Abstract is: Catecholaminergic polymorphic ventricular tachycardia (CPVT) is an inherited genetic disorder that predisposes those affected to potentially life-threatening abnormal heart rhythms or arrhythmias. The arrhythmias seen in CPVT typically occur during exercise or at times of emotional stress, and classically take the form of bidirectional ventricular tachycardia or ventricular fibrillation. Those affected may be asymptomatic, but they may also experience blackouts or even sudden cardiac death. CPVT is caused by genetic mutations affecting proteins that regulate the concentrations of calcium within cardiac muscle cells. The most commonly identified gene is RYR2, which encodes a protein included in an ion channel known as the ryanodine receptor; this channel releases calcium from a cell's internal calcium store, the sarcoplasmic reticulum, during every heartbeat. CPVT is often diagnosed from an ECG recorded during an exercise tolerance test, but it may also be diagnosed with a genetic test. The condition is treated with medication including beta-adrenoceptor blockers or flecainide, or with surgical procedures including sympathetic denervation and implantation of a defibrillator. It is thought to affect as many as one in ten thousand people and is estimated to cause 15% of all unexplained sudden cardiac deaths in young people. The condition was first defined in 1978, and the underlying genetics were described in 2001.
rare disease | Q929833 |
class of disease | Q112193867 |
monogenic disease | Q1225194 |
heart conduction disease | Q1361515 |
genetic cardiac rhythm disease | Q55785258 |
P699 | Disease Ontology ID | DOID:0060674 |
P557 | DiseasesDB | 33816 |
P10565 | Encyclopedia of China (Third Edition) ID | 579514 |
P2888 | exact match | http://identifiers.org/doid/DOID:0060674 |
http://purl.obolibrary.org/obo/DOID_0060674 | ||
http://www.orpha.net/ORDO/Orphanet_3286 | ||
P646 | Freebase ID | /m/0268hwz |
P4317 | GARD rare disease ID | 4421 |
P7464 | Genetics Home Reference Conditions ID | catecholaminergic-polymorphic-ventricular-tachycardia |
P494 | ICD-10 ID | I47.2 |
P4229 | ICD-10-CM | I47.2 |
P7807 | ICD-11 ID (Foundation) | 976309888 |
P7329 | ICD-11 ID (MMS) | BC65.5 |
P493 | ICD-9 ID | 427 |
P665 | KEGG ID | H01019 |
P6366 | Microsoft Academic ID | 2778178275 |
P492 | OMIM ID | 604772 |
604772 | ||
P10283 | OpenAlex ID | C2778178275 |
P1550 | Orphanet ID | 3286 |
P4233 | PatientsLikeMe condition ID | catecholaminergic-polymorphic-ventricular-tachycardia |
P5806 | SNOMED CT ID | 419671004 |
P2892 | UMLS CUI | C5574922 |
P11143 | WikiProjectMed ID | Catecholaminergic polymorphic ventricular tachycardia |
P2293 | genetic association | RYR2 | Q18031341 |
P1995 | health specialty | cardiology | Q10379 |
P5008 | on focus list of Wikimedia project | WikiProject Medicine | Q4099686 |
P780 | symptoms and signs | ventricular tachycardia | Q56002 |
Q28024494 | catecholaminergic polymorphic ventricular tachycardia 1 |
Q28024495 | catecholaminergic polymorphic ventricular tachycardia 2 |
Q28024496 | catecholaminergic polymorphic ventricular tachycardia 3 |
Q28024497 | catecholaminergic polymorphic ventricular tachycardia 4 |
Q28024498 | catecholaminergic polymorphic ventricular tachycardia 5 |
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Q89495906 | Efficacy of ivabradine to control ventricular arrhythmias in catecholaminergic polymorphic ventricular tachycardia |
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Q33161522 | Familial evaluation in catecholaminergic polymorphic ventricular tachycardia: disease penetrance and expression in cardiac ryanodine receptor mutation-carrying relatives |
Q38633396 | Flecainide Reduces Ventricular Arrhythmias in Patients With Genotype RYR2-positive Catecholaminergic Polymorphic Ventricular Tachycardia |
Q38032383 | Flecainide and antiarrhythmic effects in a mouse model of catecholaminergic polymorphic ventricular tachycardia. |
