G. Piscosquito

发表

Anti–amyloid β autoantibodies in cerebral amyloid angiopathy–related inflammation: Implications for amyloid‐modifying therapies

Antonio Colombo, Ricardo Nitrini, Carlo Ferrarese, 2013, Annals of neurology.

Postural stabilization and balance assessment of Charcot-Marie-Tooth types 1A, 2 and X1

M. Ferrarin, M. Rabuffetti, L. Padua, 2014 .

Monitoring effectiveness and safety of Tafamidis in transthyretin amyloidosis in Italy: a longitudinal multicenter study in a non-endemic area

M. Russo, D. Pareyson, A. Schenone, 2016, Journal of Neurology.

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.

Generalized anhidrosis as first clinical presentation of systemic lupus erythematosus

L. Santoro, M. Nolano, V. Provitera, 2018, Lupus.

Combined central and peripheral demyelination: Clinical features, diagnostic findings, and treatment

E. Marchioni, A. Pichiecchio, D. Pareyson, 2016, Journal of the Neurological Sciences.

Exercise training effects on elderly and middle-age patients with chronic heart failure after acute decompensation: A randomized, controlled trial.

G. Furgi, R. Incalzi, P. Scicchitano, 2016, International journal of cardiology.

Responsiveness of gait parameters to changes in locomotor impairments induced by CMT disease: A 12 months follow-up study

M. Ferrarin, M. Rabuffetti, D. Pareyson, 2015 .

A longitudinal study of CMT1A using Rasch analysis based CMT neuropathy and examination scores

R. Finkel, S. Züchner, F. Muntoni, 2020, Neurology.

Genotype-phenotype characteristics and baseline natural history of heritable neuropathies caused by mutations in the MPZ gene.

R. Finkel, F. Muntoni, D. Herrmann, 2015, Brain : a journal of neurology.

A slowly progressive mitochondrial encephalomyopathy widens the spectrum of AIFM1 disorders

E. Lamantea, D. Pareyson, D. Ghezzi, 2015, Neurology.

Adult-onset leukodystrophies from respiratory chain disorders: do they exist?

M. Zeviani, E. Lamantea, G. Uziel, 2013, Journal of Neurology.

Mitochondrial dynamics and inherited peripheral nerve diseases

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

An update on clinical trials in Charcot-Marie-Tooth Disease

D. Pareyson, G. Piscosquito, 2014 .

A novel insertional mutation in the prion protein gene: clinical and bio-molecular findings

F. Tagliavini, C. Coppola, G. Giaccone, 2008, Journal of Neurology, Neurosurgery, and Psychiatry.

Validation of the Italian version of the pediatric CMT quality of life outcome measure

D. Pareyson, A. Ardissone, E. Pagliano, 2022, Journal of the peripheral nervous system : JPNS.

Peripheral neuropathy in mitochondrial disorders

M. Zeviani, D. Pareyson, E. Salsano, 2013, The Lancet Neurology.

The influence of somatosensory and muscular deficits on postural stabilization: Insights from an instrumented analysis of subjects affected by different types of Charcot–Marie–Tooth disease

M. Ferrarin, M. Rabuffetti, L. Padua, 2015, Neuromuscular Disorders.

A novel NDRG1 mutation in a non‐Romani patient with CMT4D/HMSN‐Lom

D. Pareyson, F. Taroni, S. Magri, 2017, Journal of the peripheral nervous system : JPNS.

CMT subtypes and disease burden in patients enrolled in the Inherited Neuropathies Consortium natural history study: a cross-sectional analysis

Jun Yu Li, R. Finkel, S. Züchner, 2014, Journal of Neurology, Neurosurgery & Psychiatry.

Cross-sectional analysis of a large cohort with X-linked Charcot-Marie-Tooth disease (CMTX1)

R. Lewis, R. Horvath, D. Herrmann, 2017, Neurology.

A progranulin mutation associated with cortico-basal syndrome in an Italian family expressing different phenotypes of fronto-temporal lobar degeneration

F. Tagliavini, D. Saracino, G. Rossi, 2012, Neurological Sciences.

A novel synonymous mutation in the MPZ gene causing an aberrant splicing pattern and Charcot-Marie-Tooth disease type 1b

D. Pareyson, R. Cantello, F. Taroni, 2016, Neuromuscular Disorders.

Inherited neuropathies: an update

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

Adherence and Reactogenicity to Vaccines against SARS-COV-2 in 285 Patients with Neuropathy: A Multicentric Study

F. Brighina, A. Firenze, V. Di Stefano, 2022, Brain sciences.

2018 Peripheral Nerve Society Annual Meeting 21‐25 July, 2018 Baltimore, Maryland

J. Polke, M. Reilly, F. Taroni, 2018, Journal of the Peripheral Nervous System.

Mutational mechanisms in MFN2‐related neuropathy: compound heterozygosity for recessive and semidominant mutations

D. Pareyson, F. Taroni, S. Magri, 2015, Journal of the peripheral nervous system : JPNS.

Relative lymphocyte count as an indicator of 3-year mortality in elderly people with severe COPD

R. Maestri, R. Antonelli-Incalzi, A. Zito, 2018, BMC Pulmonary Medicine.

A Model to Study Myelinated Fiber Degeneration and Regeneration in Human Skin

L. Santoro, M. Nolano, V. Provitera, 2019, Annals of neurology.

Outcome measures in the clinical evaluation of ambulatory Charcot-Marie-Tooth 1A subjects.

