CEREDA, CRISTINA
CEREDA, CRISTINA
Dipartimento di Scienze Biomediche e Cliniche
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
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
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
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
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
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
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
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
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
Novel frontiers in aicardi-goutières syndrome: association between a rnu7-1 variant and histone dysfunctions
2024 E. Maghraby, F. Rey, L. Esposito, M. Leone, A. Mauri, R. Allevi, S. Mazzucchelli, G. Zuccotti, D. Tonduti, S. Carelli, C. Cereda
P.47 Association between cobalamin deficiency detected through newborn screening and creatine levels in mothers and their offspring in the neonatal period
2024 M. Tosi, L. Fiori, C. Montanari, L. Alberti, A. Meta, V. Tagi, G. Zuccotti, C. Cereda, E. Verduci
Transcriptional profiling and functional characterization of three genetic variants in SLC16A2 gene
2024 L. Esposito, F. Rey, E. Maghraby, L. Messa, M. Elli, F. Bruschi, G. Zuccotti, L. Alberti, D. Tonduti, S. Carelli, C. Cereda
Functional characterization and transcriptional profiling of fibroblasts from patients with mutations in SLC16A2 gene
2024 L. Esposito, F. Rey, E. Maghraby, L. Messa, F. Bruschi, G. Zuccotti, D. Tonduti, S. Carelli, C. Cereda
Further insights into Allan-Herndon-Dudley syndrome: a novel SLC16A2 splice site variant
2024 L. Esposito, A. Mauri, F. Rey, E. Maghraby, B. Castellotti, G. Zuccotti, D. Tonduti, S. Carelli, C. Cereda
Transcriptional profiling and functional characterization of 3 patient-derived skin fibroblasts affected by Allan-Herndon-Dudley syndrome
2024 L. Esposito, F. Rey, E. Maghraby, L. Messa, M. Elli, F. Bruschi, G. Zuccotti, D. Tonduti, S. Carelli, C. Cereda
Functional Study of SNCA p.V15A Variant: Further Linking α-Synuclein and Glucocerebrosidase
2024 M. Avenali, S. Cerri, I. Palmieri, G. Ongari, R. Stiuso, G. Buongarzone, C. Tassorelli, T. Biagini, M. Valente, C. Cereda, T. Mazza, S. Gana, C. Pacchetti, E.M. Valente
Cobalamin deficiency in the maternal-newborn dyad identified by neonatal screening: preliminary data from an observational study
2024 C. Montanari, M. Tosi, L. Fiori, A. Lugotti, A. Bosetti, E. Bonaventura, D. Tonduti, L. Alberti, L. Assunta Saielli, C. Cereda, G. Zuccotti, E. Verduci