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Results: 1-18 |
Results: 18
How will the human genome project change cardiovascular medicine?
Authors: Komajda, M Charron, P
Citation: M. Komajda et P. Charron, How will the human genome project change cardiovascular medicine?, HEART, 86(2), 2001, pp. 123-124
The heart of genomics
Authors: Komajda, M Charron, P
Citation: M. Komajda et P. Charron, The heart of genomics, NAT MED, 7(3), 2001, pp. 287-288
Are we ready for pharmacogenomics in heart failure?
Authors: Charron, P Komajda, M
Citation: P. Charron et M. Komajda, Are we ready for pharmacogenomics in heart failure?, EUR J PHARM, 417(1-2), 2001, pp. 1-9
Between France and Flanders: Manuscript illumination in Amiens in the fifteen century
Authors: Charron, P
Citation: P. Charron, Between France and Flanders: Manuscript illumination in Amiens in the fifteen century, BURLINGTON, 143(1176), 2001, pp. 164-165
A new locus for autosomal dominant dilated cardiomyopathy identified on chromosome 6q12-q14
Authors: Sylvius, N Tesson, F Gayet, C Charron, P Benaiche, A Mangin, L Peuchmaurd, M Duboscq-Bidot, L Feingold, J Beckmann, JS Bouchier, C Komajda, M
Citation: N. Sylvius et al., A new locus for autosomal dominant dilated cardiomyopathy identified on chromosome 6q12-q14, AM J HU GEN, 68(1), 2001, pp. 241-246
Epidemiology of desmin and cardiac actin gene mutations in a European population of dilated cardiomyopathy
Authors: Tesson, F Sylvius, N Pilotto, A Dubosq-Bidot, L Peuchmaurd, M Bouchier, C Benaiche, A Mangin, L Charron, P Gavazzi, A Tavazzi, L Arbustini, E Komajda, M
Citation: F. Tesson et al., Epidemiology of desmin and cardiac actin gene mutations in a European population of dilated cardiomyopathy, EUR HEART J, 21(22), 2000, pp. 1872-1876
Painters, stained glass artists and illuminators in Lille at the beginningof the 16th century as seen through the unpublished statutes of their corporation
Authors: Charron, P
Citation: P. Charron, Painters, stained glass artists and illuminators in Lille at the beginningof the 16th century as seen through the unpublished statutes of their corporation, REV NORD, 82(337), 2000, pp. 723-738
Homozygotes for a R869G mutation in the beta-myosin heavy chain gene have a severe form of familial hypertrophic cardiomyopathy
Authors: Richard, P Charron, P Leclercq, C Ledeuil, C Carrier, L Dubourg, O Desnos, M Bouhour, JB Schwartz, K Daubert, JC Komajda, M Hainque, B
Citation: P. Richard et al., Homozygotes for a R869G mutation in the beta-myosin heavy chain gene have a severe form of familial hypertrophic cardiomyopathy, J MOL CEL C, 32(8), 2000, pp. 1575-1583
Familial dilated cardiomyopathy: clinical features in French families
Authors: Mangin, L Charron, P Tesson, F Mallet, A Dubourg, O Desnos, M Benaische, A Gayet, C Gibelin, P Davy, JM Bonnet, J Sidi, D Schwartz, K Komajda, M
Citation: L. Mangin et al., Familial dilated cardiomyopathy: clinical features in French families, EUR J HE FA, 1(4), 1999, pp. 353-361
Genetic aspects of heart failure
Authors: Komajda, M Charron, P Tesson, F
Citation: M. Komajda et al., Genetic aspects of heart failure, EUR J HE FA, 1(2), 1999, pp. 121-126
Genetics of dilated cardiomyopathy
Authors: Tesson, F Charron, P Schwartz, K Komajda, M
Citation: F. Tesson et al., Genetics of dilated cardiomyopathy, M S-MED SCI, 15(3), 1999, pp. 369-375
Screening for familial hypertrophic cardiomyopathy using brain natriureticpeptide - Reply
Authors: Charron, P Komajda, M
Citation: P. Charron et M. Komajda, Screening for familial hypertrophic cardiomyopathy using brain natriureticpeptide - Reply, EUR HEART J, 20(7), 1999, pp. 550-550
Identification of a genetic risk factor for idiopathic dilated cardiomyopathy - Involvement of a polymorphism in the endothelin receptor type A gene
Authors: Charron, P Tesson, F Poirier, O Nicaud, V Peuchmaurd, M Tiret, L Cambien, F Amouyel, P Dubourg, O Bouhour, JB Millaire, A Juilliere, Y Bareiss, P Andre-Fouet, X Pouillart, F Arveiler, D Ferrieres, J Dorent, R Roizes, G Schwartz, K Desnos, M Komajda, M
Citation: P. Charron et al., Identification of a genetic risk factor for idiopathic dilated cardiomyopathy - Involvement of a polymorphism in the endothelin receptor type A gene, EUR HEART J, 20(21), 1999, pp. 1587-1591
Guidelines for the study of familial dilated cardiomyopathies
Authors: Mestroni, L Maisch, B McKenna, WJ Schwartz, K Charron, P Rocco, C Tesson, F Richter, A Wilke, A Komajda, M
Citation: L. Mestroni et al., Guidelines for the study of familial dilated cardiomyopathies, EUR HEART J, 20(2), 1999, pp. 93-102
Characterization of a unique genetic variant in the beta(1)-adrenooeptor gene and evaluation of its role in idiopathic dilated cardiomyopathy
Authors: Tesson, F Charron, P Peuchmaurd, M Nicaud, V Cambien, F Tiret, L Poirier, O Desnos, M Jullieres, Y Amouyel, P Roizes, G Dorent, R Schwartz, K Komajda, M
Citation: F. Tesson et al., Characterization of a unique genetic variant in the beta(1)-adrenooeptor gene and evaluation of its role in idiopathic dilated cardiomyopathy, J MOL CEL C, 31(5), 1999, pp. 1025-1032
Double heterozygosity for mutations in the beta-myosin heavy chain and in the cardiac myosin binding protein C genes in a family with hypertrophic cardiomyopathy
Authors: Richard, P Isnard, R Carrier, L Dubourg, O Donatien, Y Mathieu, B Bonne, G Gary, F Charron, P Hagege, A Komajda, M Schwartz, K Hainque, B
Citation: P. Richard et al., Double heterozygosity for mutations in the beta-myosin heavy chain and in the cardiac myosin binding protein C genes in a family with hypertrophic cardiomyopathy, J MED GENET, 36(7), 1999, pp. 542-545
Clinical expression in patients with hypertrophic cardiomyopathy caused bycardiac myosin-binding protein C gene mutation - Response
Authors: Charron, P Bennaceur, M Isnard, R Komajda, M Carrier, L Bonne, G Schwartz, K Camproux, AC Richard, P Hainque, B Dubourg, O Desnos, M Hagege, A Langlard, JM Bouhour, JB
Citation: P. Charron et al., Clinical expression in patients with hypertrophic cardiomyopathy caused bycardiac myosin-binding protein C gene mutation - Response, CIRCULATION, 100(4), 1999, pp. 449-449
Diagnosis of hypertrophic cardiomyopathy: Validation of criteria by genetics.
Authors: Charron, P
Citation: P. Charron, Diagnosis of hypertrophic cardiomyopathy: Validation of criteria by genetics., ARCH MAL C, 91(12), 1998, pp. 65-68
Risultati: 1-18 |