N. Smania, L. Padua, D. Pareyson, 2019, European journal of physical and rehabilitation medicine.

Sex differences in neuromuscular disorders

F. Ginanneschi, F. Brighina, C. Balistreri, 2023, Mechanisms of Ageing and Development.

Overlapping phenotypes in complex spastic paraplegias SPG11, SPG15, SPG35 and SPG48.

B. Castellotti, C. Gellera, D. Pareyson, 2014, Brain : a journal of neurology.

Mutations in noncoding regions of GJB1 are a major cause of X-linked CMT

H. Houlden, D. Pareyson, J. Polke, 2017, Neurology.

Electromyographic and biomechanical analysis of step negotiation in Charcot Marie Tooth subjects whose level walk is not impaired.

M. Ferrarin, M. Rabuffetti, L. Padua, 2018, Gait & posture.

Responsiveness of gait analysis parameters in a cohort of 71 CMT subjects

Maurizio Ferrarin, Davide Pareyson, Isabella Moroni, 2017, Neuromuscular Disorders.

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.

Novel loss‐of‐function mutation of the HINT1 gene in a patient with distal motor axonal neuropathy without neuromyotonia

D. Pareyson, F. Boaretto, C. Briani, 2015, Muscle & nerve.

Different nerve ultrasound patterns in charcot‐marie‐tooth types and hereditary neuropathy with liability to pressure palsies

L. Padua, M. Lucchetta, D. Pareyson, 2018, Muscle & nerve.

Responsiveness of clinical outcome measures in Charcot−Marie−Tooth disease

D. Radice, A. Quattrone, L. Padua, 2015, European journal of neurology.

Postural stabilization and balance assessment in Charcot–Marie–Tooth 1A subjects

M. Ferrarin, M. Rabuffetti, L. Padua, 2014, Gait & posture.

Neurofascin-155 as a putative antigen in combined central and peripheral demyelination

E. Marchioni, D. Pareyson, J. Devaux, 2016, Neurology: Neuroimmunology & Neuroinflammation.

Charcot-Marie-Tooth Type 2B: A New Phenotype Associated with a Novel RAB7A Mutation and Inhibited EGFR Degradation

P. Fossa, E. Cichero, D. Pareyson, 2020, Cells.

Screening for SH3TC2 gene mutations in a series of demyelinating recessive Charcot‐Marie‐Tooth disease (CMT4)

Davide Pareyson, Isabella Moroni, Franco Taroni, 2016, Journal of the peripheral nervous system : JPNS.

Psychometrics evaluation of Charcot‐Marie‐Tooth Neuropathy Score (CMTNSv2) second version, using Rasch analysis

D. Pareyson, C. Bacon, M. Shy, 2014, Journal of the peripheral nervous system : JPNS.

Coexistence of Charcot‐Marie‐Tooth disease type 1A and anti‐MAG neuropathy

D. Pareyson, E. Salsano, M. Morbin, 2013, Journal of the peripheral nervous system : JPNS.

Anterior lumbosacral polyradiculoneuropathy following intrathecal methotrexate administration: a case report and literature update

G. Piscosquito, C. Vinciguerra, M. C. Russillo, 2022, Neurological Sciences.

Charcot-Marie-Tooth Disease and Related Hereditary Neuropathies: From Gene Function to Associated Phenotypes.

D. Pareyson, P. Saveri, G. Piscosquito, 2014, Current molecular medicine.

Starting eculizumab as rescue therapy in refractory myasthenic crisis

G. Piscosquito, C. Vinciguerra, A. Toriello, 2023, Neurological Sciences.

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.

Case report: Asp194Ala variant in MFN2 is associated with ALS-FTD in an Italian family

S. Cuoco, E. Monfrini, A. Di Fonzo, 2023, Frontiers in genetics.

Miller Fisher syndrome: an updated narrative review

G. Piscosquito, C. Vinciguerra, A. Toriello, 2023, Frontiers in Neurology.

Is overwork weakness relevant in Charcot–Marie–Tooth disease?

D. Radice, L. Santoro, A. Quattrone, 2014, Journal of Neurology, Neurosurgery & Psychiatry.

Treadmill training in patients affected by Charcot–Marie–Tooth neuropathy: results of a multicenter, prospective, randomized, single‐blind, controlled study

N. Smania, L. Marinelli, L. Padua, 2019, European journal of neurology.

Chronic inflammatory demyelinating polyneuropathy after SARS-CoV2 vaccination: update of the literature and patient characterization.

F. Ginanneschi, G. Piscosquito, C. Vinciguerra, 2023, Immunologic research.

A slowly progressive mitochondrial encephalomyopathy widens the spectrum of AIFM1 disorders

E. Lamantea, D. Pareyson, D. Ghezzi, 2015, Neurology.

Small fiber pathology parallels disease progression in Parkinson disease: a longitudinal study

L. Santoro, M. Nolano, V. Provitera, 2018, Acta Neuropathologica.

The analysis of epidermal nerve fibre spatial distribution improves the diagnostic yield of skin biopsy

M. Nolano, V. Provitera, G. Caporaso, 2020, Neuropathology and applied neurobiology.