All Stories

  1. Problems in the diagnosis of discordant atrioventricular with concordant ventriculo-arterial connections: anatomical considerations, surgical management, and long-term outcome
  2. Anatomy of the ventricular septal defect in outflow tract defects: Similarities and differences
  3. Myocardial inflammation on cardiovascular magnetic resonance predicts left ventricular function recovery in children with recent dilated cardiomyopathy
  4. Incidence and predictors of Melody® valve endocarditis: A prospective study
  5. 0487: Dilatable pulmonary artery band: results of interventional dilatation and clinical outcome
  6. 0458: Outcomes of pediatric hypertrophic cardiomyopathy associated with Rasopathy
  7. 0489: Incidence and outcomes of right sided endocarditis in patients with congenital heart diseases with surgical or transcatheter pulmonary valve implantation
  8. 0483: Cardiac magnetic resonance imaging and left ventricular diastolic function in children with hypertrophic cardiomyopathy
  9. 0238: Quality of life of patients with pulmonary arterial hypertension associated with congenital heart disease: the multicenter cross-sectional Achille study
  10. 0462: Chest CT findings in idiopathic and heritable pediatric pulmonary arterial hypertension
  11. 0459: MRI evaluation of coronary anatomy and myocardial perfusion after arterial switch for transposition of great arteries
  12. 0241: Knowledge-based 3D reconstruction compared to MRI for evaluation of right ventricular volumes and function in congenital heart diseases affecting the right ventricle
  13. 0491: Extracardiac or chromosomal anomalies strongly influence parental treatment decision and postnatal survival of neonates with prenatally diagnosed congenital heart diseases
  14. 0523: Feasibility and accuracy of left ventricular volumes and ejection fraction measured by different echocardiographic methods in congenital heart diseases involving the right ventricle
  15. 0449: Prognostic value of right ventricle echocardiographic parameters in children with idiopathic pulmonary hypertension
  16. 0484: Outcome of coronary artery lesions after neonatal arterial switch operation
  17. 0460: Radiation dose reduction in pediatric coronary CT: assessment of effective dose and image quality
  18. Melody® transcatheter pulmonary valve implantation: Results from a French registry
  19. Incidence and outcomes of right-sided endocarditis in patients with congenital heart disease after surgical or transcatheter pulmonary valve implantation
  20. Case of a healthy infant born following antenatal enterovirus myocarditis and hydrops
  21. Computational modeling of blood flow in the aorta—insights into eccentric dilatation of the ascending aorta after surgery for coarctation
  22. Executive Functions Development in 5- to 7-Year-Old Children With Transposition of the Great Arteries: A Longitudinal Study
  23. Closure of Fontan fenestration with the use of covered stents: short- and mid-term results in a cohort of 50 patients
  24. Anomalous Left Coronary Artery Connected to the Pulmonary Artery Associated With Other Cardiac Defects: A Difficult Joint Diagnosis
  25. Novel method of surgical preparation for transcatheter completion of Fontan circulation: Creation of an extracardiac pathway
  26. Severe Nocturnal and Postexercise Hypoxia in Children and Adolescents with Sickle Cell Disease
  27. Association between Prenatal Exposure to Antiretroviral Therapy and Birth Defects: An Analysis of the French Perinatal Cohort Study (ANRS CO1/CO11)
  28. Pulmonary Hypoplasia Associated with Congenital Heart Diseases: A Fetal Study
  29. Hyperacute flash pulmonary oedema after transcatheter pulmonary valve implantation: The melody of an overwhelmed left ventricle
  30. Coronary artery compression during intention to treat right ventricle outflow with percutaneous pulmonary valve implantation: Incidence, diagnosis, and outcome
