CEREDA, CRISTINA
CEREDA, CRISTINA
Dipartimento di Scienze Biomediche e Cliniche
Development and characterization of 3D spinal cord organoids to advance the study of amyotrophic lateral sclerosis
2026 M. Bordoni, E. Scarian, L. Messa, M. Garofalo, E. Jacchetti, M.T. Raimondi, L. Diamanti, S. Gagliardi, S. Carelli, C. Cereda, O. Pansarasa
Predicting congenital hypothyroidism in newborns with complex risk profiles by using thyroid-stimulating hormone variations across serial dried blood spots
2026 L. Cappelletti, A. Gaviglio, S. Moggia, S. Lucchi, L. Lalli, S. Fede, L. Cannella, M.C. Vigone, G. Zuccotti, A. Zambon, C. Cereda, S. Ferraro
Study of POLR3A variants in a family trio suggests mutation-specific pathogenetic mechanisms: insights from integrative OMIC approaches
2026 F. Rey, A. Casamassa, S. Di Cristofano, L. Esposito, A.A. Soriano, L. Messa, C. Berardo, M. Hazrati, I. Ferrone, M. Bonnet, F. Bruschi, Y. Vaia, M. Marano, E. Bertini, F. Nicita, D. Tonduti, G. Zuccotti, A.L. Vescovi, D. Raimondo, J. Rosati, S. Carelli, C. Cereda
Metformin Reduces Oxidative Damage in RNASEH2-Mutant Aicardi-Goutières Cells
2025 F. Dragoni, J. Garau, B. Rizzo, S. Orcesi, C. Varesio, R. Di Gerlando, M. Bordoni, E. Scarian, C. Cereda, O. Pansarasa, S. Gagliardi
Gene expression analysis in subcutaneous adipose tissue reveals a predominant influence of lncRNAs during growth
2025 F. Rey, L. Messa, C. Berardo, A. Mauri, G. Zuccotti, C. Cereda, S. Carelli
Landscape Analysis of COL6A1, COL6A2, and COL6A3 Pathogenic Variants in a Large Italian Cohort Presenting with Collagen VI-Related Myopathies: A Nationwide Report
2025 F. Fortunato, L. Fiocco, A. Margutti, M. Neri, A. D'Amico, E. Bertini, E. Ricci, E.M. Mercuri, M. Pane, R. Massa, G. Greco, A.L. Berardinelli, C. Cereda, A. Pini, L. Merlini, C. Fusco, C. Rodolico, S. Messina, C. Fiorillo, C. Bruno, M. Pedemonte, M. Traverso, I. Moroni, L. Maggi, S. Gibertini, E. Pegoraro, E. Picillo, L. Politano, M. Scutifero, F. Vercellino, F. Massaro, M. Filosto, P. Gasparini, F. Ricci, T.E. Mongini, R. Selvatici, A. Ferlini, F. Gualandi
Newborn Screening of X-Linked Adrenoleukodystrophy in Italy: Clinical and Biochemical Outcomes from a 4-Year Pilot Study
2025 E. Bonaventura, F. Bruschi, L. Alberti, C. Antonello, F. Arrigoni, M. Balestriero, B. Borsani, L. Cappelletti, E. Cattaneo, M. Ferrario, G. Fiore, M. Iascone, G. Izzo, S. Lucchi, C. Parazzini, M. Perrone Donnorso, L. Spaccini, Y. Vaia, P. Veggiotti, E. Verduci, G. Zuccotti, C. Cereda, D. Tonduti, X. Study Group
Medium-Chain Acyl-CoA Dehydrogenase Deficiency (MCADD) Newborn Screening in Italy: Five Years’ Experience from a Nationwide Program
2025 M. Ruoppolo, C. Cereda, T. Giovanniello, S. Malvagia, S. Boenzi, F. Teofoli, O. Behalf Of The Simmesn Italian Newborn Screening Group, A. Burlina
Expanded Newborn Screening in Italy: The First Report of Lombardy Region
