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Neuropsychological tests at the Italian Centers for Cognitive Disorders and Dementias: results from a survey on 450 specialized services.
Vaccaro R, Lorenzini P, Giaquinto F, Matascioli F, Carnevale G, Sciancalepore F, Gasparini M, Salvi E, Corbo M, Locuratolo N, Vanacore N, Bacigalupo I; Permanent Table of the National Dementia Plan Study Group; CCDDs Study Group. Vaccaro R, et al. Aging Clin Exp Res. 2024 Dec 20;37(1):1. doi: 10.1007/s40520-024-02869-6. Aging Clin Exp Res. 2024. PMID: 39704981 Free PMC article.
A new national survey of centers for cognitive disorders and dementias in Italy.
Bacigalupo I, Giaquinto F, Salvi E, Carnevale G, Vaccaro R, Matascioli F, Remoli G, Vanacore N, Lorenzini P; Permanent Table of the National Dementia Plan Study Group and the CCDDs Study Group. Bacigalupo I, et al. Neurol Sci. 2024 Feb;45(2):525-538. doi: 10.1007/s10072-023-06958-8. Epub 2023 Aug 18. Neurol Sci. 2024. PMID: 37592124 Free PMC article.
Improving Discharge Safety in a Pediatric Emergency Department.
Paydar-Darian N, Stack AM, Volpe D, Gerling MJ, Seneski A, Eisenberg MA, Hickey E, Toomey Lindsay K, Moriarty L, Hudgins JD, Falvo F, Portillo EN, Creedon JK, Perron CE. Paydar-Darian N, et al. Among authors: falvo f. Pediatrics. 2022 Nov 1;150(5):e2021054307. doi: 10.1542/peds.2021-054307. Pediatrics. 2022. PMID: 36222092
Renal involvement in paediatric Fabry disease.
Sestito S, Falvo F, Sallemi A, Petrisano M, Scuderi MG, Tarsitano F, D'Angelo G, Betta P, Roppa K, Parisi F, Pensabene L, Fede C, Chimenz R, Concolino D. Sestito S, et al. Among authors: falvo f. J Biol Regul Homeost Agents. 2019 Sep-Oct;33(5 Suppl. 1):59-63. Special Issue: Focus on Pediatric Nephrology. J Biol Regul Homeost Agents. 2019. PMID: 31630715
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: falvo f. 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: falvo f. 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.
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: falvo f. Curr Gene Ther. 2018;18(2):90-95. doi: 10.2174/1566523218666180404155759. Curr Gene Ther. 2018. PMID: 29618310 Review.
28 results