Sfoglia per Autore
Extensive placental methylation profiling in normal pregnancies
2021 O. Rondinone, A. Murgia, J. Costanza, S. Tabano, M. Camanni, L. Corsaro, L. Fontana, P. Colapietro, L. Calzari, S. Motta, C. Santaniello, T. Radaelli, E. Ferrazzi, S. Bosari, D. Gentilini, S.M. Sirchia, M. Miozzo
A novel de novo DDX3X missense variant in a female with brachycephaly and intellectual disability : a case report
2021 G. Moresco, J. Costanza, C. Santaniello, O. Rondinone, F. Grilli, E. Prada, S. Orcesi, I. Coro, A. Pichiecchio, P. Marchisio, M. Miozzo, L. Fontana, D. Milani
MMP1 drives tumor progression in large cell carcinoma of the lung through fibroblast senescence
2021 M. Gabasa, E.S. Radisky, R. Ikemori, G. Bertolini, M. Arshakyan, A. Hockla, P. Duch, O. Rondinone, A. Llorente, M. Maqueda, A. Davalos, E. Gavilan, A. Perera, J. Ramirez, P. Gascon, N. Reguart, L. Roz, D.C. Radisky, J. Alcaraz
Unraveling the genetic causes of Moebius syndrome
2022 G. Moresco, O. Rondinone, J. Costanza, C. Santaniello, L. Fontana, A. Mauri, M. Venturin, O. Picciolini, R. Villa, M. Miozzo, M.F. Bedeschi
Pitfalls of whole exome sequencing in undefined clinical conditions with a suspected genetic etiology
2022 G. Moresco, O. Rondinone, A. Mauri, J. Costanza, C. Santaniello, P. Colapietro, E. Micaglio, G. Marfia, C. Pesenti, F. Grilli, B. Rinaldi, E. Prada, G. Scuvera, R. Villa, M.F. Bedeschi, M.R. Miozzo, D. Milani, L. Fontana
Case report: Chorea and cognitive decline in a young woman: instrumental and genetic assessment of a case originally diagnosed as multiple sclerosis
2023 C. Dato, E. Micaglio, G. Moresco, O. Rondinone, P. Vitali, C. Pappone, L. Fontana, M. Miozzo, L. Bet
The Genetic Basis, Lung Involvement, and Therapeutic Options in Niemann–Pick Disease: A Comprehensive Review
2024 C. Tirelli, O. Rondinone, M. Italia, S. Mira, L.A. Belmonte, M. De Grassi, G. Guido, S. Maggioni, M. Mondoni, M.R. Miozzo, S. Centanni
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