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Novel alpha-galactosidase A mutation in a female with recurrent strokes.
Tuttolomondo A, Duro G, Miceli S, Di Raimondo D, Pecoraro R, Serio A, Albeggiani G, Nuzzo D, Iemolo F, Pizzo F, Sciarrino S, Licata G, Pinto A. Tuttolomondo A, et al. Among authors: miceli s. Clin Biochem. 2012 Nov;45(16-17):1525-30. doi: 10.1016/j.clinbiochem.2012.07.085. Epub 2012 Jul 20. Clin Biochem. 2012. PMID: 22820434
Anderson-Fabry disease: a multiorgan disease.
Tuttolomondo A, Pecoraro R, Simonetta I, Miceli S, Pinto A, Licata G. Tuttolomondo A, et al. Among authors: miceli s. Curr Pharm Des. 2013;19(33):5974-96. doi: 10.2174/13816128113199990352. Curr Pharm Des. 2013. PMID: 23448451 Review.
Neurological complications of Anderson-Fabry disease.
Tuttolomondo A, Pecoraro R, Simonetta I, Miceli S, Arnao V, Licata G, Pinto A. Tuttolomondo A, et al. Among authors: miceli s. Curr Pharm Des. 2013;19(33):6014-30. doi: 10.2174/13816128113199990387. Curr Pharm Des. 2013. PMID: 23448452 Review.
Inter-familial and intra-familial phenotypic variability in three Sicilian families with Anderson-Fabry disease.
Tuttolomondo A, Simonetta I, Duro G, Pecoraro R, Miceli S, Colomba P, Zizzo C, Nucera A, Daidone M, Di Chiara T, Scaglione R, Della Corte V, Corpora F, Vogiatzis D, Pinto A. Tuttolomondo A, et al. Among authors: miceli s. Oncotarget. 2017 May 29;8(37):61415-61424. doi: 10.18632/oncotarget.18250. eCollection 2017 Sep 22. Oncotarget. 2017. PMID: 28977874 Free PMC article.
Genetics and Gene Therapy of Anderson-Fabry Disease.
Simonetta I, Tuttolomondo A, Di Chiara T, Miceli S, Vogiatzis D, Corpora F, Pinto A. Simonetta I, et al. Among authors: miceli s. Curr Gene Ther. 2018;18(2):96-106. doi: 10.2174/1566523218666180404161315. Curr Gene Ther. 2018. PMID: 29618309 Review.
Treatment of Anderson-Fabry Disease.
Simonetta I, Tuttolomondo A, Daidone M, Miceli S, Pinto A. Simonetta I, et al. Among authors: miceli s. Curr Pharm Des. 2020;26(40):5089-5099. doi: 10.2174/1381612826666200317142412. Curr Pharm Des. 2020. PMID: 32183665 Review.
171 results