Search Results - "Tozza, Stefano"

Parallel Neurological and Cardiac Progression in Hereditary Transthyretin Amyloidosis: An Integrated Clinical and Imaging Study.

Authors: Canciello, Grazia Tozza, Stefano Ordine, Leopoldo et al.

Source: Diagnostics (2075-4418). Sep2025, Vol. 15 Issue 17, p2143. 11p.

A novel de novo variant in POLR3B gene associated with a primary axonal involvement of the largest nerve fibers.

Authors: Geroldi, Alessandro Tozza, Stefano Fiorillo, Chiara et al.

Source: Journal of the Peripheral Nervous System. Dec2023, Vol. 28 Issue 4, p620-628. 9p.

Charcot-Marie-Tooth type 2CC misdiagnosed as Chronic Inflammatory Demyelinating Polyradiculoneuropathy.

Authors: Di Sarno, Isabella Tozza, Stefano Santorelli, Filippo Maria et al.

Source: Neurological Sciences. Dec2024, Vol. 45 Issue 12, p5933-5937. 5p.

Subjects: Chronic inflammatory demyelinating polyradiculoneuropathy, Nerve conduction studies, Muscle weakness, Tibial nerve, Peroneal nerve

Acute onset anti-MAG neuropathy and paradoxical worsening to rituximab: a challenging case.

Authors: Cassano, Emanuele Iodice, Rosa Di Sarno, Isabella et al.

Source: Neurological Sciences. Jul2025, Vol. 46 Issue 7, p3291-3294. 4p.

Subjects: Medical sciences, Neural conduction, Antibody titer, Neuropathy, Ataxia

Heterogenous electrophysiological features in early stage of hereditary transthyretin amyloidosis neuropathy.

Authors: Tozza, Stefano Palumbo, Giovanni Severi, Daniele et al.

Source: Neurological Sciences. Apr2024, Vol. 45 Issue 4, p1685-1689. 5p.

Subjects: Cardiac amyloidosis, Nerve conduction studies, Electrophysiology, Neuropathy, Transthyretin, Amyloidosis

Multiple cranial neuropathy due to varicella zoster virus reactivation without vesicular rash: a challenging diagnosis.

Authors: Stornaiuolo, Antonio Iodice, Rosa De Simone, Roberto et al.

Source: Neurological Sciences. Oct2023, Vol. 44 Issue 10, p3687-3689. 3p.

Subjects: Varicella-zoster virus, Virus reactivation, Cranial nerves, Facial nerve, Neuropathy, Herpes zoster, Facial paralysis

The spectrum of anti-GQ1B antibody syndrome: beyond Miller Fisher syndrome and Bickerstaff brainstem encephalitis.

Authors: Noioso, Ciro Maria Bevilacqua, Liliana Acerra, Gabriella Maria et al.

Source: Neurological Sciences. Dec2024, Vol. 45 Issue 12, p5657-5669. 13p.

Subjects: Central nervous system, Guillain-Barré syndrome, Encephalitis, Brain stem, Immunoglobulin G

Global longitudinal strain in pre-symptomatic patients with mutation for transthyretin amyloidosis.

Authors: Canciello, Grazia Tozza, Stefano Todde, Gaetano et al.

Source: Orphanet Journal of Rare Diseases. 12/5/2024, Vol. 19 Issue 1, p1-10. 10p.

Telemedicine application to headache: a critical review.

Authors: Spina, Emanuele Tedeschi, Gioacchino Russo, Antonio et al.

Source: Neurological Sciences. Jun2022, Vol. 43 Issue 6, p3795-3801. 7p. 1 Chart.

Subjects: Telemedicine, Headache, Child patients, Neurologic examination, Health equity

A case of severe increase of liver enzymes in a ATTRv patient after one year of inotersen treatment.

Authors: Severi, Daniele Palumbo, Giovanni Spina, Emanuele et al.

Source: Neurological Sciences. Apr2023, Vol. 44 Issue 4, p1419-1422. 4p. 1 Graph.

