| P2093 | author name string | Philippe Mabo | |
| | Julien Baruteau | |
| | Alban-Elouen Baruteau | |
| P2860 | cites work | Catecholaminergic polymorphic ventricular tachycardia | Q28287523 |
| | Catecholaminergic polymorphic ventricular tachycardia. | Q33152560 |
| | Clinical aspects and prognosis of Brugada syndrome in children | Q33154976 |
| | Identification of a possible pathogenic link between congenital long QT syndrome and epilepsy | Q33156860 |
| | Clinical experiences of patients with catecholaminergic polymorphic ventricular tachycardia | Q33156954 |
| | Misdiagnosis of long QT syndrome as epilepsy at first presentation | Q33157207 |
| | Catecholaminergic polymorphic ventricular tachycardia in children. A 7-year follow-up of 21 patients | Q33173888 |
| | Brugada syndrome: report of the second consensus conference: endorsed by the Heart Rhythm Society and the European Heart Rhythm Association. | Q34385271 |
| | Cardiorespiratory findings in sudden unexplained/unexpected death in epilepsy (SUDEP). | Q35769298 |
| | Inherited arrhythmias: a National Heart, Lung, and Blood Institute and Office of Rare Diseases workshop consensus report about the diagnosis, phenotyping, molecular mechanisms, and therapeutic approaches for primary cardiomyopathies of gene mutation | Q36999467 |
| | Brugada syndrome masquerading as febrile seizures. | Q40453234 |
| | Woman with Brugada syndrome and epilepsy: a unifying diagnosis? | Q50448352 |
| | Epilepsy, Brugada syndrome and the risk of sudden unexpected death | Q73101179 |
| | Torsades de pointes in a child | Q83484084 |
| P433 | issue | 1 | |
| P304 | page(s) | 111-112 | |
| P577 | publication date | 2010-01-13 | |
| P1433 | published in | Cardiology in the Young | Q2041555 |
| P1476 | title | The differential diagnosis of primary electrical diseases from seizures in childhood | |
| P478 | volume | 20 | |