Výsledky vyhledávání - "J B, Bouhour"

Genetic testing and genetic counselling in hypertrophic cardiomyopathy: the French experience

Autor: P, Charron, D, Héron, M, Gargiulo, P, Richard, O, Dubourg, M, Desnos, J B, Bouhour, J, Feingold, L, Carrier, B, Hainque, K, Schwartz, M, Komajda

Publikováno v: Journal of Medical Genetics. 39:741-746

A major breakthrough in the molecular genetics of hypertrophic cardiomyopathy (HCM) has made genetic testing now available in clinical practice, raising new questions about its implications, potential benefits, and the organisation of the procedure.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1c2f3ea662a6c5dbb677844793b7a4f3
https://doi.org/10.1136/jmg.39.10.741

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Relation between QT duration and maximal wall thickness in familial hypertrophic cardiomyopathy

Autor: X, Jouven, A, Hagege, P, Charron, L, Carrier, O, Dubourg, J M, Langlard, S, Aliaga, J B, Bouhour, K, Schwartz, M, Desnos, M, Komajda

Publikováno v: Heart. 88:153-157

Background: QT abnormalities have been reported in left ventricular hypertrophy and hypertrophic cardiomyopathy. Objective: To determine the relation between left ventricular hypertrophy and increased QT interval in familial hypertrophic cardiomyopat

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c2fc48f2e1cb5f75b65c2d3a35455d84
https://doi.org/10.1136/heart.88.2.153

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Ambulatory heart failure management in private practice in France

Autor: J.-B. Bouhour, E. Rougemond, F. Delahaye, E. Leutenegger, I. Croce, E. Vicaut, Philippe Amouyel, F. Vuittenez, Michel Komajda

Publikováno v: European Journal of Heart Failure. 3:503-507

Management of ambulatory heart failure was assessed in a group of 600 patients, mean age 73, 64% males, NYHA I: 9%; II: 52%; III: 33%; IV: 6%; followed up by a representative sample of private cardiologists. Fifty-two percent of patients had been pre

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d85b2781f0acb68bb27ce09879966ab2
https://doi.org/10.1016/s1388-9842(01)00172-6

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Identification of a genetic risk factor for idiopathic dilated cardiomyopathy. Involvement of a polymorphism in the endothelin receptor type A gene

Publikováno v: European Heart Journal. 20:1587-1591

Background Idiopathic dilated cardiomyopathy is a frequent cause of heart failure, a major concern of public health. Although idiopathic dilated cardiomyopathy may be familial, most cases are sporadic and the disease is considered to be multifactoria

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::97624af29f51aed857eb2e9e80e7c7ba
https://doi.org/10.1053/euhj.1999.1696

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Diagnostic value of electrocardiography and echocardiography for familial hypertrophic cardiomyopathy in genotyped children

Autor: P, Charron, O, Dubourg, M, Desnos, J B, Bouhour, R, Isnard, A, Hagege, L, Carrier, G, Bonne, F, Tesson, P, Richard, B, Hainque, K, Schwartz, M, Komajda

Publikováno v: European Heart Journal. 19:1377-1382

The aim of the study was to evaluate electrocardiography and echocardiography in the diagnosis of familial hypertrophic cardiomyopathy in children, using the genetic status as the criterion of reference.We analysed 35 children (18 years) from 13 fami

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::02d02319fe0a81f593a02925795f76be
https://doi.org/10.1053/euhj.1998.1049

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Genotype–phenotype correlations in familial hypertrophic cardiomyopathy A comparison between mutations in the cardiac protein-C and the beta-myosin heavy chain genes

Autor: P, Charron, O, Dubourg, M, Desnos, R, Isnard, A, Hagege, G, Bonne, L, Carrier, F, Tesson, J B, Bouhour, J C, Buzzi, J, Feingold, K, Schwartz, M, Komajda

Publikováno v: European Heart Journal. 19:139-145

Background The gene involved in familial hypertrophic cardiomyopathy on chromosome 11 was recently identified as the cardiac myosin binding protein-C (MyBP-C) gene. The phenotype of two families associated with mutation in this gene is described here

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6d1f02a89b9c4a76cb71d91abc212da3
https://doi.org/10.1053/euhj.1997.0575

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Factors predicting mortality in idiopathic dilated cardiomyopathy

Autor: J. B. Bouhour, Y. Juillieres, Jean-Philippe Jais, Y. Grosgogeat, Lanfranchi J, B. Goldfarb, Michel Komajda, Ph. Geslin, Didier Carrié, P. Peycelon, F. Reeves

Publikováno v: European Heart Journal. 11:824-831

A study of factors predicting mortality was performed in 201 patients with dilated cardiomyopathy (163 men, 38 women, mean age: 48 +/- 11 years) by multivariate analysis (Cox Model) of 51 clinical, electrocardiographic, echocardiographic and haemodyn

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c7c4c715029edb667c08fd1f83be6013
https://doi.org/10.1093/oxfordjournals.eurheartj.a059803

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Accuracy of European diagnostic criteria for familial hypertrophic cardiomyopathy in a genotyped population

Autor: Olivier Dubourg, Richard Isnard, Michel Komajda, Jean-François Forissier, Albert A. Hagège, Michel Desnos, J B Bouhour, Philippe Charron, P. Richard, Amara Me, Ketty Schwartz, A. Benaiche

Publikováno v: International journal of cardiology. 90(1)

Background: Since the sensitivity of conventional diagnostic criteria for familial hypertrophic cardiomyopathy (HCM) is low, new diagnostic criteria were proposed by a European collaboration. However, their diagnostic value remains unknown. The aim o

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d41caf6cd0b07f907bab756020da4b31
https://pubmed.ncbi.nlm.nih.gov/12821216

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