المؤلفون: Lee, W.Y., Tam, C.S., Yan, P.Y., Lam, Y.Y., Duchatelet, S., Peat, R.A., Denjoy, I., Itoh, H., Berthet, M., Crotti, L., Ohno, S., Pedrazzini, M., Klug, D., Schwartz, P.J., Shimizu, W., Horie, M., Tregouet, D.A., Guicheney, P., Tiong, W.N., Hwang, S.S., Fong, A.Y.Y., Wee, C.C., Lai, L.Y.H., Tiong, L.L., Chang, B.C., Ong, T.K., Garg, P., Ashraffi, R., Chuah, S., Baho, H., Draz, S., Mously, F., Atta, J., Kouatly, A., Hussian, A., Abu zeid, H., Courtney, A., Hamilton-Craig, C., Strugnell, W., Slaughter, R., Luis, C.R., Habibian, M., Luis, S.A., Raffel, O.C., Tung, T.H., Hsiung, M.C., Wei, J., Clements, I.P., Hodge, D.O., Scott, C.G., Chai, S.C., Liew, M., Leong, G., Peng, H., Ding, J., Peng, Y., Zhang, Q., Xu, Y., Chao, X., Tian, H., Zhang, Y., Liu, Y., Tong, W.J., Liu, Y.Y., Wang, J., Zhang, Y.H., Wong, M.C.S., Yan, B., Tam, W.W.S., Wang, H.H.X., Liu, K.S.D., Liu, K.Q., Cheung, C.S.K., Tong, E.L.H., Sek, A.C.H., Cheung, N.T., Yu, C.M., Leeder, S., Griffiths, S., Poon, K.K.C., Wong, H.L., Ng, S.H., Kwok, W.T., Yeung, C.L., Yu, S.Y., Wan, Y.P., Wan, S., Underwood, M.J., Chan, P.H., Alegria-Barrero, E., Price, S., Kelleher, A., Moat, N., Mario, C.D., Franzen, O., Zhang, Y.C., Lee, A.P., Lin, Q.S., Fang, F., Underwood, M., Mirhoseini, S.J., Frouzannia, S.K., Mostafavi Pour Manshadi, S.M.Y., Naderi, N., Sayegh, S., Dandekar, P.G., Verma, Y.

مصطلحات موضوعية: Arrhythmia

وصف الملف: text/html

العلاقة: http://eurheartjsupp.oxfordjournals.org/cgi/content/short/14/suppl_A/A3Test; http://dx.doi.org/10.1093/eurheartj/sur021Test

الإتاحة: https://doi.org/10.1093/eurheartj/sur021Test
http://eurheartjsupp.oxfordjournals.org/cgi/content/short/14/suppl_A/A3Test

المؤلفون: Itoh, H, Crotti, L, Aiba, T, Spazzolini, C, Denjoy, I, Fressart, V, Hayashi, K, Nakajima, T, Ohno, S, Makiyama, T, Wu, J, Hasegawa, K, Mastantuono, E, Dagradi, F, Pedrazzini, M, Yamagishi, M, Berthet, M, Murakami, Y, Shimizu, W, Guicheney, P, Schwartz, P, Horie, M

المساهمون: Itoh, H, Crotti, L, Aiba, T, Spazzolini, C, Denjoy, I, Fressart, V, Hayashi, K, Nakajima, T, Ohno, S, Makiyama, T, Wu, J, Hasegawa, K, Mastantuono, E, Dagradi, F, Pedrazzini, M, Yamagishi, M, Berthet, M, Murakami, Y, Shimizu, W, Guicheney, P, Schwartz, P, Horie, M

مصطلحات موضوعية: acquired long qt syndrome, genetic, disease causing mutation, cascade screening, family members, MED/11 - MALATTIE DELL'APPARATO CARDIOVASCOLARE, MED/03 - GENETICA MEDICA

وصف الملف: STAMPA

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/26715165; info:eu-repo/semantics/altIdentifier/wos/WOS:000375404500011; volume:37; issue:18; firstpage:1456; lastpage:1464; numberofpages:9; journal:EUROPEAN HEART JOURNAL; http://hdl.handle.net/10281/182195Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84975852981; https://www.ncbi.nlm.nih.gov/pubmed/?term=26715165Test

الإتاحة: https://doi.org/10.1093/eurheartj/ehv695Test
http://hdl.handle.net/10281/182195Test
https://www.ncbi.nlm.nih.gov/pubmed/?term=26715165Test

المؤلفون: Furlong, M, Bower, R.G., Crain, R.A., Schaye, J, Theuns, T, Trayford, J.W., Qu, Y., Schaller, M., Berthet, M., Helly, J.C.

