Detalhe da pesquisa
1.
Left Ventricular Systolic Dysfunction in Patients Diagnosed With Hypertrophic Cardiomyopathy During Childhood: Insights From the SHaRe Registry.
Circulation
; 148(5): 394-404, 2023 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-37226762
2.
Current management of inherited arrhythmia syndromes associated with the cardiac ryanodine receptor.
Curr Opin Cardiol
; 38(4): 390-395, 2023 07 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37016946
3.
Gene Therapy for Catecholaminergic Polymorphic Ventricular Tachycardia.
Heart Lung Circ
; 32(7): 790-797, 2023 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-37032191
4.
Cascade testing for inherited cardiac conditions: Risk perception and screening after a negative genetic test result.
J Genet Couns
; 31(6): 1273-1281, 2022 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-35763674
5.
Exercise Recommendations in Pediatric HCM: Variation and Influence of Provider Characteristics.
Pediatr Cardiol
; 43(1): 132-141, 2022 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-34406429
6.
An International Multicenter Evaluation of Type 5 Long QT Syndrome: A Low Penetrant Primary Arrhythmic Condition.
Circulation
; 141(6): 429-439, 2020 02 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-31941373
7.
An International Multicenter Evaluation of Inheritance Patterns, Arrhythmic Risks, and Underlying Mechanisms of CASQ2-Catecholaminergic Polymorphic Ventricular Tachycardia.
Circulation
; 142(10): 932-947, 2020 09 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-32693635
8.
Lead age as a predictor for failure in pediatrics and congenital heart disease.
Pacing Clin Electrophysiol
; 44(4): 586-594, 2021 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-33432629
9.
Gene Therapy for Catecholaminergic Polymorphic Ventricular Tachycardia by Inhibition of Ca2+/Calmodulin-Dependent Kinase II.
Circulation
; 140(5): 405-419, 2019 07 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-31155924
10.
Insights Into the Pathogenesis of Catecholaminergic Polymorphic Ventricular Tachycardia From Engineered Human Heart Tissue.
Circulation
; 140(5): 390-404, 2019 07 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-31311300
11.
Value of provocative electrophysiology testing in the management of pediatric patients after congenital heart surgery.
Pacing Clin Electrophysiol
; 43(9): 901-907, 2020 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-32329521
12.
Premature ventricular contractions in children and young adults: natural history and clinical implications.
Europace
; 26(3)2024 Mar 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-38441283
13.
SCN5A mutations in 442 neonates and children: genotype-phenotype correlation and identification of higher-risk subgroups.
Eur Heart J
; 39(31): 2879-2887, 2018 08 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-30059973
14.
Causal Genetic Variants in Stillbirth.
N Engl J Med
; 383(27): 2687, 2020 12 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-33382937
15.
How to develop a clinic for sudden cardiac arrest survivors and families of non-survivors.
Cardiol Young
; 27(S1): S3-S9, 2017 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-28084954
16.
Radiofrequency ablation of atrial tachyarrhythmias in adults with tetralogy of Fallot - predictors of success and outcome.
Cardiol Young
; 27(2): 284-293, 2017 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-27225323
17.
Clinical Management of Catecholaminergic Polymorphic Ventricular Tachycardia: The Role of Left Cardiac Sympathetic Denervation.
Circulation
; 131(25): 2185-93, 2015 Jun 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-26019152
18.
The DSPII splice variant is crucial for desmosome-mediated adhesion in HaCaT keratinocytes.
J Cell Sci
; 125(Pt 12): 2853-61, 2012 Jun 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-22454510
19.
Inflammatory skin and bowel disease linked to ADAM17 deletion.
N Engl J Med
; 365(16): 1502-8, 2011 Oct 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-22010916
20.
The use of an integrated electroanatomic mapping system and intracardiac echocardiography to reduce radiation exposure in children and young adults undergoing ablation of supraventricular tachycardia.
Europace
; 16(2): 277-83, 2014 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-23928735