CEREDA, CRISTINA
CEREDA, CRISTINA
Dipartimento di Scienze Biomediche e Cliniche
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
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
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
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
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
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
Extended Lombardy’s Neonatal Screening Dataset
2025 G. Lopiano, L. Alberti, C. Cereda, F. Cabitza
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
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
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
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
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
Mechanism-free repurposing of drugs for C9orf72-related ALS/FTD using large-scale genomic data
2024 S. Saez-Atienzar, C.D.S. Souza, R. Chia, S.N. Beal, I. Lorenzini, R. Huang, J. Levy, C. Burciu, J. Ding, J.R. Gibbs, A. Jones, R. Dewan, V. Pensato, S. Peverelli, L. Corrado, J.J.F.A. van Vugt, W. van Rheenen, C. Tunca, E. Bayraktar, M. Xia, A. Iacoangeli, A. Shatunov, C. Tiloca, N. Ticozzi, F. Verde, L. Mazzini, K. Kenna, A. Al Khleifat, S. Opie-Martin, F. Raggi, M. Filosto, S.C. Piccinelli, A. Padovani, S. Gagliardi, M. Inghilleri, A. Ferlini, R. Vasta, A. Calvo, C. Moglia, A. Canosa, U. Manera, M. Grassano, J. Mandrioli, G. Mora, C. Lunetta, R. Tanel, F. Trojsi, P. Cardinali, S. Gallone, M. Brunetti, D. Galimberti, M. Serpente, C. Fenoglio, E. Scarpini, G.P. Comi, S. Corti, R. Del Bo, M. Ceroni, G.L. Pinter, F. Taroni, E.D. Bella, E. Bersano, C.J. Curtis, S.H. Lee, R. Chung, H. Patel, K.E. Morrison, J. Cooper-Knock, P.J. Shaw, G. Breen, R.J.B. Dobson, C.L. Dalgard, S.W. Scholz, A. Al-Chalabi, L.H. van den Berg, R. Mclaughlin, O. Hardiman, C. Cereda, G. Sorarù, S. D'Alfonso, S. Chandran, S. Pal, A. Ratti, C. Gellera, K. Johnson, T. Doucet-O'Hare, N. Pasternack, T. Wang, A. Nath, G. Siciliano, V. Silani, A.N. Başak, J.H. Veldink, W. Camu, J.D. Glass, J.E. Landers, A. Chiò, R. Sattler, C.E. Shaw, L. Ferraiuolo, I. Fogh, B.J. Traynor
Exploring the anti-inflammatory effects of curcumin encapsulated within ferritin nanocages: a comprehensive in vivo and in vitro study in Alzheimer’s disease
2024 C. Morasso, M. Truffi, V. Tinelli, P. Stivaktakis, R. Di Gerlando, F. Dragoni, G. Perini, M. Faisal, J. Aid, B. Noridov, B. Lee, L. Barbieri, S. Negri, D. Nikitovic, L. Thrapsanioti, A. Tsatsakis, C. Cereda, A. Bonizzi, S. Mazzucchelli, D. Prosperi, M.A. Hickey, F. Corsi, S. Gagliardi
Activated Human Adipose Tissue Transplantation Promotes Sensorimotor Recovery after Acute Spinal Cord Contusion in Rats
2024 M. Bonnet, C. Ertlen, M. Seblani, J. Brezun, T. Coyle, C. Cereda, G. Zuccotti, M. Colli, C. Desouches, P. Decherchi, S. Carelli, T. Marqueste
Characterization of the molecular dysfunctions occurring in Aicardi-Goutières syndrome patients with mutations in ADAR1
2024 S. Al Wardat, L. Frassinelli, E. Orecchini, F. Rey, S.A. Ciafre, S. Galardi, J. Garau, S. Gagliardi, S. Orcesi, D. Tonduti, S. Carelli, C. Cereda, E. Picardi, A. Michienzi