Cargando…

Prognostic Usefulness of Motor Unit Number Index (MUNIX) in Patients Newly Diagnosed with Amyotrophic Lateral Sclerosis

The MUNIX technique allows us to estimate the number and size of surviving motor units (MUs). Previous studies on ALS found correlations between MUNIX and several clinical measures, but its potential role as a predictor of disease progression rate (DPR) has not been thoroughly evaluated to date. We...

Descripción completa

Detalles Bibliográficos
Autores principales:	Risi, Barbara, Cotti Piccinelli, Stefano, Gazzina, Stefano, Labella, Beatrice, Caria, Filomena, Damioli, Simona, Poli, Loris, Padovani, Alessandro, Filosto, Massimiliano
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	MDPI 2023
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10420094/ https://www.ncbi.nlm.nih.gov/pubmed/37568439 http://dx.doi.org/10.3390/jcm12155036

Ejemplares similares

Hereditary transthyretin amyloidosis: a comprehensive review with a focus on peripheral neuropathy
por: Poli, Loris, et al.
Publicado: (2023)

A Comprehensive Update on Late-Onset Pompe Disease
por: Labella, Beatrice, et al.
Publicado: (2023)

Juvenile-Onset Recurrent Rhabdomyolysis Due to Compound Heterozygote Variants in the ACADVL Gene
por: Labella, Beatrice, et al.
Publicado: (2023)

Leprosy Neuropathy in a Non-Endemic Area: A Clinical and Pathological Study
por: Cotti Piccinelli, Stefano, et al.
Publicado: (2023)

Leveraging process mining for modeling progression trajectories in amyotrophic lateral sclerosis
por: Tavazzi, Erica, et al.
Publicado: (2023)

Mitochondrial Neurogastrointestinal Encephalomyopathy (MNGIE-MTDPS1)
por: Filosto, Massimiliano, et al.
Publicado: (2018)

Late and Severe Myopathy in a Patient With Glycogenosis VII Worsened by Cyclosporine and Amiodarone
por: Filosto, Massimiliano, et al.
Publicado: (2019)

Does the MUNIX Method Reflect Clinical Dysfunction in Amyotrophic Lateral Sclerosis: A Practical Experience
por: Gawel, Malgorzata, et al.
Publicado: (2016)

A Novel CAPN1 Mutation Causes a Pure Hereditary Spastic Paraplegia in an Italian Family
por: Cotti Piccinelli, Stefano, et al.
Publicado: (2019)

Advances in Quantitative Imaging of Genetic and Acquired Myopathies: Clinical Applications and Perspectives
por: Paoletti, Matteo, et al.
Publicado: (2019)

Electrophysiological features of acute inflammatory demyelinating polyneuropathy associated with SARS-CoV-2 infection
por: Uncini, Antonino, et al.
Publicado: (2021)

Combinatory Biomarker Use of Cortical Thickness, MUNIX, and ALSFRS-R at Baseline and in Longitudinal Courses of Individual Patients With Amyotrophic Lateral Sclerosis
por: Wirth, Anna M., et al.
Publicado: (2018)

A Preliminary Study of Effects of Channel Number and Location on the Repeatability of Motor Unit Number Index (MUNIX)
por: Gao, Farong, et al.
Publicado: (2020)

A Novel Mutation in the Stalk Domain of KIF5A Causes a Slowly Progressive Atypical Motor Syndrome
por: Filosto, Massimiliano, et al.
Publicado: (2018)

Modified motor unit number index (MUNIX) algorithm for assessing excitability of alpha motor neuron in spasticity
por: Uslu, Serkan, et al.
Publicado: (2018)

Motor unit number index (MUNIX) in the D50 disease progression model reflects disease accumulation independently of disease aggressiveness in ALS
por: Ebersbach, Theresa, et al.
Publicado: (2022)

Quality Control of Motor Unit Number Index (MUNIX) Measurements in 6 Muscles in a Single-Subject “Round-Robin” Setup
por: Neuwirth, Christoph, et al.
Publicado: (2016)

