C. Gronier

发表

Patent foramen ovale closure in children without cardiopathy: Child-PFO study.

C. Dauphin, P. Aldebert, C. Karsenty, 2020, Archives of cardiovascular diseases.

A systematic variant screening in familial cases of congenital heart defects demonstrates the usefulness of molecular genetics in this field

J. Lusson, P. Acar, J. Roume, 2015, European Journal of Human Genetics.

Position paper concerning the competence, performance and environment required for the practice of ablation in children and in congenital heart disease.

L. Fauchier, É. Marijon, F. Sacher, 2020, Archives of cardiovascular diseases.

Long-Term Outcomes After Percutaneous Closure of Ostium Secundum Atrial Septal Defect in the Young: A Nationwide Cohort Study.

J. Lusson, C. Dauphin, X. Pillois, 2018, JACC. Cardiovascular interventions.

Long-Term Outcomes After Percutaneous Closure of Ostium Secundum Atrial Septal Defect in€the€Young

J. Lusson, C. Dauphin, X. Pillois, 2018 .

Familial Recurrence Patterns in Congenitally Corrected Transposition of the Great Arteries: An International Study

R. Redon, E. Bacha, C. Dina, 2021, Circulation. Genomic and precision medicine.

Cardiovascular events in perimembranous ventricular septal defect with left ventricular volume overload: a French prospective cohort study (FRANCISCO).

P. Helms, L. Iserin, N. Combes, 2021, Cardiology in the young.

Hopes and fears of Generation Y congenital cardiac interventionists.

N. Combes, C. Karsenty, S. Hascoet, 2019, Archives of cardiovascular diseases.

Small infantile haemangioma and breast hypoplasia

D. Lipsker, C. Velter, C. Gronier, 2017, Journal of the European Academy of Dermatology and Venereology : JEADV.

[Infantile segmental hemangioma without facial involvement: A cutaneous marker of vascular malformations such as in PHACE syndrome?].

D. Lipsker, C. Gronier, M. Huther, 2015, Annales de dermatologie et de vénéréologie.

Off-label use of Lifetech KONAR-MF™ ventricular septal defect occluder for large patent ductus arteriosus closure in <6 kg infants

Q. Hauet, N. Benbrik, A. Baruteau, 2021, International Journal of Cardiology Congenital Heart Disease.

Bifid nose as the sole manifestation of BNAR syndrome, a FREM1‐related condition

F. Alkuraya, L. Van Maldergem, F. Nobili, 2020, Clinical genetics.

Clinical utility gene card for: Arterial tortuosity syndrome

X. Jeunemaître, P. Moceri, J. Albuisson, 2015, European Journal of Human Genetics.

Familial Recurrence Patterns in Congenitally Corrected Transposition of the Great Arteries: An International Study

R. Redon, E. Bacha, C. Dina, 2022, Circulation. Genomic and precision medicine.