يعرض 1 - 10 نتائج من 70 نتيجة بحث عن '"Fressart, V"', وقت الاستعلام: 1.24s تنقيح النتائج
  1. 1
    دورية أكاديمية
    A Systematic Analysis of the Clinical Outcome Associated with Multiple Reclassified Desmosomal Gene Variants in Arrhythmogenic Right Ventricular Cardiomyopathy Patients

    المؤلفون: Nagyova, E, Hoorntje, ET, Rijdt, WPT, Bosman, LP, Syrris, P, Protonotarios, A, Elliott, PM, Tsatsopoulou, A, Mestroni, L, Taylor, MRG, Sinagra, G, Merlo, M, Wada, Y, Horie, M, Mogensen, J, Christensen, AH, Gerull, B, Song, L, Yao, Y, Fan, S, Saguner, AM, Duru, F, Koskenvuo, JW, Cruz Marino, T, Tichnell, C, Judge, DP, Dooijes, D, Lekanne Deprez, RH, Basso, C, Pilichou, K, Bauce, B, Wilde, AAM, Charron, P, Fressart, V, van der Heijden, JF, van den Berg, MP, Asselbergs, FW, James, CA, Jongbloed, JDH, Harakalova, M, van Tintelen, JP

    المصدر: Journal of Cardiovascular Translational Research (2023) (In press).

    مصطلحات موضوعية: ARVC, Arrhythmia, Composite endpoint, Desmosomal genes, Genetics, Multiple variants

    وصف الملف: text

    العلاقة: https://discovery.ucl.ac.uk/id/eprint/10173573/1/s12265-023-10403-8.pdfTest; https://discovery.ucl.ac.uk/id/eprint/10173573Test/

    الإتاحة: https://discovery.ucl.ac.uk/id/eprint/10173573/1/s12265-023-10403-8.pdfTest
    https://discovery.ucl.ac.uk/id/eprint/10173573Test/

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  2. 2
    دورية أكاديمية
    Study of the diagnostic yield of gene panels in long QT syndrome in pediatrics

    المؤلفون: Daire, E., Dirani, S., Klug, D., Dhaenens, C.M., Kyndt, F., Fressart, V., Jedraszak, G.

    المصدر: Archives of Cardiovascular Diseases Supplements ; volume 14, issue 3-4, page 244 ; ISSN 1878-6480

    مصطلحات موضوعية: Cardiology and Cardiovascular Medicine

    الإتاحة: https://doi.org/10.1016/j.acvdsp.2022.07.050Test
    https://api.elsevier.com/content/article/PII:S1878648022002257?httpAccept=text/xmlTest
    https://api.elsevier.com/content/article/PII:S1878648022002257?httpAccept=text/plainTest

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  3. 3
    دورية أكاديمية
    Prevalence and significance of atrial tachyarrhythmias in arrhythmogenic right ventricular cardiomyopathy

    المؤلفون: Proukhnitzky, J., Maupain, C., Waintraub, X., Badenco, N., Duthoit, G., Hidden-Lucet, F., Himbert, C., Pousset, F., Redheuil, A., Hebert, J.L., Bordet, C., Fedida, J., Laredo, M., Fressart, V., Charron, P., Gandjbakhch, E.

    المصدر: Archives of Cardiovascular Diseases Supplements ; volume 13, issue 2, page 234 ; ISSN 1878-6480

    مصطلحات موضوعية: Cardiology and Cardiovascular Medicine

    الإتاحة: https://doi.org/10.1016/j.acvdsp.2021.04.209Test
    https://api.elsevier.com/content/article/PII:S1878648021002111?httpAccept=text/xmlTest
    https://api.elsevier.com/content/article/PII:S1878648021002111?httpAccept=text/plainTest

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  4. 4
    دورية أكاديمية
    A Systematic Analysis of the Clinical Outcome Associated with Multiple Reclassified Desmosomal Gene Variants in Arrhythmogenic Right Ventricular Cardiomyopathy Patients

    المؤلفون: Nagyova E., Hoorntje E. T., Rijdt W. P., Bosman L. P., Syrris P., Protonotarios A., Elliott P. M., Tsatsopoulou A., Mestroni L., Taylor M. R. G., Sinagra G., Merlo M., Wada Y., Horie M., Mogensen J., Christensen A. H., Gerull B., Song L., Yao Y., Fan S., Saguner A. M., Duru F., Koskenvuo J. W., Cruz Marino T., Tichnell C., Judge D. P., Dooijes D., Lekanne Deprez R. H., Basso C., Pilichou K., Bauce B., Wilde A. A. M., Charron P., Fressart V., van der Heijden J. F., van den Berg M. P., Asselbergs F. W., James C. A., Jongbloed J. D. H., Harakalova M., van Tintelen J. P.

