المؤلفون: Migliore F., Biffi M., Viani S., Pittorru R., Francia P., Pieragnoli P., De Filippo P., Bisignani G., Nigro G., Dello Russo A., Pisano E., Palmisano P., Rapacciuolo A., Silvetti M. S., Lavalle C., Curcio A., Rordorf R., Lovecchio M., Valsecchi S., D'Onofrio A., Botto G. L.

المساهمون: Migliore, F., Biffi, M., Viani, S., Pittorru, R., Francia, P., Pieragnoli, P., De Filippo, P., Bisignani, G., Nigro, G., Dello Russo, A., Pisano, E., Palmisano, P., Rapacciuolo, A., Silvetti, M. S., Lavalle, C., Curcio, A., Rordorf, R., Lovecchio, M., Valsecchi, S., D'Onofrio, A., Botto, G. L.

مصطلحات موضوعية: cardiomyopathie, channelopathie, implantable defibrillator, inappropriate shock, subcutaneous

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/37536671; info:eu-repo/semantics/altIdentifier/wos/WOS:001051445700001; volume:25; issue:9; firstpage:1; lastpage:11; numberofpages:11; journal:EUROPACE; https://hdl.handle.net/11573/1688170Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85168316056

الإتاحة: https://doi.org/10.1093/europace/euad239Test
https://hdl.handle.net/11573/1688170Test

المؤلفون: Picci, Giacomo, Marchesan, Silvia, Caltagirone, Claudia

المساهمون: Picci, Giacomo, Marchesan, Silvia, Caltagirone, Claudia

مصطلحات موضوعية: ion channel, ion transporter, ionophore, ion carrier, channelopathie, cystic fibrosi, AMP, peptide, supramolecular medicinal chemistry, nanotubes

العلاقة: info:eu-repo/semantics/altIdentifier/wos/WOS:000786882500001; volume:10; issue:4; firstpage:"-"; lastpage:"-"; numberofpages:23; journal:BIOMEDICINES; https://hdl.handle.net/11368/3017565Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85129137237; https://www.mdpi.com/2227-9059/10/4/885Test

الإتاحة: https://doi.org/10.3390/biomedicines10040885Test
https://hdl.handle.net/11368/3017565Test
https://www.mdpi.com/2227-9059/10/4/885Test

المؤلفون: Silvia Castelletti, Belinda Gray, Cristina Basso, Elijah R Behr, Lia Crotti, Perry M Elliott, Cecilia M Gonzalez Corcia, Flavio D'Ascenzi, Jodie Ingles, Bart Loeys, Antonis Pantazis, Guido E Pieles, Johan Saenen, Georgia Sarquella Brugada, Maria Sanz de la Garza, Sanjay Sharma, Emeline M Van Craenebroek, Arthur Wilde, Michael Papadakis

المساهمون: Castelletti, S, Gray, B, Basso, C, R Behr, E, Crotti, L, M Elliott, P, M Gonzalez Corcia, C, D'Ascenzi, F, Ingles, J, Loeys, B, Pantazis, A, E Pieles, G, Saenen, J, Sarquella Brugada, G, Sanz de la Garza, M, Sharma, S, M Van Craenebroek, E, Wilde, A, Papadakis, M

مصطلحات موضوعية: Athlete, Cardiomyopathie, Channelopathie, Genetic testing, Inherited cardiac condition, Sudden cardiac death

وصف الملف: ELETTRONICO

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/36070487; info:eu-repo/semantics/altIdentifier/wos/WOS:000851196000004; volume:29; issue:12; firstpage:1582; lastpage:1591; numberofpages:10; journal:EUROPEAN JOURNAL OF PREVENTIVE CARDIOLOGY; http://hdl.handle.net/10281/392936Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85137515547

الإتاحة: https://doi.org/10.1093/eurjpc/zwac080Test
http://hdl.handle.net/10281/392936Test

المؤلفون: Pagliarani, Serena, Meola, Giovanni, Filareti, Melania, Comi, Giacomo Pietro, Lucchiari, Sabrina

المساهمون: S. Pagliarani, G. Meola, M. Filareti, G.P. Comi, S. Lucchiari

مصطلحات موضوعية: CLCN1, SCN4A, channelopathie, myotonia, paramyotonia, Settore MED/26 - Neurologia

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/36081873; info:eu-repo/semantics/altIdentifier/wos/WOS:000859444300001; volume:13; firstpage:1; lastpage:6; numberofpages:6; journal:FRONTIERS IN NEUROLOGY; https://hdl.handle.net/2434/944645Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85139253573

الإتاحة: https://doi.org/10.3389/fneur.2022.845383Test
https://hdl.handle.net/2434/944645Test

المؤلفون: Kochi A. N., Vettor G., Dessanai M. A., Pizzamiglio F., Tondo C.

المساهمون: A.N. Kochi, G. Vettor, M.A. Dessanai, F. Pizzamiglio, C. Tondo

مصطلحات موضوعية: Arrhythmogenic right ventricular cardiomyopathy, Athlete, Channelopathie, Hypertrophic cardiomyopathy, ICD implant, Myocarditi, Sudden cardiac death, Ventricular arrhythmias, Settore MED/11 - Malattie dell'Apparato Cardiovascolare

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/33673000; info:eu-repo/semantics/altIdentifier/wos/WOS:000622758900001; volume:57; issue:2; firstpage:1; lastpage:15; numberofpages:15; journal:MEDICINA; http://hdl.handle.net/2434/827637Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85101923757

الإتاحة: https://doi.org/10.3390/medicina57020168Test
http://hdl.handle.net/2434/827637Test

المؤلفون: Maggi L., Brugnoni R., Canioni E., Tonin P., Saletti V., Sola P., Piccinelli S. C., Colleoni L., Ferrigno P., Pini A., Masson R., Manganelli F., Lietti D., Vercelli L., Ricci G., Bruno C., Tasca G., Pizzuti A., Padovani A., Fusco C., Pegoraro E., Ruggiero L., Ravaglia S., Siciliano G., Morandi L., Dubbioso R., Mongini T., Filosto M., Tramacere I., Mantegazza R., Bernasconi P.

