Published in Neth Heart J on November 01, 2004
A single Na(+) channel mutation causing both long-QT and Brugada syndromes. Circ Res (2000) 3.68
Possible bradycardic mode of death and successful pacemaker treatment in a large family with features of long QT syndrome type 3 and Brugada syndrome. J Cardiovasc Electrophysiol (2001) 2.57
Long-term prognosis of patients diagnosed with Brugada syndrome: Results from the FINGER Brugada Syndrome Registry. Circulation (2010) 2.53
Identification of a possible pathogenic link between congenital long QT syndrome and epilepsy. Neurology (2008) 2.21
Is T-wave alternans testing feasible in candidates for prophylactic implantable defibrillators? Neth Heart J (2011) 1.89
Bibliometric data in clinical cardiology revisited. The case of 37 Dutch professors. Neth Heart J (2011) 1.79
Catecholaminergic polymorphic ventricular tachycardia: RYR2 mutations, bradycardia, and follow up of the patients. J Med Genet (2005) 1.78
Novel Brugada syndrome-causing mutation in ion-conducting pore of cardiac Na+ channel does not affect ion selectivity properties. Acta Physiol Scand (2005) 1.67
[Initial diagnostic strategy in the case of transient losses of consciousness: the importance of the medical history]. Ned Tijdschr Geneeskd (2003) 1.55
Genetic knowledge and counselling skills of Dutch cardiologists: sufficient for the genomics era? Eur Heart J (2003) 1.52
[Genetic identification of patients and families with a long-QT syndrome: large regional differences in the result of 10 years]. Ned Tijdschr Geneeskd (2007) 1.46
The works of Dirk Durrer (1918-1984). Neth Heart J (2012) 1.39
[Medication for ADHD and the risk of cardiovascular mortality]. Ned Tijdschr Geneeskd (2006) 1.39
The Hirsch-index: a simple, new tool for the assessment of scientific output of individual scientists: The case of Dutch professors in clinical cardiology. Neth Heart J (2009) 1.30
The use of genotype-phenotype correlations in mutation analysis for the long QT syndrome. J Med Genet (2003) 1.13
The cardiac sodium channel displays differential distribution in the conduction system and transmural heterogeneity in the murine ventricular myocardium. Basic Res Cardiol (2009) 1.11
Electrical cardioversion during pregnancy: safe or not? Neth Heart J (2011) 1.00
Impact of cardiac complications on outcome after aneurysmal subarachnoid hemorrhage: a meta-analysis. Neurology (2009) 1.00
Family and population strategies for screening and counselling of inherited cardiac arrhythmias. Ann Med (2004) 0.98
Rationale and design of the Measuring Athlete's Risk of Cardiovascular events (MARC) study : The role of coronary CT in the cardiovascular evaluation of middle-aged sportsmen. Neth Heart J (2015) 0.96
Fever-triggered ventricular arrhythmias in Brugada syndrome and type 2 long-QT syndrome. Neth Heart J (2010) 0.94
First experience with the wearable cardioverter defibrillator in the Netherlands. Neth Heart J (2012) 0.94
Recurrent and founder mutations in the Netherlands-Phospholamban p.Arg14del mutation causes arrhythmogenic cardiomyopathy. Neth Heart J (2013) 0.94
Left cardiac sympathetic denervation in the Netherlands for the treatment of inherited arrhythmia syndromes. Neth Heart J (2014) 0.93
Ethnic differences in ventricular hypertrabeculation on cardiac MRI in elite football players. Neth Heart J (2012) 0.93
Short-coupled variant of torsade de pointes. Neth Heart J (2008) 0.93
Founder mutations in hypertrophic cardiomyopathy patients in the Netherlands. Neth Heart J (2010) 0.92
The sense and nonsense of direct-to-consumer genetic testing for cardiovascular disease. Neth Heart J (2011) 0.91
Recurrent and founder mutations in the Netherlands : Plakophilin-2 p.Arg79X mutation causing arrhythmogenic right ventricular cardiomyopathy/dysplasia. Neth Heart J (2010) 0.91
Rationale and design of the CAREFUL study : The yield of CARdiogenetic scrEening in First degree relatives of sudden cardiac and UnexpLained death victims <45 years. Neth Heart J (2010) 0.90
