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Inherited rare variants in homologous recombination and neurodevelopmental genes are associated with increased risk of neuroblastoma.
Bonfiglio F, Lasorsa VA, Cantalupo S, D'Alterio G, Aievola V, Boccia A, Ardito M, Furini S, Renieri A, Morini M, Stainczyk S, Westermann F, Paolella G, Eva A, Iolascon A, Capasso M. Bonfiglio F, et al. Among authors: ardito m. EBioMedicine. 2023 Jan;87:104395. doi: 10.1016/j.ebiom.2022.104395. Epub 2022 Dec 6. EBioMedicine. 2023. PMID: 36493725 Free PMC article.
Emerging multisystem biomarkers in hereditary transthyretin amyloidosis: a pilot study.
Luigetti M, Vitali F, Romano A, Sciarrone MA, Guglielmino V, Ardito M, Sabino A, Servidei S, Piro G, Carbone C, Graziani F, Lillo R, Ferraro PM, Primiano G. Luigetti M, et al. Among authors: ardito m. Sci Rep. 2024 Aug 7;14(1):18281. doi: 10.1038/s41598-024-69123-x. Sci Rep. 2024. PMID: 39112608 Free PMC article.
Immune Tolerance-Adjusted Personalized Immunogenicity Prediction for Pompe Disease.
De Groot AS, Desai AK, Lelias S, Miah SMS, Terry FE, Khan S, Li C, Yi JS, Ardito M, Martin WD, Kishnani PS. De Groot AS, et al. Among authors: ardito m. Front Immunol. 2021 Jun 16;12:636731. doi: 10.3389/fimmu.2021.636731. eCollection 2021. Front Immunol. 2021. PMID: 34220802 Free PMC article. Clinical Trial.
34 results