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C Patrono

Showing results (191-200 of 227) with videos related to

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Neuromuscular Disorders : NMD|July 19, 2000
A novel SURF1 mutation results in Leigh syndrome with peripheral neuropathy caused by cytochrome c oxidase deficiencyL Santoro, R Carrozzo, A Malandrini, et al.
Clinical Pharmacology and Therapeutics|November 24, 2001
The human pharmacology of monocyte cyclooxygenase 2 inhibition by cortisol and synthetic glucocorticoidsG Santini, P Patrignani, M G Sciulli, et al.
Circulation|January 1, 1990
Comparison of low-dose aspirin and coronary vasodilators in acute unstable anginaM Vejar, D Hackett, C Brunelli, et al.
Advances in Prostaglandin, Thromboxane, and Leukotriene Research|January 1, 1985
Drugs, prostaglandins, and renal functionC Patrono, G Ciabattoni, P Filabozzi, et al.
European Heart Journal|May 1, 1985
Low-dose aspirin in patients recovering from myocardial infarction. Evidence for a selective inhibition of thromboxane-related platelet functionR De Caterina, D Giannessi, W Bernini, et al.
Thrombosis and Haemostasis|March 28, 2014
In vivo prostacyclin biosynthesis and effects of different aspirin regimens in patients with essential thrombocythaemiaV Cavalca, B Rocca, I Squellerio, et al.
American Journal of Medical Genetics|April 5, 2000
Novel 7-DHCR mutation in a child with Smith-Lemli-Opitz syndromeC Patrono, C Rizzo, A Tessa, et al.
Human Mutation|April 11, 2001
Identification of novel WFS1 mutations in Italian children with Wolfram syndromeA Tessa, I Carbone, M C Matteoli, et al.
The New England Journal of Medicine|February 2, 1984
Effects of sulindac and ibuprofen in patients with chronic glomerular disease. Evidence for the dependence of renal function on prostacyclinG Ciabattoni, G A Cinotti, A Pierucci, et al.
Molecular and Cellular Probes|September 25, 2002
Two novel mutations of the human delta7-sterol reductase (DHCR7) gene in children with Smith-Lemli-Opitz syndromeC Patrono, C Dionisi-Vici, A Giannotti, et al.
Pageof 23

Showing results (191-200 of 227) with videos related to

Sort By:
Pageof 23
Neuromuscular Disorders : NMD|July 19, 2000
A novel SURF1 mutation results in Leigh syndrome with peripheral neuropathy caused by cytochrome c oxidase deficiencyL Santoro, R Carrozzo, A Malandrini, et al.
Clinical Pharmacology and Therapeutics|November 24, 2001
The human pharmacology of monocyte cyclooxygenase 2 inhibition by cortisol and synthetic glucocorticoidsG Santini, P Patrignani, M G Sciulli, et al.
Circulation|January 1, 1990
Comparison of low-dose aspirin and coronary vasodilators in acute unstable anginaM Vejar, D Hackett, C Brunelli, et al.
Advances in Prostaglandin, Thromboxane, and Leukotriene Research|January 1, 1985
Drugs, prostaglandins, and renal functionC Patrono, G Ciabattoni, P Filabozzi, et al.
European Heart Journal|May 1, 1985
Low-dose aspirin in patients recovering from myocardial infarction. Evidence for a selective inhibition of thromboxane-related platelet functionR De Caterina, D Giannessi, W Bernini, et al.
Thrombosis and Haemostasis|March 28, 2014
In vivo prostacyclin biosynthesis and effects of different aspirin regimens in patients with essential thrombocythaemiaV Cavalca, B Rocca, I Squellerio, et al.
American Journal of Medical Genetics|April 5, 2000
Novel 7-DHCR mutation in a child with Smith-Lemli-Opitz syndromeC Patrono, C Rizzo, A Tessa, et al.
Human Mutation|April 11, 2001
Identification of novel WFS1 mutations in Italian children with Wolfram syndromeA Tessa, I Carbone, M C Matteoli, et al.
The New England Journal of Medicine|February 2, 1984
Effects of sulindac and ibuprofen in patients with chronic glomerular disease. Evidence for the dependence of renal function on prostacyclinG Ciabattoni, G A Cinotti, A Pierucci, et al.
Molecular and Cellular Probes|September 25, 2002
Two novel mutations of the human delta7-sterol reductase (DHCR7) gene in children with Smith-Lemli-Opitz syndromeC Patrono, C Dionisi-Vici, A Giannotti, et al.
Pageof 23