CARELLI, STEFANA
CARELLI, STEFANA
Dipartimento di Scienze Biomediche e Cliniche
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
Transcriptomic and metabolomic changes might predict frailty in SAMP8 mice
2024 L. Dacomo, P. Lavitola, L. Brunelli, L. Messa, E. Micotti, L. Artioli, E. Sinopoli, G. Cecutti, S. Leva, S. Gagliardi, O. Pansarasa, S. Carelli, A. Guaita, R. Pastorelli, G. Forloni, C. Cereda, C. Balducci
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
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
Production of an induced pluripotent stem cell line CSSi018-A (14192) from a patient with hypomyelinating leukodystrophy 7 (HLD7) carrying biallelic variants of POLR3A (c.1802 T > A; c.4072G > A)
2024 A. Casamassa, G. Rotundo, C. Ceresoni, E.M. Turco, I. Torrente, O. Candido, F. Nicita, D. Tonduti, E. Bertini, M. Marano, D. Ferrari, C. Cereda, M. Pennuto, A.L. Vescovi, S. Carelli, J. Rosati
Insights on ZEB1-AS1: emerging roles from cancer to neurodegeneration
2024 S. Carelli, F. Rey, E. Maghraby, C. Cereda
Non-Negative Matrix Tri-Factorization for Representation Learning in Multi-Omics Datasets with Applications to Drug Repurposing and Selection
2024 L. Messa, C. Testa, S. Carelli, F. Rey, E. Jacchetti, C. Cereda, M.T. Raimondi, S. Ceri, P. Pinoli
3D photopolymerized microstructured scaffolds influence nuclear deformation, nucleo/cytoskeletal protein organization, and gene regulation in mesenchymal stem cells
2023 F. Donnaloja, M.T. Raimondi, L. Messa, B. Barzaghini, F. Carnevali, E. Colombo, D. Mazza, C. Martinelli, L. Boeri, F. Rey, C. Cereda, R. Osellame, G. Cerullo, S. Carelli, M. Soncini, E. Jacchetti
TDP-43 PROTEINOPATHIES: THE ROLE OF EXTRACELLULAR VESICLES
2023 E. Casarotto, L. Messa, M. Chierichetti, L. Cornaggia, M. Cozzi, R. Cristofani, V. Ferrari, M. Galbiati, G. Patelli, M. Piccolella, P. Pramaggiore, P. Rusmini, B. Tedesco, S. Gagliardi, S. Carelli, C. Cereda, A. Poletti, V. Crippa
lncRNAs at the interplay between neurodegeneration and cancer: a role for MINCR
2023 C. Pandini, I. Cassotti, M. Garofalo, F. Rey, S. Carelli, C. Cereda, S. Gagliardi, P. Gandellini
Further insights into Allan-Herndon-Dudley syndrome: characterization of two genetic variants in SLC16A2 gene
2023 L. Esposito, F. Rey, E. Maghraby, G. Zuccotti, D. Tonduti, S. Carelli, C. Cereda
Identification of a novel pathway in sporadic Amyotrophic Lateral Sclerosis mediated by the long non-coding RNA ZEB1-AS1
2023 F. Rey, E. Maghraby, L. Messa, L. Esposito, B. Barzaghini, C. Pandini, M. Bordoni, S. Gagliardi, L. Diamanti, M.T. Raimondi, M. Mazza, G. Zuccotti, S. Carelli, C. Cereda
How PQC inhibition modulates miRNA loading in large and small extracellular vesicles
2022 E. Casarotto, M. Garofalo, L. Messa, D. Sproviero, S. Carelli, M. Cozzi, M. Chierichetti, R. Cristofani, V. Ferrari, M. Galbiati, F. Mina, M. Piccolella, P. Rusmini, B. Tedesco, P. Pramaggiore, C. Cereda, S. Gagliardi, A. Poletti, V. Crippa
SNCA-AS1 in aging and Parkinson's disease
2022 S. Carelli, F. Rey, C. Cereda
Correspondence on “Expanded phenotype of AARS1-related white matter disease” by Helman et al
2022 A. Leidi, R. Previtali, C. Parazzini, F. Raviglione, S. Carelli, M.I. Mendes, G.S. Salomons, M. Iascone, D. Tonduti
Patients’ Stem Cells Differentiation in a 3D Environment as a Promising Experimental Tool for the Study of Amyotrophic Lateral Sclerosis
2022 E. Scarian, M. Bordoni, V. Fantini, E. Jacchetti, M.T. Raimondi, L. Diamanti, S. Carelli, C. Cereda, O. Pansarasa
COMPUTATIONAL AND BIOLOGICAL VALIDATION OF A NEW NICHOID SCAFFOLD OPTIMIZED FOR HUMAN MESENCHYMAL STEM CELLS
2022 B. Barzaghini, L. Messa, F. Rey, F. Fanizza, M. Antonella Sforazzini, G.V. Zuccotti, R. Osellame, G. Cerullo, E. Jacchetti, S. Carelli, M. Teresa Raimondi
Mitochondrial dysfunctions in neurodegenerative diseases: role in disease pathogenesis, strategies for analysis and therapeutic prospects
2022 F. Rey, S. Ottolenghi, G. Zuccotti, M. Samaja, S. Carelli
Oxygen sensing in neurodegenerative diseases: current mechanisms, implication of transcriptional response and pharmacological modulation
2022 F. Rey, L. Messa, E. Maghraby, G. Casili, S. Ottolenghi, B. Barzaghini, M.T. Raimondi, C. Cereda, S. Cuzzocrea, G.V. Zuccotti, E. Esposito, I. Paterniti, S. Carelli