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Page 1
Role of inflammation in pediatric irritable bowel syndrome.
Di Nardo G, Cremon C, Staiano A, Stanghellini V, Borrelli O, Strisciuglio C, Romano C, Mallardo S, Scarpato E, Marasco G, Salvatore S, Zenzeri L, Felici E, Pensabene L, Sestito S, Francavilla R, Quitadamo P, Baldassarre M, Giorgio V, Tambucci R, Ziparo C, Parisi P, Barbaro MR, Barbara G; Neurogastroenterology Study Group of the Italian Society of Pediatric Gastroenterology Hepatology, Nutrition (SIGENP). Di Nardo G, et al. Among authors: sestito s. Neurogastroenterol Motil. 2023 Mar;35(3):e14365. doi: 10.1111/nmo.14365. Epub 2022 Mar 27. Neurogastroenterol Motil. 2023. PMID: 35340083 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.
Genetic variants associated with gastrointestinal symptoms in Fabry disease.
Di Martino MT, Scionti F, Sestito S, Nicoletti A, Arbitrio M, Hiram Guzzi P, Talarico V, Altomare F, Sanseviero MT, Agapito G, Pisani A, Riccio E, Borrelli O, Concolino D, Pensabene L. Di Martino MT, et al. Among authors: sestito s. Oncotarget. 2016 Dec 27;7(52):85895-85904. doi: 10.18632/oncotarget.13135. Oncotarget. 2016. PMID: 27825144 Free PMC article.
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.
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
Werner syndrome: a rare mutation.
Castagna A, Gareri P, Falvo F, Sestito S, Rocca M, Pensabene L, Concolino D, Coppolino G, Ruotolo G. Castagna A, et al. Among authors: sestito s. Aging Clin Exp Res. 2019 Mar;31(3):425-429. doi: 10.1007/s40520-018-0982-1. Epub 2018 Jun 6. Aging Clin Exp Res. 2019. PMID: 29876830 No abstract available.
105 results