Publications by authors named "Alessandra Govoni"

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High Prevalence of GALC Gene Variants in Adults With Neurodegenerative Conditions.
Federica Feo, Luciana Tramacere, Silvia Ramat, Alessandra Govoni, Luca Caremani

Eur J Neurol· May 2025

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genotype-Parkinson's phenotype correlation in a cohort of 252 Italian patients from the Tuscany region.
Rodolfo Tonin, Silvia Ramat, Marina Rinaldi, Silvia Falliano, Federica Feo, Alessandra Govoni

Clin Park Relat Disord· April 2025

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Dopaminergic therapy disrupts decision-making in impulsive-compulsive Parkinsonian patients.
Fabio Taddeini, Erica Ordali, Alessandra Govoni, Francesca Piattellini, Simone Valente

Ann Clin Transl Neurol· March 2025

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Correction to: Spinocerebellar ataxia 27B: a frequent and slowly progressive autosomal-dominant cerebellar ataxia-experience from an Italian cohort.
Sara Satolli, Salvatore Rossi, Elisa Vegezzi, David Pellerin, Maria Laura Manca, Alessandra Govoni

J Neurol· December 2024

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Six-minute walk test as outcome measure of fatigability in adults with spinal muscular atrophy treated with nusinersen.
Alessandra Govoni, Giulia Ricci, Silvia Bonanno, Luca Bello, Francesca Magri

Muscle Nerve· October 2024

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Spinocerebellar ataxia 27B: a frequent and slowly progressive autosomal-dominant cerebellar ataxia-experience from an Italian cohort.
Sara Satolli, Salvatore Rossi, Elisa Vegezzi, David Pellerin, Maria Laura Manca, Alessandra Govoni

J Neurol· August 2024

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The Frequency of Intermediate Alleles in Patients with Cerebellar Phenotypes.
Elena Capacci, Silvia Bagnoli, Giulia Giacomucci, Costanza Maria Rapillo, Alessandra Govoni

Cerebellum· June 2024

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Characterization of Phenotypic Variability in Becker Muscular Dystrophy for Clinical Practice and Towards Trial Readiness: A Two-Years Follow up Study.
Giulia Ricci, Alessandra Govoni, Francesca Torri, Guja Astrea, Bianca Buchignani

J Neuromuscul Dis· March 2024

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Respiratory function in a large cohort of treatment-naïve adult spinal muscular atrophy patients: a cross-sectional study.
Alex Vicino, Luca Bello, Silvia Bonanno, Alessandra Govoni, Federica Cerri

Neuromuscul Disord· December 2023

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Proposal of a new clinical protocol for evaluating fatigability in adult SMA patients.
Giulia Ricci, Francesca Torri, Alessandra Govoni, Roberto Chiappini, Laura Manca

Acta Myol· December 2023

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Multi-omics profiling of CSF from spinal muscular atrophy type 3 patients after nusinersen treatment: a 2-year follow-up multicenter retrospective study.
Irene Faravelli, Delia Gagliardi, Elena Abati, Megi Meneri, Jessica Ongaro, Alessandra Govoni

Cell Mol Life Sci· August 2023

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Ischemic optic neuropathy as first presentation in patient with m.3243 A > G MELAS classic mutation.
Simone Scarcella, Laura Dell'Arti, Delia Gagliardi, Francesca Magri, Alessandra Govoni

BMC Neurol· April 2023

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Adults with spinal muscular atrophy: a large-scale natural history study shows gender effect on disease.
Lorenzo Maggi, Luca Bello, Silvia Bonanno, Alessandra Govoni, Claudia Caponnetto

J Neurol Neurosurg Psychiatry· December 2022

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Bridging the Gap: Gene Therapy in a Patient With Spinal Muscular Atrophy Type 1.
Gianluca Costamagna, Alessandra Govoni, Adina Wise, Stefania Corti

Neurology· November 2022

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Molecular analysis of SMARD1 patient-derived cells demonstrates that nonsense-mediated mRNA decay is impaired.
Michela Taiana, Alessandra Govoni, Sabrina Salani, Nicole Kleinschmidt, Noemi Galli

J Neurol Neurosurg Psychiatry· August 2022

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CACNA1S mutation associated with a case of juvenile-onset congenital myopathy.
Eleonora Mauri, Daniela Piga, Serena Pagliarani, Francesca Magri, Arianna Manini, Alessandra Govoni

J Neurol Sci· December 2021

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Early Findings in Neonatal Cases of -Related Congenital Myopathies.
Eleonora Mauri, Daniela Piga, Alessandra Govoni, Roberta Brusa, Serena Pagliarani

Front Neurol· June 2021

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Diagnostic and prognostic value of CSF neurofilaments in a cohort of patients with motor neuron disease: A cross-sectional study.
Delia Gagliardi, Irene Faravelli, Megi Meneri, Domenica Saccomanno, Alessandra Govoni

J Cell Mol Med· April 2021

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Acute inflammatory demyelinating polyneuritis in association with an asymptomatic infection by SARS-CoV-2.
Martina Bracaglia, Ilaria Naldi, Alessandra Govoni, Donatella Brillanti Ventura, Patrizia De Massis

J Neurol· November 2020

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Nusinersen safety and effects on motor function in adult spinal muscular atrophy type 2 and 3.
Lorenzo Maggi, Luca Bello, Silvia Bonanno, Alessandra Govoni, Claudia Caponnetto

J Neurol Neurosurg Psychiatry· November 2020

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Current understanding of and emerging treatment options for spinal muscular atrophy with respiratory distress type 1 (SMARD1).
Martina G L Perego, Noemi Galli, Monica Nizzardo, Alessandra Govoni, Michela Taiana

Cell Mol Life Sci· September 2020

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Estimating the impact of COVID-19 pandemic on services provided by Italian Neuromuscular Centers: an Italian Association of Myology survey of the acute phase.
Eleonora Mauri, Elena Abati, Olimpia Musumeci, Carmelo Rodolico, Maria Grazia D'Angelo, Alessandra Govoni

Acta Myol· June 2020

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Limb girdle muscular dystrophy due to gene mutations: new mutations expand the clinical spectrum of a still challenging diagnosis.
Francesca Magri, Roberta Brusa, Luca Bello, Lorenzo Peverelli, Roberto Del Bo, Alessandra Govoni

Acta Myol· June 2020

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Nusinersen treatment and cerebrospinal fluid neurofilaments: An explorative study on Spinal Muscular Atrophy type 3 patients.
Irene Faravelli, Megi Meneri, Domenica Saccomanno, Daniele Velardo, Elena Abati, Alessandra Govoni

J Cell Mol Med· March 2020

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Spinal muscular atrophy with respiratory distress type 1: Clinical phenotypes, molecular pathogenesis and therapeutic insights.
Matteo Saladini, Monica Nizzardo, Alessandra Govoni, Michela Taiana, Nereo Bresolin

J Cell Mol Med· January 2020

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