  31. Type 2 short QT syndrome and vestibular dysfunction: Mirror of the Jervell and Lange-Nielsen syndrome?
  32. Facial expression recognition and emotion understanding in children after neonatal open-heart surgery for transposition of the great arteries
  33. Correction: Circulating Endothelial Cells in Refractory Pulmonary Hypertension in Children: Markers of Treatment Efficacy and Clinical Worsening
  34. Assessing the role of multiple pregnancies in the association between tetralogy of Fallot and assisted reproductive techniques: a path-analysis approach
  35. EIF2AK4 mutations cause pulmonary veno-occlusive disease, a recessive form of pulmonary hypertension
  36. Pediatric Pulmonary Hypertension
  37. Congenital Heart Defects in Patients with Deletions Upstream ofSOX9
  38. Use of Early Remedial Services in Children with Transposition of the Great Arteries
  39. Hypertension after repair of aortic coarctation — A systematic review
  40. Inferior vena cava into the left atrium
  41. Anatomy of the ventricular septal defect in congenital heart defects: Random or systemic association?
  42. Atrioventricular discordance with ventriculo-arterial concordance: Diagnostic challenge, surgical management and long-term outcome
  43. Systematic description of cardiac phenotype based on the anatomical and clinical classification (ACC-CHD) in a DNA bank for congenital heart disease
  44. Coronary artery compression during transcatheter right-ventricular outflow tract treatment: Incidence, diagnosis and outcome
  45. TAPSE is correlated with right ventricle ejection fraction in children with native congenital heart disease but not after cardiac surgery
  46. Anomalous left coronary artery from the pulmonary artery associated with other cardiac defects: A difficult joint diagnosis
  47. Cardiomyopathies and congenital heart diseases in Shwachman–Diamond syndrome: A national survey
  48. Circulating Endothelial Cells in Refractory Pulmonary Hypertension in Children: Markers of Treatment Efficacy and Clinical Worsening
  49. Key issues of daily life in adults with congenital heart disease
  50. Mechanisms of coronary complications after the arterial switch for transposition of the great arteries
  51. Structure and function of the ascending aorta in palliated transposition of the great arteries
  52. Early neonatal death and congenital left coronary abnormalities: Ostial atresia, stenosis and anomalous aortic origin
  53. Risk of cancer associated with cardiac catheterization procedures during childhood: a cohort study in France
  54. INCIDENCE, DIAGNOSIS AND OUTCOMES OF CORONARY ARTERY COMPRESSION DURING PERCUTANEOUS PULMONARY VALVE IMPLANTATION
  55. Respiratory Outcome in Children with Scimitar Syndrome
  56. FOXgene cluster defects in alveolar capillary dysplasia associated with congenital heart disease
  57. Determination of the efficacious and safe dose of ivabradine in paediatric patients with dilated cardiomyopathy and symptomatic chronic heart failure from ages 6 months to 18 years
  58. The pattern of the coronary arterial orifices in hearts with congenital malformations of the outflow tracts: a marker of rotation of the outflow tract during cardiac development?
  59. 266: Cardiac Magnetic Resonance in Children with Acute Myocarditis
  60. 274: Is valvulation of Fontan circulation of clinical value?
  61. 272: Long-term outcome of 117 patients with univentricular heart and common atrioventricular valve
  62. 275: Percutaneous insertion of a Melody valve in tricuspid position: technical aspects
  63. 282: Distribution of causes and outcomes of pulmonary hypertensions in a tertiary pediatric hospital
  64. Impact of right ventricular outflow tract size and substrate on outcomes of percutaneous pulmonary valve implantation
  65. Optimal follow-up in adult patients with congenital heart disease and chronic pulmonary regurgitation: Towards tailored use of cardiac magnetic resonance imaging
  66. 268: Right ventricular function with standard and speckle-tracking echocardiography and clinical tolerance in adults with D-transposition of the great arteries post atrial switch
  67. 278: Congenital left coronary ostial atresia or stenosis - a series of four neonatal fatal cases
  68. 276: Potts’ shunt in children with idiopathic pulmonary arterial hypertension: long-term results
  69. 281: Use of covered stents for closure of fenestration in extracardiac cavopulmonary connection: technical aspects and mid-term results
  70. 089: Expanding the phenotype associated with a desmoplakin dominant mutation: Carvajal/Naxos syndrome associated with leukonychia and oligodentia
  71. 292: Pulmonary arterial hypertension complicating arterial switch surgery for simple transposition of the great arteries-prevalence and outcomes
  72. 280: Circulating endothelial cell levels decrease after vasodilator therapy and are a biomarker of deterioration in pediatric pulmonary hypertension
