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Results: 1-25 | 26-26
Results: 1-25/26
CARDIAC MYOSIN-BINDING PROTEIN-C AND HYPERTROPHIC CARDIOMYOPATHY
Authors: CARRIER L BONNE G SCHWARTZ K
Citation: L. Carrier et al., CARDIAC MYOSIN-BINDING PROTEIN-C AND HYPERTROPHIC CARDIOMYOPATHY, Trends in cardiovascular medicine, 8(4), 1998, pp. 151-157
IDENTIFICATION OF 2 NOVEL MUTATIONS IN THE VENTRICULAR REGULATORY MYOSIN LIGHT-CHAIN GENE (MYL2) ASSOCIATED WITH FAMILIAL AND CLASSICAL FORMS OF HYPERTROPHIC CARDIOMYOPATHY
Authors: FLAVIGNY J RICHARD P ISNARD R CARRIER L CHARRON P BONNE G FORISSIER JF DESNOS M DUBOURG O KOMAJDA M SCHWARTZ K HAINQUE B
Citation: J. Flavigny et al., IDENTIFICATION OF 2 NOVEL MUTATIONS IN THE VENTRICULAR REGULATORY MYOSIN LIGHT-CHAIN GENE (MYL2) ASSOCIATED WITH FAMILIAL AND CLASSICAL FORMS OF HYPERTROPHIC CARDIOMYOPATHY, Journal of molecular medicine, 76(3-4), 1998, pp. 208-214
GENETICS OF FAMILIAR HYPERTROPHIC CARDIOMYOPATHY
Authors: BONNE G CARRIER L RICHARD P HAINQUE B TESSON F KOMAJDA M SCHWARTZ K
Citation: G. Bonne et al., GENETICS OF FAMILIAR HYPERTROPHIC CARDIOMYOPATHY, MS. Medecine sciences, 14(10), 1998, pp. 1054-1066
DIAGNOSTIC-VALUE OF ELECTROCARDIOGRAPHY AND ECHOCARDIOGRAPHY FOR FAMILIAL HYPERTROPHIC CARDIOMYOPATHY IN GENOTYPED CHILDREN
Authors: CHARRON P DUBOURG O DESNOS M BOUHOUR JB ISNARD R HAGEGE A CARRIER L BONNE G TESSON F RICHARD P HAINQUE B SCHWARTZ K KOMAJDA M
Citation: P. Charron et al., DIAGNOSTIC-VALUE OF ELECTROCARDIOGRAPHY AND ECHOCARDIOGRAPHY FOR FAMILIAL HYPERTROPHIC CARDIOMYOPATHY IN GENOTYPED CHILDREN, European heart journal, 19(9), 1998, pp. 1377-1382
FAMILIAL HYPERTROPHIC CARDIOMYOPATHY - CARDIAC ULTRASONIC ABNORMALITIES IN GENETICALLY AFFECTED SUBJECTS WITHOUT ECHOCARDIOGRAPHIC EVIDENCEOF LEFT-VENTRICULAR HYPERTROPHY
Authors: HAGEGE AA DUBOURG O DESNOS M MIROCHNIK R ISNARD G BONNE G CARRIER L GUICHENEY P BOUHOUR JB SCHWARTZ K KOMAJDA M
Citation: Aa. Hagege et al., FAMILIAL HYPERTROPHIC CARDIOMYOPATHY - CARDIAC ULTRASONIC ABNORMALITIES IN GENETICALLY AFFECTED SUBJECTS WITHOUT ECHOCARDIOGRAPHIC EVIDENCEOF LEFT-VENTRICULAR HYPERTROPHY, European heart journal, 19(3), 1998, pp. 490-499
GENOTYPE-PHENOTYPE CORRELATIONS IN FAMILIAL HYPERTROPHIC CARDIOMYOPATHY - A COMPARISON BETWEEN MUTATIONS IN THE CARDIAC PROTEIN-C AND THE BETA-MYOSIN HEAVY-CHAIN GENES
Authors: CHARRON P DUBOURG O DESNOS M ISNARD R HAGEGE A BONNE G CARRIER L TESSON F BOUHOUR JB BUZZI JC FEINGOLD J SCHWARTZ K KOMAJDA M
Citation: P. Charron et al., GENOTYPE-PHENOTYPE CORRELATIONS IN FAMILIAL HYPERTROPHIC CARDIOMYOPATHY - A COMPARISON BETWEEN MUTATIONS IN THE CARDIAC PROTEIN-C AND THE BETA-MYOSIN HEAVY-CHAIN GENES, European heart journal, 19(1), 1998, pp. 139-145
