PHILIPPE CHARRON
Centre de référence maladies cardiaques héréditaires, Hôpital Ambroise Paré & Hôpital Pitié-Salpêtrière · +33 (0)1 42 16 13 47 · PITIE SALPETRIERE HOSPITAL, PARIS, FRANCE
Built from public records under this name as ClinicalTrials.gov spells it. A name can belong to more than one person, so each section says how its rows were tied to this name. No contact details are shown.
Trials
Studies that name PHILIPPE CHARRON as principal investigator, study chair or study director, newest first. Live from ClinicalTrials.gov, fetched 2026-11-12 01:32 UTC. Open this list on ClinicalTrials.gov
- N/ANCT03846297 · Optimisation of Decision Making for Defibrillator Implantation in Hypertrophic CardiomyopathyAssistance Publique - Hôpitaux de Paris · recruiting · Hypertrophic Cardiomyopathy · principal investigator
- N/ANCT02920203 · Genetic Autopsy and Sudden DeathAssistance Publique - Hôpitaux de Paris · unknown · Sudden Death · study director
- Ph3NCT01583114 · PREclinical Mutation CARriers From Families With DIlated Cardiomyopathy and ACE InhibitorsInstitut National de la Santé Et de la Recherche Médicale, France · terminated · Dilated Cardiomyopathy · principal investigator
- N/ANCT00999947 · Arrhythmogenic Right Ventricular Dysplasia/CardiomyopathyAssistance Publique - Hôpitaux de Paris · completed · Cardiomyopathy, Arrhythmogenic Right Ventricular Dysplasia · principal investigator
Grants
NIH projects from RePORTER, fetched 2026-11-12 01:32 UTC. A project is listed only when its grant number is on one of the trials above, or when the awardee institution matches an affiliation the registry gives for this name. Coverage is US federal funding only; UK and EU funders are not searched yet.
No NIH project could be tied to this name by a shared trial or a matching institution.
Most cited trial papers
Clinical-trial papers with this author name, ranked by citations from NIH iCite, fetched 2026-11-12 01:32 UTC. The ranking covers the 200 most relevant of 4 PubMed records, and a shared surname and initials can bring in a namesake. All 4 on PubMed
- Characterization of a unique genetic variant in the beta1-adrenoceptor gene and evaluation of its role in idiopathic dilated cardiomyopathy. CARDIGENE Group.J Mol Cell Cardiol · 1999107 citationsRCR 2.6
- Diagnostic value of electrocardiography and echocardiography for familial hypertrophic cardiomyopathy in genotyped children.Eur Heart J · 199849 citationsRCR 1.2
- Cardiopulmonary Fitness and Physical Activity Among Children and Adolescents With Inherited Cardiac Disease.JAMA Netw Open · 202512 citationsRCR 5.4
- Strong increase of leukocyte apha-galactosidase A activity in two male patients with Fabry disease following oral chaperone therapy.Mol Genet Genomic Med · 20197 citationsRCR 0.4