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Year | Number of Results |
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2013 | 2 |
2014 | 2 |
2015 | 2 |
2017 | 1 |
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2024 | 0 |
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Coexistence of epilepsy and Brugada syndrome in a family with SCN5A mutation.
Epilepsy Res. 2013 Aug;105(3):415-8. doi: 10.1016/j.eplepsyres.2013.02.024. Epub 2013 Mar 25.
Epilepsy Res. 2013.
PMID: 23538271
Genetic and forensic implications in epilepsy and cardiac arrhythmias: a case series.
Partemi S, Vidal MC, Striano P, Campuzano O, Allegue C, Pezzella M, Elia M, Parisi P, Belcastro V, Casellato S, Giordano L, Mastrangelo M, Pietrafusa N, Striano S, Zara F, Bianchi A, Buti D, La Neve A, Tassinari CA, Oliva A, Brugada R.
Partemi S, et al. Among authors: vidal mc.
Int J Legal Med. 2015 May;129(3):495-504. doi: 10.1007/s00414-014-1063-4. Epub 2014 Aug 15.
Int J Legal Med. 2015.
PMID: 25119684
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Genetic analysis, in silico prediction, and family segregation in long QT syndrome.
Riuró H, Campuzano O, Berne P, Arbelo E, Iglesias A, Pérez-Serra A, Coll-Vidal M, Partemi S, Mademont-Soler I, Picó F, Allegue C, Oliva A, Gerstenfeld E, Sarquella-Brugada G, Castro-Urda V, Fernández-Lozano I, Mont L, Brugada J, Scornik FS, Brugada R.
Riuró H, et al. Among authors: coll vidal m.
Eur J Hum Genet. 2015 Jan;23(1):79-85. doi: 10.1038/ejhg.2014.54. Epub 2014 Mar 26.
Eur J Hum Genet. 2015.
PMID: 24667783
Free PMC article.
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Sudden Death without a Clear Cause after Comprehensive Investigation: An Example of Forensic Approach to Atypical/Uncertain Findings.
Grassi S, Vidal MC, Campuzano O, Arena V, Alfonsetti A, Rossi SS, Scarnicci F, Iglesias A, Brugada R, Oliva A.
Grassi S, et al. Among authors: vidal mc.
Diagnostics (Basel). 2021 May 17;11(5):886. doi: 10.3390/diagnostics11050886.
Diagnostics (Basel). 2021.
PMID: 34067575
Free PMC article.
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Mild Beckwith-Wiedemann and severe long-QT syndrome due to deletion of the imprinting center 2 on chromosome 11p.
Gurrieri F, Zollino M, Oliva A, Pascali V, Orteschi D, Pietrobono R, Camporeale A, Coll Vidal M, Partemi S, Brugada R, Bellocci F, Neri G.
Gurrieri F, et al. Among authors: coll vidal m.
Eur J Hum Genet. 2013 Sep;21(9):965-9. doi: 10.1038/ejhg.2012.280. Epub 2013 Mar 20.
Eur J Hum Genet. 2013.
PMID: 23511928
Free PMC article.
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Juvenile myoclonic epilepsy and Brugada type 1 ECG pattern associated with (a novel) plakophillin 2 mutation.
Gigli L, Bertero G, Vidal MC, Iglesias A, Campuzano O, Striano P, Oliva A, Brugada R.
Gigli L, et al. Among authors: vidal mc.
J Neurol. 2017 Apr;264(4):792-795. doi: 10.1007/s00415-017-8414-2. Epub 2017 Feb 20.
J Neurol. 2017.
PMID: 28220292
No abstract available.
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