Q47673840 | Flecainide in CASQ2-mediated catecholaminergic polymorphic ventricular tachycardia: the gift that keeps on giving |
Q95429683 | Flecainide in patient with aggressive catecholaminergic polymorphic ventricular tachycardia due to novel RYR2 mutation |
Q86550491 | Flecainide monotherapy for catecholaminergic polymorphic ventricular tachycardia: Perspectives and limitations |
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Q34629553 | Flecainide therapy reduces exercise-induced ventricular arrhythmias in patients with catecholaminergic polymorphic ventricular tachycardia |
Q33163165 | Flecainide therapy suppresses exercise-induced ventricular arrhythmias in patients with CASQ2-associated catecholaminergic polymorphic ventricular tachycardia |
Q98946460 | Flipping syncope: The case of an adolescent athlete with syncopal episodes ultimately diagnosed with catecholaminergic polymorphic ventricular tachycardia |
Q35675536 | Gender Differences in the Inheritance Mode of RYR2 Mutations in Catecholaminergic Polymorphic Ventricular Tachycardia Patients |
Q92475159 | Gene Therapy for Catecholaminergic Polymorphic Ventricular Tachycardia by Inhibition of Ca2+/Calmodulin-Dependent Kinase II |
Q52714512 | Gene Transfer of Engineered Calmodulin Alleviates Ventricular Arrhythmias in a Calsequestrin-Associated Mouse Model of Catecholaminergic Polymorphic Ventricular Tachycardia. |
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Q90466227 | High-dose flecainide with low-dose β-blocker therapy in catecholaminergic polymorphic ventricular tachycardia: A case report and review of the literature |
Q27011445 | How to perform and interpret provocative testing for the diagnosis of Brugada syndrome, long-QT syndrome, and catecholaminergic polymorphic ventricular tachycardia |
Q90919947 | Identification of a novel exon3 deletion of RYR2 in a family with catecholaminergic polymorphic ventricular tachycardia |
Q90660340 | Implantable cardioverter-defibrillator use in catecholaminergic polymorphic ventricular tachycardia: A systematic review |
Q92404510 | Implantable cardioverter-defibrillators in previously undiagnosed patients with catecholaminergic polymorphic ventricular tachycardia resuscitated from sudden cardiac arrest |
Q83821934 | Importance of ventricular tachycardia storms not terminated by implantable cardioverter defibrillators shocks in patients with CASQ2 associated catecholaminergic polymorphic ventricular tachycardia |
Q57820983 | In Vivo Ryr2 Editing Corrects Catecholaminergic Polymorphic Ventricular Tachycardia |
Q36667578 | In silico prediction of drug therapy in catecholaminergic polymorphic ventricular tachycardia. |
Q34313368 | In situ confocal imaging in intact heart reveals stress-induced Ca(2+) release variability in a murine catecholaminergic polymorphic ventricular tachycardia model of type 2 ryanodine receptor(R4496C+/-) mutation |
Q33157356 | Incidence and risk factors of arrhythmic events in catecholaminergic polymorphic ventricular tachycardia |
Q33551271 | Increased Ca2+ sensitivity of the ryanodine receptor mutant RyR2R4496C underlies catecholaminergic polymorphic ventricular tachycardia |
Q114014605 | Increased susceptibility to ventricular arrhythmia at low–normal and moderately low levels of extracellular potassium in catecholaminergic polymorphic ventricular tachycardia |
Q90377976 | Inefficacious ICD shocks treated with left cardiac sympathetic denervation in a patient with catecholaminergic polymorphic ventricular tachycardia |
Q51518257 | Inherited catecholaminergic polymorphic ventricular tachycardia due to RYR2 mutation. |
Q34160930 | Inhibition of cardiac Ca2+ release channels (RyR2) determines efficacy of class I antiarrhythmic drugs in catecholaminergic polymorphic ventricular tachycardia. |
Q91929825 | Insights Into the Pathogenesis of Catecholaminergic Polymorphic Ventricular Tachycardia From Engineered Human Heart Tissue |