FAMILIAL HYPERTROPHIC CARDIOMYOPATHY FROM MUTATIONS TO FUNCTIONAL DEFECTS
Authors: BONNE G CARRIER L RICHARD P HAINQUE B SCHWARTZ K
Citation: G. Bonne et al., FAMILIAL HYPERTROPHIC CARDIOMYOPATHY FROM MUTATIONS TO FUNCTIONAL DEFECTS, Circulation research, 83(6), 1998, pp. 580-593
IMPACT OF C-TERMINAL TRUNCATION OF HUMAN CARDIAC MYOSIN BINDING-PROTEIN C ON MYOSIN FILAMENT ORGANIZATION
Authors: SEBILLION P BONNE G FLAVIGNY J VENIN S WISNEWSKY C VIKSTROM K LEINWAND L CARRIER L SCHWARTZ K
Citation: P. Sebillion et al., IMPACT OF C-TERMINAL TRUNCATION OF HUMAN CARDIAC MYOSIN BINDING-PROTEIN C ON MYOSIN FILAMENT ORGANIZATION, Circulation, 98(17), 1998, pp. 1219-1219
CLINICAL PRESENTATION AND GENETIC LOCALIZATION OF A NEW FORM OF AUTOSOMAL-DOMINANT DILATED CARDIOMYOPATHY
Authors: DUBOC D BONNE G BECANE HM DIBARLETTA MR VARNOUS S ELHADI H URTIZBEREA JA TONIOLO D FARDEAU M SCHWARTZ K
Citation: D. Duboc et al., CLINICAL PRESENTATION AND GENETIC LOCALIZATION OF A NEW FORM OF AUTOSOMAL-DOMINANT DILATED CARDIOMYOPATHY, Circulation, 98(17), 1998, pp. 1552-1552
CLINICAL-FEATURES AND PROGNOSTIC IMPLICATIONS OF FAMILIAL HYPERTROPHIC CARDIOMYOPATHY RELATED TO THE CARDIAC MYOSIN-BINDING PROTEIN-C GENE
Authors: CHARRON P DUBOURG O DESNOS M BENNACEUR M CARRIER L CAMPROUX AC ISNARD R HAGEGE A LANGLARD JM BONNE G RICHARD P HAINQUE B BOUHOUR JB SCHWARTZ K KOMAJDA M
Citation: P. Charron et al., CLINICAL-FEATURES AND PROGNOSTIC IMPLICATIONS OF FAMILIAL HYPERTROPHIC CARDIOMYOPATHY RELATED TO THE CARDIAC MYOSIN-BINDING PROTEIN-C GENE, Circulation, 97(22), 1998, pp. 2230-2236
ORGANIZATION AND SEQUENCE OF HUMAN CARDIAC MYOSIN-BINDING-PROTEIN-C GENE (MYBPC3) AND IDENTIFICATION OF MUTATIONS PREDICTED TO PRODUCE TRUNCATED PROTEINS IN FAMILIAL HYPERTROPHIC CARDIOMYOPATHY
Authors: CARRIER L BONNE G BAHREND E YU B RICHARD P NIEL F HAINQUE B CRUAUD C GARY F LABEIT S BOUHOUR JB DUBOURG O DESNOS M HAGEGE AA TRENT RJ KOMAJDA M FISZMAN M SCHWARTZ K
Citation: L. Carrier et al., ORGANIZATION AND SEQUENCE OF HUMAN CARDIAC MYOSIN-BINDING-PROTEIN-C GENE (MYBPC3) AND IDENTIFICATION OF MUTATIONS PREDICTED TO PRODUCE TRUNCATED PROTEINS IN FAMILIAL HYPERTROPHIC CARDIOMYOPATHY, Circulation research, 80(3), 1997, pp. 427-434
THE ONSET OF THE DISEASE IS DELAYED IN FAMILIAL HYPERTROPHIC CARDIOMYOPATHY RELATED TO CARDIAC MYOSIN-BINDING-PROTEIN-C GENE
Authors: CHARRON P CARRIER L BONNE G BENNACEUR M DUBOURG O ISNARD R HAGEGE A DESNOS M BOUHOUR JB SCHWARTZ K KOMAJDA M
Citation: P. Charron et al., THE ONSET OF THE DISEASE IS DELAYED IN FAMILIAL HYPERTROPHIC CARDIOMYOPATHY RELATED TO CARDIAC MYOSIN-BINDING-PROTEIN-C GENE, Circulation, 96(8), 1997, pp. 3612-3612
