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R Sarges

Showing results (11-20 of 25) with videos related to

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Der Anaesthesist|January 1, 1990
[Intraoperative suppression of spasticity using intrathecal baclofen]H Müller, R Sarges, J Jouaux, et al.
Advances in Experimental Medicine and Biology|January 1, 1979
Inhibition of polyol pathway activity in diabetic and galactosemic rats by the aldose reductase inhibitor CP-45,634M J Peterson, R Sarges, C E Aldinger, et al.
Journal of Medicinal Chemistry|May 1, 1976
Sulfamylurea hypoglycemic agents. 6. High-potency derivativesR Sarges, D E Kuhla, H E Wiedermann, et al.
Journal of Medicinal Chemistry|September 1, 1985
Synthesis and dopamine autoreceptor activity of a 5-(methylmercapto)methyl-substituted derivative of (+/-)-3-PPP (3-(3-hydroxyphenyl)-1-n-propylpiperidine)T R Kelly, H R Howard, B K Koe, et al.
Journal of Medicinal Chemistry|September 17, 1993
Inhibition of bone resorption by H+/K(+)-ATPase inhibitorsR Sarges, A Gallagher, T J Chambers, et al.
Metabolism: Clinical and Experimental|April 1, 1979
CP-45,634: a novel aldose reductase inhibitor that inhibits polyol pathway activity in diabetic and galactosemic ratsM J Peterson, R Sarges, C E Aldinger, et al.
Journal of Medicinal Chemistry|November 1, 1984
Nontricyclic antidepressant agents derived from cis- and trans-1-amino-4-aryltetralinsW M Welch, A R Kraska, R Sarges, et al.
Journal of Medicinal Chemistry|January 1, 1988
Spiro hydantoin aldose reductase inhibitorsR Sarges, R C Schnur, J L Belletire, et al.
Journal of Medicinal Chemistry|May 1, 1977
Analgesic and tranquilizing activity of 5,8-disubstituted 1-tetralone Mannich basesW M Welch, C A Harbert, R Sarges, et al.
Journal of Medicinal Chemistry|October 1, 1986
Neuroleptics from the 4a,9b-trans-2,3,4,4a,5,9b-hexahydro-1H-pyrido[4,3-b]indole series. 3. Carboxamidoalkyl derivativesW M Welch, C A Harbert, R Sarges, et al.
Pageof 3

Showing results (11-20 of 25) with videos related to

Sort By:
Pageof 3
Der Anaesthesist|January 1, 1990
[Intraoperative suppression of spasticity using intrathecal baclofen]H Müller, R Sarges, J Jouaux, et al.
Advances in Experimental Medicine and Biology|January 1, 1979
Inhibition of polyol pathway activity in diabetic and galactosemic rats by the aldose reductase inhibitor CP-45,634M J Peterson, R Sarges, C E Aldinger, et al.
Journal of Medicinal Chemistry|May 1, 1976
Sulfamylurea hypoglycemic agents. 6. High-potency derivativesR Sarges, D E Kuhla, H E Wiedermann, et al.
Journal of Medicinal Chemistry|September 1, 1985
Synthesis and dopamine autoreceptor activity of a 5-(methylmercapto)methyl-substituted derivative of (+/-)-3-PPP (3-(3-hydroxyphenyl)-1-n-propylpiperidine)T R Kelly, H R Howard, B K Koe, et al.
Journal of Medicinal Chemistry|September 17, 1993
Inhibition of bone resorption by H+/K(+)-ATPase inhibitorsR Sarges, A Gallagher, T J Chambers, et al.
Metabolism: Clinical and Experimental|April 1, 1979
CP-45,634: a novel aldose reductase inhibitor that inhibits polyol pathway activity in diabetic and galactosemic ratsM J Peterson, R Sarges, C E Aldinger, et al.
Journal of Medicinal Chemistry|November 1, 1984
Nontricyclic antidepressant agents derived from cis- and trans-1-amino-4-aryltetralinsW M Welch, A R Kraska, R Sarges, et al.
Journal of Medicinal Chemistry|January 1, 1988
Spiro hydantoin aldose reductase inhibitorsR Sarges, R C Schnur, J L Belletire, et al.
Journal of Medicinal Chemistry|May 1, 1977
Analgesic and tranquilizing activity of 5,8-disubstituted 1-tetralone Mannich basesW M Welch, C A Harbert, R Sarges, et al.
Journal of Medicinal Chemistry|October 1, 1986
Neuroleptics from the 4a,9b-trans-2,3,4,4a,5,9b-hexahydro-1H-pyrido[4,3-b]indole series. 3. Carboxamidoalkyl derivativesW M Welch, C A Harbert, R Sarges, et al.
Pageof 3