| human | Q5 |
| P6178 | Dimensions author ID | 01047727355.47 |
| P9844 | IRIS UNIPV author ID | 03278 |
| P2798 | Loop ID | 22909 |
| P496 | ORCID iD | 0000-0002-6122-9939 |
| P1153 | Scopus author ID | 15761982400 |
| P108 | employer | New York University School of Medicine | Q3100195 |
| P735 | given name | Marina | Q1120708 |
| Marina | Q1120708 | ||
| P106 | occupation | researcher | Q1650915 |
| P21 | sex or gender | female | Q6581072 |
| Q106767284 | 4965Non-transcriptional disruption of Ca2+i homeostasis and Cx43 function in the right ventricle precedes overt arrhythmogenic cardiomyopathy in PKP2-deficient mice |
| Q38189169 | Arrhythmogenic cardiomyopathy and Brugada syndrome: diseases of the connexome |
| Q28595062 | Arrhythmogenic mechanisms in a mouse model of catecholaminergic polymorphic ventricular tachycardia |
| Q92562779 | Beyond the One Gene-One Disease Paradigm: Complex Genetics and Pleiotropy in Inheritable Cardiac Disorders |
| Q33152686 | Bidirectional ventricular tachycardia and fibrillation elicited in a knock-in mouse model carrier of a mutation in the cardiac ryanodine receptor. |
| Q60046472 | Blockade of the Adenosine 2A Receptor Mitigates the Cardiomyopathy Induced by Loss of Plakophilin-2 Expression |
| Q92563268 | Calmodulin mutations and life-threatening cardiac arrhythmias: insights from the International Calmodulinopathy Registry |
| Q51775633 | Catecholaminergic Polymorphic Ventricular Tachycardia. |
| Q27349514 | Connexin43 contributes to electrotonic conduction across scar tissue in the intact heart. |
| Q47652735 | Controversies in Brugada syndrome |
| Q42408111 | Desmosomal junctions are necessary for adult sinus node function. |
| Q28236522 | Desmosomes and the sodium channel complex: implications for arrhythmogenic cardiomyopathy and Brugada syndrome |
| Q53360198 | Discerning From the Good, the Bad, and the Ugly. |
| Q91963652 | Disruption of Ca2+i Homeostasis and Connexin 43 Hemichannel Function in the Right Ventricle Precedes Overt Arrhythmogenic Cardiomyopathy in Plakophilin-2-Deficient Mice |
| Q37521891 | ECG non-specific ST-T and QTc abnormalities in patients with systemic lupus erythematosus compared with rheumatoid arthritis |
| Q38376971 | Efficacy of Flecainide in the Treatment of Catecholaminergic Polymorphic Ventricular Tachycardia: A Randomized Clinical Trial |
| Q40740395 | Electrocardiographic features of sudden unexpected death in epilepsy |
| Q61640621 | Exercise: A Risky Subject in Arrhythmogenic Cardiomyopathy |
| Q36446436 | Experimental therapy of genetic arrhythmias: disease-specific pharmacology. |
| Q61640649 | Fast-slow and slow-slow form of atrioventricular nodal reentrant tachycardia sustained by the same reentrant circuit: a case report |
| Q36117207 | Genetic arrhythmias. |
| Q37727681 | Genetic testing for inherited cardiac arrhythmias. |
| Q51955831 | Genetic testing in the long QT syndrome: development and validation of an efficient approach to genotyping in clinical practice. |
| Q35242478 | Genetically engineered SCN5A mutant pig hearts exhibit conduction defects and arrhythmias. |
| Q37997324 | Genetics of ion-channel disorders. |
| Q37863374 | Genetics of sudden death: focus on inherited channelopathies. |
| Q92892261 | Impact of RNA testing on cardiac variant interpretation and patient management |
| Q58596427 | Implantable Loop Recorder in Inherited Arrhythmia Diseases: A Critical Tool for Symptom Diagnosis and Advanced Risk Stratification |
| Q36692867 | KCNJ2 mutation in short QT syndrome 3 results in atrial fibrillation and ventricular proarrhythmia |
| Q33151232 | Left cardiac sympathetic denervation in the management of high-risk patients affected by the long-QT syndrome |
| Q28304358 | Missense mutations in plakophilin-2 cause sodium current deficit and associate with a Brugada syndrome phenotype |
| Q60304954 | Molecular autopsy: using the discovery of a novel de novo pathogenic variant in the KCNH2 gene to inform healthcare of surviving family |
| Q61640648 | Molecular genetics: is it making an impact in the management of inherited arrhythmogenic syndromes? |
| Q51204140 | Multilevel analyses of SCN5A mutations in arrhythmogenic right ventricular dysplasia/cardiomyopathy suggest non-canonical mechanisms for disease pathogenesis. |
| Q91220220 | Multimodality Imaging of Danon Disease in a Patient with a Novel LAMP2 Mutation |
| 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 |
| Q41107820 | Plakophilin-2 is required for transcription of genes that control calcium cycling and cardiac rhythm. |
| Q60949634 | Pleiotropic Phenotypes Associated With PKP2 Variants |
| Q36709335 | Relationship Between Arrhythmogenic Right Ventricular Cardiomyopathy and Brugada Syndrome: New Insights From Molecular Biology and Clinical Implications. |
| Q43670831 | Risk indicators in long QT syndrome: does location matter? |
| Q61640642 | Routine electrocardiogram and medical history in syncope: a simple approach can identify most high-risk patients |
| Q28270379 | Sodium current deficit and arrhythmogenesis in a murine model of plakophilin-2 haploinsufficiency. |
| Q36693417 | Universal scaling law of electrical turbulence in the mammalian heart |
| Q50708618 | Up-regulation of the inward rectifier K+ current (I K1) in the mouse heart accelerates and stabilizes rotors. |
| Q61640650 | [Brugada's syndrome] |
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