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P S Thornton

Showing results (11-20 of 28) with videos related to

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The Journal of Pediatric Endocrinology|October 1, 1994
The new highly sensitive adrenocorticotropin assay improves detection of patients with partial adrenocorticotropin deficiency in a short-term metyrapone testP S Thornton, C A Alter, L E Katz, et al.
The Journal of Pediatrics|November 1, 1991
Familial and sporadic hyperinsulinism: histopathologic findings and segregation analysis support a single autosomal recessive disorderP S Thornton, A E Sumner, E D Ruchelli, et al.
The Journal of Clinical Endocrinology and Metabolism|August 15, 2001
Acute insulin responses to leucine in children with the hyperinsulinism/hyperammonemia syndromeA Kelly, D Ng, R J Ferry, et al.
Archives of Disease in Childhood|April 8, 1999
Hyperinsulinism: molecular aetiology of focal diseaseF Ryan, D Devaney, C Joyce, et al.
Diabetes|July 30, 1999
Hyperinsulinism caused by paternal-specific inheritance of a recessive mutation in the sulfonylurea-receptor geneB Glaser, F Ryan, M Donath, et al.
Hormone Research in Paediatrics|September 12, 2013
A four-year, open-label, multi-center, randomized, two-arm study of Genotropin® in patients with idiopathic short stature: comparison of an individualized, target-driven treatment regimen to standard dosing of Genotropin® - analysis of two-year dataD R Counts, L A Silverman, M E Geffner, et al.
Diabetes|November 28, 2001
p57(KIP2) expression in normal islet cells and in hyperinsulinism of infancyS A Kassem, I Ariel, P S Thornton, et al.
The Journal of Pediatrics|August 1, 1997
Insulin-like growth factor binding protein-1 levels in the diagnosis of hypoglycemia caused by hyperinsulinismL E Levitt Katz, M S Satin-Smith, P Collett-Solberg, et al.
Pediatric Research|January 1, 1994
In vitro and in vivo effects of granulocyte colony-stimulating factor on neutrophils in glycogen storage disease type 1B: granulocyte colony-stimulating factor therapy corrects the neutropenia and the defects in respiratory burst activity and Ca2+ mobilizationL J McCawley, H M Korchak, S D Douglas, et al.
Human Molecular Genetics|June 9, 1998
Genetic heterogeneity in familial hyperinsulinismA Nestorowicz, B Glaser, B A Wilson, et al.
Pageof 3

Showing results (11-20 of 28) with videos related to

Sort By:
Pageof 3
The Journal of Pediatric Endocrinology|October 1, 1994
The new highly sensitive adrenocorticotropin assay improves detection of patients with partial adrenocorticotropin deficiency in a short-term metyrapone testP S Thornton, C A Alter, L E Katz, et al.
The Journal of Pediatrics|November 1, 1991
Familial and sporadic hyperinsulinism: histopathologic findings and segregation analysis support a single autosomal recessive disorderP S Thornton, A E Sumner, E D Ruchelli, et al.
The Journal of Clinical Endocrinology and Metabolism|August 15, 2001
Acute insulin responses to leucine in children with the hyperinsulinism/hyperammonemia syndromeA Kelly, D Ng, R J Ferry, et al.
Archives of Disease in Childhood|April 8, 1999
Hyperinsulinism: molecular aetiology of focal diseaseF Ryan, D Devaney, C Joyce, et al.
Diabetes|July 30, 1999
Hyperinsulinism caused by paternal-specific inheritance of a recessive mutation in the sulfonylurea-receptor geneB Glaser, F Ryan, M Donath, et al.
Hormone Research in Paediatrics|September 12, 2013
A four-year, open-label, multi-center, randomized, two-arm study of Genotropin® in patients with idiopathic short stature: comparison of an individualized, target-driven treatment regimen to standard dosing of Genotropin® - analysis of two-year dataD R Counts, L A Silverman, M E Geffner, et al.
Diabetes|November 28, 2001
p57(KIP2) expression in normal islet cells and in hyperinsulinism of infancyS A Kassem, I Ariel, P S Thornton, et al.
The Journal of Pediatrics|August 1, 1997
Insulin-like growth factor binding protein-1 levels in the diagnosis of hypoglycemia caused by hyperinsulinismL E Levitt Katz, M S Satin-Smith, P Collett-Solberg, et al.
Pediatric Research|January 1, 1994
In vitro and in vivo effects of granulocyte colony-stimulating factor on neutrophils in glycogen storage disease type 1B: granulocyte colony-stimulating factor therapy corrects the neutropenia and the defects in respiratory burst activity and Ca2+ mobilizationL J McCawley, H M Korchak, S D Douglas, et al.
Human Molecular Genetics|June 9, 1998
Genetic heterogeneity in familial hyperinsulinismA Nestorowicz, B Glaser, B A Wilson, et al.
Pageof 3