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Showing results (431-440 of 630) with videos related to

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Organic & Biomolecular Chemistry|October 8, 2016
Biphenyl urea derivatives as selective CYP1B1 inhibitorsMohd Usman Mohd Siddique, Glen J P McCann, Vinay Sonawane, et al.
Heart (British Cardiac Society)|April 12, 2013
Valvular heart disease: a call for global collaborative research initiativesJohn B Chambers, Benoy N Shah, Bernard Prendergast, et al.
European Heart Journal|December 11, 2024
Prognostic impact of inducible ischaemia in ischaemic left ventricular dysfunction: the REVIVED-BCIS2 trialHolly Morgan, Muhummad Sohaib Nazir, Matthew E Li Kam Wa, et al.
Journal of Magnetic Resonance Imaging : JMRI|April 5, 2014
Intertechnique agreement and interstudy reproducibility of strain and diastolic strain rate at 1.5 and 3 Tesla: a comparison of feature-tracking and tagging in patients with aortic stenosisAnvesha Singh, Christopher D Steadman, Jamal N Khan, et al.
Heart (British Cardiac Society)|December 1, 2023
Symptoms and signs in patients with heart failure: association with 3-month hospitalisation and mortalityMohammad Rizwan Ali, Carolyn S P Lam, Anna Strömberg, et al.
Scientific Reports|September 14, 2024
Effect of aortic valve replacement on myocardial perfusion and exercise capacity in patients with severe aortic stenosisSaadia Aslam, Abhishek Dattani, Aseel Alfuhied, et al.
Irish Medical Journal|October 1, 1982
Coronary bypass surgery for acute coronary insufficiency resistant to medical treatmentS Blake, C McCarthy, M Neligan, et al.
Human Molecular Genetics|April 11, 2015
Defects in optineurin- and myosin VI-mediated cellular trafficking in amyotrophic lateral sclerosisVinod Sundaramoorthy, Adam K Walker, Vanessa Tan, et al.
Human Molecular Genetics|September 1, 2017
Defects in optineurin- and myosin VI-mediated cellular trafficking in amyotrophic lateral sclerosisVinod Sundaramoorthy, Adam K Walker, Vanessa Tan, et al.
Neurobiology of Aging|September 10, 2015
Novel TBK1 truncating mutation in a familial amyotrophic lateral sclerosis patient of Chinese originKelly L Williams, Emily P McCann, Jennifer A Fifita, et al.
Pageof 63

Showing results (431-440 of 630) with videos related to

Sort By:
Pageof 63
Organic & Biomolecular Chemistry|October 8, 2016
Biphenyl urea derivatives as selective CYP1B1 inhibitorsMohd Usman Mohd Siddique, Glen J P McCann, Vinay Sonawane, et al.
Heart (British Cardiac Society)|April 12, 2013
Valvular heart disease: a call for global collaborative research initiativesJohn B Chambers, Benoy N Shah, Bernard Prendergast, et al.
European Heart Journal|December 11, 2024
Prognostic impact of inducible ischaemia in ischaemic left ventricular dysfunction: the REVIVED-BCIS2 trialHolly Morgan, Muhummad Sohaib Nazir, Matthew E Li Kam Wa, et al.
Journal of Magnetic Resonance Imaging : JMRI|April 5, 2014
Intertechnique agreement and interstudy reproducibility of strain and diastolic strain rate at 1.5 and 3 Tesla: a comparison of feature-tracking and tagging in patients with aortic stenosisAnvesha Singh, Christopher D Steadman, Jamal N Khan, et al.
Heart (British Cardiac Society)|December 1, 2023
Symptoms and signs in patients with heart failure: association with 3-month hospitalisation and mortalityMohammad Rizwan Ali, Carolyn S P Lam, Anna Strömberg, et al.
Scientific Reports|September 14, 2024
Effect of aortic valve replacement on myocardial perfusion and exercise capacity in patients with severe aortic stenosisSaadia Aslam, Abhishek Dattani, Aseel Alfuhied, et al.
Irish Medical Journal|October 1, 1982
Coronary bypass surgery for acute coronary insufficiency resistant to medical treatmentS Blake, C McCarthy, M Neligan, et al.
Human Molecular Genetics|April 11, 2015
Defects in optineurin- and myosin VI-mediated cellular trafficking in amyotrophic lateral sclerosisVinod Sundaramoorthy, Adam K Walker, Vanessa Tan, et al.
Human Molecular Genetics|September 1, 2017
Defects in optineurin- and myosin VI-mediated cellular trafficking in amyotrophic lateral sclerosisVinod Sundaramoorthy, Adam K Walker, Vanessa Tan, et al.
Neurobiology of Aging|September 10, 2015
Novel TBK1 truncating mutation in a familial amyotrophic lateral sclerosis patient of Chinese originKelly L Williams, Emily P McCann, Jennifer A Fifita, et al.
Pageof 63