Cardiac abnormalities in a follow-up study on carriers of Duchenne and Becker muscular dystrophy. Neurology (2011) 0.90
Tako Tsubo cardiomyopathy, presenting with cardiogenic shock in a 24-year-old patient with anorexia nervosa. Neth J Med (2011) 0.89
Can parents adjust to the idea that their child is at risk for a sudden death?: Psychological impact of risk for long QT syndrome. Am J Med Genet A (2005) 0.88
High distress in parents whose children undergo predictive testing for long QT syndrome. Community Genet (2005) 0.87
Prognostic value of microvolt T-wave alternans in a real-world ICD population. Twente ICD Cohort Studie (TICS). Neth Heart J (2014) 0.87
Abnormal postprandial apolipoprotein B-48 and triglyceride responses in normolipidemic women with greater than 70% stenotic coronary artery disease: a case-control study. Atherosclerosis (1996) 0.86
Preferences of cardiologists and clinical geneticists for the future organization of genetic care in hypertrophic cardiomyopathy: a survey. Clin Genet (2005) 0.85
Routine versus aggressive upstream rhythm control for prevention of early atrial fibrillation in heart failure: background, aims and design of the RACE 3 study. Neth Heart J (2013) 0.84
Clinical implementation of guidelines for cardioverter defibrillator implantation: lost in translation? Neth Heart J (2007) 0.84
Risk stratification for sudden cardiac death in hypertrophic cardiomyopathy: Dutch cardiologists and the care of mutation carriers. Neth Heart J (2009) 0.84
Pregnancy and the risk of torsades de pointes in congenital long-QT syndrome. Neth Heart J (2008) 0.83
GENCOR: a national registry for patients and families suffering from a familial heart disease in the Netherlands. Neth Heart J (2006) 0.81
Netherlands Heart Journal: accepted into PubMed Central! Neth Heart J (2006) 0.81
Bilateral optic neuritis with branch retinal artery occlusion associated with vaccination. Doc Ophthalmol (1994) 0.81
Structural abnormalities of the left ventricle in hypertrophic cardiomyopathy mutation carriers detectable before the development of hypertrophy. Neth Heart J (2007) 0.81
Letter regarding article by McNair et al, "SCN5A mutation associated with dilated cardiomyopathy, conduction disorder, and arrhythmia". Circulation (2005) 0.80
Recurrent and Founder Mutations in the Netherlands: the Long-QT Syndrome. Neth Heart J (2010) 0.80
Recurrent and founder mutations in inherited cardiac diseases in the Netherlands. Neth Heart J (2009) 0.80
Founder mutations in the Netherlands: familial idiopathic ventricular fibrillation and DPP6. Neth Heart J (2011) 0.80
[Hypertrophic cardiomyopathy: a genetically-carried heart disease]. Ned Tijdschr Geneeskd (2002) 0.79
Percutaneous pulmonary valve replacement: a new development in the lifetime strategy for patients with congenital heart disease. Neth Heart J (2007) 0.79
A large family characterised by nocturnal sudden death. Neth Heart J (2002) 0.77
Flush after syncope: not always an arrhythmia. J Cardiovasc Electrophysiol (2006) 0.77
How to perform pulmonary vein isolation for the treatment of atrial fibrillation: use of the LocaLisa catheter navigation system. Europace (2004) 0.77
Towards a better risk stratification for sudden cardiac death in patients with structural heart disease. Neth Heart J (2009) 0.77
Arrhythmogenic right ventricular cardiomyopathy: asymptomatic to life threatening as illustrated by the cases of two sisters. Neth Heart J (2007) 0.77
T-wave alternans in a patient with long-QT syndrome type 3. Neth Heart J (2006) 0.77
De novo mutation in the KCNQ1 gene causal to Jervell and Lange-Nielsen syndrome. Clin Genet (2013) 0.76
Genetic predisposition for sudden cardiac death in myocardial ischaemia: the Arrhythmia Genetics in the NEtherlandS study. Neth Heart J (2011) 0.76
It's not what you think it is. Neth Heart J (2005) 0.75