  73. Natural history of Barth syndrome: a national cohort study of 22 patients
  74. Expanding the phenotype associated with a desmoplakin dominant mutation: Carvajal/Naxos syndrome associated with leukonychia and oligodontia
  75. Immunodeficiency, autoinflammation and amylopectinosis in humans with inherited HOIL-1 and LUBAC deficiency
  76. Total Anomalous Pulmonary Venous Connection to the Unroofed Coronary Sinus in a Neonate
  77. Acquired coronary disease in children: the role of multimodality imaging
  78. Managing pulmonary hypertension in patients with congenital heart disease
  79. Potts Shunt in Children With Idiopathic Pulmonary Arterial Hypertension: Long-Term Results
  80. Outcomes and safety of transcatheter pulmonary valve replacement in patients with large patched right ventricular outflow tracts
  81. Impact of Prenatal Diagnosis on Neurocognitive Outcomes in Children with Transposition of the Great Arteries
  82. Fatal Rhabdomyolysis in 2 Children with LPIN1 Mutations
  83. Right Ventricular Systolic Strain Is Altered in Children with Sickle Cell Disease
  84. Midterm results of percutaneous closure of very large atrial septal defects in children: role of multislice computed tomography
  85. Atypical malignant late infective endocarditis of Melody valve
  86. Clinical features of paediatric pulmonary hypertension: a registry study
  87. Can “Inoperable” Congenital Heart Defects Become Operable in Patients with Pulmonary Arterial Hypertension? Dream or Reality?
  88. 354 Evolution of right ventricle volumes and function from childhood to adulthood
  89. 328 Optimal dosing of warfarin in a pediatric cohort: height, INR range, VKORC1 and CYP2C9 genotypes are the main contributors of the dose requirement
  90. 323 Congenital heart defects in twin pregnancies: A series of 226 cases
  91. 340 Population-based evaluation of a suggested anatomic and clinical classification of congenital heart defects based on the International Paediatric and Congenital Cardiac Code
  92. 330 Characteristics of patients with pulmonary arterial hypertension associated with congenital heart disease in the registry of the French PAH network
  93. 335 Characteristics of PAH associated with pretricuspid shunts in the registry of the French PAH network
  94. 324 Anatomy and position of the coronary orifices on the aortic/truncal circumference in cardiac outflow tract defects: A marker of outflow tract rotation
  95. Successful Treatment of Severe Cardiomyopathy in Glycogen Storage Disease Type III With D,L-3-Hydroxybutyrate, Ketogenic and High-Protein Diet
  96. Measurement of nuchal translucency for prenatal screening of congenital heart defects: a population-based evaluation
  97. Anaemia is a predictor of early death or cardiac transplantation in children with idiopathic dilated cardiomyopathy
  98. Mutations in the TGFβ Binding-Protein-Like Domain 5 of FBN1 Are Responsible for Acromicric and Geleophysic Dysplasias
  99. Loan applications in adult patients with congenital heart disease: A French study
  100. Add-On Therapy with Subcutaneous Treprostinil for Refractory Pediatric Pulmonary Hypertension
  101. Prognosis Factors in Probands With an FBN1 Mutation Diagnosed Before the Age of 1 Year
  102. 293 Anomalies of coronary artery ostia in common arterial trunk
  103. 295 Pulmonary arterial hypertension after bone marrow transplantation in children
  104. 310 Aorto-pulmonary anastomosis in tuberous sclerosis and cardiac tumor with severe right ventricular outflow tract obstruction (a case report)
  105. Population-based evaluation of a suggested anatomic and clinical classification of congenital heart defects based on the International Paediatric and Congenital Cardiac Code
  106. Isolated Congenital Asplenia: A French Nationwide Retrospective Survey of 20 Cases
  107. Treprostinil increases the number and angiogenic potential of endothelial progenitor cells in children with pulmonary hypertension
  108. Nontoxinogenic Corynebacterium Diphtheriae as a Rare Cause of Native Endocarditis in Childhood
  109. Executive function and theory of mind in school-aged children after neonatal corrective cardiac surgery for transposition of the great arteries
  110. Traitement de l’hypertension artérielle pulmonaire
  111. Traitement de l’hypertension artérielle pulmonaire de l’enfant
  112. Intramural coronary arteries and outcome of neonatal arterial switch operation
  113. Caractéristiques et suivi prospectif sur deux ans des enfants atteints d’hypertension artérielle pulmonaire en France
  114. Arterial alterations in severely obese children with obstructive sleep apnoea
  115. Subcutaneous Treprostinil In Pediatric Pulmonary Arterial Hypertension
  116. Post-operative cardiac lesions after cardiac surgery in childhood
  117. Postnatal growth retardation, facial dysmorphism, spondylocarpal synostosis, cardiac defect, and inner ear malformation (cardiospondylocarpofacial syndrome?)-A distinct syndrome?
