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Page 1
Cardiovascular complications in children with chronic kidney injury.
Meo F, Salpietro A, Ceravolo G, Concolino D, De Sarro R, Gitto E, Viola I, Sestito S, Cucinotta U, Giannitto N, Cuppari C, Corso M, Ceravolo MD, Calabrò MP, Chimenz R. Meo F, et al. Among authors: concolino d. J Biol Regul Homeost Agents. 2020 Jul-Aug;34(4 Suppl. 2):43-46. SPECIAL ISSUE: FOCUS ON PEDIATRIC CARDIOLOGY. J Biol Regul Homeost Agents. 2020. PMID: 33000599 No abstract available.
Acid sphingomyelinase deficiency (ASMD): addressing knowledge gaps in unmet needs and patient journey in Italy-a Delphi consensus.
Scarpa M, Barbato A, Bisconti A, Burlina A, Concolino D, Deodato F, Di Rocco M, Dionisi-Vici C, Donati MA, Fecarotta S, Fiumara A, Galeone C, Giona F, Giuffrida G, Manna R, Mariani P, Pession A, Scopinaro A, Spada M, Spandonaro F, Trifirò G, Carubbi F, Cappellini MD. Scarpa M, et al. Among authors: concolino d. Intern Emerg Med. 2023 Apr;18(3):831-842. doi: 10.1007/s11739-023-03238-3. Epub 2023 Mar 7. Intern Emerg Med. 2023. PMID: 36882619
Anderson-Fabry disease in children.
Sestito S, Ceravolo F, Concolino D. Sestito S, et al. Among authors: concolino d. 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: concolino d. Gastroenterol Res Pract. 2016;2016:9712831. doi: 10.1155/2016/9712831. Epub 2015 Dec 31. Gastroenterol Res Pract. 2016. PMID: 26880903 Free PMC article.
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: concolino d. Nephrol Dial Transplant. 2018 Feb 1;33(2):318-323. doi: 10.1093/ndt/gfx009. Nephrol Dial Transplant. 2018. PMID: 28371803
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. Among authors: concolino d. Curr Gene Ther. 2018;18(2):90-95. doi: 10.2174/1566523218666180404155759. Curr Gene Ther. 2018. PMID: 29618310 Review.
149 results