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Page 1
The Diagnosis and Management of Chronic Constipation in Italy: Results from a Survey Conducted among Italian Gastroenterologists.
Lambiase C, D'Alba L, Galeazzi F, Bassotti G, Consalvo D, Battaglia E, Cataudella G, Neri MC, Londoni C, Rossitti P, Valenzi E, Annibale B, Soncini M, Parodi MC, Bellini M. Lambiase C, et al. Among authors: consalvo d. J Clin Med. 2024 Oct 10;13(20):6047. doi: 10.3390/jcm13206047. J Clin Med. 2024. PMID: 39457997 Free PMC article.
Identification and management of gastrointestinal manifestations of hereditary transthyretin amyloidosis: Recommendations from an Italian group of experts.
Cappello M, Barbara G, Bellini M, Consalvo D, Di Sabatino A, Marasco G, Principi M, Savarino EV, Tortora A, Obici L. Cappello M, et al. Among authors: consalvo d. Dig Liver Dis. 2024 Jun;56(6):1014-1020. doi: 10.1016/j.dld.2023.11.025. Epub 2023 Dec 17. Dig Liver Dis. 2024. PMID: 38105149 Free article.
A familiar study on self-limited childhood epilepsy patients using hIPSC-derived neurons shows a bias towards immaturity at the morphological, electrophysiological and gene expression levels.
Casalia ML, Casabona JC, García C, Cavaliere Candedo V, Quintá HR, Farías MI, Gonzalez J, Gonzalez Morón D, Córdoba M, Consalvo D, Mostoslavsky G, Urbano FJ, Pasquini J, Murer MG, Rela L, Kauffman MA, Pitossi FJ. Casalia ML, et al. Among authors: consalvo d. Stem Cell Res Ther. 2021 Nov 25;12(1):590. doi: 10.1186/s13287-021-02658-2. Stem Cell Res Ther. 2021. PMID: 34823607 Free PMC article.
Diverse genetic causes of polymicrogyria with epilepsy.
Epilepsy Phenome/Genome Project, Epi4K Consortium. Epilepsy Phenome/Genome Project, Epi4K Consortium. Epilepsia. 2021 Apr;62(4):973-983. doi: 10.1111/epi.16854. Epub 2021 Apr 5. Epilepsia. 2021. PMID: 33818783 Free PMC article.
The odyssey of complex neurogenetic disorders: From undetermined to positive.
Salinas V, Vega P, Marsili L, Pérez-Maturo J, Martínez N, Zavala L, González-Morón D, Medina N, Rodriguez-Quiroga SA, Amartino H, Maxit C, Sturchio A, Grimberg B, Duque K, Comas B, Silva W, Consalvo D, Sfaello I, Espay AJ, Kauffman MA. Salinas V, et al. Among authors: consalvo d. Am J Med Genet C Semin Med Genet. 2020 Dec;184(4):876-884. doi: 10.1002/ajmg.c.31848. Epub 2020 Oct 20. Am J Med Genet C Semin Med Genet. 2020. PMID: 33084218
Identification of a somatic mutation in the RHEB gene through high depth and ultra-high depth next generation sequencing in a patient with Hemimegalencephaly and drug resistant Epilepsy.
Salinas V, Vega P, Piccirilli MV, Chicco C, Ciraolo C, Christiansen S, Consalvo D, Perez-Maturo J, Medina N, González-Morón D, Novaro V, Perrone C, García MDC, Agosta G, Silva W, Kauffman M. Salinas V, et al. Among authors: consalvo d. Eur J Med Genet. 2019 Nov;62(11):103571. doi: 10.1016/j.ejmg.2018.11.005. Epub 2018 Nov 8. Eur J Med Genet. 2019. PMID: 30414531
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