المصدر: Monthly notices of the Royal Astronomical Society, 2017, Vol.465(1), pp.722-738 [Peer Reviewed Journal]

وصف الملف: application/pdf

العلاقة: dro:21308; http://dro.dur.ac.uk/21308Test/; https://doi.org/10.1093/mnras/stw2740Test; http://dro.dur.ac.uk/21308/1/21308.pdfTest

الإتاحة: https://doi.org/10.1093/mnras/stw2740Test
http://dro.dur.ac.uk/21308Test/
http://dro.dur.ac.uk/21308/1/21308.pdfTest

المؤلفون: Behr, E, Savio-Galimberti, E, Barc, J, Holst, AG, Petropoulou, E, Prins, B, Jabbari, J, Torchio, M, Berthet, M, Mizusawa, Y, Yang, T, Nannenberg, E, Dagradi, F, Weeke, P, Bastiaenan, R, Ackerman, M, Haunso, S, Leenhardt, A, Kääb, S, Probst, V, Redon, R, Sharma, S, Wilde, A, Tfelt-Hansen, J, Schwartz, P, Roden, D, Bezzina, C, Olesen, M, Darbar, D, Guicheney, P, Crotti, L, Jamshidi, Y

المساهمون: Behr, E, Savio-Galimberti, E, Barc, J, Holst, A, Petropoulou, E, Prins, B, Jabbari, J, Torchio, M, Berthet, M, Mizusawa, Y, Yang, T, Nannenberg, E, Dagradi, F, Weeke, P, Bastiaenan, R, Ackerman, M, Haunso, S, Leenhardt, A, Kääb, S, Probst, V, Redon, R, Sharma, S, Wilde, A, Tfelt-Hansen, J, Schwartz, P, Roden, D, Bezzina, C, Olesen, M, Darbar, D, Guicheney, P, Crotti, L, Jamshidi, Y

مصطلحات موضوعية: Brugada syndrome, Genetic, QRS duration, Rare variant, SCN10A, MED/11 - MALATTIE DELL'APPARATO CARDIOVASCOLARE, BIO/18 - GENETICA, MED/01 - STATISTICA MEDICA

وصف الملف: STAMPA

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/25691538; info:eu-repo/semantics/altIdentifier/wos/WOS:000359088400019; volume:106; issue:3; firstpage:520; lastpage:529; numberofpages:10; journal:CARDIOVASCULAR RESEARCH; http://hdl.handle.net/10281/182204Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84930331925; http://www.ncbi.nlm.nih.gov/pubmed/25691538Test

الإتاحة: https://doi.org/10.1093/cvr/cvv042Test
http://hdl.handle.net/10281/182204Test
http://www.ncbi.nlm.nih.gov/pubmed/25691538Test

المؤلفون: Yoshitaka Murakami, Tadashi Nakajima, Myriam Berthet, Carla Spazzolini, Isabelle Denjoy, Jie Wu, Elisa Mastantuono, Kenshi Hayashi, Federica Dagradi, Kanae Hasegawa, Seiko Ohno, Matteo Pedrazzini, Takeshi Aiba, Pascale Guicheney, Minoru Horie, Hideki Itoh, Véronique Fressart, Wataru Shimizu, Masakazu Yamagishi, Takeru Makiyama, Lia Crotti, Peter J. Schwartz

المساهمون: Itoh, H, Crotti, L, Aiba, T, Spazzolini, C, Denjoy, I, Fressart, V, Hayashi, K, Nakajima, T, Ohno, S, Makiyama, T, Wu, J, Hasegawa, K, Mastantuono, E, Dagradi, F, Pedrazzini, M, Yamagishi, M, Berthet, M, Murakami, Y, Shimizu, W, Guicheney, P, Schwartz, P, Horie, M

المصدر: Eur. Heart J. 37, 1456-1464 (2016)

مصطلحات موضوعية: Proband, Male, congenital, hereditary, and neonatal diseases and abnormalities, cascade screening, MED/03 - GENETICA MEDICA, Long QT syndrome, hERG, Torsades de pointes, 030204 cardiovascular system & hematology, Ventricular tachycardia, QT interval, Acquired Long Qt Syndrome, Congenital Long Qt Syndrome, Drug-induced Long Qt Syndrome, Genetics, 03 medical and health sciences, Electrocardiography, 0302 clinical medicine, Japan, Clinical Research, medicine, Humans, KvLQT1, cardiovascular diseases, Genetic Testing, Genetic testing, biology, medicine.diagnostic_test, business.industry, family members, MED/11 - MALATTIE DELL'APPARATO CARDIOVASCOLARE, Middle Aged, medicine.disease, acquired long qt syndrome, Long QT Syndrome, disease causing mutation, Italy, Mutation, biology.protein, Female, France, genetic, Cardiology and Cardiovascular Medicine, business, 030217 neurology & neurosurgery

