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Results: 1-14 |
Results: 14

Authors: NEYROUD N MAISONBLANCHE P DENJOY I CHEVRET S DONGER C DAUSSE E FAYN J BADILINI F MENHABI N SCHWARTZ K GUICHENEY P COUMEL P
Citation: N. Neyroud et al., DIAGNOSTIC PERFORMANCE OF QT INTERVAL VARIABLES FROM 24-H ELECTROCARDIOGRAPHY IN THE LONG QT SYNDROME, European heart journal, 19(1), 1998, pp. 158-165

Authors: BOIZIAU C DAUSSE E MISHRA R DUCONGE F TOULME JJ
Citation: C. Boiziau et al., IDENTIFICATION OF APTAMERS AGAINST THE DNA-TEMPLATE FOR IN-VITRO TRANSCRIPTION OF THE HIV-1 TAR ELEMENT, ANTISENSE & NUCLEIC ACID DRUG DEVELOPMENT, 7(4), 1997, pp. 369-380

Authors: DAUSSE E BERTHET M DENJOY I ANDREFOUET X CRUAUD C BENNACEUR M FAURE S COUMEL P SCHWARTZ K GUICHENEY P
Citation: E. Dausse et al., A MUTATION IN HERG ASSOCIATED WITH NOTCHED T-WAVES IN LONG QT SYNDROME, Journal of Molecular and Cellular Cardiology, 28(8), 1996, pp. 1609-1615

Authors: DAUSSE E DENJOY I KAHLEM P BENNACEUR M FAURE S WEISSENBACH J COUMEL P SCHWARTZ K GUICHENEY P
Citation: E. Dausse et al., READJUSTING THE LOCALIZATION OF LONG QT SYNDROME GENE ON CHROMOSOME 11P15, Comptes rendus de l'Academie des sciences. Serie 3, Sciences de la vie, 318(8), 1995, pp. 879-885

Authors: DAUSSE E QUEMENEUR E SCHWARTZ K
Citation: E. Dausse et al., P-33 AND BETA-IMAGER - APPLICATION FOR GENOTYPING OF MICROSATELLITE MARKERS, BioTechniques, 18(3), 1995, pp. 426

Authors: ROY N KAHLEM P DAUSSE E BENNACEUR M FAURE S WEISSENBACH J KOMAJDA M DENJOY I COUMEL P SCHWARTZ K GUICHENEY P
Citation: N. Roy et al., EXCLUSION OF HRAS FROM LONG QT LOCUS, Nature genetics, 8(2), 1994, pp. 113-114

Authors: DUFOUR C DAUSSE E FETLER L DUBOURG O BOUHOUR JB VOSBERG HP GUICHENEY P KOMAJDA M SCHWARTZ K
Citation: C. Dufour et al., IDENTIFICATION OF A MUTATION NEAR A FUNCTIONAL SITE OF THE BETA-CARDIAC MYOSIN HEAVY-CHAIN GENE IN A FAMILY WITH HYPERTROPHIC CARDIOMYOPATHY, Journal of Molecular and Cellular Cardiology, 26(9), 1994, pp. 1241-1247

Authors: GUICHENEY P DENJOY I KAHLEM P DAUSSE E ROY N KOMAJDA M SCHWARTZ K COUMEL P
Citation: P. Guicheney et al., FAMILIES WITH LONG QT SYNDROME LINKED TO CHROMOSOME-11 - PHENOTYPIC HETEROGENEITY, The Journal of general physiology, 104(6), 1994, pp. 10000011-10000011

Authors: GUICHENEY P DENJOY I DAUSSE E ROY N KAHLEM P KOMAJDA M SCHWARTZ K COUMEL P
Citation: P. Guicheney et al., PHENOTYPIC HETEROGENEITY IN FRENCH FAMILIES WITH LONG QT SYNDROME LINKED TO CHROMOSOME-11, Circulation, 90(4), 1994, pp. 313-313

Authors: GUICHENEY P DENJOY I DAUSSE E ROY N KAHLEM P KOMAJDA M SCHWARTZ K COUMEL P
Citation: P. Guicheney et al., PHENOTYPIC HETEROGENEITY IN FRENCH FAMILIES WITH LONG QT SYNDROME LINKED TO CHROMOSOME-11, Circulation, 90(4), 1994, pp. 313-313

Authors: CARRIER L HENGSTENBERG C BECKMANN JS GUICHENEY P DUFOUR C BERCOVICI J DAUSSE E BEREBBIBERTRAND I WISNEWSKY C PULVENIS D FETLER L VIGNAL A WEISSENBACH J HILLAIRE D FEINGOLD J BOUHOUR JB HAGEGE A DESNOS M ISNARD R DUBOURG O KOMAJDA M SCHWARTZ K
Citation: L. Carrier et al., MAPPING OF A NOVEL GENE FOR FAMILIAL HYPERTROPHIC CARDIOMYOPATHY TO CHROMOSOME-11, Nature genetics, 4(3), 1993, pp. 311-313

Authors: DUFOUR C CARRIER L HENGSTENBERG C BERCOVICI J DAUSSE E WEISSENBACH J DUBOURG O KOMAJDA M SCHWARTZ K BECKMANN JS
Citation: C. Dufour et al., EXCLUSION OF GENES-CODING FOR PROTEINS OF THE CYTOSKELETON AND THE EXTRACELLULAR-MATRIX IN FAMILIAL HYPERTROPHIC CARDIOMYOPATHY USING A CANDIDATE GENE APPROACH, Comptes rendus de l'Academie des sciences. Serie 3, Sciences de la vie, 316(5), 1993, pp. 474-481

Authors: DAUSSE E KOMAJDA M FETLER L DUBOURG O DUFOUR C CARRIER L WISNEWSKY C BERCOVICI J HENGSTENBERG C ALMAHDAWI S ISNARD R HAGEGE A BOUHOUR JB DESNOS M BECKMANN J WEISSENBACH J SCHWARTZ K GUICHENEY P
Citation: E. Dausse et al., FAMILIAL HYPERTROPHIC CARDIOMYOPATHY - MICROSATELLITE HAPLOTYPING ANDIDENTIFICATION OF A HOT-SPOT FOR MUTATIONS IN THE BETA-MYOSIN HEAVY-CHAIN GENE, The Journal of clinical investigation, 92(6), 1993, pp. 2807-2813

Authors: DAUSSE E DUFOUR C FETLER L DUBOURG O VOSBERG HP KOMAJDA M SCHWARTZ K GUICHENEY P
Citation: E. Dausse et al., IDENTIFICATION OF 3 NEW MUTATIONS IN THE BETA-MYOSIN HEAVY-CHAIN GENEIN FRENCH FAMILIES WITH HYPERTROPHIC CARDIOMYOPATHY, Circulation, 88(4), 1993, pp. 572-572
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