    المساهمون: Nagyova, E., Hoorntje, E. T., Rijdt, W. P., Bosman, L. P., Syrris, P., Protonotarios, A., Elliott, P. M., Tsatsopoulou, A., Mestroni, L., Taylor, M. R. G., Sinagra, G., Merlo, M., Wada, Y., Horie, M., Mogensen, J., Christensen, A. H., Gerull, B., Song, L., Yao, Y., Fan, S., Saguner, A. M., Duru, F., Koskenvuo, J. W., Cruz Marino, T., Tichnell, C., Judge, D. P., Dooijes, D., Lekanne Deprez, R. H., Basso, C., Pilichou, K., Bauce, B., Wilde, A. A. M., Charron, P., Fressart, V., van der Heijden, J. F., van den Berg, M. P., Asselbergs, F. W., James, C. A., Jongbloed, J. D. H., Harakalova, M., van Tintelen, J. P.

    مصطلحات موضوعية: Arrhythmia, ARVC, Composite endpoint, Desmosomal gene, Genetic, Multiple variants

    العلاقة: info:eu-repo/semantics/altIdentifier/pmid/37418234; info:eu-repo/semantics/altIdentifier/wos/WOS:001027955800001; journal:JOURNAL OF CARDIOVASCULAR TRANSLATIONAL RESEARCH; https://hdl.handle.net/11577/3493663Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85164170998

    الإتاحة: https://doi.org/10.1007/s12265-023-10403-8Test
    https://hdl.handle.net/11577/3493663Test

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  5. 5
    دورية أكاديمية
    A new SCN5A mutation responsible for Multifocal Ectopic Purkinje-Related Premature Contractions

    المؤلفون: Doisne, Nicolas, Waldmann, V., Fressart, V., Redheuil, Alban, Fosse, L., Waintraub, Xavier, Hidden-Lucet, F., Neyroud, N., Gandjbakhch, E.

    المصدر: Archives of Cardiovascular Diseases Supplements ; volume 11, issue 1, page 81-82 ; ISSN 1878-6480

    مصطلحات موضوعية: Cardiology and Cardiovascular Medicine

    الإتاحة: https://doi.org/10.1016/j.acvdsp.2018.10.180Test
    https://api.elsevier.com/content/article/PII:S187864801830435X?httpAccept=text/xmlTest
    https://api.elsevier.com/content/article/PII:S187864801830435X?httpAccept=text/plainTest

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  6. 6
    دورية أكاديمية
    SCN5A mutations in 442 neonates and children: genotype-phenotype correlation and identification of higher-risk subgroups

    المؤلفون: Baruteau, A-E, Kyndt, F, Behr, ER, Vink, AS, Lachaud, M, Joong, A, Schott, J-J, Horie, M, Denjoy, I, Crotti, L, Shimizu, W, Bos, JM, Stephenson, EA, Wong, L, Abrams, DJ, Davis, AM, Winbo, A, Dubin, AM, Sanatani, S, Liberman, L, Kaski, JP, Rudic, B, Kwok, SY, Rieubland, C, Tfelt-Hansen, J, Van Hare, GF, Guyomarc'h-Delasalle, B, Blom, NA, Wijeyeratne, YD, Gourraud, J-B, Le Marec, H, Ozawa, J, Fressart, V, Lupoglazoff, J-M, Dagradi, F, Spazzolini, C, Aiba, T, Tester, DJ, Zahavich, LA, Beauséjour-Ladouceur, V, Jadhav, M, Skinner, JR, Franciosi, S, Krahn, AD, Abdelsayed, M, Ruben, PC, Yung, T-C, Ackerman, MJ, Wilde, AA, Schwartz, PJ, Probst, V

    المصدر: European Heart Journal , 39 (31) pp. 2879-2887. (2018)

