Richard P - Search Results

1

Contribution of exome sequencing for genetic diagnostic in arrhythmogenic right ventricular cardiomyopathy/dysplasia.

Fedida J, Fressart V, Charron P, Surget E, Hery T, Richard P, Donal E, Keren B, Duthoit G, Hidden-Lucet F, Villard E, Gandjbakhch E. Fedida J, et al. Among authors: richard p. PLoS One. 2017 Aug 2;12(8):e0181840. doi: 10.1371/journal.pone.0181840. eCollection 2017. PLoS One. 2017. PMID: 28767663 Free PMC article.

2

Hypertrophic cardiomyopathy: distribution of disease genes, spectrum of mutations, and implications for a molecular diagnosis strategy.

Richard P, Charron P, Carrier L, Ledeuil C, Cheav T, Pichereau C, Benaiche A, Isnard R, Dubourg O, Burban M, Gueffet JP, Millaire A, Desnos M, Schwartz K, Hainque B, Komajda M; EUROGENE Heart Failure Project. Richard P, et al. Circulation. 2003 May 6;107(17):2227-32. doi: 10.1161/01.CIR.0000066323.15244.54. Epub 2003 Apr 21. Circulation. 2003. PMID: 12707239

3

Prenatal molecular diagnosis in hypertrophic cardiomyopathy: report of the first case.

Charron P, Héron D, Gargiulo M, Feingold J, Oury JF, Richard P, Komajda M. Charron P, et al. Among authors: richard p. Prenat Diagn. 2004 Sep;24(9):701-3. doi: 10.1002/pd.969. Prenat Diagn. 2004. PMID: 15386449

4

Diagnostic accuracy of a 2D left ventricle hypertrophy score for familial hypertrophic cardiomyopathy.

Forissier JF, Charron P, Tezenas du Montcel S, Hagège A, Isnard R, Carrier L, Richard P, Desnos M, Bouhour JB, Schwartz K, Komajda M, Dubourg O. Forissier JF, et al. Among authors: richard p. Eur Heart J. 2005 Sep;26(18):1882-6. doi: 10.1093/eurheartj/ehi276. Epub 2005 Apr 28. Eur Heart J. 2005. PMID: 15860513

5

A familial form of conduction defect related to a mutation in the PRKAG2 gene.

Charron P, Genest M, Richard P, Komajda M, Pochmalicki G. Charron P, et al. Among authors: richard p. Europace. 2007 Aug;9(8):597-600. doi: 10.1093/europace/eum071. Epub 2007 May 4. Europace. 2007. PMID: 17483151

6

Early identification of mutation carriers in familial hypertrophic cardiomyopathy by combined echocardiography and tissue Doppler imaging.

Gandjbakhch E, Gackowski A, Tezenas du Montcel S, Isnard R, Hamroun A, Richard P, Komajda M, Charron P. Gandjbakhch E, et al. Among authors: richard p. Eur Heart J. 2010 Jul;31(13):1599-607. doi: 10.1093/eurheartj/ehq101. Epub 2010 May 3. Eur Heart J. 2010. PMID: 20439259

7

High cardiovascular morbidity and mortality in myofibrillar myopathies due to DES gene mutations: a 10-year longitudinal study.

Wahbi K, Béhin A, Charron P, Dunand M, Richard P, Meune C, Vicart P, Laforêt P, Stojkovic T, Bécane HM, Kuntzer T, Duboc D. Wahbi K, et al. Among authors: richard p. Neuromuscul Disord. 2012 Mar;22(3):211-8. doi: 10.1016/j.nmd.2011.10.019. Epub 2011 Dec 5. Neuromuscul Disord. 2012. PMID: 22153487 Free article.

8

Advising a cardiac disease gene positive yet phenotype negative or borderline abnormal athlete: is sporting disqualification really necessary?

Richard P, Denjoy I, Fressart V, Wilson MG, Carré F, Charron P. Richard P, et al. Br J Sports Med. 2012 Nov;46 Suppl 1:i59-68. doi: 10.1136/bjsports-2012-091318. Br J Sports Med. 2012. PMID: 23097481 Free article. Review.

9

A novel genetic variant in the transcription factor Islet-1 exerts gain of function on myocyte enhancer factor 2C promoter activity.

Friedrich FW, Dilanian G, Khattar P, Juhr D, Gueneau L, Charron P, Fressart V, Vilquin JT, Isnard R, Gouya L, Richard P, Hammoudi N, Komajda M, Bonne G, Eschenhagen T, Dubourg O, Villard E, Carrier L. Friedrich FW, et al. Among authors: richard p. Eur J Heart Fail. 2013 Mar;15(3):267-76. doi: 10.1093/eurjhf/hfs178. Epub 2012 Nov 14. Eur J Heart Fail. 2013. PMID: 23152444 Free article.

10

Genetic advances in sarcomeric cardiomyopathies: state of the art.

Ho CY, Charron P, Richard P, Girolami F, Van Spaendonck-Zwarts KY, Pinto Y. Ho CY, et al. Among authors: richard p. Cardiovasc Res. 2015 Apr 1;105(4):397-408. doi: 10.1093/cvr/cvv025. Epub 2015 Jan 29. Cardiovasc Res. 2015. PMID: 25634555 Free PMC article. Review.

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