Disease: Ventricular familial preexcitation syndrome
- A Case Series on Cardiac and Skeletal Involvement in Two Families with PRKAG2 Mutations
- A Frequent Observation of Wolff-Parkinson-White Syndrome and Fasciculoventricular Pathways in Patients With Danon Disease
- A novel PRKAG2 mutation in a Chinese family with cardiac hypertrophy and ventricular pre-excitation
- Abnrormality of ventricular repolarization of a familial type
- Adenosine monophosphate-activated protein kinase disease mimicks hypertrophic cardiomyopathy and Wolff-Parkinson-White syndrome: natural history
- An Interesting Case of Wolf-Parkinson-White Syndrome in a Young Patient With Sensorineural Deafness
- Atrial Flutter in PRKAG2 Syndrome: Clinical and Electrophysiological Characteristics
- Atriofascicular connection or a nodoventricular Mahaim fiber? Electrophysiologic elucidation of the pathway and associated reentrant circuit
- Cardiac arrhythmias in patients with Danon disease
- Cardiac MR manifestations in two cases of PRKAG2 mutations in a Chinese family
- Cardiac syncope in children
- Cardiovascular Screening before Sports Participation: Results of 11487 Children
- Clinical and evolutive aspects in ventricular preexcitation syndromes in child
- Clinical and genetic investigation of pediatric cases of Wolff-Parkinson-White syndrome in Tunisian families
- Clinical and molecular characterization of seven patients with Danon disease
- Clinical Features and Natural History of PRKAG2 Variant Cardiac Glycogenosis
- Clinical manifestations and MRI features of Danon disease: a case series
- Constitutively active AMP kinase mutations cause glycogen storage disease mimicking hypertrophic cardiomyopathy
- CRISPR correction of the PRKAG2 gene mutation in the patient's induced pluripotent stem cell-derived cardiomyocytes eliminates electrophysiological and structural abnormalities
- Danon disease as an underrecognized cause of hypertrophic cardiomyopathy in children
- Deceptive surgical results in three siblings with familial Wolff-Parkinson-White syndrome
- Duplication of 20p12.3 associated with familial Wolff-Parkinson-White syndrome
- Electrophysiologic characteristics of accessory atrioventricular connections in an inherited form of Wolff-Parkinson-White syndrome
- Electrophysiological determinants of antidromic reentry induced during atrial extrastimulation. Insights from a pacing model of Wolff-Parkinson-White syndrome
- Familial conduction system disease associated with hypertrophic cardiomyopathy
- Familial forms of hypertrophic cardiomyopathy
- Familial hypertrophic cardiomyopathy associated with Wolff-Parkinson-White syndrome
- Familial hypertrophic cardiomyopathy with Wolff-Parkinson-White syndrome progressing to ventricular dilation
- Familial occurrence of endocardial fibroelastosis in three siblings, including identical twins
- Familial occurrence of Wolff-Parkinson-White syndrome. Report of a family group and review of the literature
- Familial pseudo-Wolff-Parkinson-White syndrome
- Familial sudden death in preexcitation syndrome. Surgical interruption of the anomalous pathways in two brothers (author's transl)
- Familial variants of cardiac rhythm and conductivity disorders
- Familial Wolff-Parkinson-White Syndrome: a disease of glycogen storage or ion channel dysfunction?