    مصطلحات موضوعية: Brugada syndrome, Genotype–phenotype correlation, Long QT syndrome, Progressive cardiac conduction disorders, SCN5A, Sodium channelopathy

    وصف الملف: text

    العلاقة: https://discovery.ucl.ac.uk/id/eprint/10055497/1/EURHEARTJ-D-17-02626_R1-3%20copy.pdfTest; https://discovery.ucl.ac.uk/id/eprint/10055497Test/

    الإتاحة: https://discovery.ucl.ac.uk/id/eprint/10055497/1/EURHEARTJ-D-17-02626_R1-3%20copy.pdfTest
    https://discovery.ucl.ac.uk/id/eprint/10055497Test/

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  7. 7
    دورية أكاديمية
    High prevalence of ventricular repolarization abnormalities in people carrying TGFβR2 mutations

    المؤلفون: Extramiana, F., Milleron, O., Elbitar, S., Uccellini, A., Langeois, M., Spentchian, M., Delorme, G., Arnoult, F., Denjoy, I., Bouleti, C., Fressart, V., Iserin, F., Maison-Blanche, P., Abifadel, M., Leenhardt, A., Boileau, C., Jondeau, G.

    المصدر: Scientific Reports ; volume 8, issue 1 ; ISSN 2045-2322

    مصطلحات موضوعية: Multidisciplinary

    الإتاحة: https://doi.org/10.1038/s41598-018-31298-5Test
    https://www.nature.com/articles/s41598-018-31298-5.pdfTest
    https://www.nature.com/articles/s41598-018-31298-5Test

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  8. 8
    دورية أكاديمية
    745High risk of heart failure in desmoglein-2 mutation carriers in arrhythmogenic right ventricular dysplasia/cardiomyopathy

    المؤلفون: Hermida, A., Fressart, V., Hidden-Lucet, F., Donal, E., Probst, V., Deharo, JC., Chevalier, P., Klug, D., Mansencal, N., Delacretaz, E., Cosnay, P., Scanu, P., Extramiana, F., Charron, P., Gandjbakhch, E.

    المصدر: EP Europace ; volume 19, issue suppl_3, page iii132-iii132 ; ISSN 1099-5129 1532-2092

    مصطلحات موضوعية: Physiology (medical), Cardiology and Cardiovascular Medicine

    الإتاحة: https://doi.org/10.1093/ehjci/eux146Test
    http://academic.oup.com/europace/article-pdf/19/suppl_3/iii132/17902589/eux146.pdfTest

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  9. 9
    دورية أكاديمية
    High risk of heart failure in desmoglein -2 mutation carriers in arrhythmogenic right ventricular dysplasia/cardiomyopathy

    المؤلفون: Hermida, A., Fressart, V., Hidden-Lucet, F., Donal, E., Probst, V., Deharo, J.C., Chevalier, P., Klug, D., Mansencal, N., Delacretaz, E., Cosnay, P., Scanu, P., Extramiana, F., Keller, D., Charron, P., Gandjbakhch, E.

    المصدر: Archives of Cardiovascular Diseases Supplements ; volume 9, issue 1, page 89 ; ISSN 1878-6480

    مصطلحات موضوعية: Cardiology and Cardiovascular Medicine

    الإتاحة: https://doi.org/10.1016/s1878-6480Test(17)30272-0
    https://api.elsevier.com/content/article/PII:S1878648017302720?httpAccept=text/xmlTest
    https://api.elsevier.com/content/article/PII:S1878648017302720?httpAccept=text/plainTest

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  10. 10
    دورية أكاديمية
    ECG descriptors of ventricular repolarization are associated with cardiac events in a gene-specific manner in long QT syndrome patients

    المؤلفون: Morgat, C, Denjoy, I, Fressart, V, Badilini, F, Vaglio, M, Messali, A, Maison-Blanche, P, Leenhardt, A, Extramiana, F

    المصدر: EP Europace ; volume 24, issue Supplement_1 ; ISSN 1099-5129 1532-2092

    مصطلحات موضوعية: Physiology (medical), Cardiology and Cardiovascular Medicine

    الإتاحة: https://doi.org/10.1093/europace/euac053.555Test
    https://academic.oup.com/europace/article-pdf/24/Supplement_1/euac053.555/43769773/euac053.555.pdfTest

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