A. Sagnelli

发表

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

Y. Hayashi, I. Nishino, A. Pichiecchio, 2018, European journal of neurology.

Clinical features and lifestyle of patients with amyotrophic lateral sclerosis in Campania: brief overview of an Italian database.

F. Izzo, G. Tedeschi, G. Savettieri, 2012, Annali dell'Istituto superiore di sanita.

X‐linked Charcot‐Marie‐Tooth type 1: stroke‐like presentation of a novel GJB1 mutation

D. Pareyson, L. Chiapparini, F. Taroni, 2014, Journal of the peripheral nervous system : JPNS.

Amyotrophic Lateral Sclerosis and Multiple Sclerosis Overlap: A Case Report

F. Izzo, G. Tedeschi, G. Cirillo, 2012, Case reports in medicine.

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

J. Finsterer, A. Ludolph, D. Pareyson, 2016, Journal of Molecular Neuroscience.

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

D. Pareyson, G. Scigliuolo, E. Salsano, 2017, Journal of the Neurological Sciences.

Mitochondrial dynamics and inherited peripheral nerve diseases

D. Pareyson, P. Saveri, A. Sagnelli, 2015, Neuroscience Letters.

Inherited neuropathies: an update

D. Pareyson, A. Sagnelli, G. Piscosquito, 2013, Journal of Neurology.

Search for compensation postures with videofluoromanometric investigation in dysphagic patients affected by amyotrophic lateral sclerosis

A. Reginelli, G. Tedeschi, N. Martino, 2011, La radiologia medica.

Tauroursodeoxycholic acid in the treatment of patients with amyotrophic lateral sclerosis

A. Albanese, G. Tedeschi, V. La Bella, 2015, European journal of neurology.

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

J. Finsterer, A. Ludolph, D. Pareyson, 2016, Journal of Molecular Neuroscience.

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

D. Pareyson, F. Taroni, D. D. Di Bella, 2017, Journal of the peripheral nervous system : JPNS.

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

A. Ludolph, D. Pareyson, A. Rosenbohm, 2015, Journal of Molecular Neuroscience.

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

M. D. Di Battista, C. Scavone, A. Capuano, 2021, Brain sciences.

Human Adipose-Derived Mesenchymal Stem Cells as a New Model of Spinal and Bulbar Muscular Atrophy

E. Parati, C. Gellera, D. Pareyson, 2014, PloS one.

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

Monica Consonni, D. Pareyson, L. Chiapparini, 2016, Journal of Neurology.

Adult polyglucosan body disease in a patient originally diagnosed with Fabry’s disease

D. Pareyson, M. Mora, A. Mazzeo, 2014, Neuromuscular Disorders.

Erythropoietin in amyotrophic lateral sclerosis: a multicentre, randomised, double blind, placebo controlled, phase III study

E. Granieri, A. Chiò, G. Mora, 2015, Journal of Neurology, Neurosurgery & Psychiatry.

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

N. Bresolin, G. Tedeschi, D. Pareyson, 2014, Neurology.

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

A. Ludolph, D. Pareyson, A. Rosenbohm, 2016, Journal of Molecular Neuroscience.

Interaction between aging and neurodegeneration in amyotrophic lateral sclerosis

Fabrizio Esposito, Alessandro Tessitore, Gioacchino Tedeschi, 2012, Neurobiology of Aging.

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

Mariana Rippa, K. Longo, V. Manzo, 2020, Neurological Sciences.

Amyotrophic lateral sclerosis: sonographic evaluation of dysphagia

A. Reginelli, A. Solazzo, L. Vecchio, 2010, La radiologia medica.

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

C. Gellera, V. Scaioli, D. Pareyson, 2015, Neuromuscular Disorders.

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

C. Gellera, M. Pennuto, D. Pareyson, 2016, European journal of neurology.

Widespread Microstructural White Matter Involvement in Amyotrophic Lateral Sclerosis: A Whole-Brain DTI Study

F. Esposito, G. Tedeschi, M. Monsurrò, 2012, American Journal of Neuroradiology.

Clinical features and lifestyle of patients with amyotrophic lateral sclerosis in Campania: brief overview of an Italian database.

F. Izzo, G. Tedeschi, G. Savettieri, 2012, Annali dell'Istituto superiore di sanita.

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

D. Pareyson, F. Taroni, D. D. Di Bella, 2014, Neurology.