Protein-sensitive and fasting hypoglycemia in children with the hyperinsulinism/hyperammonemia syndrome

Hyperinsulinism and Hyperammonemia in Infants with Regulatory Mutations of the Glutamate Dehydrogenase Gene

Charles A. Stanley, Yen K. Lieu, Betty Y.L. Hsu et al. · New England Journal of Medicine · 1998 · 672 citations · Full text

Medicine, Genetics, Molecular Genetics +17

Mitochondrial glutamate acts as a messenger in glucose-induced insulin exocytosis

Pierre Maechler, Claes B. Wollheim · Nature · 1999 · 506 citations · Full text

Life Sciences, Cell Biology, Neuroscience +14

FAMILIAL HYPOGLYCEMIA PRECIPITATED BY AMINO ACIDS

W. A. Cochrane, W. W. Payne, M. J. Simpkiss et al. · Journal of Clinical Investigation · 1956 · 246 citations · Full text

Life Sciences, Endocrinology, Physiology +17

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.

Charles A. Stanley, Jun Fang, K Kutyna et al. · Diabetes · 2000 · 171 citations

Life Sciences, Endocrinology, Genetics +17

IDIOPATHIC SPONTANEOUSLY OCCURRING HYPOGLYCEMIA IN INFANTS<subtitle>Clinical Significance of Problem and Treatment</subtitle>

Irvine G. McQuarrie · Archives of Pediatrics and Adolescent Medicine · 1954 · 169 citations

Medicine, Endocrinology, Pediatrics +9