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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 syndromes
Grace 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 infarction
Axel 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 strategies
Oksana 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 Injury
Erik Kadesjö, Andreas Roos, Anwar J Siddiqui, et al.
Heart (British Cardiac Society)
|
July 25, 2019
Acute versus chronic myocardial injury and long-term outcomes
Erik 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 Pain
Andreas 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 syndrome
Nadine Schönherr, Esther Meyer, Andreas Roos, et al.
Analytical Chemistry
|
November 15, 2017
Quantifying Missing (Phospho)Proteome Regions with the Broad-Specificity Protease Subtilisin
Humberto 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 Study
Adela 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 process
Frederik Braun, Andrea Gangfuß, Petra Stöbe, et al.
Page
of 21
Search research articles
Search
Showing results (31-40 of 209) with videos related to
Sort By:
Page
of 21
Human Molecular Genetics
|
February 21, 2018
The beta-adrenergic agonist salbutamol modulates neuromuscular junction formation in zebrafish models of human myasthenic syndromes
Grace 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 infarction
Axel 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 strategies
Oksana 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 Injury
Erik Kadesjö, Andreas Roos, Anwar J Siddiqui, et al.
Heart (British Cardiac Society)
|
July 25, 2019
Acute versus chronic myocardial injury and long-term outcomes
Erik 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 Pain
Andreas 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 syndrome
Nadine Schönherr, Esther Meyer, Andreas Roos, et al.
Analytical Chemistry
|
November 15, 2017
Quantifying Missing (Phospho)Proteome Regions with the Broad-Specificity Protease Subtilisin
Humberto 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 Study
Adela 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 process
Frederik Braun, Andrea Gangfuß, Petra Stöbe, et al.
Page
of 21