GAGLIARDI, DELIA
GAGLIARDI, DELIA
Dipartimento di Fisiopatologia Medico-Chirurgica e dei Trapianti
High Prevalence of SOD1 Pathogenic Variants in the UK Biobank: Implications for Early Intervention in Amyotrophic Lateral Sclerosis
2026 D. Gagliardi, C. Villella, M. Zanovello, V. Iacobelli, S. Corti, G.P. Comi, P. Fratta, H. Houlden, A. Tucci, D. Ronchi
Investigating the role of serum NfL, FGF21, NCAM1 and GDF15 as disease biomarkers for Charcot-Marie-Tooth type 2A
2026 E. Abati, D. Saccomanno, C. Alberti, A. Anastasia, D. Gagliardi, E. Ferri, B. Arosio, G. D Angelo, R. Cima, M.T. Bassi, S. Oldoni, G.P. Comi, P. Rizzo, S.P. Corti
MYBPC1-associated congenital myopathy with tremor: further delineation of the clinical and pathological phenotype in the first Italian case
2026 D. Velardo, C. Alberti, D. Gagliardi, R. Del Bo, P. Ciscato, L. Napoli, S. Zanotti, M. Ripolone, M.G. Croce, G. Cosentino, G. Tumminello, M. Locatelli, G.P. Comi, S. Corti, S. Ravaglia, D. Ronchi
Skeletal muscle in spinal muscular atrophy: Critical insights from pathogenesis to therapeutic strategies
2026 L. Ottoboni, C. Panicucci, G. Magni, D. Gagliardi, M. Ripolone, L. Napoli, M. Moggio, G.P. Comi, C. Bruno, S.P. Corti
Beyond motor neurons: peripheral TDP-43 pathology in skeletal muscle and intramuscular nerves in amyotrophic lateral sclerosis
2026 S. Corti, C. Alberti, L. Ottoboni, G. Magni, D. Gagliardi, F. Marcotti, S. Zanotti, M. Moggio, G.P. Comi
Late-onset severe axonal polyneuropathy in mut0 methylmalonic acidemia after liver-kidney transplantation: a genotype-informed case report
2026 M. Griffo, F. Magri, F. Furlan, E. Bernardi, F. Menni, F. Tagliaferri, S. Testa, D. Ronchi, S. Petrillo, F. Piemonte, D. Gagliardi, M. Parisi, S. Padelli, D. Velardo, N. Molitierno, S. Corti, G.P. Comi
FcRn antagonist and C5 complement inhibitor as early rescue strategies in severe Myasthenia Gravis: a two-case report
2026 M. Parisi, N. Molitierno, C. Alberti, D. Gagliardi, D. Velardo, G.P. Comi, S.P. Corti
Single Nucleotide SMN1 Variants in a Cohort of Individuals With Spinal Muscular Atrophy
2025 M. Rimoldi, F. Magri, M. Meneri, D. Gagliardi, V. Ada Sansone, E. Albamonte, L. Ottoboni, G.P. Comi, E. Mercuri, F.D. Tiziano, D. Ronchi, S. Corti
Exploring the relationship between dystonia and STN-DBS in Parkinson’s disease: insights from a single-centre cohort
2025 L.G. Remore, D. Gagliardi, L. Borellini, A. Fasano, V.L. Faso, F. Cogiamanian, E. Mailand, G. Valcamonica, E. Pirola, L. Schisano, A.M. Ampollini, G.A. Bertani, G. Fiore, A. D'Ammando, L. Tariciotti, G. Marfia, S.E. Navone, S. Barbieri, M. Locatelli
Case Report: Acute onset hemiparesis in a young man: do not miss Crohn's disease
2025 V. Iacobelli, S. Tagliabue, B. Modello, D. Velardo, E. Abati, F. Triulzi, G.P. Comi, S. Corti, D. Gagliardi, M. Parisi
Unveiling amyotrophic lateral sclerosis complexity: insights from proteomics, metabolomics and microbiomics
2025 S. Scarcella, L. Brambilla, L. Quetti, M. Rizzuti, V. Melzi, N. Galli, L. Sali, G. Costamagna, G.P. Comi, S. Corti, D. Gagliardi
A rare case of focal myositis affecting the sternocleidomastoid muscle: diagnostic challenges and management strategies
2025 N. Molitierno, M. Parisi, D. Gagliardi, S. Corti, D. Velardo
LEVERAGING THREE-DIMENSIONAL IN VITRO MODELS TO IDENTIFY EARLY NEURONAL VULNERABILITY AND TO TEST THERAPEUTIC STRATEGIES IN AMYOTROPHIC LATERAL SCLEROSIS
2024 D. Gagliardi
Early spinal muscular atrophy treatment following newborn screening: A 20‐month review of the first Italian regional experience
2024 D. Gagliardi, E. Canzio, P. Orsini, P. Conti, V. Sinisi, C. Maggiore, M. Carla Santarsia, G. Lagioia, G. Lupis, I. Roppa, G. Scianatico, D. Mancini, S. Corti, G.P. Comi, M. Gentile, D. Gagliardi
Unleashing the potential of mRNA therapeutics for inherited neurological diseases
2024 E. Monfrini, G. Baso, D. Ronchi, M. Meneri, D. Gagliardi, L. Quetti, F. Verde, N. Ticozzi, A. Ratti, A. Di Fonzo, G.P. Comi, L. Ottoboni, S. Corti
Investigating the prevalence of MFN2 mutations in amyotrophic lateral sclerosis: insights from an Italian cohort
2024 E. Abati, D. Gagliardi, A. Manini, R. Del Bo, D. Ronchi, M. Meneri, F. Beretta, A. Sarno, F. Rizzo, E. Monfrini, A. Di Fonzo, M.T. Pellecchia, A. Brusati, V. Silani, G.P. Comi, A. Ratti, F. Verde, N. Ticozzi, S. Corti
Correlation between clinical phenotype and electromyographic parameters in amyotrophic lateral sclerosis
2023 E. Colombo, A. Doretti, F. Scheveger, A. Maranzano, G. Pata, D. Gagliardi, M. Meneri, S. Messina, F. Verde, C. Morelli, S. Corti, L. Maderna, V. Silani, N. Ticozzi
The impact of upper motor neuron involvement on clinical features, disease progression and prognosis in amyotrophic lateral sclerosis
2023 E. Colombo, F. Gentile, A. Maranzano, A. Doretti, F. Verde, M. Olivero, D. Gagliardi, M. Faré, M. Meneri, B. Poletti, L. Maderna, S. Corti, M. Corbo, C. Morelli, V. Silani, N. Ticozzi
NOTCH2NLC GGC repeats are not expanded in Italian amyotrophic lateral sclerosis patients
2023 A. Manini, D. Gagliardi, M. Meneri, S. Antognozzi, R. Del Bo, G.P. Comi, S. Corti, D. Ronchi
Genomic and transcriptomic advances in amyotrophic lateral sclerosis
2023 M. Rizzuti, L. Sali, V. Melzi, S. Scarcella, G. Costamagna, L. Ottoboni, L. Quetti, L. Brambilla, D. Papadimitriou, F. Verde, A. Ratti, N. Ticozzi, G.P. Comi, S. Corti, D. Gagliardi