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Atherosclerosis|November 2, 2024
Publication bias in pharmacogenetics of statin-associated muscle symptoms: A meta-epidemiological studyA Gougeon, I Aribi, S Guernouche, et al.
Journal of Cardiovascular Pharmacology|January 1, 1991
Once- vs. twice-daily nitrendipine in the treatment of mild to moderate hypertension, Canadian Nitrendipine Study GroupP Bolli, J Cobby, S P Handa, et al.
Pharmaceutical Research|July 15, 2017
Optimizing the Bioavailability of Subcutaneously Administered Biotherapeutics Through Mechanochemical DriversD S Collins, L C Kourtis, N R Thyagarajapuram, et al.
American Journal of Medical Genetics|June 1, 1985
Osteogenesis imperfecta with unusual skeletal lesions: report of three familiesL S Levin, J M Wright, D L Byrd, et al.
The Journal of Pharmacology and Experimental Therapeutics|January 22, 1998
A new genetic defect in human CYP2C19: mutation of the initiation codon is responsible for poor metabolism of S-mephenytoinR J Ferguson, S M De Morais, S Benhamou, et al.
American Journal of Veterinary Research|July 1, 1996
Immunohistochemical analysis of an equine model of synovitis-induced arthritisP G Todhunter, S A Kincaid, R J Todhunter, et al.
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