Motor unit number index (MUNIX) loss of 50% occurs in half the time of 50% functional loss according to the D50 disease progression model of ALS
por: Ebersbach, Theresa, et al.
Publicado: (2023)

Predictors of “brain fog” 1 year after COVID-19 disease
por: Cristillo, Viviana, et al.
Publicado: (2022)

Neurologic disease and COVID-19: A comparative study between first and second wave hospitalized patients in Brescia, Lombardia, Italy
por: Cristillo, Viviana, et al.
Publicado: (2021)

Premorbid vulnerability and disease severity impact on Long-COVID cognitive impairment
por: Cristillo, Viviana, et al.
Publicado: (2022)

Motor unit properties do not correlate between MUNIX and needle EMG in remote polio in the biceps brachii muscle
por: Sandberg, A.
Publicado: (2022)

Effect of RNS60 in amyotrophic lateral sclerosis: a phase II multicentre, randomized, double‐blind, placebo‐controlled trial
por: Beghi, Ettore, et al.
Publicado: (2022)

A complex craniovertebral junction malformation in a patient with late onset glycogenosis 2
por: Cotelli, Mariasofia, et al.
Publicado: (2014)

Current and emerging treatments for amyotrophic lateral sclerosis
por: Zoccolella, Stefano, et al.
Publicado: (2009)

Newly Diagnosed Amyotrophic Lateral Sclerosis in a Patient with Multiple-System Atrophy
por: Choi, Moonkyung, et al.
Publicado: (2020)

Decreased Levels of Foldase and Chaperone Proteins Are Associated with an Early-Onset Amyotrophic Lateral Sclerosis
por: Filareti, Melania, et al.
Publicado: (2017)

Subcortical and Deep Cortical Atrophy in Frontotemporal Dementia due to Granulin Mutations
por: Premi, Enrico, et al.
Publicado: (2014)

The environmental effects of the “twin” green and digital transition in European regions
por: Bianchini, Stefano, et al.
Publicado: (2022)

Mitochondrial diseases: advances and issues
por: Scarpelli, Mauro, et al.
Publicado: (2017)

Guillain-barré syndrome and COVID-19: An observational multicenter study
por: Piccinelli, Stefano Cotti, et al.
Publicado: (2021)

An overview of motor unit number index reproducibility in amyotrophic lateral sclerosis
por: Fathi, Davood, et al.
Publicado: (2019)

Long-term neurological manifestations of COVID-19: prevalence and predictive factors
por: Pilotto, Andrea, et al.
Publicado: (2021)

Oligodendrocyte Dysfunction in Amyotrophic Lateral Sclerosis: Mechanisms and Therapeutic Perspectives
por: Raffaele, Stefano, et al.
Publicado: (2021)

Increased Axonal Ribosome Numbers Is an Early Event in the Pathogenesis of Amyotrophic Lateral Sclerosis
por: Verheijen, Mark H. G., et al.
Publicado: (2014)

Exercise Combined with Electrotherapy Enhances Motor Function in an Adolescent with Spinal Muscular Atrophy Type III
por: Gobbo, Massimiliano, et al.
Publicado: (2019)

Microglial crosstalk with astrocytes and immune cells in amyotrophic lateral sclerosis
por: Calafatti, Matteo, et al.
Publicado: (2023)

The Cortical Signature of Amyotrophic Lateral Sclerosis
por: Agosta, Federica, et al.
Publicado: (2012)

An overview on amyotrophic lateral sclerosis and cadmium
por: Oggiano, Riccardo, et al.
Publicado: (2020)

The first year of neurology and COVID-19: The importance of understanding neurological and biopsychosocial symptoms in acute and post neurocovid disease
por: Leonardi, Matilde, et al.
Publicado: (2021)

Cannot write session to /tmp/vufind_sessions/sess_g516r3j54erb5qv9c3c32phbom