المساهمون: Maggi, L., Brugnoni, R., Canioni, E., Tonin, P., Saletti, V., Sola, P., Piccinelli, S. C., Colleoni, L., Ferrigno, P., Pini, A., Masson, R., Manganelli, F., Lietti, D., Vercelli, L., Ricci, G., Bruno, C., Tasca, G., Pizzuti, A., Padovani, A., Fusco, C., Pegoraro, E., Ruggiero, L., Ravaglia, S., Siciliano, G., Morandi, L., Dubbioso, R., Mongini, T., Filosto, M., Tramacere, I., Mantegazza, R., Bernasconi, P.

مصطلحات موضوعية: channelopathie, myotonia, periodic paralysi, SCN4A gene mutation, SNEL, voltage-gated sodium channel Na, 1.4

وصف الملف: ELETTRONICO

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/32849172; info:eu-repo/semantics/altIdentifier/wos/WOS:000561451700001; volume:11; firstpage:646; numberofpages:8; journal:FRONTIERS IN NEUROLOGY; http://hdl.handle.net/11577/3395083Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85089420709

الإتاحة: https://doi.org/10.3389/fneur.2020.00646Test
http://hdl.handle.net/11577/3395083Test

المؤلفون: Barretta F., Mirra B., Monda E., Caiazza M., Lombardo B., Tinto N., Scudiero O., Frisso G., Mazzaccara C.

المساهمون: Barretta, F., Mirra, B., Monda, E., Caiazza, M., Lombardo, B., Tinto, N., Scudiero, O., Frisso, G., Mazzaccara, C.

مصطلحات موضوعية: Athlete, Cardiomyopathie, Channelopathie, Genetic test, Next generation sequencing, Preventive medicine, Sudden cardiac death

العلاقة: info:eu-repo/semantics/altIdentifier/wos/WOS:000581393700001; volume:21; issue:18; firstpage:1; lastpage:26; numberofpages:26; journal:INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES; http://hdl.handle.net/11588/819556Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85090558359

الإتاحة: https://doi.org/10.3390/ijms21186682Test
http://hdl.handle.net/11588/819556Test

المؤلفون: Kotta M. -C., Torchio M., Bayliss P., Cohen M. C., Quarrell O., Wheeldon N., Marton T., Gentilini D., Crotti L., Coombs R. C., Schwartz P. J.

المساهمون: Kotta, M, Torchio, M, Bayliss, P, Cohen, M, Quarrell, O, Wheeldon, N, Marton, T, Gentilini, D, Crotti, L, Coombs, R, Schwartz, P

مصطلحات موضوعية: channelopathie, molecular autopsy, sudden infant death syndrome, sudden unexplained death in childhood

وصف الملف: ELETTRONICO

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/37589201; info:eu-repo/semantics/altIdentifier/wos/WOS:001062730000046; volume:12; issue:17; journal:JOURNAL OF THE AMERICAN HEART ASSOCIATION. CARDIOVASCULAR AND CEREBROVASCULAR DISEASE; https://hdl.handle.net/10281/467703Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85169847762

الإتاحة: https://doi.org/10.1161/JAHA.122.029100Test
https://hdl.handle.net/10281/467703Test

المؤلفون: Crotti L., Brugada P., Calkins H., Chevalier P., Conte G., Finocchiaro G., Postema P. G., Probst V., Schwartz P. J., Behr E. R.

المساهمون: Crotti, L, Brugada, P, Calkins, H, Chevalier, P, Conte, G, Finocchiaro, G, Postema, P, Probst, V, Schwartz, P, Behr, E

مصطلحات موضوعية: Cardiomyopathie, Channelopathie, Gene therapy, Genetic, Polygenic risk score, Sudden cardiac death

وصف الملف: STAMPA

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/37622577; volume:25; issue:8; journal:EUROPACE; https://hdl.handle.net/10281/467702Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85171806454

الإتاحة: https://doi.org/10.1093/europace/euad180Test
https://hdl.handle.net/10281/467702Test

المؤلفون: Guerrini, Renzo, Conti, Valerio, Mantegazza, Massimo, Balestrini, Simona, Galanopoulou, Aristea S, Benfenati, Fabio

المساهمون: Guerrini, Renzo, Conti, Valerio, Mantegazza, Massimo, Balestrini, Simona, Galanopoulou, Aristea S, Benfenati, Fabio

مصطلحات موضوعية: channelopathie, developmental and epileptic encephalopathie, epileptogenesi, personalized treatment approache, synaptopathie, Animal, Genetic Heterogeneity, Mutation, Epilepsy

وصف الملف: STAMPA

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/35951482; info:eu-repo/semantics/altIdentifier/wos/WOS:000895991800002; volume:103; firstpage:433; lastpage:513; numberofpages:81; journal:PHYSIOLOGICAL REVIEWS; https://hdl.handle.net/11567/1146137Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85140144534

الإتاحة: https://doi.org/10.1152/physrev.00063.2021Test
https://hdl.handle.net/11567/1146137Test