Search Results - "Gérard, Hilla"
-
1
Identification of non-synonymous variations in ROBO1 and GATA5 genes in a family with bicuspid aortic valve disease
Published in Journal of human genetics (01-09-2022)“…Bicuspid aortic valve (BAV) is the most common congenital heart defect with a high index of heritability. Patients with BAV have different clinical courses and…”
Get full text
Journal Article -
2
Expanding the phenome and variome of the ROBO-SLIT pathway in congenital heart defects: toward improving the genetic testing yield of CHD
Published in Journal of translational medicine (28-02-2023)“…Recent studies have shown the implication of the ROBO-SLIT pathway in heart development. Within this study, we aimed to further assess the implication of the…”
Get full text
Journal Article -
3
Left atrial dysfunction as marker of poor outcome in patients with hypertrophic cardiomyopathy
Published in Archives of cardiovascular diseases (01-02-2021)“…The incremental prognostic value of left atrial (LA) dysfunction, emerging in various clinical contexts, remains poorly explored in hypertrophic cardiomyopathy…”
Get full text
Journal Article -
4
Prognosis of Adults With Isolated Left Ventricular Non-Compaction: Results of a Prospective Multicentric Study
Published in Frontiers in cardiovascular medicine (02-05-2022)“…Whether left ventricular non-compaction (LVNC) bears a different prognosis than dilated cardiomyopathy (DCM) is still a matter of debate. From a multicenter…”
Get full text
Journal Article -
5
Unexpected coronary thrombosis complicating COVID-19 infection in young adult
Published in Acta Cardiologica (01-04-2024)Get full text
Journal Article -
6
Phenotype/Genotype Relationship in Left Ventricular Noncompaction: Ion Channel Gene Mutations Are Associated With Preserved Left Ventricular Systolic Function and Biventricular Noncompaction: Phenotype/Genotype of Noncompaction
Published in Journal of cardiac failure (01-06-2021)“…Few data exist concerning genotype-phenotype relationships in left ventricular noncompaction (LVNC). From a multicenter French Registry, we report the genetic…”
Get full text
Journal Article -
7
Phenotype/Genotype Relationship in Left Ventricular Noncompaction: Ion Channel Gene Mutations Are Associated With Preserved Left Ventricular Systolic Function and Biventricular Noncompaction
Published in Journal of cardiac failure (01-06-2021)“…Background: Few data exist concerning genotype-phenotype relationships in left ventricular noncompaction (LVNC).Methods and results: From a multicenter French…”
Get full text
Journal Article -
8
Phenotype/Genotype Relationship in Left Ventricular Noncompaction: Ion Channel Gene Mutations Are Associated With Preserved Left Ventricular Systolic Function and Biventricular Noncompaction
Published in Journal of cardiac failure (01-06-2021)“…Few data exist concerning genotype–phenotype relationships in left ventricular noncompaction (LVNC). From a multicenter French Registry, we report the genetic…”
Get full text
Journal Article