Q48105793 | Integration of 60,000 exomes and ACMG guidelines question the role of Catecholaminergic Polymorphic Ventricular Tachycardia-associated variants. |
Q51061793 | Interpreting Incidentally Identified Variants in Genes Associated With Catecholaminergic Polymorphic Ventricular Tachycardia in a Large Cohort of Clinical Whole-Exome Genetic Test Referrals. |
Q85005791 | Intravenous epinephrine infusion test in diagnosis of catecholaminergic polymorphic ventricular tachycardia |
Q60307232 | Investigation of Catecholaminergic Polymorphic Ventricular Tachycardia Children in China: Clinical Characteristics, Delay to Diagnosis, and Misdiagnosis |
Q28216442 | Involvement of the cardiac ryanodine receptor/calcium release channel in catecholaminergic polymorphic ventricular tachycardia |
Q95503814 | Left Cardiac Sympathetic Denervation in Patients with CASQ2-Associated Catecholaminergic Polymorphic Ventricular Tachycardia |
Q28279395 | Left cardiac sympathetic denervation for catecholaminergic polymorphic ventricular tachycardia |
Q33161560 | Left cardiac sympathetic denervation for the management of life-threatening ventricular tachyarrhythmias in young patients with catecholaminergic polymorphic ventricular tachycardia and long QT syndrome |
Q51636642 | Left cardiac sympathetic denervation for the treatment of long QT syndrome and catecholaminergic polymorphic ventricular tachycardia using video-assisted thoracic surgery. |
Q90763897 | Left cardiac sympathetic denervation in the management of long QT syndrome and catecholaminergic polymorphic ventricular tachycardia: A meta-regression |
Q87159192 | Letter by Gow Regarding Article, "Clinical Management of Catecholaminergic Polymorphic Ventricular Tachycardia: The Role of Left Cardiac Sympathetic Denervation" |
Q87159189 | Letter by Patanè Regarding Article, "Clinical Management of Catecholaminergic Polymorphic Ventricular Tachycardia: The Role of Left Cardiac Sympathetic Denervation" |
Q88645882 | Letter by Ruiz-Guerrero et al Regarding Article, "Yield of the RYR2 Genetic Test in Suspected Catecholaminergic Polymorphic Ventricular Tachycardia and Implications for Test Interpretation" |
Q91251306 | Linking the heart and the brain: Neurodevelopmental disorders in patients with catecholaminergic polymorphic ventricular tachycardia |
Q33173930 | Long term course of catecholaminergic polymorphic ventricular tachycardia in children. Apropos of 20 cases with an 8 year-follow-up |
Q87630294 | Long-QT Syndrome, Brugada Syndrome, and Catecholaminergic Polymorphic Ventricular Tachycardia: A Tale of 3 Diseases |
Q51572294 | Long-Term Prognosis of Catecholaminergic Polymorphic Ventricular Tachycardia Patients With Ryanodine Receptor (RYR2) Mutations. |
Q33163179 | Long-term outcomes and factors for predicting ventricular arrhythmia in patients with catecholaminergic polymorphic ventricular tachycardia |
Q129198625 | MULTIPLE GENETIC VARIANTS IN CATECHOLAMINERGIC POLYMORPHIC VENTRICULAR TACHYCARDIA: A CLINICAL AND MOLECULAR REPORT FROM THE PACES CPVT REGISTRY |
Q59200863 | Management of Gene-Positive Catecholaminergic Polymorphic Ventricular Tachycardia: Are the Long Term Outcomes on Therapy Really So Poor? |
Q88754258 | Management of Gene-Positive Catecholaminergic Polymorphic Ventricular Tachycardia: Are the Long Term Outcomes on Therapy Really So Poor? - Reply |
Q84875153 | Mechanism of antiarrhythmic effects of flecainide in catecholaminergic polymorphic ventricular tachycardia |
Q84842571 | Mechanism underlying catecholaminergic polymorphic ventricular tachycardia and approaches to therapy |
Q33157630 | Mechanisms and clinical management of inherited channelopathies: long QT syndrome, Brugada syndrome, catecholaminergic polymorphic ventricular tachycardia, and short QT syndrome |
Q52576349 | Mechanisms of abnormal calcium homeostasis in mutations responsible for catecholaminergic polymorphic ventricular tachycardia. |
Q33163102 | Modeling Catecholaminergic Polymorphic Ventricular Tachycardia using Induced Pluripotent Stem Cell-derived Cardiomyocytes |
