Zobrazeno 1 - 10
of 100
pro vyhledávání: '"Cardiomyopathies/genetics"'
Publikováno v:
Cardiovascular Innovations and Applications, Vol 2, Iss 2, p 297 (2017)
Inherited cardiomyopathies are major causes of morbidity and mortality and include a group of cardiac disorders such as hypertrophic cardiomyopathy (HCM), dilated cardiomyopathy, arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C), lef
Externí odkaz:
https://doaj.org/article/82d09efc791243b792372ebb2f843f62
Akademický článek
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Publikováno v:
Cardiovascular Innovations and Applications, Vol 2, Iss 2, Pp 297-308 (2017)
Inherited cardiomyopathies are major causes of morbidity and mortality and include a group of cardiac disorders such as hypertrophic cardiomyopathy (HCM), dilated cardiomyopathy, arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C), lef
Autor:
Di Toro, Alessandro, Urtis, Mario, Narula, Nupoor, Giuliani, Lorenzo, Grasso, Maurizia, Pasotti, Michele, Pellegrini, Carlo, Serio, Alessandra, Pilotto, Andrea, Antoniazzi, Elena, Rampino, Teresa, Magrassi, Lorenzo, Valentini, Adele, Cavallini, Anna, Scelsi, Laura, Ghio, Stefano, Abelli, Massimo, Olivotto, Iacopo, Porcu, Maurizio, Gavazzi, Antonello, Kodama, Takahide, Arbustini, Eloisa
Publikováno v:
In Journal of the American College of Cardiology 11 October 2022 80(15):1431-1443
Autor:
Tayal, Upasana, Verdonschot, Job A.J., Hazebroek, Mark R., Howard, James, Gregson, John, Newsome, Simon, Gulati, Ankur, Pua, Chee Jian, Halliday, Brian P., Lota, Amrit S., Buchan, Rachel J., Whiffin, Nicola, Kanapeckaite, Lina, Baruah, Resham, Jarman, Julian W.E., O’Regan, Declan P., Barton, Paul J.R., Ware, James S., Pennell, Dudley J., Adriaans, Bouke P., Bekkers, Sebastiaan C.A.M., Donovan, Jackie, Frenneaux, Michael, Cooper, Leslie T., Januzzi, James L., Jr., Cleland, John G.F., Cook, Stuart A., Deo, Rahul C., Heymans, Stephane R.B., Prasad, Sanjay K.
Publikováno v:
In Journal of the American College of Cardiology 7 June 2022 79(22):2219-2232
Akademický článek
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In de laatste decennia zijn er belangrijke doorbraken geweest die hebben geleid tot het bekend worden van genetische factoren betrokken bij het ontstaan van erfelijke hartspierziekten (cardiomyopathieën). Dit is met name van belang voor naaste famil
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::9d82acbe2119f6486c2ffcc852dda87e
https://pure.amc.nl/en/publications/inherited-cardiomyopathies-genetics-and-geneenvironment-interactions(7995b812-05f9-47b8-9eb9-fb247484552a).html
https://pure.amc.nl/en/publications/inherited-cardiomyopathies-genetics-and-geneenvironment-interactions(7995b812-05f9-47b8-9eb9-fb247484552a).html
Autor:
Yu, Bing, Roberts, Mary B., Raffield, Laura M., Zekavat, Seyedeh Maryam, Nguyen, Ngoc Quynh H., Biggs, Mary L., Brown, Michael R., Griffin, Gabriel, Desai, Pinkal, Correa, Adolfo, Morrison, Alanna C., Shah, Amil M., Niroula, Abhishek, Uddin, Md Mesbah, Honigberg, Michael C., Ebert, Benjamin L., Psaty, Bruce M., Whitsel, Eric A., Manson, JoAnn E., Kooperberg, Charles, Bick, Alexander G., Ballantyne, Christie M., Reiner, Alex P., Natarajan, Pradeep, Eaton, Charles B.
Publikováno v:
In Journal of the American College of Cardiology 6 July 2021 78(1):42-52
Autor:
Sheppard, M.N., van der Wal, A.C., Banner, J., d'Amati, G., De Gaspari, M., De Gouveia, R., Di Gioia, C., Giordano, C., Larsen, M.K., Lynch, M.J., Lucena, J., Molina, P., Parsons, S., Suarez-Mier, M.P., Rizzo, S., Suvarna, S.K., Rijdt, WPT, Thiene, G., Vink, A., Westaby, J., Michaud, K., Basso, C.
Publikováno v:
Virchows Archiv, vol. 482, no. 4, pp. 653-669
Cardiomyopathies (CMP) comprise a heterogenous group of diseases affecting primarily the myocardium, either genetic and/or acquired in origin. While many classification systems have been proposed in the clinical setting, there is no internationally a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______1900::3adde79061492d2bbe81cf970a668bb1
https://serval.unil.ch/resource/serval:BIB_3FCA281023B9.P001/REF.pdf
https://serval.unil.ch/resource/serval:BIB_3FCA281023B9.P001/REF.pdf