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Author

Daniele Severi

Observed names: D Severi, D. Severi
ORCID: 0000-0003-3131-032X
Observed ORCID: 0000-0003-3131-032X
OpenAlex ID: A5085857415
Aging, Cognitive Decline and Hearing Loss: Effects of Auditory Rehabilitation and Training with Hearing Aids and Cochlear Implants on Cognitive Function and Depression among Older Adults
2016 · Alessandro Castiglione, Alice Benatti, et al. · Audiology and Neurotology · 218
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The neuropathy in hereditary transthyretin amyloidosis : A narrative review
2021 · Stefano Tozza, Daniele Severi, et al. · Journal of the Peripheral Nervous System · 74
CSF sphingomyelin: a new biomarker of demyelination in the diagnosis and management of CIDP and GBS
2020 · Giovanna Capodivento, Chiara De Michelis, et al. · Journal of Neurology Neurosurgery & Psychiatry · 48
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Brain Plasticity in Charcot-Marie-Tooth Type 1A Patients? A Combined Structural and Diffusion MRI Study
2020 · Giuseppe Pontillo, Raffaele Dubbioso, et al. · Frontiers in Neurology · 14
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Quantitative Sensory Testing in Late-Onset ATTRv Presymptomatic Subjects: A Single Center Experience
2022 · Stefano Tozza, Daniele Severi, et al. · Biomedicines · 13
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A novel family with axonal Charcot‐Marie‐Tooth disease caused by a mutation in the EGR2 gene
2019 · Stefano Tozza, Stefania Magri, et al. · Journal of the Peripheral Nervous System · 12
A compound score to screen patients with hereditary transthyretin amyloidosis
2022 · Stefano Tozza, Daniele Severi, et al. · Journal of Neurology · 10
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Proximal weakness involvement in the first Italian case of Charcot‐Marie‐Tooth 2CC harboring a novel frameshift variant in NEFH
2021 · Francesco Aruta, Daniele Severi, et al. · Journal of the Peripheral Nervous System · 10
The impact of symptoms on daily life as perceived by patients with Charcot-Marie-Tooth type 1A disease
2021 · Stefano Tozza, Dario Bruzzese, et al. · Neurological Sciences · 10
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Can we identify hereditary TTR amyloidosis by the screening of carpal tunnel syndrome patients?
2022 · Daniele Severi, Francesco Aruta, et al. · Neurological Sciences · 6
Diffuse brain connectivity changes in Charcot–Marie–Tooth type 1a patients: a resting‐state functional magnetic resonance imaging study
2020 · G. Pontillo, S. Tozza, et al. · European Journal of Neurology · 6
Neuropathic pain experience in symptomatic and presymptomatic subjects carrying a transthyretin gene mutation
2023 · Stefano Tozza, Marco Luigetti, et al. · Frontiers in Neurology · 5
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Heterogenous electrophysiological features in early stage of hereditary transthyretin amyloidosis neuropathy
2023 · Stefano Tozza, Giovanni Palumbo, et al. · Neurological Sciences · 3
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A case of severe increase of liver enzymes in a ATTRv patient after one year of inotersen treatment
2022 · Daniele Severi, Giovanni Palumbo, et al. · Neurological Sciences · 2
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The first two-year follow-up in a patient with isolated sensory neuronopathy due to biallelic expansion in RFC1 gene
2022 · Stefano Tozza, Riccardo Currò, et al. · Acta Neurologica Belgica · 2
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Proximal weakness involvement in the first Italian case of Charcot-Marie-Tooth 2CC harboring a novel frameshift variant in NEFH
2021 · Francesco Aruta, Daniele Severi, et al. · Journal of the Neurological Sciences · 1
67 Guillain-Barrè Syndrome presenting with proximal weakness: electrophysiology means diagnosis
2026 · Mele Giulia, Luana Durante, et al. · Clinical Neurophysiology
A Comprehensive Description of the Roadmap to Identify and Validate a Myelin Biomarker
2025 · Giovanna Capodivento, Davide Visigalli, et al. · Biomarker Insights
Global longitudinal strain and quantitative sensory testing in pre-symptomatic patients with mutation for transthyretin amyloidosis
2022 · G Canciello, S Tozza, et al. · European Heart Journal
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Title Page / Table of Contents
2016 · Carmelita Velardita, Diego Favaro, et al. · Audiology and Neurotology
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Works count: 20
Citation count: 434
H-index: 9
I10-index: 9
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