Torsten Bloch Rasmussen
Torsten Bloch Rasmussen
Department of Cardiology, Aarhus University Hospital
Geverifieerd e-mailadres voor rm.dk
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RBM20 regulates circular RNA production from the titin gene
MAF Khan, YJ Reckman, S Aufiero, MMG van den Hoogenhof, ...
Circulation research 119 (9), 996-1003, 2016
Development of a novel risk prediction model for sudden cardiac death in childhood hypertrophic cardiomyopathy (HCM Risk-Kids)
G Norrish, T Ding, E Field, L Ziˇłkowska, I Olivotto, G Limongelli, ...
JAMA cardiology 4 (9), 918-927, 2019
Cardiac involvement in juvenile neuronal ceroid lipofuscinosis (Batten disease)
JR ěstergaard, TB Rasmussen, H M°lgaard
Neurology 76 (14), 1245-1251, 2011
A mutation in the glutamate-rich region of RNA-binding motif protein 20 causes dilated cardiomyopathy through missplicing of titin and impaired Frank–Starling mechanism
A Beqqali, IAE Bollen, TB Rasmussen, MM van den Hoogenhof, ...
Cardiovascular research 112 (1), 452-463, 2016
The TMEM43 Newfoundland mutation p.S358L causing ARVC-5 was imported from Europe and increases the stiffness of the cell nucleus
H Milting, B Klauke, AH Christensen, J MŘsebeck, V Walhorn, ...
European heart journal 36 (14), 872-881, 2015
Pathogenic RBM20-Variants Are Associated With a Severe Disease Expression in Male Patients With Dilated Cardiomyopathy
TM Hey, TB Rasmussen, T Madsen, MM Aagaard, M Harbo, H M°lgaard, ...
Circulation: Heart Failure 12 (3), e005700, 2019
Randomized trial of metoprolol in patients with obstructive hypertrophic cardiomyopathy
AM Dybro, TB Rasmussen, RR Nielsen, MJ Andersen, MK Jensen, ...
Journal of the American College of Cardiology 78 (25), 2505-2517, 2021
Clinical Features and Natural History of PRKAG2 Variant Cardiac Glycogenosis
A Lopez-Sainz, F Dominguez, LR Lopes, JP Ochoa, R Barriales-Villa, ...
Journal of the American College of Cardiology 76 (2), 186-197, 2020
Truncating plakophilin-2 mutations in arrhythmogenic cardiomyopathy are associated with protein haploinsufficiency in both myocardium and epidermis
TB Rasmussen, PH Nissen, J Palmfeldt, K Gehmlich, S Dalager, ...
Circulation: Cardiovascular Genetics 7 (3), 230-240, 2014
Protein expression studies of desmoplakin mutations in cardiomyopathy patients reveal different molecular disease mechanisms
TB Rasmussen, J Hansen, PH Nissen, J Palmfeldt, S Dalager, UB Jensen, ...
Clinical Genetics 84 (1), 20-30, 2013
Mutated desmoglein‐2 proteins are incorporated into desmosomes and exhibit dominant‐negative effects in arrhythmogenic right ventricular cardiomyopathy
TB Rasmussen, J Palmfeldt, PH Nissen, R Magnoni, S Dalager, ...
Human Mutation 34 (5), 697-705, 2013
Association of left ventricular systolic dysfunction among carriers of truncating variants in filamin C with frequent ventricular arrhythmia and end-stage heart failure
MM Akhtar, M Lorenzini, M Pavlou, JP Ochoa, C O’mahony, ...
JAMA cardiology 6 (8), 891-901, 2021
Statin-associated rhabdomyolysis triggered by drug–drug interaction with itraconazole
AM Dybro, P Damkier, TB Rasmussen, M Hellfritzsch
Case Reports 2016, bcr2016216457, 2016
The role of the electrocardiographic phenotype in risk stratification for sudden cardiac death in childhood hypertrophic cardiomyopathy
G Norrish, C Topriceanu, C Qu, E Field, H Walsh, L Ziˇłkowska, I Olivotto, ...
European Journal of Preventive Cardiology 29 (4), 645-653, 2022
Natural History of MYH7-Related Dilated Cardiomyopathy
F De Frutos, JP Ochoa, M Navarro-Pe˝alver, A Baas, JV Bjerre, E Zorio, ...
Journal of the American College of Cardiology 80 (15), 1447-1461, 2022
Effects of metoprolol on exercise hemodynamics in patients with obstructive hypertrophic cardiomyopathy
AM Dybro, TB Rasmussen, RR Nielsen, BT Ladefoged, MJ Andersen, ...
Journal of the American College of Cardiology 79 (16), 1565-1575, 2022
The LMNA mutation p. Arg321Ter associated with dilated cardiomyopathy leads to reduced expression and a skewed ratio of lamin A and lamin C proteins
R Al-Saaidi, TB Rasmussen, J Palmfeldt, PH Nissen, A Beqqali, J Hansen, ...
Experimental Cell Research 319 (19), 3010-3019, 2013
Clinical features and natural history of preadolescent nonsyndromic hypertrophic cardiomyopathy
G Norrish, A Cleary, E Field, E Cervi, O Boleti, L Ziˇłkowska, I Olivotto, ...
Journal of the American College of Cardiology 79 (20), 1986-1997, 2022
The clinical outcome of LMNA missense mutations can be associated with the amount of mutated protein in the nuclear envelope
RA Al‐Saaidi, TB Rasmussen, RID Birkler, J Palmfeldt, A Beqqali, ...
European Journal of Heart Failure 20 (10), 1404-1412, 2018
Dilated cardiomyopathy caused by truncating titin variants: long-term outcomes, arrhythmias, response to treatment and sex differences
CR Vissing, TB Rasmussen, AM Dybro, MS Olesen, LN Pedersen, ...
Journal of Medical Genetics 58 (12), 832-841, 2021
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