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Journal of the American College of Cardiology|February 1, 1988
Acute myocardial infarction associated with single vessel coronary artery disease: an analysis of clinical outcome and the prognostic importance of vessel patency and residual ischemic myocardiumW W Wilson, R S Gibson, T W Nygaard, et al.
Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine|July 1, 1981
Quantitative thallium-201 exercise scintigraphy for detection of coronary artery diseaseB C Berger, D D Watson, G J Taylor, et al.
The Journal of Physical Chemistry. A|August 18, 2006
Amine-hydrogen halide complexes: experimental electric dipole moments and a theoretical decomposition of dipole moments and binding energiesCarolyn S Brauer, Matthew B Craddock, Jacob Kilian, et al.
Bipolar Disorders|March 17, 2001
No evidence of association from transmission disequilibrium analysis of the hKCa3 gene in bipolar disorderT Bowen, L Ashworth, G Kirov, et al.
Psychiatric Genetics|July 26, 2000
Association analysis of the proneurotensin gene and bipolar disorderJ Austin, B Hoogendoorn, P Buckland, et al.
Molecular Psychiatry|September 17, 2002
Evidence that variation at the serotonin transporter gene influences susceptibility to attention deficit hyperactivity disorder (ADHD): analysis and pooled analysisL Kent, U Doerry, E Hardy, et al.
Journal of the American College of Cardiology|November 1, 1985
A prospective clinical, scintigraphic, angiographic and functional evaluation of patients after inferior myocardial infarction with and without right ventricular dysfunctionD E Haines, G A Beller, D D Watson, et al.
Circulation|August 1, 1983
Prediction of cardiac events after uncomplicated myocardial infarction: a prospective study comparing predischarge exercise thallium-201 scintigraphy and coronary angiographyR S Gibson, D D Watson, G B Craddock, et al.
American Journal of Medical Genetics|March 2, 1999
No association between a polymorphic CAG repeat in the human potassium channel gene hKCa3 and bipolar disorderC A Guy, T Bowen, N Williams, et al.
Psychiatric Genetics|June 21, 2001
Systematic screening for mutations in the glycine receptor alpha2 subunit gene (GLRA2) in patients with schizophrenia and other psychiatric diseasesJ Feng, N Craddock, I R Jones, et al.
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