DIAGNOSTIC-VALUE OF ELECTROCARDIOGRAPHY AND ECHOCARDIOGRAPHY FOR FAMILIAL HYPERTROPHIC CARDIOMYOPATHY IN A GENOTYPED ADULT-POPULATION
Authors: CHARRON P DUBOURG O DESNOS M ISNARD R HAGEGE A MILLAIRE A CARRIER L BONNE G TESSON F RICHARD P BOUHOUR JB SCHWARTZ K KOMAJDA M
Citation: P. Charron et al., DIAGNOSTIC-VALUE OF ELECTROCARDIOGRAPHY AND ECHOCARDIOGRAPHY FOR FAMILIAL HYPERTROPHIC CARDIOMYOPATHY IN A GENOTYPED ADULT-POPULATION, Circulation, 96(1), 1997, pp. 214-219
FAMILIAL HYPERTROPHIC CARDIOMYOPATHY - ULTRASONIC ABNORMALITIES IN GENETICALLY AFFECTED SUBJECTS WITHOUT ECHOCARDIOGRAPHIC EVIDENCE OF LEFT-VENTRICULAR HYPERTROPHY
Authors: HAGEGE AA DUBOURG O DESNOS M BESSE B BONNE G CARRIER L ISNARD R GUICHENEY P BOUHOUR JB SCHWARTZ K KOMAJDA M
Citation: Aa. Hagege et al., FAMILIAL HYPERTROPHIC CARDIOMYOPATHY - ULTRASONIC ABNORMALITIES IN GENETICALLY AFFECTED SUBJECTS WITHOUT ECHOCARDIOGRAPHIC EVIDENCE OF LEFT-VENTRICULAR HYPERTROPHY, Circulation, 94(8), 1996, pp. 478-478
ECHOCARDIOGRAPHIC SCREENING IN FAMILIAL HYPERTROPHIC CARDIOMYOPATHY -INFLUENCE OF AGE AND HEIGHT ON THE INTEREST OF WALL THICKNESS MEASUREMENT
Authors: HAGEGE AA DUBOURG O MARIE FN DESNOS M ISNARD R CARRIER LI BONNE G SCHWARTZ K KOMAJDA M
Citation: Aa. Hagege et al., ECHOCARDIOGRAPHIC SCREENING IN FAMILIAL HYPERTROPHIC CARDIOMYOPATHY -INFLUENCE OF AGE AND HEIGHT ON THE INTEREST OF WALL THICKNESS MEASUREMENT, Circulation, 94(8), 1996, pp. 1578-1578
2 NEW MUTATIONS IN THE CARDIAC C-PROTEIN GENE ASSOCIATED WITH FAMILIAL HYPERTROPHIC CARDIOMYOPATHY ARE PREDICTED TO PRODUCE TRUNCATED PROTEINS
Authors: CARRIER L BAHREND E BONNE G RICHARD P GAUTEL M LABEIT S KOMAJDA M SCHWARTZ K
Citation: L. Carrier et al., 2 NEW MUTATIONS IN THE CARDIAC C-PROTEIN GENE ASSOCIATED WITH FAMILIAL HYPERTROPHIC CARDIOMYOPATHY ARE PREDICTED TO PRODUCE TRUNCATED PROTEINS, Circulation, 94(8), 1996, pp. 2488-2488
CODON-102 OF THE CARDIAC TROPONIN-T GENE IS A PUTATIVE HOT-SPOT FOR MUTATIONS IN FAMILIAL HYPERTROPHIC CARDIOMYOPATHY
Authors: FORISSIER JF CARRIER L FARZA H BONNE G BERCOVICI J RICHARD P HAINQUE B TOWNSEND PJ YACOUB MH FAURE S DUBOURG O MILLAIRE A HAGEGE AA DESNOS M KOMAJDA M SCHWARTZ K
Citation: Jf. Forissier et al., CODON-102 OF THE CARDIAC TROPONIN-T GENE IS A PUTATIVE HOT-SPOT FOR MUTATIONS IN FAMILIAL HYPERTROPHIC CARDIOMYOPATHY, Circulation, 94(12), 1996, pp. 3069-3073
MUSCLE P-31-NMR IN A MITOCHONDRIAL ENCEPHALOMYELOPATHY DUE TO A SPECIFIC DEFECT IN PYRUVATE-DEHYDROGENASE
Authors: JEHENSON P MARSAC C DUBOC D STANSBIE D BONNE G COUSIN J BENELLI C LEROUX JP LINDSAY G SYROTA A
