about
Screening for cognitive dysfunction in ALS: validation of the Edinburgh Cognitive and Behavioural ALS Screen (ECAS) using age and education adjusted normative data.Cognitive impairment in amyotrophic lateral sclerosis.Functional Connectivity Changes in Resting-State EEG as Potential Biomarker for Amyotrophic Lateral Sclerosis.Predicting prognosis in amyotrophic lateral sclerosis: a simple algorithmCognitive and clinical characteristics of patients with amyotrophic lateral sclerosis carrying a C9orf72 repeat expansion: a population-based cohort study.Measurement of Social Cognition in Amyotrophic Lateral Sclerosis: A Population Based Study.Multiparametric MRI study of ALS stratified for the C9orf72 genotype.The Irish epilepsy surgery experience: Long-term follow-up.Social cognition in neurodegenerative disorders: a systematic review.The economic cost of nonepileptic attack disorder in Ireland.Metacognitive and online error awareness deficits after prefrontal cortex lesions.Becoming comfortable with "my" epilepsy: Strategies that patients use in the journey from diagnosis to acceptance and disclosure.Mismatch Negativity as an Indicator of Cognitive Sub-Domain Dysfunction in Amyotrophic Lateral Sclerosis.A Cross-sectional population-based investigation into behavioral change in amyotrophic lateral sclerosis: subphenotypes, staging, cognitive predictors, and survival.Caregivers of patients with amyotrophic lateral sclerosis: investigating quality of life, caregiver burden, service engagement, and patient survival.Basal ganglia involvement in amyotrophic lateral sclerosis.Cognitive changes predict functional decline in ALS: a population-based longitudinal study.Discordant performance on the 'Reading the Mind in the Eyes' Test, based on disease onset in amyotrophic lateral sclerosis.A comparison of propofol and amobarbital for use in the Wada test.The effects of immunologic brainstem encephalopathy on cognitive function following awakening from a progressive autoimmune coma.Grey matter correlates of clinical variables in amyotrophic lateral sclerosis (ALS): a neuroimaging study of ALS motor phenotype heterogeneity and cortical focality.The syndrome of cognitive impairment in amyotrophic lateral sclerosis: a population-based study.Huntington's disease presenting as amyotrophic lateral sclerosis.Abstracts from the 20th International Symposium on Signal Transduction at the Blood-Brain Barriers.Characteristic Increases in EEG Connectivity Correlate With Changes of Structural MRI in Amyotrophic Lateral Sclerosis.Managing cognitive impairment following stroke: protocol for a systematic review of non-randomised controlled studies of psychological interventions.Clustering of Neuropsychiatric Disease in First-Degree and Second-Degree Relatives of Patients With Amyotrophic Lateral Sclerosis.Identifying behavioural changes in ALS: Validation of the Beaumont Behavioural Inventory (BBI).Caregiver burden in amyotrophic lateral sclerosis: a cross-sectional investigation of predictors.Longitudinal predictors of caregiver burden in amyotrophic lateral sclerosis: a population-based cohort of patient-caregiver dyads.Needs of informal caregivers across the caregiving course in amyotrophic lateral sclerosis: a qualitative analysis.Measuring reliable change in cognition using the Edinburgh Cognitive and Behavioural ALS Screen (ECAS).Assessing behavioural changes in ALS: cross-validation of ALS-specific measures.The contribution of retrospective memory, attention and executive functions to the prospective and retrospective components of prospective memory following TBI.Connectivity-based characterisation of subcortical grey matter pathology in frontotemporal dementia and ALS: a multimodal neuroimaging study.Visual encoding, consolidation, and retrieval in amyotrophic lateral sclerosis: executive function as a mediator, and predictor of performance.Executive dysfunction is a negative prognostic indicator in patients with ALS without dementia.A considerable memory store.Neuroimaging patterns along the ALS-FTD spectrum: a multiparametric imaging study.The Study of Language in the Amyotrophic Lateral Sclerosis - Frontotemporal Spectrum Disorder: a Systematic Review of Findings and New Perspectives.
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P50
description
hulumtues
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researcher
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հետազոտող
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name
Niall P Pender
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Niall P. Pender
@en
Niall P. Pender
@nl
Niall P. Pender
@sl
type
label
Niall P Pender
@es
Niall P. Pender
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Niall P. Pender
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Niall P. Pender
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prefLabel
Niall P Pender
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Niall P. Pender
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Niall P. Pender
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Niall P. Pender
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P106
P1153
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P21
P31
P496
0000-0002-4172-0704
P569
2000-01-01T00:00:00Z