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Epilepsia|April 29, 1999
Criterion-based validity of an intracarotid amobarbital recognition-memory protocolJ McGlone, S E Black, J Evans, et al.Human Molecular Genetics|June 9, 1998
Genetic heterogeneity in familial hyperinsulinismA Nestorowicz, B Glaser, B A Wilson, et al.Diabetes|November 14, 1997
A nonsense mutation in the inward rectifier potassium channel gene, Kir6.2, is associated with familial hyperinsulinismA Nestorowicz, N Inagaki, T Gonoi, et al.Human Molecular Genetics|November 1, 1996
Mutations in the sulonylurea receptor gene are associated with familial hyperinsulinism in Ashkenazi JewsA Nestorowicz, B A Wilson, K P Schoor, et al.Physical Review Letters|March 17, 2011
Demonstration of ignition radiation temperatures in indirect-drive inertial confinement fusion hohlraumsS H Glenzer, B J MacGowan, N B Meezan, et al.Pageof 12