Q34322985 | Modeling of catecholaminergic polymorphic ventricular tachycardia with patient-specific human-induced pluripotent stem cells |
Q24306493 | Modulation of human ether a gogo related channels by CASQ2 contributes to etiology of catecholaminergic polymorphic ventricular tachycardia (CPVT) |
Q99236777 | Molecular adaptation to calsequestrin 2 (CASQ2) point mutations leading to catecholaminergic polymorphic ventricular tachycardia (CPVT): comparative analysis of R33Q and D307H mutants |
Q36853107 | Molecular and electrophysiological bases of catecholaminergic polymorphic ventricular tachycardia |
Q89961129 | Molecular and tissue mechanisms of catecholaminergic polymorphic ventricular tachycardia |
Q37361927 | Molecular basis of catecholaminergic polymorphic ventricular tachycardia |
Q80161603 | Molecular diagnostics of catecholaminergic polymorphic ventricular tachycardia using denaturing high-performance liquid chromatography and sequencing |
Q79833038 | Molecular pathogenesis of catecholaminergic polymorphic ventricular tachycardia: sex matters! |
Q79906106 | Mutant ryanodine receptors in catecholaminergic polymorphic ventricular tachycardia generate delayed afterdepolarizations due to increased propensity to Ca2+ waves |
Q35156823 | Mutation-linked defective interdomain interactions within ryanodine receptor cause aberrant Ca²⁺release leading to catecholaminergic polymorphic ventricular tachycardia. |
Q50085974 | Mutation-linked excessively tight interaction between the calmodulin-binding domain and c-terminal domain of the cardiac ryanodine receptor as a novel cause of catecholaminergic polymorphic ventricular tachycardia |
Q28201561 | Mutations in the cardiac ryanodine receptor gene (hRyR2) underlie catecholaminergic polymorphic ventricular tachycardia |
Q41268618 | Nadolol decreases the incidence and severity of ventricular arrhythmias during exercise stress testing compared with β1-selective β-blockers in patients with catecholaminergic polymorphic ventricular tachycardia |
Q33168311 | Nationwide experience of catecholaminergic polymorphic ventricular tachycardia caused by RyR2 mutations |
Q39395421 | Nebivolol suppresses cardiac ryanodine receptor-mediated spontaneous Ca2+ release and catecholaminergic polymorphic ventricular tachycardia |
Q30982059 | New Family With Catecholaminergic Polymorphic Ventricular Tachycardia Linked to the Triadin Gene |
Q50959364 | New data on catecholaminergic polymorphic ventricular tachycardia in Japan: from the bench to the bedside. |
Q30666264 | New exome data question the pathogenicity of genetic variants previously associated with catecholaminergic polymorphic ventricular tachycardia |
Q86091957 | Non-ventricular, Clinical, and Functional Features of the RyR2(R420Q) Mutation Causing Catecholaminergic Polymorphic Ventricular Tachycardia |
Q50579160 | Novel ryanodine receptor 2 mutation associated with a severe phenotype of catecholaminergic polymorphic ventricular tachycardia. |
Q90339840 | Novel variants in TECRL cause catecholaminergic polymorphic ventricular tachycardia |
Q113872886 | One family’s clinical odyssey from evolving phenotypic and genotypic knowledge of catecholaminergic polymorphic ventricular tachycardia and long QT syndrome |
Q33919047 | Optimizing catecholaminergic polymorphic ventricular tachycardia therapy in calsequestrin-mutant mice |
Q33163389 | Outcomes of defibrillator therapy in catecholaminergic polymorphic ventricular tachycardia. |
Q127003018 | P5025Structural insights into catecholaminergic polymorphic ventricular tachycardia-associated RyR2 mutant channels using a three-dimensional in silico model |
Q113186283 | PE-568-04 A DISTINCT AND POTENTIALLY MORE SEVERE NEUROCARDIAC PHENOTYPE AMONG PEDIATRIC PATIENTS WITH CATECHOLAMINERGIC POLYMORPHIC VENTRICULAR TACHYCARDIA |
Q33161429 | Paradoxical effect of increased diastolic Ca(2+) release and decreased sinoatrial node activity in a mouse model of catecholaminergic polymorphic ventricular tachycardia. |