- Genetic aspects of the etiology of arrhythmia
- Genetically transmitted ventricular pre-excitation in a family with hypertrophic cardiomyopathy
- Genome editing with CRISPR/Cas9 in postnatal mice corrects PRKAG2 cardiac syndrome
- High prevalence of arrhythmic and myocardial complications in patients with cardiac glycogenosis due to PRKAG2 mutations
- Identification and functional analysis of a novel PRKAG2 mutation responsible for Chinese PRKAG2 cardiac syndrome reveal an important role of non-CBS domains in regulating the AMPK pathway
- Identification of a gene responsible for familial Wolff-Parkinson-White syndrome
- Identification of a novel de novo mutation associated with PRKAG2 cardiac syndrome and early onset of heart failure
- Identification of LAMP2 Mutations in Early-Onset Danon Disease With Hypertrophic Cardiomyopathy by Targeted Next-Generation Sequencing
- Identification, clinical manifestation and structural mechanisms of mutations in AMPK associated cardiac glycogen storage disease
- Incomplete right bundle branch block: Challenges in electrocardiogram diagnosis
- Intrafamilial Phenotypical Variability Linked to PRKAG2 Mutation-Family Case Report and Review of the Literature
- Intraventricular conduction delays (left anterior hemiblock, right branch block), ventricular pre-excitation (Wolff-Parkinson-White syndrome, short PQ-normal QRS syndrome) and anomalies of ventricular repolarization of familial type
- Intraventricular conduction delays, ventricular pre-excitation and ventricular repolarization anomalies of familial character (author's transl)
- Isolated left ventricular non-compaction cardiomyopathy associated with ventricular preexcitation: a case report
- Loss of ventricular preexcitation during noninvasive testing does not exclude high-risk accessory pathways: A multicenter study of WPW in children
- Mechanisms of clinical tachycardias
- Mitochondrial DNA mutation "m.3243A>G"-Heterogeneous clinical picture for cardiologists ("m.3243A>G": A phenotypic chameleon)
- Mitral valve prolapse and the ventricular pre-excitation syndrome (author's transl)
- Molecular genetic basis of sudden cardiac death
- Molecular Pathogenesis of Familial Wolff-Parkinson-White Syndrome
- Mutation in the γ2-subunit of AMP-activated protein kinase stimulates cardiomyocyte proliferation and hypertrophy independent of glycogen storage
- Mutation of the MYH7 gene in a child with hypertrophic cardiomyopathy and Wolff-Parkinson-White syndrome
- Mutations in the gamma(2) subunit of AMP-activated protein kinase cause familial hypertrophic cardiomyopathy: evidence for the central role of energy compromise in disease pathogenesis
- Nodoventricular accessory pathways in PRKAG2-dependent familial preexcitation syndrome reveal a disorder in cardiac development
- Non-invasive Risk Stratification in Pediatric Ventricular Pre-excitation
- Noncompacted ventricular myocardium: is syncope the only warning sign?
- Novel PRKAG2 mutation responsible for the genetic syndrome of ventricular preexcitation and conduction system disease with childhood onset and absence of cardiac hypertrophy
- Novel PRKAG2 Variant Manifesting with a Cardiac Arrest in a Child
- Pharmacological testing in the diagnosis of arrhythmias
- Prevalence of electrocardiographic findings suggestive of sudden cardiac death risk in 10,867 apparently healthy young Korean men
- Prevalence of hypertrophic cardiomyopathy in highly trained athletes: relevance to pre-participation screening
- Prevalence of ventricular preexcitation in Japanese schoolchildren
- PRKAG2 cardiac syndrome: familial ventricular preexcitation, conduction system disease, and cardiac hypertrophy
- PRKAG2 syndrome, a rare hypertrophic cardiomyopathy: a Brazilian long-term follow-up with extracardiac disorders
- Rare forms of preexcitation: a case study and brief overview of familial forms of preexcitation
- Same genotype and different phenotypes in a family with PRKAG2 gene mutation
- Screening high school students in Italy for sudden cardiac death prevention by using a telecardiology device: a retrospective observational study
- Shortening of PR interval, bradycardia and polymorphic ventricular tachycardia--clinico-electrocardiografical syndrome with high risk of sudden death in children
- Sports-Related Sudden Cardiac Injury or Death
- Successful outcome in a pregnant woman with isolated noncompaction of the left ventricular myocardium
- Sudden cardiac death in the Wolff-Parkinson-White syndrome
- Sudden death risk factors in patients with hypertrophic cardiomyopathy
- The Association Between Components of Metabolic Syndrome and Abnormal Electrocardiograms in the Saudi Population: A Retrospective Study
- The genetics of cardiac arrhythmias
- The inheritance of the ventricular pre-excitation syndrome
- The role of genetic factors in determining the ECG indicators
- Three-Catheter Technique for Ablation of Left-Sided Accessory Pathways in Wolff-Parkinson-White is Less Expensive and Equally Successful When Compared to a Five-Catheter Technique
- Transgenic mouse model of ventricular preexcitation and atrioventricular reentrant tachycardia induced by an AMP-activated protein kinase loss-of-function mutation responsible for Wolff-Parkinson-White syndrome
- Using exome sequencing to identify the cause of myocardial hypertrophy in a Chinese family
- Ventricular pre-excitation and cardiac hypertrophy mimicking hypertrophic cardiomyopathy in a Turkish family with a novel PRKAG2 mutation
- Wolff-Parkinson-White syndrome and noncompaction in Leber's hereditary optic neuropathy due to the variant m.3460G>A
- Wolff-Parkinson-White syndrome and noncompaction in Leber's hereditary optic neuropathy due to the variant m.3460G>A
- Wolff-Parkinson-White Syndrome with Ventricular Hypertrophy in a Brazilian Family
- Wolff-Parkinson-White Syndrome: A Master of Disguise
- Wolff-Parkinson-White syndrome: De novo variants and evidence for mutational burden in genes associated with atrial fibrillation