Citation: P. Jehenson et al., MUSCLE P-31-NMR IN A MITOCHONDRIAL ENCEPHALOMYELOPATHY DUE TO A SPECIFIC DEFECT IN PYRUVATE-DEHYDROGENASE, Journal de chimie physique et de physico-chimie biologique, 92(10), 1995, pp. 1801-1805
CARDIAC MYOSIN BINDING PROTEIN-C GENE SPLICE ACCEPTOR SITE MUTATION IS ASSOCIATED WITH FAMILIAL HYPERTROPHIC CARDIOMYOPATHY
Authors: BONNE G CARRIER L BERCOVICI J CRUAUD C RICHARD P HAINQUE B GAUTEL M LABEIT S JAMES M BECKMANN J WEISSENBACH J VOSBERG HP FISZMAN M KOMAJDA M SCHWARTZ K
Citation: G. Bonne et al., CARDIAC MYOSIN BINDING PROTEIN-C GENE SPLICE ACCEPTOR SITE MUTATION IS ASSOCIATED WITH FAMILIAL HYPERTROPHIC CARDIOMYOPATHY, Nature genetics, 11(4), 1995, pp. 438-440
INVOLVEMENT OF C-PROTEIN IN CARDIAC CONTR ACTION UNDER FOCUS
Authors: BONNE G CARRIER L SCHWARTZ K
Citation: G. Bonne et al., INVOLVEMENT OF C-PROTEIN IN CARDIAC CONTR ACTION UNDER FOCUS, MS. Medecine sciences, 11(12), 1995, pp. 1739-1741
THE COX8 GENE IS NOT THE DISEASE GENE OF THE CMH4 LOCUS IN FAMILIAL HYPERTROPHIC CARDIOMYOPATHY
Authors: BONNE G CARRIER L SCHWARTZ K KOMAJDA M
Citation: G. Bonne et al., THE COX8 GENE IS NOT THE DISEASE GENE OF THE CMH4 LOCUS IN FAMILIAL HYPERTROPHIC CARDIOMYOPATHY, Journal of Medical Genetics, 32(8), 1995, pp. 670-671
DISTRIBUTION OF DISEASE LOCI IN 28 FRENCH FAMILIES WITH FAMILIAL HYPERTROPHIC CARDIOMYOPATHY
Authors: CARRIER L RICHARD P BONNE G BERCOVICI J TESSON F LAUTIE N FORISSIER JF HAINQUE F BENNACEUR F GUICHENEY P KOMAJDA M SCHWARTZ K
Citation: L. Carrier et al., DISTRIBUTION OF DISEASE LOCI IN 28 FRENCH FAMILIES WITH FAMILIAL HYPERTROPHIC CARDIOMYOPATHY, Circulation, 92(8), 1995, pp. 1106-1106
EXPRESSION OF CYTOCHROME-C-OXIDASE SUBUNITS ENCODED BY MITOCHONDRIAL OR NUCLEAR-DNA IN THE MUSCLE OF PATIENTS WITH ZIDOVUDINE MYOPATHY
Authors: CHARIOT P BONNE G AUTHIER FJ MARSAC C GHERARDI R
Citation: P. Chariot et al., EXPRESSION OF CYTOCHROME-C-OXIDASE SUBUNITS ENCODED BY MITOCHONDRIAL OR NUCLEAR-DNA IN THE MUSCLE OF PATIENTS WITH ZIDOVUDINE MYOPATHY, Journal of the neurological sciences, 125(2), 1994, pp. 190-193
DEFECTS OF THE HUMAN MITOCHONDRIAL GENOME
Authors: SEIBEL P JANETZKY B VILLANI G BONNE G NAUMANN M MARSAC C PAPA S REICHMANN H
Citation: P. Seibel et al., DEFECTS OF THE HUMAN MITOCHONDRIAL GENOME, Journal of muscle research and cell motility, 14(2), 1993, pp. 261-261
DEFECT IN THE LIPOYL-BEARING PROTEIN-X SUBUNIT OF THE PYRUVATE-DEHYDROGENASE COMPLEX IN 2 PATIENTS WITH ENCEPHALOMYELOPATHY
Authors: MARSAC C STANSBIE D BONNE G COUSIN J JEHENSON P BENELLI C LEROUX JP LINDSAY G
Citation: C. Marsac et al., DEFECT IN THE LIPOYL-BEARING PROTEIN-X SUBUNIT OF THE PYRUVATE-DEHYDROGENASE COMPLEX IN 2 PATIENTS WITH ENCEPHALOMYELOPATHY, The Journal of pediatrics, 123(6), 1993, pp. 915-920
Risultati: 1-25 | 26-26