Publications by authors named "Moreno Ferrarini"

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Phenotypic spectrum of myelin protein zero-related neuropathies: a large cohort study from five mutation clusters across Italy.
Alessandro Bertini, Luca Gentile, Tiziana Cavallaro, Stefano Tozza, Paola Saveri, Moreno Ferrarini

J Neurol Neurosurg Psychiatry· December 2024

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Nerve ultrasound in CANVAS-spectrum disease: Reduced nerve size distinguishes genetically confirmed CANVAS from other axonal polyneuropathies.
Alessandro Salvalaggio, Mario Cacciavillani, Benedetta Tierro, Daniele Coraci, Riccardo Currò, Moreno Ferrarini

J Peripher Nerv Syst· December 2024

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A progranulin gene deletion in frontotemporal lobar degeneration with corticobasal syndrome in a TREDEM case report.
Maurizio Gallucci, Chiara Da Ronch, Matteo Bendini, Vittorio Fiore, Licia Turolla, Moreno Ferrarini

J Alzheimers Dis Rep· December 2024

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Clinical and pathology characterization of small nerve fiber neuro(no)pathy in cerebellar ataxia with neuropathy and vestibular areflexia syndrome.
Matteo Tagliapietra, Alex Incensi, Moreno Ferrarini, Nazarena Mesiano, Alessandro Furia

Eur J Neurol· December 2023

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Clinical spectrum and frequency of Charcot-Marie-Tooth disease in Italy: Data from the National CMT Registry.
Chiara Pisciotta, Alessandro Bertini, Irene Tramacere, Fiore Manganelli, Gian Maria Fabrizi, Moreno Ferrarini

Eur J Neurol· August 2023

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Association between inflammatory central nervous system lesions and Cerebellar Ataxia, Neuropathy and Vestibular Areflexia Syndrome (CANVAS): a case series.
Matteo Azzimonti, Raffaella Fazio, Antonino Giordano, Matteo Tagliapietra, Moreno Ferrarini

J Neurol· October 2022

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Rare among Rare: Phenotypes of Uncommon CMT Genotypes.
Luca Gentile, Massimo Russo, Federica Taioli, Moreno Ferrarini, M'Hammed Aguennouz

Brain Sci· December 2021

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RFC1 AAGGG repeat expansion masquerading as Chronic Idiopathic Axonal Polyneuropathy.
Matteo Tagliapietra, Davide Cardellini, Moreno Ferrarini, Silvia Testi, Sergio Ferrari

J Neurol· November 2021

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Charcot-Marie-Tooth disease: experience from a large Italian tertiary neuromuscular center.
Luca Gentile, Massimo Russo, Gian Maria Fabrizi, Federica Taioli, Moreno Ferrarini

Neurol Sci· May 2020

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Sporadic hereditary neuropathies misdiagnosed as chronic inflammatory demyelinating polyradiculoneuropathy: Pitfalls and red flags.
Marta Campagnolo, Federica Taioli, Mario Cacciavillani, Marta Ruiz, Marco Luigetti, Moreno Ferrarini

J Peripher Nerv Syst· March 2020

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Nerve size correlates with clinical severity in Charcot-Marie-Tooth disease 1A.
Giampietro Zanette, Stefano Tamburin, Federica Taioli, Matteo Francesco Lauriola, Andrea Badari, Moreno Ferrarini

Muscle Nerve· December 2019

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Deoxysphingolipids as candidate biomarkers for a novel mutation associated with HSAN-I.
Federica Boso, Andrea Armirotti, Federica Taioli, Moreno Ferrarini, Lucilla Nobbio

Neurol Genet· December 2019

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Expanding the spectrum of genes responsible for hereditary motor neuropathies.
Stefano C Previtali, Edward Zhao, Dejan Lazarevic, Giovanni Battista Pipitone, Gian Maria Fabrizi, Moreno Ferrarini

J Neurol Neurosurg Psychiatry· October 2019

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Nerve ultrasound findings differentiate Charcot-Marie-Tooth disease (CMT) 1A from other demyelinating CMTs.
Giampietro Zanette, Gian Maria Fabrizi, Federica Taioli, Matteo Francesco Lauriola, Andrea Badari, Moreno Ferrarini

Clin Neurophysiol· November 2018

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The spectrum of Charcot-Marie-Tooth disease due to myelin protein zero: An electrodiagnostic, nerve ultrasound and histological study.
Gian Maria Fabrizi, Stefano Tamburin, Tiziana Cavallaro, Ilaria Cabrini, Moreno Ferrarini

Clin Neurophysiol· January 2018

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Progressive Myoclonus Epilepsy in Congenital Generalized Lipodystrophy type 2: Report of 3 cases and literature review.
Roberta Opri, Gian Maria Fabrizi, Gaetano Cantalupo, Moreno Ferrarini, Alessandro Simonati

Seizure· November 2016

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Erratum to "Charcot-Marie-Tooth type 2 and distal hereditary motor neuropathy: Clinical, neurophysiological and genetic findings from a single-centre experience" [Clin. Neurol. Neurosurg. 144 (2016) 67-71].
Marco Luigetti, Gian Maria Fabrizi, Giulia Bisogni, Angela Romano, Federica Taioli, Moreno Ferrarini

Clin Neurol Neurosurg· June 2016

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Charcot-Marie-Tooth type 2 and distal hereditary motor neuropathy: Clinical, neurophysiological and genetic findings from a single-centre experience.
Marco Luigetti, Gian Maria Fabrizi, Giulia Bisogni, Angela Romano, Federica Taioli, Moreno Ferrarini

Clin Neurol Neurosurg· May 2016

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A novel PSEN1 mutation in a patient with sporadic early-onset Alzheimer's disease and prominent cerebellar ataxia.
Silvia Testi, Silvio Peluso, Gian Maria Fabrizi, Antonella Antenora, Cinzia Valeria Russo, Moreno Ferrarini

J Alzheimers Dis· September 2015

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Charcot-Marie-Tooth 2F: phenotypic presentation of the Arg136Leu HSP27 mutation in a multigenerational family.
Claudia Stancanelli, Gian Maria Fabrizi, Moreno Ferrarini, Tiziana Cavallaro, Federica Taioli

Neurol Sci· June 2015

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Parental mosaicism of a novel PMP22 mutation with a minimal neuropathic phenotype.
Federica Taioli, Laura Bertolasi, Domenico Ajena, Moreno Ferrarini, Ilaria Cabrini

J Peripher Nerv Syst· December 2012

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Variable presentations of TTR-related familial amyloid polyneuropathy in seventeen patients.
Manuel Cappellari, Tiziana Cavallaro, Moreno Ferrarini, Ilaria Cabrini, Federica Taioli

J Peripher Nerv Syst· June 2011

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Vascular endothelial growth factor helps differentiate neuropathies in rare plasma cell dyscrasias.
Chiara Briani, Gian Maria Fabrizi, Susanna Ruggero, Chiara Dalla Torre, Moreno Ferrarini

Muscle Nerve· February 2011

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A novel mutation of aprataxin associated with ataxia ocular apraxia type 1: phenotypical and genotypical characterization.
Moreno Ferrarini, Giovanna Squintani, Tiziana Cavallaro, Sergio Ferrari, Nicolo' Rizzuto

J Neurol Sci· September 2007

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Glycan-independent role of calnexin in the intracellular retention of Charcot-Marie-tooth 1A Gas3/PMP22 mutants.
Alessandra Fontanini, Romina Chies, Erik L Snapp, Moreno Ferrarini, Gian Maria Fabrizi

J Biol Chem· January 2005

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