Gain-of-Function Mutations in TRPM4 Cause Autosomal Dominant Isolated Cardiac Conduction Disease
Background—Isolated cardiac conduction block is a relatively common condition in young
and elderly populations. Genetic predisposing factors have long been suspected because of …
and elderly populations. Genetic predisposing factors have long been suspected because of …
Long QT syndrome in neonates: Conduction disorders associated with HERGmutations and sinus bradycardia with KCNQ1mutations
JM Lupoglazoff, I Denjoy, E Villain, V Fressart… - Journal of the American …, 2004 - jacc.org
Objectives: We hypothesized that neonatal long QT syndrome (LQTS) with 2: 1
atrioventricular block (AVB) could be related to HERG mutations. Background: Early onset of …
atrioventricular block (AVB) could be related to HERG mutations. Background: Early onset of …
Extracoronary echocardiographic findings as predictors of coronary artery lesions in the initial phase of Kawasaki disease
JC Lega, A Bozio, R Cimaz, M Veyrier… - Archives of disease in …, 2013 - adc.bmj.com
Objective To describe the significance of pericardial effusion (PE), mitral regurgitation (MR)
and impaired systolic function in predicting coronary artery lesions (CAL) at diagnosis and …
and impaired systolic function in predicting coronary artery lesions (CAL) at diagnosis and …
A de novo mutation of the beta cardiac myosin heavy chain gene in an infantile restrictive cardiomyopathy
S Karam, MJ Raboisson, C Ducreux… - Congenital heart …, 2008 - Wiley Online Library
Here we report the first pediatric case of restrictive cardiomyopathy secondary to a de novo
mutation in the cardiac myosin heavy chain gene MYH7. The clinical course is characterized …
mutation in the cardiac myosin heavy chain gene MYH7. The clinical course is characterized …
Mechanical valve in aortic position is a valid option in children and adolescents
G Champsaur, J Robin, F Tronc, A Curtil… - European journal of …, 1997 - academic.oup.com
OBJECTIVE: The choice of a valve substitute remains a challenge in youngpatients, with
numerous reports of early degeneration and calcification ofbiological valves in this age …
numerous reports of early degeneration and calcification ofbiological valves in this age …
Rabbit antithymocyte globulin as induction immunotherapy in pediatric heart transplantation
S Di Filippo, P Boissonnat, F Sassolas, J Robin… - …, 2003 - journals.lww.com
Background. There is little published data on the use of antithymocyte globulins in children.
This retrospective study describes the use of Thymoglobulin (Imtix, SangStat, Lyon, France) …
This retrospective study describes the use of Thymoglobulin (Imtix, SangStat, Lyon, France) …
The challenge of renal function in heart transplant children
S Di Filippo, P Cochat, A Bozio - Pediatric Nephrology, 2007 - Springer
Renal dysfunction may occur after pediatric heart transplantation and impacts on long-term
prognosis. This study aims to review the incidence and mechanisms of chronic nephropathy …
prognosis. This study aims to review the incidence and mechanisms of chronic nephropathy …
[HTML][HTML] Long-term clinical and hemodynamic evaluation of porcine valved conduits implanted from the right ventricle to the pulmonary artery
G Champsaur, J Robin, A Curtil, F Tronc… - The Journal of Thoracic …, 1998 - Elsevier
Objective: This retrospective study was initiated to evaluate the long-term results of valved
prosthetic conduits implanted in the right ventricular outflow tract in patients with complex …
prosthetic conduits implanted in the right ventricular outflow tract in patients with complex …
Lack of evidence for connexin 43 gene mutations in human autosomal recessive lateralization defects
S Debrus, S Tuffery, R Matsuoka, O Galal… - Journal of molecular and …, 1997 - Elsevier
Heterotaxy is the failure of the developing embryo to establish normal left–right asymmetry,
which is often associated with multiple malformations. Previous studies have identified …
which is often associated with multiple malformations. Previous studies have identified …
Focus on Echocardiographic and D oppler Analysis of Coronary Artery Abnormal Origin from the Pulmonary Trunk with Mild Myocardial Dysfunction
PY Courand, A Bozio, J Ninet, R Henaine… - …, 2013 - Wiley Online Library
Background Late presentation of abnormal origin of coronary artery from the pulmonary
artery (ACAPA) is uncommon compared with early presentation, which usually induces …
artery (ACAPA) is uncommon compared with early presentation, which usually induces …