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Page 1
Mitochondrial DNA haplogroups may influence Fabry disease phenotype.
Simoncini C, Chico L, Concolino D, Sestito S, Fancellu L, Boadu W, Sechi GP, Feliciani C, Gnarra M, Zampetti A, Salviati A, Scarpelli M, Orsucci D, Bonuccelli U, Siciliano G, Mancuso M. Simoncini C, et al. Among authors: fancellu l. Neurosci Lett. 2016 Aug 26;629:58-61. doi: 10.1016/j.neulet.2016.06.051. Epub 2016 Jun 27. Neurosci Lett. 2016. PMID: 27365132
Genetic Screening of Anderson-Fabry Disease in Probands Referred From Multispecialty Clinics.
Favalli V, Disabella E, Molinaro M, Tagliani M, Scarabotto A, Serio A, Grasso M, Narula N, Giorgianni C, Caspani C, Concardi M, Agozzino M, Giordano C, Smirnova A, Kodama T, Giuliani L, Antoniazzi E, Borroni RG, Vassallo C, Mangione F, Scelsi L, Ghio S, Pellegrini C, Zedde M, Fancellu L, Sechi G, Ganau A, Piga S, Colucci A, Concolino D, Di Mascio MT, Toni D, Diomedi M, Rapezzi C, Biagini E, Marini M, Rasura M, Melis M, Nucera A, Guidetti D, Mancuso M, Scoditti U, Cassini P, Narula J, Tavazzi L, Arbustini E. Favalli V, et al. Among authors: fancellu l. J Am Coll Cardiol. 2016 Sep 6;68(10):1037-50. doi: 10.1016/j.jacc.2016.05.090. J Am Coll Cardiol. 2016. PMID: 27585509 Free article.
Urine bikunin as a marker of renal impairment in Fabry's disease.
Lepedda AJ, Fancellu L, Zinellu E, De Muro P, Nieddu G, Deiana GA, Canu P, Concolino D, Sestito S, Formato M, Sechi G. Lepedda AJ, et al. Among authors: fancellu l. Biomed Res Int. 2013;2013:205948. doi: 10.1155/2013/205948. Epub 2013 Jun 12. Biomed Res Int. 2013. PMID: 23841057 Free PMC article.
Primary motor cortex hyperexcitability in Fabry's disease.
Ortu E, Fancellu L, Sau G, Falchi P, Traccis S, Pes GM, Ganau A, Sechi G. Ortu E, et al. Among authors: fancellu l. Clin Neurophysiol. 2013 Jul;124(7):1381-9. doi: 10.1016/j.clinph.2013.02.005. Epub 2013 Mar 7. Clin Neurophysiol. 2013. PMID: 23474053
11 results