Q37465444 | Paralogue annotation identifies novel pathogenic variants in patients with Brugada syndrome and catecholaminergic polymorphic ventricular tachycardia. |
Q52687047 | Pathogenic mechanism of a catecholaminergic polymorphic ventricular tachycardia causing-mutation in cardiac calcium release channel RyR2. |
Q28067569 | Patient Specific Induced Pluripotent Stem Cell-Derived Cardiomyocytes for Drug Development and Screening In Catecholaminergic Polymorphic Ventricular Tachycardia |
Q36409821 | Patient-Specific Drug Screening Using a Human Induced Pluripotent Stem Cell Model of Catecholaminergic Polymorphic Ventricular Tachycardia Type 2. |
Q36169155 | Patient-Specific Human Induced Pluripotent Stem Cell Model Assessed with Electrical Pacing Validates S107 as a Potential Therapeutic Agent for Catecholaminergic Polymorphic Ventricular Tachycardia |
Q33168745 | Percutaneous renal sympathetic denervation in catecholaminergic polymorphic ventricular tachycardia |
Q99729619 | Peripartum management of a patient with catecholaminergic polymorphic ventricular tachycardia |
Q37396106 | Phospholamban knockout breaks arrhythmogenic Ca²⁺ waves and suppresses catecholaminergic polymorphic ventricular tachycardia in mice |
Q33166057 | Physical and Psychological Consequences of Left Cardiac Sympathetic Denervation in Long-QT Syndrome and Catecholaminergic Polymorphic Ventricular Tachycardia |
Q91207510 | Plakophilin-2 Truncation Variants in Patients Clinically Diagnosed With Catecholaminergic Polymorphic Ventricular Tachycardia and Decedents With Exercise-Associated Autopsy Negative Sudden Unexplained Death in the Young |
Q84288373 | Possible targets of therapy for catecholaminergic polymorphic ventricular tachycardia. - Insight from a theoretical model - |
Q50700554 | Post-natal heart adaptation in a knock-in mouse model of calsequestrin 2-linked recessive catecholaminergic polymorphic ventricular tachycardia. |
Q39163186 | Postexertional supraventricular tachycardia in children with catecholaminergic polymorphic ventricular tachycardia |
Q35242390 | Postpacing abnormal repolarization in catecholaminergic polymorphic ventricular tachycardia associated with a mutation in the cardiac ryanodine receptor gene. |
Q92533570 | Pregnancy in Catecholaminergic Polymorphic Ventricular Tachycardia |
Q30498471 | Prevention of Ventricular Arrhythmia and Calcium Dysregulation in a Catecholaminergic Polymorphic Ventricular Tachycardia Mouse Model Carrying Calsequestrin-2 Mutation |
Q97878645 | Protein expression profiles in murine ventricles modeling catecholaminergic polymorphic ventricular tachycardia: effects of genotype and sex |
Q37396920 | Protein kinase A-dependent biophysical phenotype for V227F-KCNJ2 mutation in catecholaminergic polymorphic ventricular tachycardia |
Q47644451 | Psychosocial Implications of Living with Catecholaminergic Polymorphic Ventricular Tachycardia in Adulthood |
Q42701447 | Purkinje cell calcium dysregulation is the cellular mechanism that underlies catecholaminergic polymorphic ventricular tachycardia |
Q42377056 | Questioning flecainide's mechanism of action in the treatment of catecholaminergic polymorphic ventricular tachycardia |
Q44292826 | RYR2 and CASQ2 mutations in patients suffering from catecholaminergic polymorphic ventricular tachycardia |
Q61451117 | Radiofrequency catheter ablation for drug-refractory atrial tachyarrhythmias in a patient with catecholaminergic polymorphic ventricular tachycardia: A case report |
Q99634561 | Rare RYR2 p.Thr85Ile variant is associated with catecholaminergic polymorphic ventricular tachycardia |
Q61632859 | Rarity and phenotypic heterogeneity provide challenges in the diagnosis of Andersen–Tawil syndrome: Two cases presenting with ECGs mimicking catecholaminergic polymorphic ventricular tachycardia (CPVT) |
