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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: feriozzi s. 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
[Fabry disease].
Feriozzi S, Faraggiana T. Feriozzi S, et al. G Ital Nefrol. 2005 Nov-Dec;22 Suppl 33:S34-8. G Ital Nefrol. 2005. PMID: 16419004 Italian.
Early markers of Fabry disease revealed by proteomics.
Matafora V, Cuccurullo M, Beneduci A, Petrazzuolo O, Simeone A, Anastasio P, Mignani R, Feriozzi S, Pisani A, Comotti C, Bachi A, Capasso G. Matafora V, et al. Among authors: feriozzi s. Mol Biosyst. 2015 Jun;11(6):1543-51. doi: 10.1039/c4mb00707g. Mol Biosyst. 2015. PMID: 25666440
Parapelvic cysts, a distinguishing feature of renal Fabry disease.
Pisani A, Petruzzelli Annicchiarico L, Pellegrino A, Bruzzese D, Feriozzi S, Imbriaco M, Tedeschi E, Cocozza S, De Rosa D, Mignani R, Veroux M, Battaglia Y, Concolino D, Sestito S, Pieruzzi F, Caroti L, Manna R, Zizzo C, Santangelo M, Sabbatini M, Riccio E. Pisani A, et al. Among authors: feriozzi s. Nephrol Dial Transplant. 2018 Feb 1;33(2):318-323. doi: 10.1093/ndt/gfx009. Nephrol Dial Transplant. 2018. PMID: 28371803
Corpus callosum involvement: a useful clue for differentiating Fabry Disease from Multiple Sclerosis.
Cocozza S, Olivo G, Riccio E, Russo C, Pontillo G, Ugga L, Migliaccio S, de Rosa D, Feriozzi S, Veroux M, Battaglia Y, Concolino D, Pieruzzi F, Tuttolomondo A, Caronia A, Russo CV, Lanzillo R, Brescia Morra V, Imbriaco M, Brunetti A, Tedeschi E, Pisani A. Cocozza S, et al. Among authors: feriozzi s. Neuroradiology. 2017 Jun;59(6):563-570. doi: 10.1007/s00234-017-1829-8. Epub 2017 Apr 6. Neuroradiology. 2017. PMID: 28386689 Free article.
Redefining the Pulvinar Sign in Fabry Disease.
Cocozza S, Russo C, Pisani A, Olivo G, Riccio E, Cervo A, Pontillo G, Feriozzi S, Veroux M, Battaglia Y, Concolino D, Pieruzzi F, Mignani R, Borrelli P, Imbriaco M, Brunetti A, Tedeschi E, Palma G. Cocozza S, et al. Among authors: feriozzi s. AJNR Am J Neuroradiol. 2017 Dec;38(12):2264-2269. doi: 10.3174/ajnr.A5420. Epub 2017 Oct 19. AJNR Am J Neuroradiol. 2017. PMID: 29051208 Free PMC article.
Glomerular Hyperfiltration: An Early Marker of Nephropathy in Fabry Disease.
Riccio E, Sabbatini M, Bruzzese D, Annicchiarico Petruzzelli L, Pellegrino A, Spinelli L, Esposito R, Imbriaco M, Feriozzi S, Pisani A; on behalf of AFFIINITY Group. Riccio E, et al. Among authors: feriozzi s. Nephron. 2019;141(1):10-17. doi: 10.1159/000493469. Epub 2018 Nov 22. Nephron. 2019. PMID: 30466100
Mutations in the GLA Gene and LysoGb3: Is It Really Anderson-Fabry Disease?
Duro G, Zizzo C, Cammarata G, Burlina A, Burlina A, Polo G, Scalia S, Oliveri R, Sciarrino S, Francofonte D, Alessandro R, Pisani A, Palladino G, Napoletano R, Tenuta M, Masarone D, Limongelli G, Riccio E, Frustaci A, Chimenti C, Ferri C, Pieruzzi F, Pieroni M, Spada M, Castana C, Caserta M, Monte I, Rodolico MS, Feriozzi S, Battaglia Y, Amico L, Losi MA, Autore C, Lombardi M, Zoccali C, Testa A, Postorino M, Mignani R, Zachara E, Giordano A, Colomba P. Duro G, et al. Among authors: feriozzi s. Int J Mol Sci. 2018 Nov 23;19(12):3726. doi: 10.3390/ijms19123726. Int J Mol Sci. 2018. PMID: 30477121 Free PMC article.
129 results