Brugada Syndrome |
1. |
Skinner JR, Chung SK, Montgomery D, McCulley CH, Crawford J, French J, Rees MI. |
|
Near-miss SIDS due to Brugada
syndrome. |
2. |
||
Double SCN5A mutation underlying
asymptomatic Brugada syndrome. |
3. |
Newton-Cheh C, Larson MG, Corey DC, Benjamin EJ, Herbert AG, Levy D, D'Agostino RB, O'donnell CJ. |
|
QT interval is a heritable
quantitative trait with evidence of linkage to chromosome 3 in a genome-wide
linkage analysis: The Framingham Heart Study. |
4. |
||
Are all sodium channel blockers
created equal? Clinical-basic correlations based on observations in Brugada
syndrome. |
5. |
||
Intravenous drug challenge
using flecainide and ajmaline in patients with Brugada syndrome. |
6. |
||
Spontaneous onset of ventricular
fibrillation in Brugada syndrome with J wave and ST-segment elevation
in the inferior leads. |
WPW |
1. |
||
Exercise Testing in Wolff-Parkinson-White
Syndrome: Case Report With ECG and Literature Review. |
2. |
Moraes PL, Gerken LM, Gontijo Filho B, Vicente WV, Evora PR. |
|
[Wolff-Parkinson-White syndrome
and the sinus venosus atrial septal defect association.] |
3. |
||
[CME-ECG solution. Tibial
fracture. WPW with posteroseptal accessory pathway] |
4. |
||
The earliest published electrocardiogram
showing ventricular preexcitation. |
5. |
Brembilla-Perrot B, Marcon F, Bosser G, Lucron H, Burger G, Beurrier D, Houriez P. |
|
[Feasibility and significance of a transoesophageal electrophysiological
investigation in children and adolescents with Wolff-Parkinson-White syndrome] |
6. |
Sarubbi B, D'Alto M, Vergara P, Calvanese R, Mercurio B, Russo MG, Calabro R. |
|
Electrophysiological evaluation
of asymptomatic ventricular pre-excitation in children and adolescents. |
7. |
||
History of Wolff-Parkinson-White
syndrome. |
8. |
Oh S, Choi YS, Choi EK, Kim HS, Sohn DW, Oh BH, Lee MM, Park YB. |
|
Electrocardiographic characteristics
of fasciculoventricular pathways. |
CPVT. |
1. |
||
A novel mutation in FKBP12.6
binding region of the human cardiac ryanodine receptor gene (R2401H) in
a Japanese patient with catecholaminergic polymorphic ventricular tachycardia. |
2. |
|||
Unusual clinical presentation
in a family with catecholaminergic polymorphic ventricular tachycardia
due to a G14876A ryanodine receptor gene mutation. |
LQT
Autonomic control of cardiac
action potentials: role of potassium channel kinetics in response to sympathetic
stimulation. |
Idiopathic Ventricular Fibrillation
1. |
|||
ECG Repolarization Waves: Their Genesis and Clinical Implications. |
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2. |
Brilakis ES, Friedman PA, Maounis TN, Rokas SG, Shen WK, Stamatelopoulos SF, Cokkinos DV. |
||
Programmed ventricular stimulation in patients with idiopathic
dilated cardiomyopathy and syncope receiving implantable cardioverter-defibrillators:
a case series and a systematic review of the literature. |
|||
3. |
|||
Recurrent cardiac events in patients with idiopathic ventricular
fibrillation, excluding patients with the Brugada syndrome. |
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