Q33168156 | Recurrent syncope related to catecholaminergic polymorphic ventricular tachycardia due to de novo RyR2-R2401H mutation |
Q87630298 | Reply: Long-QT Syndrome, Brugada Syndrome, and Catecholaminergic Polymorphic Ventricular Tachycardia: A Tale of 3 Diseases : Ibutilide as a Torsade de Pointes Stress Test |
Q88645884 | Response by Kapplinger et al to Letter Regarding Article, "Yield of the RYR2 Genetic Test in Suspected Catecholaminergic Polymorphic Ventricular Tachycardia and Implications for Test Interpretation" |
Q48747281 | Response to Letters Regarding Article, "Clinical Management of Catecholaminergic Polymorphic Ventricular Tachycardia: The Role of Left Cardiac Sympathetic Denervation". |
Q37852300 | Role of calmodulin kinase in catecholaminergic polymorphic ventricular tachycardia |
Q33168540 | RyR2R420Q catecholaminergic polymorphic ventricular tachycardia mutation induces bradycardia by disturbing the coupled clock pacemaker mechanism |
Q92547582 | Ryanodine receptor-bound calmodulin is essential to protect against catecholaminergic polymorphic ventricular tachycardia |
Q44605812 | S4153R is a gain-of-function mutation in the cardiac Ca(2+) release channel ryanodine receptor associated with catecholaminergic polymorphic ventricular tachycardia and paroxysmal atrial fibrillation. |
Q92813180 | Safety and efficacy of flecainide for patients with catecholaminergic polymorphic ventricular tachycardia: A systematic review and meta-analysis |
Q95935026 | Scared to death-A novel mutation in catecholaminergic polymorphic ventricular tachycardia |
Q33157114 | Search for cardiac calcium cycling gene mutations in familial ventricular arrhythmias resembling catecholaminergic polymorphic ventricular tachycardia. |
Q87177194 | Sensitivity and negative predictive value of treadmill exercise stress testing for the diagnosis of catecholaminergic polymorphic ventricular tachycardia |
Q87234314 | Sensitivity and negative predictive value of treadmill exercise stress testing for the diagnosis of catecholaminergic polymorphic ventricular tachycardia. Response |
Q41659299 | Serotonin and catecholaminergic polymorphic ventricular tachycardia : a possible therapeutic role for SSRIs? |
Q44073503 | Short communication: flecainide exerts an antiarrhythmic effect in a mouse model of catecholaminergic polymorphic ventricular tachycardia by increasing the threshold for triggered activity. |
Q42215203 | Single delivery of an adeno-associated viral construct to transfer the CASQ2 gene to knock-in mice affected by catecholaminergic polymorphic ventricular tachycardia is able to cure the disease from birth to advanced age. |
Q38238961 | Sinus node dysfunction in catecholaminergic polymorphic ventricular tachycardia: risk factor and potential therapeutic target? |
Q92974112 | Slow and steady or fast and furious? Sinus node dysfunction in catecholaminergic polymorphic ventricular tachycardia |
Q51591524 | Slowed depolarization and irregular repolarization in catecholaminergic polymorphic ventricular tachycardia: a study from cellular Ca2+ transients and action potentials to clinical monophasic action potentials and electrocardiography. |
Q96585524 | Structural Abnormalities on Cardiac Magnetic Resonance Imaging in Patients With Catecholaminergic Polymorphic Ventricular Tachycardia |
Q88317300 | Successful Treatment of Refractory Cardiac Arrest With β-Blockade and Extracorporeal Life Support in a Pediatric Patient With Catecholaminergic Polymorphic Ventricular Tachycardia: A Case Report |
Q83447670 | Successful catheter ablation of bidirectional ventricular premature contractions triggering ventricular fibrillation in catecholaminergic polymorphic ventricular tachycardia with RyR2 mutation |
Q28292607 | Successful treatment of catecholaminergic polymorphic ventricular tachycardia with bilateral thoracoscopic sympathectomy |
Q37835555 | Successful treatment of catecholaminergic polymorphic ventricular tachycardia with flecainide: a case report and review of the current literature |
