David J. Dick
Norwich, ENG, United Kingdom
Last Updated: 09/26/2026
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Found 15 publications
Self-reported initiation apathy is related to worse quality of life in amyotrophic lateral sclerosis.
Journal: Amyotrophic lateral sclerosis & frontotemporal degeneration
Published: October 23, 2025
Impact of apathy over the course of disease in amyotrophic lateral sclerosis.
Journal: Amyotrophic lateral sclerosis & frontotemporal degeneration
Published: April 29, 2025
Acceptance and Commitment Therapy for people living with motor neuron disease: an uncontrolled feasibility study.
Journal: Pilot and feasibility studies
Published: March 13, 2023
Measuring coping in people with amyotrophic lateral sclerosis using the Coping Index-ALS: A patient derived, Rasch compliant scale.
Journal: Journal of the neurological sciences
Published: August 10, 2020
Measuring quality of life in ALS/MND: validation of the WHOQOL-BREF.
Journal: Amyotrophic lateral sclerosis & frontotemporal degeneration
Published: June 27, 2020
Clinical and Genetic Features in a Series of Eight Unrelated Patients with Neuropathy Due to Glycyl-tRNA Synthetase (GARS) Variants.
Journal: Journal of neuromuscular diseases
Published: January 28, 2020
Reliability and validity of the brief dimensional apathy scale.
Journal: Archives of clinical neuropsychology : the official journal of the National Academy of Neuropsychologists
Published: September 24, 2019
The relationships between symptoms, disability, perceived health and quality of life in amyotrophic lateral sclerosis/motor neuron disease.
Journal: Amyotrophic lateral sclerosis & frontotemporal degeneration
Published: May 23, 2019
Development and validation of Spasticity Index-Amyotrophic Lateral Sclerosis.
Journal: Acta neurologica Scandinavica
Published: January 23, 2018
A multicentre evaluation of oropharyngeal secretion management practices in amyotrophic lateral sclerosis.
Journal: Amyotrophic lateral sclerosis & frontotemporal degeneration
Published: September 01, 2016
Zebra body myopathy is caused by a mutation in the skeletal muscle actin gene (ACTA1).
Journal: Neuromuscular disorders : NMD
Published: November 28, 2014
Mutations in the SPG7 gene cause chronic progressive external ophthalmoplegia through disordered mitochondrial DNA maintenance.
Journal: Brain : a journal of neurology
Published: April 15, 2014
Last Updated: 09/26/2026