Hyperinsulinism and Hyperammonemia in Infants with Regulatory Mutations of the Glutamate Dehydrogenase Gene von Stanley, Charles A, Lieu, Yen K, Hsu, Betty Y.L, Burlina, Alberto B, Greenberg, Cheryl R, Hopwood, Nancy J, Perlman, Kusiel, Rich, Barry H, Zammarchi, Enrico, Poncz, Mortimer

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Effects of a GTP-insensitive Mutation of Glutamate Dehydrogenase on Insulin Secretion in Transgenic Mice von Li, Changhong, Matter, Andrea, Kelly, Andrea, Petty, Thomas J., Najafi, Habiba, MacMullen, Courtney, Daikhin, Yevgeny, Nissim, Ilana, Lazarow, Adam, Kwagh, Jae, Collins, Heather W., Hsu, Betty Y.L., Nissim, Itzhak, Yudkoff, Marc, Matschinsky, Franz M., Stanley, Charles A.

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Fasting Hypoketotic Coma in a Child with Deficiency of Mitochondrial 3-Hydroxy-3-Methylglutaryl-CoA Synthase von Thompson, Geoffrey N, Hsu, Betty Y.L, Pitt, James J, Treacy, Eileen, Stanley, Charles A

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“Leucine Sensitive Hypoglycemia” Caused by a Dominantly-inherited Mutation of Glutamate Dehydrogenase • 442 von Hsu, Betty YL, Kharlip, Julia, Fang, Jie, Poncz, Mortimer, Glaser, Benjamin, Stanley, Charles A

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