2025 C. Berardo, A. Vasco, A. Mauri, S. Lucchi, L. Cappelletti, L. Saielli, M. Rizzetto, D. Biganzoli, C. Montrasio, D. Postorivo, E. Pratiffi, A. Meta, S. Carelli, A. Amorosi, S. Paci, G. Cefalo, F. Furlan, F. Menni, S. Gasperini, V. Crescitelli, G. Banderali, G. Zuccotti, L. Alberti, C. Cereda
Mitochondrial Acetoacetyl-CoA Thiolase Deficiency: Three New Cases Detected by Newborn Screening Confirming the Significance of C4OH Elevation
2025 A. Vasco, C. Berardo, S. Lucchi, L. Cappelletti, G. Tamburello, S. Fazzone, A. Mauri, F. Fiumani, D. Postorivo, L. Alberti, M. Perrone Donnorso, S. Gasperini, F. Furlan, L. Fiori, S. Carelli, L.A. Saielli, C. Montrasio, C. Cereda
Prediction of evolution to epilepsy or genetic epilepsy with febrile seizures plus (GEFS+) in children presenting with febrile seizures: a retrospective multicenter longitudinal study
2025 P. Baso, S. Masnada, M.M. Lodi, F. Teutonico, A. Vignoli, E. Ricci, M.P. Canevini, F. Brustia, M. Viri, C. Cereda, L. Lalli, S. Ferraro, P. Veggiotti
Amino Acid Patterns in Childdren with Autistic Spectrum Disorder: A Preliminary Biochemical Evaluation
2025 S. Ferraro, L. Saielli, D. Biganzoli, M. Tosi, L. Guidi, R. Longo, F. Severino, S. Carelli, M. Rossi, L. Pisciotta, E. Ricci, F. Brustia, E. Verduci, G. Zuccotti, M. Mussap, C. Cereda
Extended Lombardy’s Neonatal Screening Dataset
2025 G. Lopiano, L. Alberti, C. Cereda, F. Cabitza
Dietary pattginern and nutritional assessment in a cohort of mothers identified by neonatal screening for cobalamin deficiency in offspring: an Italian single center experience
2025 M. Tosi, V.M. Tagi, A. Colombo, A. Cecchini, M. Zobele, C. Montanari, S. Ferraro, A. Bosetti, E. Bonaventura, F. Bruschi, D. De Zan, G. Fiore, C. Cereda, G. Zuccotti, E. Verduci
Beyond newborn screening: the role of reverse cascade testing in familial disease detection
2025 A. Gaviglio, K. Petritis, V. Tagi, A. Vasco, A. Mauri, G. Zuccotti, E. Verduci, C. Cereda, S. Ferraro
Newborn screening for congenital adrenal hyperplasia due to 21 hydroxylase deficiency: the Italian experience 2006–2019
2025 F. Baronio, E. Abrigo, S. Azzolini, P. Cavarzere, C. Cereda, L. De Sanctis, S.L.C. Meroni, J. Munarin, F. Righetti, G. Russo, F. Teofoli, A. Balsamo
Modeling unknowns: A vision for uncertainty-aware machine learning in healthcare
2025 A. Campagner, E.M. Biganzoli, C. Balsano, C. Cereda, F. Cabitza
Newborn Screening for Metachromatic Leukodystrophy in Tuscany: The Paradigm of a Successful Preventive Medicine Program
2025 S. Malvagia, A. Bettiol, M. Porcaro, M. Mura, S. Funghini, D. Ombrone, G. Forni, E. Scolamiero, F. Coppi, R. Damiano, C. Cereda, S. Simonetti, A. Lonetti, M. Daniotti, A. Caciotti, A. Morrone, V. Calbi, F. Fumagalli, A. Aiuti, E. Procopio, R. Guerrini, G. La Marca
Biochemical evidence of vitamin B12 deficiency: a crucial issue to address supplementation in pregnant women
2025 S. Ferraro, C. Cereda, G. Zuccotti
Vitamin B12 Deficiency and New Recommendations by the National Institute for Health and Care Excellence: A Challenging Clinical and Laboratory Topic
2025 S. Ferraro, S. Da Molin, C. Cereda, G. Zuccotti, S. Marcovina, B.M. Cesana