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American Journal of Human Genetics|October 30, 1998
A range of clinical phenotypes associated with mutations in CRX, a photoreceptor transcription-factor geneM M Sohocki, L S Sullivan, H A Mintz-Hittner, et al.
Nuclear Medicine and Biology|May 1, 1994
Evaluation of 3-[18F]fluoro-alpha-fluoromethyl-p-tyrosine as a tracer for striatal tyrosine hydroxylase activityO T DeJesus, D Murali, R Kitchen, et al.
Cell Proliferation|November 1, 1993
Cell kinetic characterization of the epidermal growth factor dependent BALB/MK line using flow cytometric analysis of DNA content and iododeoxyuridine incorporationC A van Hooijdonk, P E van Erp, R L Freund, et al.
The New England Journal of Medicine|September 28, 1989
A placebo-controlled, double-blind, randomized trial of cyclosporine therapy in active chronic Crohn's diseaseJ Brynskov, L Freund, S N Rasmussen, et al.
Scandinavian Journal of Gastroenterology|July 1, 1991
Final report on a placebo-controlled, double-blind, randomized, multicentre trial of cyclosporin treatment in active chronic Crohn's diseaseJ Brynskov, L Freund, S Nørby Rasmussen, et al.
Ugeskrift for Laeger|February 6, 1989
[Liver transplantation undertaken on Danes abroad]S Keiding, L Freund, N Hobolth, et al.
Kidney International|October 9, 2003
Relationship between duration of brain death and hemodynamic (in)stability on progressive dysfunction and increased immunologic activation of donor kidneysJoost A B van der Hoeven, Grietje Molema, Gert J Ter Horst, et al.
American Journal of Medical Genetics|January 1, 1992
Clinical, biochemical, and neuropsychiatric evaluation of a patient with a contiguous gene syndrome due to a microdeletion Xp11.3 including the Norrie disease locus and monoamine oxidase (MAOA and MAOB) genesF A Collins, D L Murphy, A L Reiss, et al.
The Annals of Thoracic Surgery|February 1, 2005
Combining robotic mitral valve repair and microwave atrial fibrillation ablation: techniques and initial resultsClifton C Reade, James O Johnson, Gil Bolotin, et al.
Investigative Ophthalmology & Visual Science|November 6, 1998
Retinal degenerations with truncation mutations in the cone-rod homeobox (CRX) geneS G Jacobson, A V Cideciyan, Y Huang, et al.
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