FONTANA, LAURA
FONTANA, LAURA
Dipartimento di Scienze della Salute
High-phosphate Causes Endothelial Extracellular Matrix Calcification by Inducing Endothelial Cell Mesenchymal Transition and Osteoblastic Differentiation
2025 P. Ciceri, L. Artioli, M. Molinaro, M. Falleni, D. Tosi, C. Martinelli, N. Santo, O. Rondinone, M. Miozzo, P. Bianchi, U. Gianelli, L. Fontana, M. Cozzolino
Metabolic reprogramming and altered ATP content impair neuroprotective functions of microglia in β-glucocerebrosidase deficiency models
2025 E. Brunialti, A. Villa, E.M. Szego, P. La Vitola, D. Drago, R. Pavlovic, L. Fontana, D. Tuna, A. Panzeri, C. Meda, C. Weissleder, O. Rondinone, M. Pitasi, M. Miozzo, M. Deleidi, A. Andolfo, D.A. Di Monte, P. Ciana
Dysfunction in IGF2R Pathway and Associated Perturbations in Autophagy and WNT Processes in Beckwith–Wiedemann Syndrome Cell Lines
2024 S. Pileggi, E.A. Colombo, S. Ancona, R. Quadri, C. Bernardelli, P. Colapietro, M. Taiana, L. Fontana, M. Miozzo, E. Lesma, S.M. Sirchia
Testing calpain inhibition in tumor endothelial cells: novel targetable biomarkers against glioblastoma malignancy
2024 L. Guarnaccia, S.E. Navone, L. Begani, E. Barilla, E. Garzia, R. Campanella, M. Miozzo, L. Fontana, G. Alotta, C. Cordiglieri, C. Gaudino, L. Schisano, A. Ampollini, L. Riboni, M. Locatelli, G. Marfia
Exploring the Impact of Genetics in a Large Cohort of Moebius Patients by Trio Whole Exome Sequencing
2024 G. Moresco, M.F. Bedeschi, M. Venturin, R. Villa, J. Costanza, A. Mauri, C. Santaniello, O. Picciolini, L. Messina, F. Triulzi, M.R. Miozzo, O. Rondinone, L. Fontana
Non-invasive biomarkers for sperm retrieval in non-obstructive patients: a comprehensive review
2024 L. Fontana, S.M. Sirchia, C. Pesenti, G.M. Colpi, M.R. Miozzo
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
Novel pathogenetic variants in PTHLH and TRPS1 genes causing syndromic brachydactyly
2022 F.M. Elli, D. Mattinzoli, C. Lucca, M. Piu, M.A. Maffini, J. Costanza, L. Fontana, C. Santaniello, C. Forino, D. Milani, M.T. Bonati, A. Secco, R. Gastaldi, C. Alfieri, P. Messa, M. Miozzo, M. Arosio, G. Mantovani
Assessment of pregnancy dietary intake and association with maternal and neonatal outcomes
2022 J. Costanza, M. Camanni, M.M. Ferrari, V. De Cosmi, S. Tabano, L. Fontana, T. Radaelli, G. Privitera, D. Alberico, P. Colapietro, S. Motta, S. Sirchia, T. Stampalija, C. Tabasso, P. Roggero, F. Parazzini, F. Mosca, E. Ferrazzi, S. Bosari, M. Miozzo, C. Agostoni
Preferential X Chromosome Inactivation as a Mechanism to Explain Female Preponderance in Myasthenia Gravis
2022 V. Nicol(`(i)), S.M. Tabano, P. Colapietro, M. Maestri, R. Ricciardi, A. Stoccoro, L. Fontana, M. Guida, M.R. Miozzo, F. Copped(`(e)), L. Migliore
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
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
Epigenetics of functional hypothalamic amenorrhea
2022 L. Fontana, E. Garzia, G. Marfia, V. Galiano, M. Miozzo
The Genetic and Epigenetic Footprint in Idiopathic Pulmonary Fibrosis and Familial Pulmonary Fibrosis: A State-of-the-Art Review
2022 C. Tirelli, C. Pesenti, M. Miozzo, M. Mondoni, L. Fontana, S. Centanni
Mental health and the effects on methylation of stress-related genes in front-line versus other health care professionals during the second wave of COVID-19 pandemic: an Italian pilot study
2022 S. Tabano, L. Tassi, M. Cannone, G. Brescia, G. Gaudioso, M. Ferrara, P. Colapietro, L. Fontana, M. Miozzo, G. Croci, M. Seia, C. Piuma, M. Solbiati, E. Tobaldini, S. Ferrero, N. Montano, G. Costantino, M. Buoli
Cohesin mutations induce chromatin conformation perturbation of the H19/IGF2 imprinted region and gene expression dysregulation in Cornelia de Lange syndrome cell lines
2021 S. Pileggi, M. La Vecchia, E.A. Colombo, L. Fontana, P. Colapietro, D. Rovina, A. Morotti, S.M. Tabano, G. Porta, M. Alcalay, C.C.G. Gervasini, M.R. Miozzo, S.M. Sirchia
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
Forecasting the burden of COVID-19 hospitalized patients during the SARS-CoV-2 second wave in Lombardy, Italy
2021 A.G. Gerli, M. Miozzo, S. Centanni, L. Fontana, D. Chiumello, G. Sotgiu, C. La Vecchia
Decreased serum level of sphingosine-1-phosphate: a novel predictor of clinical severity in COVID-19
2021 G. Marfia, S. Navone, L. Guarnaccia, R. Campanella, M. Mondoni, M. Locatelli, A. Barassi, L. Fontana, F. Palumbo, E. Garzia, G. Ciniglio Appiani, D. Chiumello, M. Miozzo, S. Centanni, L. Riboni
Clinical and molecular diagnosis of beckwith-wiedemann syndrome with single-or multi-locus imprinting disturbance
2021 L. Fontana, S. Tabano, S. Maitz, P. Colapietro, E. Garzia, A.G. Gerli, S.M. Sirchia, M. Miozzo