Anna Sagnelli

Naples, 80131, Italy

Last Updated: 09/26/2026

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Found 20 publications

Influenza Vaccine Hesitancy in Patients with Multiple Sclerosis: A Monocentric Observational Study.

Influenza Vaccine Hesitancy in Patients with Multiple Sclerosis: A Monocentric Observational Study.

Journal: Brain sciences

Published: June 04, 2021

One year experience with erenumab: real-life data in 30 consecutive patients.

One year experience with erenumab: real-life data in 30 consecutive patients.

Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology

Published: August 27, 2020

Altered TDP-43-dependent splicing in HSPB8-related distal hereditary motor neuropathy and myofibrillar myopathy.

Altered TDP-43-dependent splicing in HSPB8-related distal hereditary motor neuropathy and myofibrillar myopathy.

Journal: European journal of neurology

Published: June 08, 2017

Lack of benefit of acetyl-dl-leucine in patients with multiple system atrophy of the cerebellar type.

Lack of benefit of acetyl-dl-leucine in patients with multiple system atrophy of the cerebellar type.

Journal: Journal of the neurological sciences

Published: March 02, 2017

Hereditary gelsolin amyloidosis (HGA): a neglected cause of bilateral progressive or recurrent facial palsy.

Hereditary gelsolin amyloidosis (HGA): a neglected cause of bilateral progressive or recurrent facial palsy.

Journal: Journal of the peripheral nervous system : JPNS

Published: November 02, 2016

No effect of AR polyG polymorphism on spinal and bulbar muscular atrophy phenotype.

No effect of AR polyG polymorphism on spinal and bulbar muscular atrophy phenotype.

Journal: European journal of neurology

Published: December 02, 2015

Towards a European Registry and Biorepository for Patients with Spinal and Bulbar Muscular Atrophy.

Towards a European Registry and Biorepository for Patients with Spinal and Bulbar Muscular Atrophy.

Journal: Journal of molecular neuroscience : MN

Published: November 18, 2015

Early-onset progressive spastic paraplegia caused by a novel TUBB4A mutation: brain MRI and FDG-PET findings.

Early-onset progressive spastic paraplegia caused by a novel TUBB4A mutation: brain MRI and FDG-PET findings.

Journal: Journal of neurology

Published: November 10, 2015

Clinical Trials in Spinal and Bulbar Muscular Atrophy-Past, Present, and Future.

Clinical Trials in Spinal and Bulbar Muscular Atrophy-Past, Present, and Future.

Journal: Journal of molecular neuroscience : MN

Published: November 01, 2015

Spinal and bulbar muscular atrophy and Charcot-Marie-Tooth type 1A: Co-existence of two rare neuromuscular genetic diseases in the same patient.

Spinal and bulbar muscular atrophy and Charcot-Marie-Tooth type 1A: Co-existence of two rare neuromuscular genetic diseases in the same patient.

Journal: Neuromuscular disorders : NMD

Published: April 28, 2015

Mitochondrial dynamics and inherited peripheral nerve diseases.

Mitochondrial dynamics and inherited peripheral nerve diseases.

Journal: Neuroscience letters

Published: January 22, 2015

Subclinical leukodystrophy and infertility in a man with a novel homozygous CLCN2 mutation.

Subclinical leukodystrophy and infertility in a man with a novel homozygous CLCN2 mutation.

Journal: Neurology

Published: August 17, 2014

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Last Updated: 09/26/2026