وصف الملف: application/pdf; STAMPA

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::edd62c316e5f24e6586f77d4ed1c1473Test
https://europepmc.org/articles/PMC4914885Test/

المؤلفون: Peter Weeke, Bram P. Prins, Yalda Jamshidi, Stefan Kääb, Margherita Torchio, Evmorfia Petropoulou, Dan M. Roden, Sanjay Sharma, Eline A. Nannenberg, Lia Crotti, Pascale Guicheney, Javad Jabbari, Julien Barc, Tao Yang, Peter J. Schwartz, Anders G. Holst, Eleonora Savio-Galimberti, Morten S. Olesen, Michael J. Ackerman, Connie R. Bezzina, Vincent Probst, Yuka Mizusawa, Dawood Darbar, Elijah R. Behr, Arthur A.M. Wilde, Myriam Berthet, Rachel Bastiaenan, Richard Redon, Antoine Leenhardt, Federica Dagradi, Stig Haunsø, Jacob Tfelt-Hansen

المساهمون: Behr, E, Savio-Galimberti, E, Barc, J, Holst, A, Petropoulou, E, Prins, B, Jabbari, J, Torchio, M, Berthet, M, Mizusawa, Y, Yang, T, Nannenberg, E, Dagradi, F, Weeke, P, Bastiaenan, R, Ackerman, M, Haunso, S, Leenhardt, A, Kääb, S, Probst, V, Redon, R, Sharma, S, Wilde, A, Tfelt-Hansen, J, Schwartz, P, Roden, D, Bezzina, C, Olesen, M, Darbar, D, Guicheney, P, Crotti, L, Jamshidi, Y, Academic Medical Center - Academisch Medisch Centrum [Amsterdam] (AMC), University of Amsterdam [Amsterdam] (UvA), Physiopathologie et thérapie du muscle strié, Université Pierre et Marie Curie - Paris 6 (UPMC)-IFR14-Institut National de la Santé et de la Recherche Médicale (INSERM), School of Chemical Engineering [Anshan], University of Science and Technology LiaoNing (USTL), Rigshospitalet [Copenhagen], Copenhagen University Hospital, Service de Cardiologie, AP-HP - Hôpital Bichat - Claude Bernard [Paris], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Université Paris Diderot - Paris 7 (UPD7)-PRES Sorbonne Paris Cité-Centre de Référence Maladies Cardiaques Héréditaires, unité de recherche de l'institut du thorax UMR1087 UMR6291 (ITX), Université de Nantes - UFR de Médecine et des Techniques Médicales (UFR MEDECINE), Université de Nantes (UN)-Université de Nantes (UN)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS), Unité de recherche de l'institut du thorax (ITX-lab), Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Université de Nantes - UFR de Médecine et des Techniques Médicales (UFR MEDECINE), Université de Nantes (UN)-Université de Nantes (UN), Cardiology, ACS - Amsterdam Cardiovascular Sciences, Human Genetics

المصدر: Cardiovascular Research
Cardiovascular Research, Oxford University Press (OUP), 2015, Equipe 3 Equipe 4, 106 (3), pp.520--529. ⟨10.1093/cvr/cvv042⟩
Cardiovascular Research, 2015, Equipe 3 Equipe 4, 106 (3), pp.520--529. ⟨10.1093/cvr/cvv042⟩
Cardiovascular research, 106(3), 520-529. Oxford University Press

مصطلحات موضوعية: Male, SCN10A, Candidate gene, QRS duration, Heredity, Physiology, [SDV]Life Sciences [q-bio], DNA Mutational Analysis, Action Potentials, Gene Frequency, Risk Factors, Databases, Genetic, Odds Ratio, humans, Exome sequencing, Brugada syndrome, Genetics, adult, Single Nucleotide, Middle Aged, Pedigree, 3. Good health, Europe, Phenotype, Female, Corrigendum, Cardiology and Cardiovascular Medicine, Saudi Arabia, BIO/18 - GENETICA, Biology, Transfection, Polymorphism, Single Nucleotide, Sudden death, Cell Line, NAV1.8 Voltage-Gated Sodium Channel, Databases, Genetic, Physiology (medical), Cardiac conduction, medicine, Genetic Predisposition to Disease, Polymorphism, Allele, Allele frequency, Genetic Association Studies, MED/01 - STATISTICA MEDICA, Aged, Genetic heterogeneity, Computational Biology, Rare variant, Rare variants, Original Articles, MED/11 - MALATTIE DELL'APPARATO CARDIOVASCOLARE, medicine.disease, United States, Case-Control Studies

وصف الملف: STAMPA

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f1cdb672ac45c09cf337599dad400da7Test
http://hdl.handle.net/10281/182204Test