Q126812813 | Sudden Death by Catecholaminergic Polymorphic Ventricular Tachycardia in Children |
Q33165068 | Sudden cardiac arrest during sex in patients with either catecholaminergic polymorphic ventricular tachycardia or long-QT syndrome: a rare but shocking experience |
Q83976705 | Sudden cardiac death and genetic ion channelopathies: long QT, Brugada, short QT, catecholaminergic polymorphic ventricular tachycardia, and idiopathic ventricular fibrillation |
Q91948071 | Sudden cardiac death in Long QT syndrome (LQTS), Brugada syndrome, and catecholaminergic polymorphic ventricular tachycardia (CPVT) |
Q51061333 | Sudden death due to catecholaminergic polymorphic ventricular tachycardia following negative stress-test outcome: genetics and clinical implications. |
Q33156361 | Sudden death in a young man with catecholaminergic polymorphic ventricular tachycardia and paroxysmal atrial fibrillation |
Q85229026 | Sympathectomy for Patients With Catecholaminergic Polymorphic Ventricular Tachycardia: Should We Have the Nerve? |
Q33160226 | Targeting intracellular calcium cycling in catecholaminergic polymorphic ventricular tachycardia: a theoretical investigation |
Q36797556 | Teenage pregnancy with catecholaminergic polymorphic ventricular tachycardia and documented ICD discharges |
Q83504637 | Ten-year follow-up of cardiac sympathectomy in a young woman with catecholaminergic polymorphic ventricular tachycardia and an implantable cardioverter defibrillator |
Q48504966 | Tetracaine derivatives for catecholaminergic polymorphic ventricular tachycardia: new drugs for correction of diastolic Ca2+ leak? |
Q89494185 | The Hyperpolarization-Activated Cyclic-Nucleotide-Gated Channel Blocker Ivabradine Does Not Prevent Arrhythmias in Catecholaminergic Polymorphic Ventricular Tachycardia |
Q28265202 | The RYR2-encoded ryanodine receptor/calcium release channel in patients diagnosed previously with either catecholaminergic polymorphic ventricular tachycardia or genotype negative, exercise-induced long QT syndrome: a comprehensive open reading [...] |
Q33167418 | The Role of Flecainide in the Management of Catecholaminergic Polymorphic Ventricular Tachycardia |
Q28576166 | The catecholaminergic polymorphic ventricular tachycardia mutation R33Q disrupts the N-terminal structural motif that regulates reversible calsequestrin polymerization |
Q92033310 | The challenge of implantable cardioverter-defibrillator programming and shock interpretation in treatment-refractory catecholaminergic polymorphic ventricular tachycardia |
Q44819523 | The clinical and genetic spectrum of catecholaminergic polymorphic ventricular tachycardia: findings from an international multicentre registry. |
Q50070682 | The genetics underlying idiopathic ventricular fibrillation: A special role for catecholaminergic polymorphic ventricular tachycardia? |
Q37551201 | The long QT syndrome and catecholaminergic polymorphic ventricular tachycardia |
Q28306389 | The mechanism of catecholaminergic polymorphic ventricular tachycardia may be triggered activity due to delayed afterdepolarization |
Q33155204 | The molecular basis of catecholaminergic polymorphic ventricular tachycardia: what are the different hypotheses regarding mechanisms? |
Q33161368 | The phenotype of a CASQ2 mutation in a Saudi family with catecholaminergic polymorphic ventricular tachycardia |
Q33161041 | The role of stress test for predicting genetic mutations and future cardiac events in asymptomatic relatives of catecholaminergic polymorphic ventricular tachycardia probands |
Q46895569 | The role of thoracic epidural blockade in predicting responsiveness to left sympathetic denervation in patients with catecholaminergic polymorphic ventricular tachycardia |
Q33160416 | Therapeutic approach for patients with catecholaminergic polymorphic ventricular tachycardia: state of the art and future developments |
