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Progress in Clinical and Biological Research
|
January 1, 1992
Detection and quantitation of acylcarnitines in plasma and blood spots from patients with inborn errors of fatty acid oxidation
E Schmidt-Sommerfeld, D Penn, M Duran, et al.
Lancet (London, England)
|
May 22, 1982
Fetal and neonatal hazards of maternal hydration with 5% dextrose before caesarean section
N B Kenepp, S Kumar, W C Shelley, et al.
Human Mutation
|
August 14, 1999
Intragenic single nucleotide polymorphism haplotype analysis of SUR1 mutations in familial hyperinsulinism
B Glaser, J Furth, C A Stanley, et al.
The Journal of Pediatrics
|
March 10, 2001
Protein-sensitive and fasting hypoglycemia in children with the hyperinsulinism/hyperammonemia syndrome
B Y Hsu, A Kelly, P S Thornton, et al.
Diabetes
|
June 28, 2000
Molecular basis and characterization of the hyperinsulinism/hyperammonemia syndrome: predominance of mutations in exons 11 and 12 of the glutamate dehydrogenase gene. HI/HA Contributing Investigators
C A Stanley, J Fang, K Kutyna, et al.
The Journal of Clinical Endocrinology and Metabolism
|
December 16, 1998
Dual regulation of insulin-like growth factor binding protein-1 levels by insulin and cortisol during fasting
L E Katz, M S Satin-Smith, P Collett-Solberg, et al.
Biology of the Neonate
|
January 1, 1989
Cerebral metabolic response and mitochondrial activity following insulin-induced hypoglycemia in newborn lambs
J Belik, L C Wagerle, C A Stanley, et al.
The Journal of Clinical Endocrinology and Metabolism
|
September 16, 1999
Suppression of insulin oversecretion by subcutaneous recombinant human insulin-like growth factor I in children with congenital hyperinsulinism due to defective beta-cell sulfonylurea receptor
L E Katz, R J Ferry, C A Stanley, et al.
The Journal of Pediatrics
|
December 18, 2001
Acarbose treatment of postprandial hypoglycemia in children after Nissen fundoplication
D D Ng, R J Ferry, A Kelly, et al.
The Journal of Pediatrics
|
November 1, 1991
Familial and sporadic hyperinsulinism: histopathologic findings and segregation analysis support a single autosomal recessive disorder
P S Thornton, A E Sumner, E D Ruchelli, et al.
Page
of 11
Search research articles
Search
Showing results (61-70 of 106) with videos related to
Sort By:
Page
of 11
Progress in Clinical and Biological Research
|
January 1, 1992
Detection and quantitation of acylcarnitines in plasma and blood spots from patients with inborn errors of fatty acid oxidation
E Schmidt-Sommerfeld, D Penn, M Duran, et al.
Lancet (London, England)
|
May 22, 1982
Fetal and neonatal hazards of maternal hydration with 5% dextrose before caesarean section
N B Kenepp, S Kumar, W C Shelley, et al.
Human Mutation
|
August 14, 1999
Intragenic single nucleotide polymorphism haplotype analysis of SUR1 mutations in familial hyperinsulinism
B Glaser, J Furth, C A Stanley, et al.
The Journal of Pediatrics
|
March 10, 2001
Protein-sensitive and fasting hypoglycemia in children with the hyperinsulinism/hyperammonemia syndrome
B Y Hsu, A Kelly, P S Thornton, et al.
Diabetes
|
June 28, 2000
Molecular basis and characterization of the hyperinsulinism/hyperammonemia syndrome: predominance of mutations in exons 11 and 12 of the glutamate dehydrogenase gene. HI/HA Contributing Investigators
C A Stanley, J Fang, K Kutyna, et al.
The Journal of Clinical Endocrinology and Metabolism
|
December 16, 1998
Dual regulation of insulin-like growth factor binding protein-1 levels by insulin and cortisol during fasting
L E Katz, M S Satin-Smith, P Collett-Solberg, et al.
Biology of the Neonate
|
January 1, 1989
Cerebral metabolic response and mitochondrial activity following insulin-induced hypoglycemia in newborn lambs
J Belik, L C Wagerle, C A Stanley, et al.
The Journal of Clinical Endocrinology and Metabolism
|
September 16, 1999
Suppression of insulin oversecretion by subcutaneous recombinant human insulin-like growth factor I in children with congenital hyperinsulinism due to defective beta-cell sulfonylurea receptor
L E Katz, R J Ferry, C A Stanley, et al.
The Journal of Pediatrics
|
December 18, 2001
Acarbose treatment of postprandial hypoglycemia in children after Nissen fundoplication
D D Ng, R J Ferry, A Kelly, et al.
The Journal of Pediatrics
|
November 1, 1991
Familial and sporadic hyperinsulinism: histopathologic findings and segregation analysis support a single autosomal recessive disorder
P S Thornton, A E Sumner, E D Ruchelli, et al.
Page
of 11