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Showing results (181-190 of 198) with videos related to

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Heart (British Cardiac Society)|October 16, 2004
Lack of association between baseline plasma homocysteine concentrations and restenosis rates after a first elective percutaneous coronary intervention without stentingC-K Wong, C J K Hammett, R The, et al.
Journal of the American College of Cardiology|April 24, 2007
Polymer-based, paclitaxel-eluting TAXUS Liberté stent in de novo lesions: the pivotal TAXUS ATLAS trialMark A Turco, John A Ormiston, Jeffrey J Popma, et al.
JACC. Cardiovascular Interventions|April 20, 2010
Monitoring in vivo absorption of a drug-eluting bioabsorbable stent with intravascular ultrasound-derived parameters a feasibility studyNico Bruining, Sebastiaan de Winter, Jos R T C Roelandt, et al.
Brain Communications|February 25, 2021
Magnetic resonance imaging pattern recognition in childhood bilateral basal ganglia disordersShekeeb S Mohammad, Rajeshwar Reddy Angiti, Andrew Biggin, et al.
Marine Genomics|March 3, 2018
Performance and precision of double digestion RAD (ddRAD) genotyping in large multiplexed datasets of marine fish speciesF Maroso, J E J Hillen, B G Pardo, et al.
Pain|May 3, 2019
Antibodies binding the head domain of P2X4 inhibit channel function and reverse neuropathic painWendy A Williams, John E Linley, Clare A Jones, et al.
Addiction (Abingdon, England)|March 21, 2000
Gender differences in alcohol consumption and adverse drinking consequences: cross-cultural patternsR W Wilsnack, N D Vogeltanz, S C Wilsnack, et al.
Nature Communications|July 8, 2015
Recessive mutations in POLR1C cause a leukodystrophy by impairing biogenesis of RNA polymerase IIIIsabelle Thiffault, Nicole I Wolf, Diane Forget, et al.
Neurology|April 1, 2016
Delineation of the movement disorders associated with FOXG1 mutationsApostolos Papandreou, Ruth B Schneider, Erika F Augustine, et al.
Journal of Inherited Metabolic Disease|March 18, 2021
ALG13 X-linked intellectual disability: New variants, glycosylation analysis, and expanded phenotypesHind Alsharhan, Miao He, Andrew C Edmondson, et al.
Pageof 20

Showing results (181-190 of 198) with videos related to

Sort By:
Pageof 20
Heart (British Cardiac Society)|October 16, 2004
Lack of association between baseline plasma homocysteine concentrations and restenosis rates after a first elective percutaneous coronary intervention without stentingC-K Wong, C J K Hammett, R The, et al.
Journal of the American College of Cardiology|April 24, 2007
Polymer-based, paclitaxel-eluting TAXUS Liberté stent in de novo lesions: the pivotal TAXUS ATLAS trialMark A Turco, John A Ormiston, Jeffrey J Popma, et al.
JACC. Cardiovascular Interventions|April 20, 2010
Monitoring in vivo absorption of a drug-eluting bioabsorbable stent with intravascular ultrasound-derived parameters a feasibility studyNico Bruining, Sebastiaan de Winter, Jos R T C Roelandt, et al.
Brain Communications|February 25, 2021
Magnetic resonance imaging pattern recognition in childhood bilateral basal ganglia disordersShekeeb S Mohammad, Rajeshwar Reddy Angiti, Andrew Biggin, et al.
Marine Genomics|March 3, 2018
Performance and precision of double digestion RAD (ddRAD) genotyping in large multiplexed datasets of marine fish speciesF Maroso, J E J Hillen, B G Pardo, et al.
Pain|May 3, 2019
Antibodies binding the head domain of P2X4 inhibit channel function and reverse neuropathic painWendy A Williams, John E Linley, Clare A Jones, et al.
Addiction (Abingdon, England)|March 21, 2000
Gender differences in alcohol consumption and adverse drinking consequences: cross-cultural patternsR W Wilsnack, N D Vogeltanz, S C Wilsnack, et al.
Nature Communications|July 8, 2015
Recessive mutations in POLR1C cause a leukodystrophy by impairing biogenesis of RNA polymerase IIIIsabelle Thiffault, Nicole I Wolf, Diane Forget, et al.
Neurology|April 1, 2016
Delineation of the movement disorders associated with FOXG1 mutationsApostolos Papandreou, Ruth B Schneider, Erika F Augustine, et al.
Journal of Inherited Metabolic Disease|March 18, 2021
ALG13 X-linked intellectual disability: New variants, glycosylation analysis, and expanded phenotypesHind Alsharhan, Miao He, Andrew C Edmondson, et al.
Pageof 20