  118. Comparison of Endothelial Biomarkers According to Reversibility of Pulmonary Hypertension Secondary to Congenital Heart Disease
  119. Development of a new lead forin uterofetal pacing
  120. Outcome of coronary artery bypass grafting performed in young children
  121. Characteristics and prospective 2-year follow-up of children with pulmonary arterial hypertension in France
  122. 322 Subcutaneous treprostinil in pediatric idiopathic pulmonary arterial hypertension
  123. Cardiomyopathies in Propionic Aciduria are Reversible After Liver Transplantation
  124. Transcatheter valve insertion in a model of enlarged right ventricular outflow tracts
  125. 311 Home INR monitoring of oral anticoagulation therapy in children using a point-of-care INR monitor after an education program
  126. 313 French pulmonary arterial hypertension registry in children: 2-year follow-up data
  127. 320 Clinical usefulness of cardiac MRI for making the definitive diagnosis of myocarditis in children
  128. 321 Congenital heart defects in CHARGE syndrome patients with CHD7 mutations
  129. Influence of polymorphisms in candidate genes on early vascular alterations in obese children
  130. Pharmacokinetic and clinical profile of a novel formulation of bosentan in children with pulmonary arterial hypertension: the FUTURE-1 study
  131. Rôle des centres de référence maladies rares dans la prise en charge de l’hypertension artérielle pulmonaire des cardiopathies congénitales
