Clinical characterisation and risk stratification of patients with arrhythmogenic right ventricular dysplasia/cardiomyopathy ≥50 years of age.

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Clinical characterisation and risk stratification of patients with arrhythmogenic right ventricular dysplasia/cardiomyopathy ≥50 years of age. is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1007/S12471-016-0886-7
P932PMC publication ID5120007
P698PubMed publication ID27580740

P2093author name stringM J Cramer
J F van der Heijden
P Loh
R N Hauer
A S J M Te Riele
T P Mast
M J van der Pols
P2860cites workThe Value of Cardiac Magnetic Resonance Imaging in Evaluation of Pediatric Patients for Arrhythmogenic Right Ventricular Dysplasia/CardiomyopathyQ42749505
Arrhythmogenic right ventricular dysplasia/cardiomyopathy according to revised 2010 task force criteria with inclusion of non-desmosomal phospholamban mutation carriersQ47972719
Diagnosis of arrhythmogenic right ventricular cardiomyopathy/dysplasia: proposed modification of the task force criteria.Q55638651
Impact of genotype on clinical course in arrhythmogenic right ventricular dysplasia/cardiomyopathy-associated mutation carriersQ86589091
Risk stratification in arrhythmogenic right ventricular dysplasia/cardiomyopathy-associated desmosomal mutation carriersQ86783761
Arrhythmogenic right ventricular dysplasia/cardiomyopathy: pathogenic desmosome mutations in index-patients predict outcome of family screening: Dutch arrhythmogenic right ventricular dysplasia/cardiomyopathy genotype-phenotype follow-up studyQ28238424
Sodium current deficit and arrhythmogenesis in a murine model of plakophilin-2 haploinsufficiency.Q28270379
Intercalated disc abnormalities, reduced Na(+) current density, and conduction slowing in desmoglein-2 mutant mice prior to cardiomyopathic changesQ28270388
Left-dominant arrhythmogenic cardiomyopathy in a large family: associated desmosomal or nondesmosomal genotype?Q28282279
Arrhythmogenic right ventricular dysplasia: a United States experienceQ33153393
Spectrum of clinicopathologic manifestations of arrhythmogenic right ventricular cardiomyopathy/dysplasia: a multicenter study.Q33175413
Arrhythmogenic cardiomyopathy: diagnosis, genetic background, and risk managementQ33906065
Right ventricular dysplasia: a report of 24 adult casesQ34714742
Evaluation and classification of right ventricular wall motion abnormalities in healthy subjects by 3-tesla cardiovascular magnetic resonance imagingQ34716129
Yield of serial evaluation in at-risk family members of patients with ARVD/C.Q35234588
Recurrent and founder mutations in the Netherlands-Phospholamban p.Arg14del mutation causes arrhythmogenic cardiomyopathyQ36868447
Exercise increases age-related penetrance and arrhythmic risk in arrhythmogenic right ventricular dysplasia/cardiomyopathy-associated desmosomal mutation carriers.Q37259910
The cardiac desmosome and arrhythmogenic cardiomyopathies: from gene to disease.Q37789552
Clinical Presentation, Long-Term Follow-Up, and Outcomes of 1001 Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy Patients and Family MembersQ41144205
P275copyright licenseCreative Commons Attribution 4.0 InternationalQ20007257
P6216copyright statuscopyrightedQ50423863
P433issue12
P304page(s)740-747
P577publication date2016-08-31
P1433published inNetherlands Heart JournalQ2146163
P1476titleClinical characterisation and risk stratification of patients with arrhythmogenic right ventricular dysplasia/cardiomyopathy ≥50 years of age.
P478volume24

Reverse relations

cites work (P2860)
Q54986833Ablation of idiopathic ventricular arrhythmias.
Q93171296The Netherlands Arrhythmogenic Cardiomyopathy Registry: design and status update

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