Subjects: Liver enzymes, Hepatotoxicology, Transthyretin, IgA glomerulonephritis, Aminotransferases, Amyloidosis

Can we identify hereditary TTR amyloidosis by the screening of carpal tunnel syndrome patients?

Authors: Severi, Daniele Aruta, Francesco Iovino, Aniello et al.

Source: Neurological Sciences. May2022, Vol. 43 Issue 5, p3435-3438. 4p. 2 Charts.

Subjects: Peripheral neuropathy diagnosis, Amyloid, Delayed diagnosis, Peripheral neuropathy, Carpal tunnel syndrome, Amyloidosis, Serum albumin, Disease complications

The impact of symptoms on daily life as perceived by patients with Charcot-Marie-Tooth type 1A disease.

Authors: Tozza, Stefano Bruzzese, Dario Severi, Daniele et al.

Source: Neurological Sciences. Jan2022, Vol. 43 Issue 1, p559-563. 5p. 3 Charts, 1 Graph.

Genotype and phenotype spectrum of Charcot-Marie-Tooth disease due to mutations in SORD.

Authors: Cortese, Andrea Dohrn, Maike F Curro, Riccardo et al.

Source: Brain: A Journal of Neurology; Oct2025, Vol. 148 Issue 10, p3737-3747, 11p

Electrodiagnostic accuracy in polyneuropathies: supervised learning algorithms as a tool for practitioners.

Authors: Uncini, Antonino Aretusi, Graziano Manganelli, Fiore et al.

Source: Neurological Sciences. Dec2020, Vol. 41 Issue 12, p3719-3727. 9p. 1 Diagram, 4 Charts, 1 Graph.

Subjects: Polyneuropathies, Supervised learning, Machine learning, Charcot-Marie-Tooth disease, Support vector machines, Discriminant analysis

Value of Antibody Determinations in Chronic Dysimmune Neuropathies.

Authors: Tozza, Stefano Spina, Emanuele Iovino, Aniello et al.

Source: Brain Sciences (2076-3425). Jan2023, Vol. 13 Issue 1, p37. 16p.

How to manage with telemedicine people with neuromuscular diseases?

Authors: Spina, Emanuele Trojsi, Francesca Tozza, Stefano et al.

Source: Neurological Sciences. Sep2021, Vol. 42 Issue 9, p3553-3559. 7p.

Subjects: Telemedicine, Neuromuscular diseases, Health services accessibility, Patient-professional relations, COVID-19, Digital technology, Telerehabilitation

A novel family with axonal Charcot‐Marie‐Tooth disease caused by a mutation in the EGR2 gene.

Authors: Tozza, Stefano Pisciotta, Chiara Severi, Daniele et al.

Source: Journal of the Peripheral Nervous System. Jun2019, Vol. 24 Issue 2, p219-223. 5p.

Pseudo-orthostatic tremor: description of a not typical case.

Authors: Iovino, Aniello Peluso, Silvio Manganelli, Fiore et al.

Source: Neurological Sciences. Oct2019, Vol. 40 Issue 10, p2205-2207. 3p. 1 Graph.

Subjects: Tremor, Transcranial magnetic stimulation, Hepatolenticular degeneration, Triceps, Arm, Dizziness, Electromyography, Skeletal muscle, Disease complications

Skin innervation across amyotrophic lateral sclerosis clinical stages: new prognostic biomarkers.

Authors: Nolano, Maria Provitera, Vincenzo Caporaso, Giuseppe et al.

Source: Brain: A Journal of Neurology; May2024, Vol. 147 Issue 5, p1740-1750, 11p

The SPTLC1 p.S331 mutation bridges sensory neuropathy and motor neuron disease and has implications for treatment.

Authors: Fiorillo, Chiara Capodivento, Giovanna Geroldi, Alessandro et al.

Source: Neuropathology & Applied Neurobiology. Dec2022, Vol. 48 Issue 7, p1-15. 15p.