  132. Health-e-Child Project: Mechanical Dyssynchrony in Children with Dilated Cardiomyopathy
  133. Ostial Stenosis of an Anomalous Left Coronary Artery from the Pulmonary Artery in a Teenager
  134. Common arterial trunk repair: with conduit or without?☆
  135. Acute Ischemic Cardiomyopathy after Extreme Emotional Stress in a Child
  136. Cardiac CT angiography after coronary artery surgery in children using 64-slice CT scan
  137. Surgical Management of Supravalvular Aortic Stenosis: Does Brom Three-Patch Technique Provide Superior Results?
  138. Non-invasive assessment of congenital pulmonary vein stenosis in children using cardiac-non-gated CT with 64-slice technology
  139. Percutaneous treatment of neonatal aortic coarctation presenting with severe left ventricular dysfunction as a bridge to surgery
  140. Preoperative evaluation of candidates for total cavopulmonary connection: The role of echocardiography and cardiac catheterization
  141. Cheatham Platinum (CP) and Palmaz stents for cardiac and vascular lesions treatment in patients with congenital heart disease
  142. Conotruncal defects associated with anomalous pulmonary venous connections
  143. Genetics and embryological mechanisms of congenital heart diseases
  144. Mécanismes embryologiques et génétiques des malformations des gros vaisseaux de la base du cœur
  145. Percutaneous treatment of aorto-pulmonary window in a one year old child
  146. ADAMTSL2 mutations in geleophysic dysplasia demonstrate a role for ADAMTS-like proteins in TGF-β bioavailability regulation
  147. Association of Arterial Stiffness and Endothelial Dysfunction with Metabolic Syndrome in Obese Children
  148. Late reoperations after neonatal arterial switch operation for transposition of the great arteries
  149. Right superior vena cava draining into the left atrium
  150. Collateral channels from the superior caval vein to the cardiac veins after atrial repair for transposition
  151. Retrograde catheterization of the right heart in patients with occluded femoral veins
  152. Safety and Accuracy of 64-Slice Computed Tomography Coronary Angiography in Children After the Arterial Switch Operation for Transposition of the Great Arteries
  153. CT demonstration of “chicken trachea” resulting from complete cartilaginous rings of the trachea in ring-sling complex
  154. The Ross Procedure in Infants and Young Children
  155. Acute angulation of the aortic arch predisposes a patient to ascending aortic dilatation and aortic regurgitation late after the arterial switch operation for transposition of the great arteries
  156. Increased central aortic stiffness and left ventricular mass in normotensive young subjects after successful coarctation repair
  157. Liste des auteurs
  158. Angular (Gothic) aortic arch leads to enhanced systolic wave reflection, central aortic stiffness, and increased left ventricular mass late after aortic coarctation repair: Evaluation with magnetic resonance flow mapping
  159. Pathophysiology of Williams Syndrome Arteriopathy
  160. Left coronary to right ventricle fistula in a child: management strategy based on cardiac-gated 64-slice CT
  161. Investigation of the MYH11 gene in sporadic patients with an isolated persistently patent arterial duct
  162. Pediatric Coronary Artery Bypass After Arterial Switch Operation: Noninvasive Evaluation With ECG-Gated 64-Slice CT in Routine Practice
  163. Cardiomyopathies restrictives de I’enfant : bilan et approche thérapeutique
  164. The French registry of pulmonary arterial hypertension in children: rationale and design
  165. Late coronary artery lesions after neonatal arterial switch operation: results of surgical coronary revascularization
  166. Unusual systemic venous return with absence of superior caval veins
  167. Atresia of the coronary sinus ostium: Surgical implications
  168. Vascular Remodeling After “Successful” Repair of Coarctation
  169. Impaired Apoptosis of Pulmonary Endothelial Cells Is Associated With Intimal Proliferation and Irreversibility of Pulmonary Hypertension in Congenital Heart Disease
  170. Mitral valvar regurgitation in a child with Sweet's syndrome
  171. Neonatal transcatheter closure of a large pulmonary arteriovenous fistula
  172. Neonatal Surgical Aortic Commissurotomy: Predictors of Outcome and Long-Term Results
  173. Aortic arch shape deformation after coarctation surgery: Effect on blood pressure response
  174. Presentation and Prognosis of Complete Atrioventricular Block in Childhood, According to Maternal Antibody Status
  175. Fibromuscular dysplasia as the substrate for systemic and pulmonary hypertension in the setting of Moya-Moya disease
  176. Myocardial cell lineages in the mammalian embryo: The second heart field
  177. Off-label use of an adjustable gastric banding system for pulmonary artery banding
  178. Anomalous origin of the left coronary artery from the right aortic sinus: surgery based on diagnosis by 64-slice CT
  179. Detection of coronary complications after the arterial switch operation for transposition of the great arteries: First experience with multislice computed tomography in children
