Genotype and Phenotype Correlations in 417 Children With Congenital Hyperinsulinism
Snider, K. E, Becker, S, Boyajian, L, Shyng, S.-L, MacMullen, C, Hughes, N, Ganapathy, K, Bhatti, T, Stanley, C. A, Ganguly, A
Published in The journal of clinical endocrinology and metabolism (01.02.2013)
Published in The journal of clinical endocrinology and metabolism (01.02.2013)
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Recycling endosome-dependent and -independent mechanisms for IL-10 secretion in LPS-activated macrophages
Stanley, A. C., Lieu, Z. Z., Wall, A. A., Venturato, J., Khromykh, T., Hamilton, N. A., Gleeson, P. A., Stow, J. L.
Published in Journal of leukocyte biology (01.12.2012)
Published in Journal of leukocyte biology (01.12.2012)
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Journal Article
Hyperinsulinism and Hyperammonemia in Infants with Regulatory Mutations of the Glutamate Dehydrogenase Gene
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
Published in The New England journal of medicine (07.05.1998)
Published in The New England journal of medicine (07.05.1998)
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Journal Article
Familial Hyperinsulinism Caused by an Activating Glucokinase Mutation
Glaser, Benjamin, Kesavan, Prebakaran, Heyman, Mozhgan, Davis, Elizabeth, Cuesta, Antonio, Buchs, Andreas, Stanley, Charles A, Thornton, Paul S, Permutt, M. Alan, Matschinsky, Franz M, Herold, Kevan C
Published in The New England journal of medicine (22.01.1998)
Published in The New England journal of medicine (22.01.1998)
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Diamond-based structures to collect and guide light
Castelletto, S, Harrison, J P, Marseglia, L, Stanley-Clarke, A C, Gibson, B C, Fairchild, B A, Hadden, J P, Ho, Y-L D, Hiscocks, M P, Ganesan, K, Huntington, S T, Ladouceur, F, Greentree, A D, Prawer, S, O'Brien, J L, Rarity, J G
Published in New journal of physics (21.02.2011)
Published in New journal of physics (21.02.2011)
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Journal Article
Genetic Heterogeneity in Familial Hyperinsulinism
Nestorowicz, Ann, Glaser, Benjamin, Wilson, Beth A., Shyng, Show-Ling, Nichols, Colin G., Stanley, Charles A., Thornton, Paul S., Permutt, M. Alan
Published in Human molecular genetics (01.07.1998)
Published in Human molecular genetics (01.07.1998)
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Journal Article
The personal experience of juvenile Huntington's disease: an interpretative phenomenological analysis of parents' accounts of the primary features of a rare genetic condition
Smith, JA, Brewer, HM, Eatough, V, Stanley, CA, Glendinning, NW, Quarrell, OWJ
Published in Clinical genetics (01.06.2006)
Published in Clinical genetics (01.06.2006)
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Journal Article
Hyperinsulinism caused by paternal-specific inheritance of a recessive mutation in the sulfonylurea-receptor gene
GLASER, B, RYAN, F, DONATH, M, LANDAU, H, STANLEY, C. A, BAKER, L, BARTON, D. E, THORNTON, P. S
Published in Diabetes (New York, N.Y.) (01.08.1999)
Published in Diabetes (New York, N.Y.) (01.08.1999)
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Journal Article
Dysregulation of Insulin Secretion in Children With Congenital Hyperinsulinism due to Sulfonylurea Receptor Mutations
GRIMBERG, A, FERRY, R. J, BAKER, L, STANLEY, Charles A, KELLY, A, KOO-MCCOY, S, POLONSKY, K, GLASER, B, PERMUTT, M. A, AGUILAR-BRYAN, L, STAFFORD, D, THORNTON, P. S
Published in Diabetes (New York, N.Y.) (01.02.2001)
Published in Diabetes (New York, N.Y.) (01.02.2001)
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Journal Article
A nonsense mutation in the inward rectifier potassium channel gene, Kir6.2, is associated with familial hyperinsulinism
Nestorowicz, A., Inagaki, N., Gonoi, T., Schoor, K. P., Wilson, B. A., Glaser, B., Landau, H., Stanley, C. A., Thornton, P. S., Seino, S., Permutt, M. A.
Published in Diabetes (New York, N.Y.) (01.11.1997)
Published in Diabetes (New York, N.Y.) (01.11.1997)
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Journal Article
A syndrome of congenital hyperinsulinism and hyperammonemia
Weinzimer, Stuart A., Stanley, Charles A., Berry, Gerard T., Yudkoff, Marc, Tuchman, Mendel, Thornton, Paul S.
Published in The Journal of pediatrics (01.04.1997)
Published in The Journal of pediatrics (01.04.1997)
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Journal Article
Familial hyperinsulinism with apparent autosomal dominant inheritance: Clinical and genetic differences from the autosomal recessive variant
Thornton, Paul S., Satin-Smith, Marta S., Herold, Kevan, Glaser, Benjamin, Chiu, Ken C., Nestorowicz, Ann, Permutt, M.Alan, Baker, Lester, Stanley, Charles A.
Published in The Journal of pediatrics (1998)
Published in The Journal of pediatrics (1998)
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Journal Article
Sudden neonatal death in carnitine transporter deficiency
Rinaldo, Piero, Stanley, Charles A., Hsu, Betty Y.L., Sanchez, Luis A., Stern, Harvey J.
Published in The Journal of pediatrics (01.08.1997)
Published in The Journal of pediatrics (01.08.1997)
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Journal Article
Acute fatty liver of pregnancy, hemolysis, elevated liver enzymes, and low platelets syndrome, and long chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency
Treem, W R, Shoup, M E, Hale, D E, Bennett, M J, Rinaldo, P, Millington, D S, Stanley, C A, Riely, C A, Hyams, J S
Published in The American journal of gastroenterology (01.11.1996)
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Published in The American journal of gastroenterology (01.11.1996)
Journal Article
Insulin-like growth factor binding protein-1 levels in the diagnosis of hypoglycemia caused by hyperinsulinism
Levitt Katz, Lorraine E., Satin-Smith, Marta S., Collett-Solberg, Paulo, Thornton, Paul S., Baker, Lester, Stanley, Charles A., Cohen, Pinchas
Published in The Journal of pediatrics (01.08.1997)
Published in The Journal of pediatrics (01.08.1997)
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