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Journal of Neurology|July 7, 2024
Muscle MRI as a biomarker of disease activity and progression in myotonic dystrophy type 1: a longitudinal studyLaura Fionda, Luca Leonardi, Laura Tufano, et al.
The International Journal of Biological Markers|March 1, 2023
Overordering of tumor marker for outpatients revealed by performance indicators and the impact of a health policy intervention: An observational study using administrative recordsMassimo Gion, Roberto De Gobbi, Manuel Zorzi, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|June 30, 2021
Skin biopsy and quantitative sensory assessment in an Italian cohort of ATTRv patients with polyneuropathy and asymptomatic carriers: possible evidence of early non-length dependent denervationLuca Leonardi, Eleonora Galosi, Fiammetta Vanoli, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|October 24, 2023
Detailed clinical, physiological and pathological phenotyping can impact access to disease-modifying treatments in ATTR carriersDiane Beauvais, Céline Labeyrie, Cécile Cauquil, et al.
The Lancet. Neurology|September 1, 2015
Riluzole in patients with hereditary cerebellar ataxia: a randomised, double-blind, placebo-controlled trialSilvia Romano, Giulia Coarelli, Christian Marcotulli, et al.
European Journal of Neurology|September 19, 2023
Serum neurofilament light chain: a promising early diagnostic biomarker for hereditary transthyretin amyloidosis?Angela Romano, Guido Primiano, Giovanni Antonini, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|June 13, 2023
Comparison of quantitative muscle ultrasound and whole-body muscle MRI in facioscapulohumeral muscular dystrophy type 1 patientsLaura Fionda, Fiammetta Vanoli, Antonella Di Pasquale, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|May 3, 2024
Serum neurofilament light chain levels correlate with small fiber related parameters in patients with hereditary transthyretin amyloidosis with polyneuropathy (ATTRv-PN)Eleonora Galosi, Rocco Costanzo, Francesca Forcina, et al.
Journal of Neurology|November 4, 2022
Muscle MRI in immune-mediated necrotizing myopathy (IMNM): implications for clinical management and treatment strategiesLaura Fionda, Antonio Lauletta, Luca Leonardi, et al.
Autoimmunity Reviews|February 17, 2020
Muscle involvement in myasthenia gravis: Expanding the clinical spectrum of Myasthenia-Myositis association from a large cohort of patientsMatteo Garibaldi, Laura Fionda, Fiammetta Vanoli, et al.
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