  180. Infected pulmonary artery aneurysms: CT imaging findings
  181. Diagnosis and outcome in congenital ventricular diverticulum and aneurysm
  182. Anomalies du retour veineux systémique
  183. Noonan Syndrome: Relationships between Genotype, Growth, and Growth Factors
  184. Unusual chronic pacemaker infection by Mycobacterium tuberculosis in a pediatric patient
  185. Noninvasive Assessment of Arterial Stiffness and Risk of Atherosclerotic Events in Children
  186. Complications of paediatric interventional catheterisation: an analysis of risk factors
  187. Steps Toward the Percutaneous Replacement of Atrioventricular Valves
  188. Infection by the respiratory syncytial virus in infants and young children at high risk
  189. Mid-term effects of implanting stents for relief of aortic recoarctation on systemic hypertension, carotid mechanical properties, intimal medial thickness and reflection of the pulse wave
  190. Off-pump replacement of the pulmonary valve in large right ventricular outflow tracts: A hybrid approach
  191. Scimitar syndrome associated with absence of the right pulmonary artery and a persistent primitive hepatic venous plexus
  192. Mutation in myosin heavy chain 6 causes atrial septal defect
  193. Noninvasive Assessment of Fetal Pulmonary Blood Flow in Experimental Pulmonary Hypertension in the Fetal Lamb
  194. Emergency trans-oesophageal ventricular pacing in a child
  195. Patients Operated for Tetralogy of Fallot and with Non-Sustained Ventricular Tachycardia Have Reduced Heart Rate Variability
  196. Endothelial Function and Mechanical Properties of the Common Carotid Artery in Children on Parenteral Nutrition
  197. Arterial stiffness and endothelial dysfunction in HIV-infected children
  198. Percutaneous pulmonary valve replacement in a large right ventricular outflow tract
  199. Potts Shunt in Patients with Pulmonary Hypertension
  200. Reply to the Editor
  201. Characteristics and management of cleft mitral valve
  202. Remote control of pulmonary blood flow: initial clinical experience
  203. Surprising outcome similarities between Contegra® bovine jugular vein conduit and Shelhigh No-React® porcine pulmonary valve conduit: role of immunologic reaction
  204. Use of bovine jugular vein to reconstruct the right ventricular outflow tract: early results
  205. Fluorescencein situhybridization (FISH) rather than ultrasound for the evaluation of fetuses at risk for 22q11.2 deletion
  206. Perforation of the atretic pulmonary valve
  207. Age-related aspects of balloon angioplasty for postsurgical aortic recoarctation
  208. Management and outcome of patients with abnormal ventriculo-arterial connections and mitral valve cleft
  209. Transcatheter Occlusion of a Large Aortoazygos Fistula Using the Amplatzer Device
  210. Stent supported angioplasty for coronary arterial stenosis following the arterial switch operation
  211. Elastin mutation is associated with a reduced gain of the baroreceptor - heart rate reflex in patients with Williams syndrome
  212. Cleft of the mitral valve in patients with Down's syndrome
  213. Can we predict 22q11 status of fetuses with tetralogy of Fallot?
  214. Pepper syndrome, truncus arteriosus communis and abnormal pulmonary venous return: an unusual association
  215. Selective coronary angiography in patients younger than 1 year of age
  216. Presence of increased stiffness of the common carotid artery and endothelial dysfunction in severely obese children: a prospective study
  217. Comparison of myocardial perfusion single-photon emission computed tomography with coronary artery angiography after arterial switch operation
  218. Prevalence of 22q11 deletion in fetuses with conotruncal cardiac defects: A 6-year prospective study
  219. Absorbable pulmonary artery banding in tricuspid atresia
  220. Hypertelorism-Microtia-Clefting Syndrome (Bixler syndrome): report of two unrelated cases
  221. Temporal bone anomaly proposed as a major criteria for diagnosis of CHARGE syndrome
  222. Percutaneous replacement of pulmonary valve in a right-ventricle to pulmonary-artery prosthetic conduit with valve dysfunction
  223. A new strategy for the surgical treatment of aortic coarctation associated with ventricular septal defect in infants using an absorbable pulmonary artery band
  224. Surgical angioplasty of the main coronary arteries in children☆☆☆
  225. Ebstein anomaly associated with rearrangements of chromosomal region 11q
  226. Atrio-ventricular valve dysplasia in 22 newborn infants
  227. Microsatellite DNA markers detects 95% of chromosome 22q11 deletions
  228. Microsatellite DNA markers detects 95% of chromosome 22q11 deletions
  229. Coronary Artery Obstruction After the Arterial Switch Operation for Transposition of the Great Arteries in Newborns
  230. Holt-Oram syndrome is caused by mutations in TBX5, a member of the Brachyury (T) gene family
  231. Outcome of, and risk factors for, second degree atrioventricular block in children
  232. Williams syndrome is characterized by 1 megabase deletions on 7q encompassing the elastin gene
  233. A gene for Holt–Oram syndrome maps to the distal long arm of chromosome 12