D. Keller

发表

Brugada syndrome and fever: genetic and molecular characterization of patients carrying SCN5A mutations.

J. Schläpfer, P. Guicheney, J. Rougier, 2005, Cardiovascular research.

Mouse model carrying H222P-Lmna mutation develops muscular dystrophy and dilated cardiomyopathy similar to human striated muscle laminopathies.

S. Varnous, T. Arimura, Y. Fromes, 2005, Human molecular genetics.

Desmosomal gene analysis in arrhythmogenic right ventricular dysplasia/cardiomyopathy: spectrum of mutations and clinical impact in practice.

J. Deharo, Y. Lecarpentier, P. Cosnay, 2010, Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology.

Comparison of fourteen rule-out strategies for acute myocardial infarction.

A. von Eckardstein, Ò. Miró, A. Buser, 2019, International journal of cardiology.

High risk of heart failure associated with desmoglein‐2 mutations compared to plakophilin‐2 mutations in arrhythmogenic right ventricular cardiomyopathy/dysplasia

J. Deharo, P. Cosnay, E. Donal, 2019, European journal of heart failure.

Prospective Validation of the 0/1-h Algorithm for Early Diagnosis of Myocardial Infarction.

Ò. Miró, S. Blankenberg, T. Zeller, 2018, Journal of the American College of Cardiology.

Novel Criteria for the Observe-Zone of the ESC 0/1h-hs-cTnT Algorithm

Ò. Miró, L. Newby, B. Lindahl, 2021, Circulation.

Machine learning-based CT fractional flow reserve assessment in acute chest pain: first experience.

H. Alkadhi, R. Manka, J. von Spiczak, 2020, Cardiovascular diagnosis and therapy.

Early Diagnosis of Myocardial Infarction With Point-of-Care High-Sensitivity Cardiac Troponin I.

Ò. Miró, A. Buser, R. Twerenbold, 2020, Journal of the American College of Cardiology.

Combining High-Sensitivity Cardiac Troponin I and Cardiac Troponin T in the Early Diagnosis of Acute Myocardial Infarction

J. Greenslade, Ò. Miró, J. Pickering, 2018, Circulation.

Direct Comparison of the 0/1h and 0/3h Algorithms for Early Rule-Out of Acute Myocardial Infarction.

Ò. Miró, K. Rentsch, R. Twerenbold, 2018, Circulation.

Molecular and clinical determinants of drug-induced long QT syndrome: an iatrogenic channelopathy.

T. Buclin, J. Biollaz, J. Schläpfer, 2004, Swiss medical weekly.

Erysipelothrix rhusiopathiae infection by geese to human transmission

S. Albini, D. Keller, J. Kottwitz, 2021, BMJ Case Reports.

A novel mutation in SCN5A, delQKP 1507-1509, causing long QT syndrome: role of Q1507 residue in sodium channel inactivation.

Mohamed Chahine, P. Guicheney, V. Fressart, 2003, Journal of molecular and cellular cardiology.

Genetics of familial cardiomyopathies and arrhythmias.

K. Schwartz, L. Carrier, D. Keller, 2002, Swiss medical weekly.

Diagnostic and prognostic values of the QRS‐T angle in patients with suspected acute decompensated heart failure

O. Pfister, H. Tanner, T. Breidthardt, 2020, ESC heart failure.

Biophysical, Molecular, and Pharmacological Characterization of Voltage-Dependent Sodium Channels From Induced Pluripotent Stem Cell-Derived Cardiomyocytes.

Mohamed Chahine, Olivier Thériault, M. Boutjdir, 2017, The Canadian journal of cardiology.

Diagnostic and prognostic value of ST-segment deviation scores in suspected acute myocardial infarction

Ò. Miró, R. Twerenbold, J. Boeddinghaus, 2020, European heart journal. Acute cardiovascular care.

Chest Pain in Repeated Emergency Department Visitors

M. Stucki, K. Slankamenac, D. Keller, 2020 .

Physical activity behaviour in patients with metabolic syndrome.

C. Schmied, E. Battegay, D. Keller, 2012, Swiss medical weekly.

De novo heterozygous desmoplakin mutations leading to Naxos-Carvajal disease.

P. Itin, V. Drouin‐Garraud, C. Balmer, 2012, Swiss medical weekly.

Asymmetric septal hypertrophy in heterozygous cMyBP-C null mice.

J. Ross, K. Chien, M. Fiszman, 2004, Cardiovascular research.

Value of repeated cardiac magnetic resonance imaging in patients with suspected arrhythmogenic right ventricular cardiomyopathy.

D. Conen, M. Pfisterer, P. Buser, 2006, Journal of cardiovascular magnetic resonance : official journal of the Society for Cardiovascular Magnetic Resonance.

Human homozygous R403W mutant cardiac myosin presents disproportionate enhancement of mechanical and enzymatic properties.

Y. Lecarpentier, M. Weyand, K. Amann, 2004, Journal of molecular and cellular cardiology.