Q90840280 | They Are Not Monozygotic Twins - Long QT Syndrome Type 1 (LQT1) and Catecholaminergic Polymorphic Ventricular Tachycardia (CPVT) |
Q35720196 | Thoracoscopic Left Cardiac Sympathetic Denervation for a Patient with Catecholaminergic Polymorphic Ventricular Tachycardia and Recurrent Implantable Cardioverter-Defibrillator Shocks. |
Q55365656 | Three cases of catecholaminergic polymorphic ventricular tachycardia with prolonged QT intervals including two cases of compound mutations. |
Q84645794 | Treatment for patients with catecholaminergic polymorphic ventricular tachycardia: are we in need of randomized trials? |
Q38014115 | Treatment of asymptomatic catecholaminergic polymorphic ventricular tachycardia |
Q47366125 | Treatment of catecholaminergic polymorphic ventricular tachycardia in mice using novel RyR2-modifying drugs |
Q43158949 | Triple mode of action of flecainide in catecholaminergic polymorphic ventricular tachycardia |
Q43888800 | Triple mode of action of flecainide in catecholaminergic polymorphic ventricular tachycardia: reply. |
Q46311440 | U-waves and T-wave peak to T-wave end intervals in patients with catecholaminergic polymorphic ventricular tachycardia, effects of beta-blockers |
Q82660867 | Unmasking false epilepsy: Catecholaminergic polymorphic ventricular tachycardia |
Q28254603 | Unraveling the mechanisms of catecholaminergic polymorphic ventricular tachycardia |
Q45274090 | Unusual clinical presentation in a family with catecholaminergic polymorphic ventricular tachycardia due to a G14876A ryanodine receptor gene mutation |
Q129691187 | Use of Interprofessional Simulation to Prepare for the Cardiac Emergency of Catecholaminergic Polymorphic Ventricular Tachycardia During Pregnancy |
Q91660795 | Ventricular arrhythmia suppression with ivabradine in a patient with catecholaminergic polymorphic ventricular tachycardia refractory to nadolol, flecainide, and sympathectomy |
Q40276777 | Viral delivered gene therapy to treat catecholaminergic polymorphic ventricular tachycardia (CPVT2) in mouse models |
Q87809814 | Yield of the RYR2 Genetic Test in Suspected Catecholaminergic Polymorphic Ventricular Tachycardia and Implications for Test Interpretation |
Q115428986 | Z16b, a natural compound from Ganoderma cochlear is a novel RyR2 stabilizer preventing catecholaminergic polymorphic ventricular tachycardia |
Q79381489 | [Arrhythmic storm induced by AICD discharge in a patient with catecholaminergic polymorphic ventricular tachycardia] |
Q95591726 | [CATECHOLAMINERGIC POLYMORPHIC VENTRICULAR TACHYCARDIA - CASE REPORT] |
Q72783148 | [Catecholaminergic polymorphic ventricular tachycardia in children. Differential diagnosis of epilepsy] |
Q33159029 | [Catecholaminergic polymorphic ventricular tachycardia is a rare inherited heart disease]. |
Q84985344 | [Catecholaminergic polymorphic ventricular tachycardia] |
Q52407485 | [Clinical challenges in the management of catecholaminergic polymorphic ventricular tachycardia in children]. |
Q33162225 | [Clinical features of six patients with catecholaminergic polymorphic ventricular tachycardia]. |
Q33158598 | [Genetic of catecholaminergic polymorphic ventricular tachycardia: basic concepts]. |
Q98732220 | [Research progress in pathogenesis and treatment of catecholaminergic polymorphic ventricular tachycardia] |
Category:Catecholaminergic polymorphic ventricular tachycardia | wikimedia | |
Arabic (ar / Q13955) | تسرع القلب البطيني الكاتيكولاميني متعدد الأشكال | wikipedia |
Kateholaminska polimorfna komorska tahikardija | wikipedia | |
Catecholaminergic polymorphic ventricular tachycardia | wikipedia | |
Taquicardia ventricular polimórfica catecolaminérgica | wikipedia | |
Katekoliamiiniherkkä polymorfinen kammiotakykardia | wikipedia | |
Tachycardie ventriculaire polymorphe catécholergique | wikipedia | |
Tachicardia ventricolare polimorfa catecolaminergica | wikipedia | |
Wielokształtny częstoskurcz komorowy zależny od katecholamin | wikipedia | |
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