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Recommendations for the inclusion of Fabry disease as a rare febrile condition in existing algorithms for fever of unknown origin.
Manna R, Cauda R, Feriozzi S, Gambaro G, Gasbarrini A, Lacombe D, Livneh A, Martini A, Ozdogan H, Pisani A, Riccio E, Verrecchia E, Dagna L; International Panel for RAre recurrent FUO-IPRAFUO. Manna R, et al. Among authors: verrecchia e. Intern Emerg Med. 2017 Oct;12(7):1059-1067. doi: 10.1007/s11739-017-1704-y. Epub 2017 Jul 19. Intern Emerg Med. 2017. PMID: 28726033
Functional and pharmacological evaluation of novel GLA variants in Fabry disease identifies six (two de novo) causative mutations and two amenable variants to the chaperone DGJ.
Ferri L, Malesci D, Fioravanti A, Bagordo G, Filippini A, Ficcadenti A, Manna R, Antuzzi D, Verrecchia E, Donati I, Mignani R, Cavicchi C, Guerrini R, Morrone A. Ferri L, et al. Among authors: verrecchia e. Clin Chim Acta. 2018 Jun;481:25-33. doi: 10.1016/j.cca.2018.02.021. Epub 2018 Feb 21. Clin Chim Acta. 2018. PMID: 29476735 Free article.
Right ventricular strain in Anderson-Fabry disease.
Lillo R, Graziani F, Panaioli E, Mencarelli E, Pieroni M, Camporeale A, Manna R, Sicignano LL, Verrecchia E, Lombardo A, Lanza GA, Crea F. Lillo R, et al. Among authors: verrecchia e. Int J Cardiol. 2021 May 1;330:84-90. doi: 10.1016/j.ijcard.2021.02.038. Epub 2021 Feb 15. Int J Cardiol. 2021. PMID: 33600844
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