Once-daily pravastatin in patients with primary hypercholesterolemia: A dose-response study

Author:

Jones P. H.,Farmer J. A.,Cressman M. D.,Mckenney J. M.,Wright J. T.,Proctor J. D.,Berkson D. M.,Farnham D. J.,Wolfson P. M.,Colfer H. T.,Rackley C. E.,Sigmund W. R.,Schlant R. C.,Arensberg D.,Mcgovern M. E.

Publisher

Wiley

Subject

Cardiology and Cardiovascular Medicine,General Medicine

Reference21 articles.

1. Tissue-selective acute effects of inhibitors of 3-hydroxy-3-methylglutaryl coenzyme A reductase on cholesterol biosynthesis in lens;Mosley;J Lipid Res,1989

2. Fujita H, Uno Y, Inazu A, Kajinami K, Takeda M, Koizumi J, Mabuki H, Takeda R, HOKURIKU FH-CHD Study Group: Long-term (2 years) treatment of heterozygous familial hypercholesterolemia with CS-514 (pravastatin), an inhibitor of 3-hydroxy-3 methylglutaryl coenzyme A reductase (abstract). Proc 8th International Symposium on Atherosclerosis. Rome, Italy, October 9 to 13, (1988) 272

3. Pravastatin: A tissue selective once-daily HMG-CoA reductase inhibitor in the treatment of primary hypercholesterolemia (abstr);Hunninghake;J Am Coll Cardiol,1988

4. Effects of CS-514, a new inhibitor of HMG-CoA reductase, on plasma lipids, lipoproteins, and apoproteins in patients with primary hypercholesterolemia;Kazumi;Horm Metab Res,1986

5. Long-Term Effects of CS-514 on Serum Lipoprotein Lipid and Apolipoprotein Levels in Patients with Familial Hypercholesterolemia

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