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Norrbottnian clinical variant of Gaucher disease in Southern Italy.
Sestito S, Filocamo M, Ceravolo F, Falvo F, Grisolia M, Moricca MT, Cantaffa R, Grossi S, Strisciuglio P, Concolino D. Sestito S, et al. J Hum Genet. 2017 Apr;62(4):507-511. doi: 10.1038/jhg.2016.158. Epub 2016 Dec 22. J Hum Genet. 2017. PMID: 28003644
Anderson-Fabry disease in children.
Sestito S, Ceravolo F, Concolino D. Sestito S, et al. Curr Pharm Des. 2013;19(33):6037-45. doi: 10.2174/13816128113199990345. Curr Pharm Des. 2013. PMID: 23448455 Review.
Gastrointestinal Symptoms of Patients with Fabry Disease.
Pensabene L, Sestito S, Nicoletti A, Graziano F, Strisciuglio P, Concolino D. Pensabene L, et al. Among authors: sestito s. Gastroenterol Res Pract. 2016;2016:9712831. doi: 10.1155/2016/9712831. Epub 2015 Dec 31. Gastroenterol Res Pract. 2016. PMID: 26880903 Free PMC article.
Alport's syndrome.
Bruni V, Petrisano M, Tarsitano F, Falvo F, Parisi F, Cucinotta U, Betta P, Di Benedetto V, Scuderi MG, Pensabene L, Sestito S, Cuppari C, Fede C, Chimenz R, Concolino D. Bruni V, et al. Among authors: sestito s. J Biol Regul Homeost Agents. 2019 Sep-Oct;33(5 Suppl. 1):19-24. Special Issue: Focus on Pediatric Nephrology. J Biol Regul Homeost Agents. 2019. PMID: 31630709
Genetics and Gene Therapy in Hunter Disease.
Sestito S, Falvo F, Scozzafava C, Apa R, Pensabene L, Bonapace G, Moricca MT, Concolino D. Sestito S, et al. Curr Gene Ther. 2018;18(2):90-95. doi: 10.2174/1566523218666180404155759. Curr Gene Ther. 2018. PMID: 29618310 Review.
Risk of autoimmune diseases in patients with RASopathies: systematic study of humoral and cellular immunity.
Siano MA, Marchetti V, Pagano S, Di Candia F, Alessio M, De Brasi D, De Luca A, Pinna V, Sestito S, Concolino D, Tartaglia M, Strisciuglio P, D'Esposito V, Cabaro S, Perruolo G, Formisano P, Melis D. Siano MA, et al. Among authors: sestito s. Orphanet J Rare Dis. 2021 Oct 2;16(1):410. doi: 10.1186/s13023-021-02050-6. Orphanet J Rare Dis. 2021. PMID: 34600590 Free PMC article.
105 results