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Page 1
Alagille Syndrome: A Novel Mutation in JAG1 Gene.
Fischetto R, Palmieri VV, Tripaldi ME, Gaeta A, Michelucci A, Delvecchio M, Francavilla R, Giordano P. Fischetto R, et al. Among authors: tripaldi me. Front Pediatr. 2019 May 15;7:199. doi: 10.3389/fped.2019.00199. eCollection 2019. Front Pediatr. 2019. PMID: 31157196 Free PMC article.
Substrate reduction therapy with Miglustat in pediatric patients with GM1 type 2 gangliosidosis delays neurological involvement: A multicenter experience.
Fischetto R, Palladino V, Mancardi MM, Giacomini T, Palladino S, Gaeta A, Di Rocco M, Zampini L, Lassandro G, Favia V, Tripaldi ME, Strisciuglio P, Romano A, Severino M, Morrone A, Giordano P. Fischetto R, et al. Among authors: tripaldi me. Mol Genet Genomic Med. 2020 Oct;8(10):e1371. doi: 10.1002/mgg3.1371. Epub 2020 Aug 11. Mol Genet Genomic Med. 2020. PMID: 32779865 Free PMC article.
Intervention for Dysbiosis in Children Born by C-Section.
Francavilla R, Cristofori F, Tripaldi ME, Indrio F. Francavilla R, et al. Among authors: tripaldi me. Ann Nutr Metab. 2018;73 Suppl 3:33-39. doi: 10.1159/000490847. Epub 2018 Jul 24. Ann Nutr Metab. 2018. PMID: 30041184 Review.