyperammonemia syndrome
Authors: Hsu, BYL Kelly, A Thornton, PS Greenberg, CR Dilling, LA Stanley, CA
Citation: Byl. Hsu et al., Protein-sensitive and fasting hypoglycemia in children with the hyperinsulinism/hyperammonemia syndrome, J PEDIAT, 138(3), 2001, pp. 383-389
Acute insulin responses to leucine in children with the hyperinsulinism/hyperammonemia syndrome
Authors: Kelly, A Ng, D Ferry, RJ Grimberg, A Koo-McCoy, S Thornton, PS Stanley, CA
Citation: A. Kelly et al., Acute insulin responses to leucine in children with the hyperinsulinism/hyperammonemia syndrome, J CLIN END, 86(8), 2001, pp. 3724-3728
Dysregulation of insulin secretion in children with congenital hyperinsulinism due to sulfonylurea receptor mutations
Authors: Grimberg, A Ferry, RJ Kelly, A Koo-McCoy, S Polonsky, K Glaser, B Permutt, MA Aguilar-Bryan, L Stafford, D Thornton, PS Baker, L Stanley, CA
Citation: A. Grimberg et al., Dysregulation of insulin secretion in children with congenital hyperinsulinism due to sulfonylurea receptor mutations, DIABETES, 50(2), 2001, pp. 322-328
beta-cell proliferation and apoptosis in the developing normal human pancreas and in hyperinsulinism of infancy
Authors: Kassem, SA Ariel, I Thornton, PS Scheimberg, I Glaser, B
Citation: Sa. Kassem et al., beta-cell proliferation and apoptosis in the developing normal human pancreas and in hyperinsulinism of infancy, DIABETES, 49(8), 2000, pp. 1325-1333
Intragenic single nucleotide polymorphism haplotype analysis of SUR1 mutations in familial hyperinsulinism
Authors: Glaser, B Furth, J Stanley, CA Baker, L Thornton, PS Landau, H Permutt, MA
Citation: B. Glaser et al., Intragenic single nucleotide polymorphism haplotype analysis of SUR1 mutations in familial hyperinsulinism, HUM MUTAT, 14(1), 1999, pp. 23-29
Hyperinsulinism caused by paternal-specific inheritance of a recessive mutation in the sulfonylurea-receptor gene
Authors: Glaser, B Ryan, F Donath, M Landau, H Stanley, CA Baker, L Barton, DE Thornton, PS
Citation: B. Glaser et al., Hyperinsulinism caused by paternal-specific inheritance of a recessive mutation in the sulfonylurea-receptor gene, DIABETES, 48(8), 1999, pp. 1652-1657
Clinical and molecular heterogeneity of familial hyperinsulinism
Authors: Glaser, B Thornton, PS Herold, K Stanley, CA
Citation: B. Glaser et al., Clinical and molecular heterogeneity of familial hyperinsulinism, J PEDIAT, 133(6), 1998, pp. 801-802
Hyperinsulinism plus hyperammonemia - Reply
Authors: Weinzimer, SA Glaser, B Thornton, PS Herold, K Stanley, CA
Citation: Sa. Weinzimer et al., Hyperinsulinism plus hyperammonemia - Reply, J PEDIAT, 133(6), 1998, pp. 801-801
Risultati: 1-9 |