MANINI, ARIANNA
MANINI, ARIANNA
Bridging the Gap of ALS Missing Heritability: Are Neurogenes Being Overlooked?
2025 A. Manini, A. Brusati, J. Spagliardi, S. Leoni, V. Pensato, S. Peverelli, P.J. Keagle, S. Magri, G. Scacciatella, A. Maranzano, B. Poletti, D. Gentilini, A. Doretti, S. Messina, C. Morelli, F. Verde, C. Gellera, V. Silani, A. Ratti, J.E. Landers, N. Ticozzi
KIF5Ap.Pro986Leu Risk Variant and Accelerated Progression of Amyotrophic Lateral Sclerosis
2025 A. Manini, R. Vasta, A. Brusati, F. Scheveger, S. Peverelli, A. Maranzano, A. Doretti, F. Gentile, E. Colombo, M. Brunetti, C. Moglia, A. Canosa, U. Manera, M. Grassano, D. Gentilini, S. Messina, F. Verde, C. Morelli, J.E. Landers, B.J. Traynor, A. Chiò, V. Silani, A. Calvo, A. Ratti, N. Ticozzi
Association of APOE genotype and cerebrospinal fluid Aβ and tau biomarkers with cognitive and motor phenotype in amyotrophic lateral sclerosis
2024 A. Maranzano, F. Verde, A. Dubini, S. Torre, E. Colombo, A. Doretti, F. Gentile, A. Manini, I. Milone, A. Brusati, S. Peverelli, S. Santangelo, E.G. Spinelli, E. Torresani, D. Gentilini, S. Messina, C. Morelli, B. Poletti, F. Agosta, A. Ratti, M. Filippi, V. Silani, N. Ticozzi
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
Serum levels of glial fibrillary acidic protein in patients with amyotrophic lateral sclerosis
2023 F. Verde, I. Milone, A. Maranzano, E. Colombo, S. Torre, F. Solca, A. Doretti, F. Gentile, A. Manini, R. Bonetti, S. Peverelli, S. Messina, L. Maderna, C. Morelli, B. Poletti, A. Ratti, 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
Genetic Causes of Cerebral Small Vessel Diseases: A Practical Guide for Neurologists
2023 A. Manini, L. Pantoni
Phenotypic correlates of serum neurofilament light chain levels in amyotrophic lateral sclerosis
2023 F. Verde, I. Milone, E. Colombo, A. Maranzano, F. Solca, S. Torre, A. Doretti, F. Gentile, A. Manini, R. Bonetti, S. Peverelli, S. Messina, L. Maderna, C. Morelli, B. Poletti, A. Ratti, V. Silani, N. Ticozzi
Association of the risk factor UNC13A with survival and upper motor neuron involvement in amyotrophic lateral sclerosis
2023 A. Manini, V. Casiraghi, A. Brusati, A. Maranzano, F. Gentile, E. Colombo, R. Bonetti, S. Peverelli, S. Invernizzi, D. Gentilini, S. Messina, F. Verde, B. Poletti, I. Fogh, C. Morelli, V. Silani, A. Ratti, N. Ticozzi
Expanding the Phenotypic Spectrum of Vocal Cord and Pharyngeal Weakness With Distal Myopathy due to the p.S85C MATR3 Mutation
2022 A. Manini, D. Velardo, P. Ciscato, C. Cinnante, M. Moggio, G. Comi, S. Corti, D. Ronchi
A novel RRM2B mutation associated with mitochondrial DNA depletion syndrome
2022 M. Fumagalli, D. Ronchi, M.F. Bedeschi, A. Manini, G. Cristofori, F. Mosca, R. Dilena, M. Sciacco, S. Zanotti, D. Piga, G. Ardissino, F. Triulzi, S. Corti, G.P. Comi, L. Salviati
Etiologic reclassification of cryptogenic stroke after implantable cardiac monitoring and computed tomography angiography re-assessment
2022 F. Mele, G. Scopelliti, A. Manini, C. Ferrari Aggradi, M. Baiardo, M. Schiavone, M. Viecca, A. Ianniello, P. Bertora, G.B. Forleo, L. Pantoni
Mitochondrial DNA homeostasis impairment and dopaminergic dysfunction : a trembling balance
2022 A. Manini, E. Abati, G.P. Comi, S. Corti, D. Ronchi
Adeno-Associated Virus (AAV)-mediated gene therapy for Duchenne muscular dystrophy : the issue of transgene persistence
2022 A. Manini, E. Abati, A. Nuredini, S. Corti, G.P. Comi
Analysis of HTT CAG repeat expansion in Italian patients with amyotrophic lateral sclerosis
2022 A. Manini, D. Gagliardi, M. Meneri, S. Antognozzi, R. Del Bo, C. Scaglione, G.P. Comi, S. Corti, D. Ronchi
Case Report: Thymidine Kinase 2 (TK2) Deficiency: A Novel Mutation Associated With Childhood-Onset Mitochondrial Myopathy and Atypical Progression
2022 A. Manini, M. Meneri, C. Rodolico, S. Corti, A. Toscano, G.P. Comi, O. Musumeci, D. Ronchi
Case Report: Rare Homozygous RNASEH1 Mutations Associated With Adult-Onset Mitochondrial Encephalomyopathy and Multiple Mitochondrial DNA Deletions
2022 A. Manini, L. Caporali, M. Meneri, S. Zanotti, D. Piga, I.G. Arena, S. Corti, A. Toscano, G.P. Comi, O. Musumeci, V. Carelli, D. Ronchi
Rapidly progressive dementia and intractable diarrhea: a teaching case report and a systematic review of cognitive impairment in Whipple's disease
2022 A. Manini, G. Querzola, C. Lovati, L. Pantoni
Inhibition of myostatin and related signaling pathways for the treatment of muscle atrophy in motor neuron diseases
2022 E. Abati, A. Manini, G.P. Comi, S. Corti
Clinical and genetic features of a cohort of patients with MFN2-related neuropathy
2022 E. Abati, A. Manini, D. Velardo, R. Del Bo, L. Napoli, F. Rizzo, M. Moggio, N. Bresolin, E. Bellone, M.T. Bassi, M.G. D'Angelo, G.P. Comi, S. Corti