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Andreas Roos

Showing results (31-40 of 209) with videos related to

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Human Molecular Genetics|February 21, 2018
The beta-adrenergic agonist salbutamol modulates neuromuscular junction formation in zebrafish models of human myasthenic syndromesGrace McMacken, Dan Cox, Andreas Roos, et al.
International Journal of Cardiology|November 20, 2016
High-sensitivity cardiac troponin T levels in the emergency department in patients with chest pain but no myocardial infarctionAxel C Carlsson, Nadia Bandstein, Andreas Roos, et al.
Orphanet Journal of Rare Diseases|May 4, 2018
GNE myopathy: from clinics and genetics to pathology and research strategiesOksana Pogoryelova, José Andrés González Coraspe, Nikoletta Nikolenko, et al.
The American Journal of Medicine|December 3, 2019
Causes of Death in Patients With Acute and Chronic Myocardial InjuryErik Kadesjö, Andreas Roos, Anwar J Siddiqui, et al.
Heart (British Cardiac Society)|July 25, 2019
Acute versus chronic myocardial injury and long-term outcomesErik Kadesjö, Andreas Roos, Anwar Siddiqui, et al.
Journal of the American College of Cardiology|October 28, 2017
Stable High-Sensitivity Cardiac Troponin T Levels and Outcomes in Patients With Chest PainAndreas Roos, Nadia Bandstein, Magnus Lundbäck, et al.
Journal of Medical Genetics|September 12, 2006
The centromeric 11p15 imprinting centre is also involved in Silver-Russell syndromeNadine Schönherr, Esther Meyer, Andreas Roos, et al.
Analytical Chemistry|November 15, 2017
Quantifying Missing (Phospho)Proteome Regions with the Broad-Specificity Protease SubtilisinHumberto Gonczarowska-Jorge, Stefan Loroch, Margherita Dell'Aica, et al.
Frontiers in Human Neuroscience|December 28, 2020
Long Term Follow-Up on Pediatric Cases With Congenital Myasthenic Syndromes-A Retrospective Single Centre Cohort StudyAdela Della Marina, Eva Wibbeler, Angela Abicht, et al.
Molecular Genetics & Genomic Medicine|July 21, 2021
Expansion of the mutational spectrum of BMPER leading to diaphanospondylodysostosis and description of the associated disease processFrederik Braun, Andrea Gangfuß, Petra Stöbe, et al.
Pageof 21

Showing results (31-40 of 209) with videos related to

Sort By:
Pageof 21
Human Molecular Genetics|February 21, 2018
The beta-adrenergic agonist salbutamol modulates neuromuscular junction formation in zebrafish models of human myasthenic syndromesGrace McMacken, Dan Cox, Andreas Roos, et al.
International Journal of Cardiology|November 20, 2016
High-sensitivity cardiac troponin T levels in the emergency department in patients with chest pain but no myocardial infarctionAxel C Carlsson, Nadia Bandstein, Andreas Roos, et al.
Orphanet Journal of Rare Diseases|May 4, 2018
GNE myopathy: from clinics and genetics to pathology and research strategiesOksana Pogoryelova, José Andrés González Coraspe, Nikoletta Nikolenko, et al.
The American Journal of Medicine|December 3, 2019
Causes of Death in Patients With Acute and Chronic Myocardial InjuryErik Kadesjö, Andreas Roos, Anwar J Siddiqui, et al.
Heart (British Cardiac Society)|July 25, 2019
Acute versus chronic myocardial injury and long-term outcomesErik Kadesjö, Andreas Roos, Anwar Siddiqui, et al.
Journal of the American College of Cardiology|October 28, 2017
Stable High-Sensitivity Cardiac Troponin T Levels and Outcomes in Patients With Chest PainAndreas Roos, Nadia Bandstein, Magnus Lundbäck, et al.
Journal of Medical Genetics|September 12, 2006
The centromeric 11p15 imprinting centre is also involved in Silver-Russell syndromeNadine Schönherr, Esther Meyer, Andreas Roos, et al.
Analytical Chemistry|November 15, 2017
Quantifying Missing (Phospho)Proteome Regions with the Broad-Specificity Protease SubtilisinHumberto Gonczarowska-Jorge, Stefan Loroch, Margherita Dell'Aica, et al.
Frontiers in Human Neuroscience|December 28, 2020
Long Term Follow-Up on Pediatric Cases With Congenital Myasthenic Syndromes-A Retrospective Single Centre Cohort StudyAdela Della Marina, Eva Wibbeler, Angela Abicht, et al.
Molecular Genetics & Genomic Medicine|July 21, 2021
Expansion of the mutational spectrum of BMPER leading to diaphanospondylodysostosis and description of the associated disease processFrederik Braun, Andrea Gangfuß, Petra Stöbe, et al.
Pageof 21