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Renal and brain complications in GLA p.Phe113Leu Fabry disease. Comments on "Fabry disease caused by the GLA p.Phe113Leu (p.F113L) variant: Natural history in males" by Oliveira et al. (Eur. J. Med. Genet. 2019).
Smirnova A, Di Toro A, Giuliani L, Tagliani M, Urtis M, Favalli V, Arbustini E. Smirnova A, et al. Among authors: favalli v. Eur J Med Genet. 2020 Apr;63(4):103847. doi: 10.1016/j.ejmg.2020.103847. Epub 2020 Jan 13. Eur J Med Genet. 2020. PMID: 31945513 No abstract available.
Anderson-Fabry disease.
Di Toro A, Favalli V, Arbustini E. Di Toro A, et al. Among authors: favalli v. J Cardiovasc Med (Hagerstown). 2018 Feb;19 Suppl 1:e1-e5. doi: 10.2459/JCM.0000000000000637. J Cardiovasc Med (Hagerstown). 2018. PMID: 29538136 Review. No abstract available.
Pathologic substrate of gastropathy in Anderson-Fabry disease.
Di Toro A, Narula N, Giuliani L, Concardi M, Smirnova A, Favalli V, Urtis M, Alvisi C, Antoniazzi E, Arbustini E. Di Toro A, et al. Among authors: favalli v. Orphanet J Rare Dis. 2020 Jun 22;15(1):156. doi: 10.1186/s13023-020-01436-2. Orphanet J Rare Dis. 2020. PMID: 32571412 Free PMC article.
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. 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.
Common presentation of rare diseases: Aortic aneurysms & valves.
Arbustini E, Favalli V, Di Toro A, Giuliani L, Limongelli G. Arbustini E, et al. Among authors: favalli v. Int J Cardiol. 2018 Apr 15;257:358-365. doi: 10.1016/j.ijcard.2018.01.003. Int J Cardiol. 2018. PMID: 29506732 Review.
Genetics and clinics: current applications, limitations, and future developments.
Di Toro A, Giuliani L, Favalli V, Di Giovannantonio M, Smirnova A, Grasso M, Arbustini E. Di Toro A, et al. Among authors: favalli v. Eur Heart J Suppl. 2019 Mar;21(Suppl B):B7-B14. doi: 10.1093/eurheartj/suz048. Epub 2019 Mar 29. Eur Heart J Suppl. 2019. PMID: 30948934 Free PMC article. No abstract available.
Hereditary muscle diseases and the heart: the cardiologist's perspective.
Giuliani L, Di Toro A, Urtis M, Smirnova A, Concardi M, Favalli V, Serio A, Grasso M, Arbustini E. Giuliani L, et al. Among authors: favalli v. Eur Heart J Suppl. 2020 Jun;22(Suppl E):E13-E19. doi: 10.1093/eurheartj/suaa051. Epub 2020 Mar 29. Eur Heart J Suppl. 2020. PMID: 32523431 Free PMC article. No abstract available.
Myths to debunk: the non-compacted myocardium.
Di Toro A, Giuliani L, Smirnova A, Favalli V, Serio A, Urtis M, Grasso M, Arbustini E. Di Toro A, et al. Among authors: favalli v. Eur Heart J Suppl. 2020 Nov 18;22(Suppl L):L6-L10. doi: 10.1093/eurheartj/suaa124. eCollection 2020 Nov. Eur Heart J Suppl. 2020. PMID: 33654460 Free PMC article.
64 results