Cargando…

Mismatch Negativity as an Indicator of Cognitive Sub-Domain Dysfunction in Amyotrophic Lateral Sclerosis

OBJECTIVE: To evaluate the utility of mismatch negativity (MMN), a neurophysiologic marker of non-motor cognitive processing, in amyotrophic lateral sclerosis (ALS). METHODS: 89 patients, stratified into 4 different phenotypic presentations of ALS (67 spinal-onset, 15 bulbar-onset, 7 ALS-FTD, 7 C9OR...

Descripción completa

Detalles Bibliográficos
Autores principales:	Iyer, Parameswaran Mahadeva, Mohr, Kieran, Broderick, Michael, Gavin, Brighid, Burke, Tom, Bede, Peter, Pinto-Grau, Marta, Pender, Niall P., McLaughlin, Russell, Vajda, Alice, Heverin, Mark, Lalor, Edmund C., Hardiman, Orla, Nasseroleslami, Bahman
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Frontiers Media S.A. 2017
Materias:	Neuroscience
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5559463/ https://www.ncbi.nlm.nih.gov/pubmed/28861032 http://dx.doi.org/10.3389/fneur.2017.00395

Ejemplares similares

Dysfunction of attention switching networks in amyotrophic lateral sclerosis
por: McMackin, Roisin, et al.
Publicado: (2019)

Functional Connectivity Changes in Resting-State EEG as Potential Biomarker for Amyotrophic Lateral Sclerosis
por: Iyer, Parameswaran Mahadeva, et al.
Publicado: (2015)

Patterned functional network disruption in amyotrophic lateral sclerosis
por: Dukic, Stefan, et al.
Publicado: (2019)

Resting-state EEG reveals four subphenotypes of amyotrophic lateral sclerosis
por: Dukic, Stefan, et al.
Publicado: (2021)

A Cross‐sectional population‐based investigation into behavioral change in amyotrophic lateral sclerosis: subphenotypes, staging, cognitive predictors, and survival
por: Burke, Tom, et al.
Publicado: (2017)

Neurophysiological markers of network dysfunction in neurodegenerative diseases
por: McMackin, Roisin, et al.
Publicado: (2019)

Localization of Brain Networks Engaged by the Sustained Attention to Response Task Provides Quantitative Markers of Executive Impairment in Amyotrophic Lateral Sclerosis
por: McMackin, Roisin, et al.
Publicado: (2020)

Corrigendum to: Localization of Brain Networks Engaged by the Sustained Attention to Response Task Provides Quantitative Markers of Executive Impairment in Amyotrophic Lateral Sclerosis
por: McMackin, Roisin, et al.
Publicado: (2020)

Measurement of Social Cognition in Amyotrophic Lateral Sclerosis: A Population Based Study
por: Burke, Tom, et al.
Publicado: (2016)

Cognitive and neuropsychiatric endophenotypes in amyotrophic lateral sclerosis
por: Costello, Emmet, et al.
Publicado: (2023)

Group interventions for amyotrophic lateral sclerosis caregivers in Ireland: a randomised controlled trial protocol
por: Burke, Tom, et al.
Publicado: (2019)

Cognitive and clinical characteristics of patients with amyotrophic lateral sclerosis carrying a C9orf72 repeat expansion: a population-based cohort study
por: Byrne, Susan, et al.
Publicado: (2012)

Predicting prognosis in amyotrophic lateral sclerosis: a simple algorithm
por: Elamin, Marwa, et al.
Publicado: (2015)

Determining the incidence of familiality in ALS: A study of temporal trends in Ireland from 1994 to 2016
por: Ryan, Marie, et al.
Publicado: (2018)

Virtual brain biopsies in amyotrophic lateral sclerosis: Diagnostic classification based on in vivo pathological patterns
por: Bede, Peter, et al.
Publicado: (2017)

“Switchboard” malfunction in motor neuron diseases: Selective pathology of thalamic nuclei in amyotrophic lateral sclerosis and primary lateral sclerosis
por: Chipika, Rangariroyashe H., et al.
Publicado: (2020)

The path to specialist multidisciplinary care in amyotrophic lateral sclerosis: A population- based study of consultations, interventions and costs
por: Galvin, Miriam, et al.
Publicado: (2017)