Not just any ICD device in patients with long-QT syndrome. Neth Heart J (2007) 0.75
Brugada syndrome. Eur Heart J (2002) 0.75
Primary prevention: prime time?: ICD trials (and tribulations). Neth Heart J (2004) 0.75
TDI-echocardiography: a new screening tool for long QT syndrome? Eur J Echocardiogr (2003) 0.75
Palpitations and dizziness in a 65-year-old man. Neth Heart J (2006) 0.75
Recommendations and cardiological evaluation of athletes with arrhythmias: Part 2. Neth Heart J (2004) 0.75
Primary ventricular fibrillation in acute myocardial infarction: an inherited disease? Neth Heart J (2001) 0.75
COMPANION - a friend indeed. Neth Heart J (2003) 0.75
Case histories: increasing role for major journals. Neth Heart J (2009) 0.75
Diversity in cardiac sodium channel disease phenotype in transgenic mice carrying a single SCN5A mutation. Neth Heart J (2007) 0.75
One more time: bibliometric analysis of scientific output remains complicated. Neth Heart J (2011) 0.75
Right you are. Neth Heart J (2005) 0.75
Cardiogenetic counselling in a non-university hospital. Neth Heart J (2007) 0.75
Rationale of the SEAS study: Serial Echocardiography After Subarachnoid haemorrhage, a prospective national, multicentre, multidisciplinary, cohort study to evaluate cardiac abnormalities following intracranial haemorrhage. Neth Heart J (2006) 0.75
An extended family suddenly confronted with a life-threatening hereditary arrhythmia. Neth Heart J (2005) 0.75
Should I be worried? Neth Heart J (2006) 0.75
Recent breakthroughs in the genetics of atrial fibrillation. Neth Heart J (2003) 0.75
The ECG of a (cardio)myopathy? Neth Heart J (2005) 0.75
'Brugada ECG' elicited by imipramine overdose. Neth Heart J (2004) 0.75
ECG screening of newborns to avoid sudden infant death syndrome? Neth Heart J (2006) 0.75
Familial primary arrhythmia syndromes: Nice to know or need to know. Neth Heart J (2002) 0.75
Recommendations and cardiological evaluation of athletes with arrhythmias: Part 1. Neth Heart J (2004) 0.75
A fainting lady with some extrasystoles. Neth Heart J (2004) 0.75
Percutaneous coronary and peripheral angioscopy with saline solution and carbon dioxide gas in porcine and canine arteries. Am Heart J (1991) 0.75
Reversed remodelling of dilated left sided cardiomyopathy after upgrading from VVIR to VVIR biventricular pacing. Europace (2002) 0.75
Chest wall reconstruction with degradable processed sheep dermal collagen in dogs. Ann Thorac Surg (1991) 0.75
[Eve's risk]. Ned Tijdschr Geneeskd (1992) 0.75
Laser ablation and the need for intra-arterial imaging. Int J Card Imaging (1989) 0.75
[The use of laser rays in medicine, especially in cardiology]. Ned Tijdschr Geneeskd (1986) 0.75
ICD-implantation guidelines versus clinical practice: a prospective study of out-of-hospital cardiac arrest survivors. Europace (2004) 0.75
Loss of blood platelet adhesion after heating native and cultured human subendothelium to 100 degrees Celcius. Cardiovasc Res (1990) 0.75
[Congenital long QT-syndrome: the cause of recurrent syncope and sudden death at a young age]. Ned Tijdschr Geneeskd (2007) 0.75
Genotype-phenotype analysis of Jervell and Lange-Nielsen syndrome in six families from Saudi Arabia. Clin Genet (2013) 0.75
The significance of coumarin anticoagulation in laser assisted percutaneous transluminal angioplasty of femoropopliteal arterial obstructions. Eur J Radiol (1995) 0.75
Haematemesis, abdominal pain and a diastolic murmur in a cocaine user. Stanford type-A aortic dissection. Neth J Med (2010) 0.75
[The optimal treatment of chronic heart failure with beta-blockers may be dependent upon the genetic background of the patient]. Ned Tijdschr Geneeskd (2007) 0.75
A patient with recurrent syncope and ST-elevation on the electrocardiogram. Europace (2004) 0.75
Nd:YAG laser-assisted angioplasty in femoropopliteal artery occlusions: "hot" versus "cold" recanalization with transparent contact probe. Radiology (1992) 0.75