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J Petit

Showing results (431-440 of 583) with videos related to

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Ecology Letters|May 14, 2011
Parallel declines in species and genetic diversity in tropical forest fragmentsMatthew J Struebig, Tigga Kingston, Eric J Petit, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|January 15, 2011
The CXCL16 A181V mutation selectively inhibits monocyte adhesion to CXCR6 but is not associated with human coronary heart diseaseSarah J Petit, Emma L Wise, John C Chambers, et al.
European Journal of Drug Metabolism and Pharmacokinetics|April 1, 1986
Kinetics of metapramine and its demethylated metabolites after single and chronic oral administration in manA M Bougerolle, J L Chabard, G Dordain, et al.
Cardiology in the Young|July 27, 2016
Late outcomes in children with Shone's complex: a single-centre, 20-year experienceGeorge T Nicholson, Michael S Kelleman, Caridad M De la Uz, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|January 5, 2002
Importance of radiotherapy in the outcome of patients with primary CNS lymphoma: an analysis of the CHOD/BVAM regimen followed by two different radiotherapy treatmentsE M Bessell, A López-Guillermo, S Villá, et al.
The Annals of Thoracic Surgery|October 1, 1994
Pulmonary circulation evaluation before cavopulmonary connections: the cavopulmonary bypassA Serraf, L Houyel, F Nicolas, et al.
British Journal of Haematology|November 1, 1991
Drug-induced agranulocytosis: prognostic factors in a series of 168 episodesA Juliá, M Olona, J Bueno, et al.
American Heart Journal|February 28, 2021
Total vascular resistance increases during volume-unloading in asymptomatic single ventricle patientsDanish Vaiyani, Kumiyo Matsuo, Usama Kanaan, et al.
Human Genetics|January 1, 1989
Chronic nonspherocytic hemolytic anemia (CNSHA) and glucose 6 phosphate dehydrogenase (G6PD) deficiency in a patient with familial amyloidotic polyneuropathy (FAP). Molecular study of a new variant (G6PD Clinic) with markedly acidic pH optimumJ L Vives-Corrons, M A Pujades, J Petit, et al.
The Journal of Thoracic and Cardiovascular Surgery|May 1, 1994
Surgery for tetralogy of Fallot at less than six months of ageM Sousa Uva, F Lacour-Gayet, T Komiya, et al.
Pageof 59

Showing results (431-440 of 583) with videos related to

Sort By:
Pageof 59
Ecology Letters|May 14, 2011
Parallel declines in species and genetic diversity in tropical forest fragmentsMatthew J Struebig, Tigga Kingston, Eric J Petit, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|January 15, 2011
The CXCL16 A181V mutation selectively inhibits monocyte adhesion to CXCR6 but is not associated with human coronary heart diseaseSarah J Petit, Emma L Wise, John C Chambers, et al.
European Journal of Drug Metabolism and Pharmacokinetics|April 1, 1986
Kinetics of metapramine and its demethylated metabolites after single and chronic oral administration in manA M Bougerolle, J L Chabard, G Dordain, et al.
Cardiology in the Young|July 27, 2016
Late outcomes in children with Shone's complex: a single-centre, 20-year experienceGeorge T Nicholson, Michael S Kelleman, Caridad M De la Uz, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|January 5, 2002
Importance of radiotherapy in the outcome of patients with primary CNS lymphoma: an analysis of the CHOD/BVAM regimen followed by two different radiotherapy treatmentsE M Bessell, A López-Guillermo, S Villá, et al.
The Annals of Thoracic Surgery|October 1, 1994
Pulmonary circulation evaluation before cavopulmonary connections: the cavopulmonary bypassA Serraf, L Houyel, F Nicolas, et al.
British Journal of Haematology|November 1, 1991
Drug-induced agranulocytosis: prognostic factors in a series of 168 episodesA Juliá, M Olona, J Bueno, et al.
American Heart Journal|February 28, 2021
Total vascular resistance increases during volume-unloading in asymptomatic single ventricle patientsDanish Vaiyani, Kumiyo Matsuo, Usama Kanaan, et al.
Human Genetics|January 1, 1989
Chronic nonspherocytic hemolytic anemia (CNSHA) and glucose 6 phosphate dehydrogenase (G6PD) deficiency in a patient with familial amyloidotic polyneuropathy (FAP). Molecular study of a new variant (G6PD Clinic) with markedly acidic pH optimumJ L Vives-Corrons, M A Pujades, J Petit, et al.
The Journal of Thoracic and Cardiovascular Surgery|May 1, 1994
Surgery for tetralogy of Fallot at less than six months of ageM Sousa Uva, F Lacour-Gayet, T Komiya, et al.
Pageof 59