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Showing results (241-250 of 359) with videos related to

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JACC. Cardiovascular Interventions|March 24, 2012
Long-term follow-up after treatment of coronary in-stent restenosis with a paclitaxel-coated balloon catheterBruno Scheller, Yvonne P Clever, Bettina Kelsch, et al.
Herz|July 8, 2020
[Troponin elevation in acute ischemic stroke-unspecific or acute myocardial infarction? : Diagnostics and clinical implications]M Kruska, C Fastner, J F Scheitz, et al.
Journal of Inherited Metabolic Disease|June 10, 2006
Inborn error of amino acid synthesis: human glutamine synthetase deficiencyJohannes Häberle, Boris Görg, Annick Toutain, et al.
Journal of the American Society of Echocardiography : Official Publication of the American Society of Echocardiography|March 6, 2003
Apical tissue tracking echocardiography for characterization of regional left ventricular function: comparison with magnetic resonance imaging in patients after myocardial infarctionAdrian C Borges, Dietmar Kivelitz, Torsten Walde, et al.
Journal of the American College of Cardiology|November 18, 2000
Reduced procedural risk for coronary catheter interventions in carriers of the coagulation factor VII-Gln353 geneP M Mrozikiewicz, I Cascorbi, S Ziemer, et al.
The New England Journal of Medicine|May 26, 1999
Benefit of abciximab in patients with refractory unstable angina in relation to serum troponin T levels. c7E3 Fab Antiplatelet Therapy in Unstable Refractory Angina (CAPTURE) Study InvestigatorsC W Hamm, C Heeschen, B Goldmann, et al.
Human Mutation|September 16, 2010
Cerebral arterial stenoses and stroke: novel features of Aicardi-Goutières syndrome caused by the Arg164X mutation in SAMHD1 are associated with altered cytokine expressionHolger Thiele, Marcel du Moulin, Katarzyna Barczyk, et al.
Circulation|October 1, 1993
Evaluation of ketanserin in the prevention of restenosis after percutaneous transluminal coronary angioplasty. A multicenter randomized double-blind placebo-controlled trialP W Serruys, W Klein, J P Tijssen, et al.
Psychiatry and Clinical Neurosciences|September 5, 2023
Disrupted-in-schizophrenia 1 protein aggregates in cerebrospinal fluid are elevated in patients with first-episode psychosisMarlene Pils, Julia Rutsch, Feride Eren, et al.
Journal of Inherited Metabolic Disease|February 4, 2010
A novel mutation in LMBRD1 causes the cblF defect of vitamin B(12) metabolism in a Turkish patientSusann Gailus, Terttu Suormala, Ayse Gül Malerczyk-Aktas, et al.
Pageof 36

Showing results (241-250 of 359) with videos related to

Sort By:
Pageof 36
JACC. Cardiovascular Interventions|March 24, 2012
Long-term follow-up after treatment of coronary in-stent restenosis with a paclitaxel-coated balloon catheterBruno Scheller, Yvonne P Clever, Bettina Kelsch, et al.
Herz|July 8, 2020
[Troponin elevation in acute ischemic stroke-unspecific or acute myocardial infarction? : Diagnostics and clinical implications]M Kruska, C Fastner, J F Scheitz, et al.
Journal of Inherited Metabolic Disease|June 10, 2006
Inborn error of amino acid synthesis: human glutamine synthetase deficiencyJohannes Häberle, Boris Görg, Annick Toutain, et al.
Journal of the American Society of Echocardiography : Official Publication of the American Society of Echocardiography|March 6, 2003
Apical tissue tracking echocardiography for characterization of regional left ventricular function: comparison with magnetic resonance imaging in patients after myocardial infarctionAdrian C Borges, Dietmar Kivelitz, Torsten Walde, et al.
Journal of the American College of Cardiology|November 18, 2000
Reduced procedural risk for coronary catheter interventions in carriers of the coagulation factor VII-Gln353 geneP M Mrozikiewicz, I Cascorbi, S Ziemer, et al.
The New England Journal of Medicine|May 26, 1999
Benefit of abciximab in patients with refractory unstable angina in relation to serum troponin T levels. c7E3 Fab Antiplatelet Therapy in Unstable Refractory Angina (CAPTURE) Study InvestigatorsC W Hamm, C Heeschen, B Goldmann, et al.
Human Mutation|September 16, 2010
Cerebral arterial stenoses and stroke: novel features of Aicardi-Goutières syndrome caused by the Arg164X mutation in SAMHD1 are associated with altered cytokine expressionHolger Thiele, Marcel du Moulin, Katarzyna Barczyk, et al.
Circulation|October 1, 1993
Evaluation of ketanserin in the prevention of restenosis after percutaneous transluminal coronary angioplasty. A multicenter randomized double-blind placebo-controlled trialP W Serruys, W Klein, J P Tijssen, et al.
Psychiatry and Clinical Neurosciences|September 5, 2023
Disrupted-in-schizophrenia 1 protein aggregates in cerebrospinal fluid are elevated in patients with first-episode psychosisMarlene Pils, Julia Rutsch, Feride Eren, et al.
Journal of Inherited Metabolic Disease|February 4, 2010
A novel mutation in LMBRD1 causes the cblF defect of vitamin B(12) metabolism in a Turkish patientSusann Gailus, Terttu Suormala, Ayse Gül Malerczyk-Aktas, et al.
Pageof 36