Genetic testing in ALS: A survey of current practices
por: Vajda, Alice, et al.
Publicado: (2017)

Brainstem–cortex disconnection in amyotrophic lateral sclerosis: bulbar impairment, genotype associations, asymptomatic changes and biomarker opportunities
por: Tahedl, Marlene, et al.
Publicado: (2023)

Brainstem pathology in amyotrophic lateral sclerosis and primary lateral sclerosis: A longitudinal neuroimaging study
por: Bede, Peter, et al.
Publicado: (2019)

Widespread subcortical grey matter degeneration in primary lateral sclerosis: a multimodal imaging study with genetic profiling
por: Finegan, Eoin, et al.
Publicado: (2019)

Needs of informal caregivers across the caregiving course in amyotrophic lateral sclerosis: a qualitative analysis
por: Galvin, Miriam, et al.
Publicado: (2018)

Survival prediction in Amyotrophic lateral sclerosis based on MRI measures and clinical characteristics
por: Schuster, Christina, et al.
Publicado: (2017)

The C9orf72 expansion is associated with accelerated respiratory function decline in a large Amyotrophic Lateral Sclerosis cohort
por: Rooney, James, et al.
Publicado: (2019)

Patient journey to a specialist amyotrophic lateral sclerosis multidisciplinary clinic: an exploratory study
por: Galvin, M., et al.
Publicado: (2015)

Prediction of caregiver quality of life in amyotrophic lateral sclerosis using explainable machine learning
por: Antoniadi, Anna Markella, et al.
Publicado: (2021)

Progressive brainstem pathology in motor neuron diseases: Imaging data from amyotrophic lateral sclerosis and primary lateral sclerosis
por: Bede, Peter, et al.
Publicado: (2020)

Care, burden and self-described positive aspects of caring in amyotrophic lateral sclerosis: an exploratory, longitudinal, mixed-methods study
por: Conroy, Éilís, et al.
Publicado: (2023)

Measuring reliable change in cognition using the Edinburgh Cognitive and Behavioural ALS Screen (ECAS)
por: Crockford, Christopher, et al.
Publicado: (2017)

Thalamic, hippocampal and basal ganglia pathology in primary lateral sclerosis and amyotrophic lateral sclerosis: Evidence from quantitative imaging data
por: Finegan, Eoin, et al.
Publicado: (2020)

Development of an Automated MRI-Based Diagnostic Protocol for Amyotrophic Lateral Sclerosis Using Disease-Specific Pathognomonic Features: A Quantitative Disease-State Classification Study
por: Schuster, Christina, et al.
Publicado: (2016)

Prediction of caregiver burden in amyotrophic lateral sclerosis: a machine learning approach using random forests applied to a cohort study
por: Antoniadi, Anna Markella, et al.
Publicado: (2020)

Survival Analysis of Irish Amyotrophic Lateral Sclerosis Patients Diagnosed from 1995–2010
por: Rooney, James, et al.
Publicado: (2013)

MRI data confirm the selective involvement of thalamic and amygdalar nuclei in amyotrophic lateral sclerosis and primary lateral sclerosis
por: Chipika, Rangariroyashe H., et al.
Publicado: (2020)

Burden and benefit—A mixed methods study of informal Amyotrophic Lateral Sclerosis caregivers in Ireland and the Netherlands
por: Kennedy, Polly, et al.
Publicado: (2022)

An Exploratory Spatial Analysis of ALS Incidence in Ireland over 17.5 Years (1995 – July 2013)
por: Rooney, James, et al.
Publicado: (2014)

The involvement of language‐associated networks, tracts, and cortical regions in frontotemporal dementia and amyotrophic lateral sclerosis: Structural and functional alterations
por: Tahedl, Marlene, et al.
Publicado: (2023)

Cortico-muscular coherence in primary lateral sclerosis reveals abnormal cortical engagement during motor function beyond primary motor areas
por: Bista, Saroj, et al.
Publicado: (2023)

ALS-specific cognitive and behavior changes associated with advancing disease stage in ALS
por: Crockford, Christopher, et al.
Publicado: (2018)

Patterns of cerebral and cerebellar white matter degeneration in ALS
por: Bede, P, et al.
Publicado: (2015)

Cannot write session to /tmp/vufind_sessions/sess_e3cf9an0lhc2bbtub7mst25keu