1. Availability and applicability of cardiac magnetic resonance imaging in diagnosis in cardiomyopathies: the Cardiomyopathy/Myocarditis registry of the EURObservational Research Programme of the ESC. (25th November 2020) Authors: Mizia-Stec, K; Charron, P; Blanes, J.R.G; Elliott, P; Kaski, J.P; Maggioni, A.P; Tavazzi, L; Tendera, M; Wybraniec, M; Laroche, C; Caforio, A.L.P Journal: European heart journal Issue: Volume 41:(2020)Supplement 2 Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Danon's disease as a cause of hypertrophic cardiomyopathy: a systematic survey. Issue 10 (1st October 2004) Authors: Charron, P; Villard, E; Sébillon, P; Laforêt, P; Maisonobe, T; Duboscq-Bidot, L; Romero, N; Drouin-Garraud, V; Frébourg, T; Richard, P; Eymard, B; Komajda, M Journal: Journal of medical genetics Issue: Volume 41:Issue 10(2004) Page Start: 751 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Danon's disease as a cause of hypertrophic cardiomyopathy: a systematic survey. Issue 8 (14th July 2004) Authors: Charron, P; Villard, E; Sébillon, P; Laforêt, P; Maisonobe, T; Duboscq-Bidot, L; Romero, N; Drouin-Garraud, V; Frébourg, T; Richard, P; Eymard, B; Komajda, M Journal: Heart Issue: Volume 90:Issue 8(2004) Page Start: 842 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Epidemiology of transthyretin amyloid cardiomyopathy (ATTR-CM) in France, a study based on the systeme national des donnees de sante (SNDS) the French nationwide claims database. (14th October 2021) Authors: Damy, T; Bourel, G; Slama, M; Algalarrondo, V; Lairez, O; Pelcot, F; Durand-Zaleski, I; Lilliu, H; Bartoli, M; Fievez, S; Granghaud, A; Rudant, J; De Neuville, B; Rault, C; Charron, P Journal: European heart journal Issue: Volume 42(2021)Supplement 1 Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Expanding the phenotype of LMNA mutations in dilated cardiomyopathy and functional consequences of these mutations. Issue 8 (14th August 2003) Authors: Sébillon, P; Bouchier, C; Bidot, L D; Bonne, G; Ahamed, K; Charron, P; Drouin-Garraud, V; Millaire, A; Desrumeaux, G; Benaïche, A; Charniot, J-C; Schwartz, K; Villard, E; Komajda, M Journal: Journal of medical genetics Issue: Volume 40:Issue 8(2003) Page Start: 560 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Genetic counselling and testing of adult patients with cardiomyopathies: insight from the EORP cardiomyopathy and myocarditis registry of the European Society of Cardiology. (25th November 2020) Authors: Helio, T; Elliott, P; Koskenvuo, J.W; Gimeno, J.G; Tavazzi, L; Tendera, M; Kaski, P; Maggioni, A; Laroche, C; Caforio, A.L.P; Charron, P Journal: European heart journal Issue: Volume 41:(2020)Supplement 2 Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Genetic testing and genetic counselling in hypertrophic cardiomyopathy: the French experience. Issue 10 (1st October 2002) Authors: Charron, P; Héron, D; Gargiulo, M; Richard, P; Dubourg, O; Desnos, M; Bouhour, J-B; Feingold, J; Carrier, L; Hainque, B; Schwartz, K; Komajda, M Other Names: group-author. Journal: Journal of medical genetics Issue: Volume 39:Issue 10(2002) Page Start: 741 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Genome wide association analysis in dilated cardiomyopathy revealed two new susceptibility loci for systolic heart failure. (25th November 2020) Authors: Garnier, S; Harakalova, M; Weiss, S; Mokry, M; Van Setten, J; Proust, C; Duboscq-Bidot, L; Boland, A; Deleuze, J.-F; Dorr, M; Asselbergs, F.-W; Cambien, F; Villard, E; Tregouet, D.-A; Charron, P Journal: European heart journal Issue: Volume 41:(2020)Supplement 2 Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. High prevalence of familial and genetic disease in children with cardiomyopathies: baseline paediatric data from the ESC EORP Cardiomyopathy and Myocarditis registry. (25th November 2020) Authors: Kaski, J.P; Maggioni, A.G; Charron, P; Elliott, P.M; Gimeno, J.R; Laroche, C; Tavazzi, L; Tendera, M; Caforio, A Journal: European heart journal Issue: Volume 41:(2020)Supplement 2 Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Hypertrophic cardiomyopathy and atrial fibrillation: the Cardiomyopathy/Myocarditis registry of the EURObservational Research Programme of the European Society of Cardiology. (3rd October 2022) Authors: Mizia-Stec, K; Gimeno Blanes, J R G; Charron, P; Elliott, P; Kaski, J P; Maggioni, A L; Tavazzi, L; Tendera, M; Wybraniec, M T; Caforio, A Journal: European heart journal Issue: Volume 43(2022)Supplement 2 Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