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C Patrono

Showing results (211-220 of 227) with videos related to

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Neurology|December 25, 2002
SPG3A: An additional family carrying a new atlastin mutationA Tessa, C Casali, M Damiano, et al.
Clinical Pharmacology and Therapeutics|February 1, 2017
Low-Dose Aspirin Acetylates Cyclooxygenase-1 in Human Colorectal Mucosa: Implications for the Chemoprevention of Colorectal CancerP Patrignani, A Sacco, C Sostres, et al.
Journal of Thrombosis and Haemostasis : JTH|June 20, 2014
Reappraisal of the clinical pharmacology of low-dose aspirin by comparing novel direct and traditional indirect biomarkers of drug actionP Patrignani, S Tacconelli, E Piazuelo, et al.
Journal of Thrombosis and Haemostasis : JTH|January 22, 2010
Postprandial hyperglycemia is a determinant of platelet activation in early type 2 diabetes mellitusF Santilli, G Formoso, P Sbraccia, et al.
Journal of Thrombosis and Haemostasis : JTH|February 26, 2010
Thromboxane and prostacyclin biosynthesis in heart failure of ischemic origin: effects of disease severity and aspirin treatmentF Santilli, G Davì, S Basili, et al.
Neurology|March 14, 2001
The T9176G mtDNA mutation severely affects ATP production and results in Leigh syndromeR Carrozzo, A Tessa, M E Vázquez-Memije, et al.
European Journal of Neurology|December 18, 2008
Autosomal recessive hereditary spastic paraplegia with thin corpus callosum: a novel mutation in the SPG11 gene and further evidence for genetic heterogeneityT Pippucci, E Panza, E Pompilii, et al.
Neurology|August 27, 2003
Genetic heterogeneity of megalencephalic leukoencephalopathy and subcortical cystsC Patrono, G Di Giacinto, E Eymard-Pierre, et al.
Neuromuscular Disorders : NMD|August 30, 2001
Respiratory chain defects in hereditary spastic paraplegiasF Piemonte, C Casali, R Carrozzo, et al.
Circulation|August 2, 2000
Effects of vitamin E supplementation on F(2)-isoprostane and thromboxane biosynthesis in healthy cigarette smokersP Patrignani, M R Panara, S Tacconelli, et al.
Pageof 23

Showing results (211-220 of 227) with videos related to

Sort By:
Pageof 23
Neurology|December 25, 2002
SPG3A: An additional family carrying a new atlastin mutationA Tessa, C Casali, M Damiano, et al.
Clinical Pharmacology and Therapeutics|February 1, 2017
Low-Dose Aspirin Acetylates Cyclooxygenase-1 in Human Colorectal Mucosa: Implications for the Chemoprevention of Colorectal CancerP Patrignani, A Sacco, C Sostres, et al.
Journal of Thrombosis and Haemostasis : JTH|June 20, 2014
Reappraisal of the clinical pharmacology of low-dose aspirin by comparing novel direct and traditional indirect biomarkers of drug actionP Patrignani, S Tacconelli, E Piazuelo, et al.
Journal of Thrombosis and Haemostasis : JTH|January 22, 2010
Postprandial hyperglycemia is a determinant of platelet activation in early type 2 diabetes mellitusF Santilli, G Formoso, P Sbraccia, et al.
Journal of Thrombosis and Haemostasis : JTH|February 26, 2010
Thromboxane and prostacyclin biosynthesis in heart failure of ischemic origin: effects of disease severity and aspirin treatmentF Santilli, G Davì, S Basili, et al.
Neurology|March 14, 2001
The T9176G mtDNA mutation severely affects ATP production and results in Leigh syndromeR Carrozzo, A Tessa, M E Vázquez-Memije, et al.
European Journal of Neurology|December 18, 2008
Autosomal recessive hereditary spastic paraplegia with thin corpus callosum: a novel mutation in the SPG11 gene and further evidence for genetic heterogeneityT Pippucci, E Panza, E Pompilii, et al.
Neurology|August 27, 2003
Genetic heterogeneity of megalencephalic leukoencephalopathy and subcortical cystsC Patrono, G Di Giacinto, E Eymard-Pierre, et al.
Neuromuscular Disorders : NMD|August 30, 2001
Respiratory chain defects in hereditary spastic paraplegiasF Piemonte, C Casali, R Carrozzo, et al.
Circulation|August 2, 2000
Effects of vitamin E supplementation on F(2)-isoprostane and thromboxane biosynthesis in healthy cigarette smokersP Patrignani, M R Panara, S Tacconelli, et al.
Pageof 23