How common are behavioural changes in amyotrophic lateral sclerosis? - Wikidata - wikimedia - TriplyDB

How common are behavioural changes in amyotrophic lateral sclerosis?

How common are behavioural changes in amyotrophic lateral sclerosis?

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Widespread structural and functional connectivity changes in amyotrophic lateral sclerosis: insights from advanced neuroimaging research Modeling ALS and FTD with iPSC-derived neurons Cognitive-behavioral screening reveals prevalent impairment in a large multicenter ALS cohort.Amyotrophic lateral sclerosis: improving care with a multidisciplinary approach.A systematic review of behavioural changes in motor neuron disease.Grey and white matter changes across the amyotrophic lateral sclerosis-frontotemporal dementia continuum.Caregiver burden in amyotrophic lateral sclerosis is more dependent on patients' behavioral changes than physical disability: a comparative study.Behavior matters--cognitive predictors of survival in amyotrophic lateral sclerosis.Personality disturbances in amyotrophic lateral sclerosis: a case study demonstrating changes in personality without cognitive deficits.Microstructural Correlates of Emotional Attribution Impairment in Non-Demented Patients with Amyotrophic Lateral Sclerosis ALS and Frontotemporal Dysfunction: A Review.Detailed volumetric analysis of the hypothalamus in behavioral variant frontotemporal dementia.Engaging in patient decision-making in multidisciplinary care for amyotrophic lateral sclerosis: the views of health professionals Executive Dysfunctions and Event-Related Brain Potentials in Patients with Amyotrophic Lateral Sclerosis The molecular basis of the frontotemporal lobar degeneration-amyotrophic lateral sclerosis spectrum Behavioral Symptoms in Motor Neuron Disease and Their Negative Impact on Caregiver Burden Frontotemporal dementia: diagnosis, deficits and management Exploring sarcasm detection in amyotrophic lateral sclerosis using ecologically valid measures.Development of a model to guide decision making in amyotrophic lateral sclerosis multidisciplinary care.The frontotemporal syndrome of ALS is associated with poor survival.Telephone based cognitive-behavioral screening for frontotemporal changes in patients with amyotrophic lateral sclerosis (ALS).Pathological staging of frontotemporal lobar degeneration.Depression and disease progression in amyotrophic lateral sclerosis: A comprehensive meta-regression analysis.Challenges in the Understanding and Treatment of Amyotrophic Lateral Sclerosis/Motor Neuron Disease.The Evolution of Caregiver Burden in Frontotemporal Dementia with and without Amyotrophic Lateral Sclerosis.Caregiver burden in amyotrophic lateral sclerosis: A systematic review.Depression and anxiety in individuals with amyotrophic lateral sclerosis: a systematic review.A Cross-sectional population-based investigation into behavioral change in amyotrophic lateral sclerosis: subphenotypes, staging, cognitive predictors, and survival.Extra-motor abnormalities in amyotrophic lateral sclerosis: another layer of heterogeneity.Development of patient decision support tools for motor neuron disease using stakeholder consultation: a study protocol.Cognitive and Behavioral Symptoms in ALSFTD: Detection, Differentiation, and Progression.Multidimensional apathy in ALS: validation of the Dimensional Apathy Scale.Examining the language and behavioural profile in FTD and ALS-FTD.What are the roles of carers in decision-making for amyotrophic lateral sclerosis multidisciplinary care?Response to 'Exploring limits of neuropsychological screening in ALS: the FAB problem'.When more is needed: the utility of the frontotemporal dementia scale in ALS.Comparison between home and hospital as the place of death for individuals with amyotrophic lateral sclerosis in the last stages of illness.Frontotemporal cortical thinning in amyotrophic lateral sclerosis.Clinical variability and female penetrance in X-linked familial FTD/ALS caused by a P506S mutation in UBQLN2.Emotion processing deficits distinguish pure amyotrophic lateral sclerosis from frontotemporal dementia.

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P2860

How common are behavioural changes in amyotrophic lateral sclerosis?

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How common are behavioural changes in amyotrophic lateral sclerosis?

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How common are behavioural changes in amyotrophic lateral sclerosis?

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How common are behavioural changes in amyotrophic lateral sclerosis?

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How common are behavioural changes in amyotrophic lateral sclerosis?

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Amyotrophic Lateral Sclerosis and Other Motor Neuron Disorders

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P2860

Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis

TDP-43 proteinopathy: the neuropathology underlying major forms of sporadic and familial frontotemporal lobar degeneration and motor neuron disease

Frontotemporal lobar degeneration: a consensus on clinical diagnostic criteria

El Escorial revisited: revised criteria for the diagnosis of amyotrophic lateral sclerosis

The short-form version of the Depression Anxiety Stress Scales (DASS-21): construct validity and normative data in a large non-clinical sample.

Establishing subtypes of the continuum of frontal lobe impairment in amyotrophic lateral sclerosis.

Sensitivity of current criteria for the diagnosis of behavioral variant frontotemporal dementia.

Are amyotrophic lateral sclerosis patients cognitively normal?

The nosological position of apathy in clinical practice.

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