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Supportive and symptomatic management of amyotrophic lateral sclerosis

Nature reviews. Neurology, 2016-09, Vol.12 (9), p.526

2016

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Factors influencing decisions people with motor neuron disease make about gastrostomy placement and ventilation: A qualitative evidence synthesis

Health expectations : an international journal of public participation in health care and health policy, 2023-08, Vol.26 (4), p.1418-1435

2023

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Improving clinical trial outcomes in amyotrophic lateral sclerosis

Nature reviews. Neurology, 2021-02, Vol.17 (2), p.104-118

2021

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Value of systematic genetic screening of patients with amyotrophic lateral sclerosis

Journal of neurology, neurosurgery and psychiatry, 2021-05, Vol.92 (5), p.510

2021

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Diagnosis and management of motor neurone disease

BMJ (British Medical Journal), 2008-03, Vol.336 (7645), p.658-662

International edition, 2008

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Clinico-pathological features in amyotrophic lateral sclerosis with expansions in C9ORF72

Brain (London, England : 1878), 2012-03, Vol.135 (Pt 3), p.751-764

2012

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A review of Mendelian randomization in amyotrophic lateral sclerosis

Brain (London, England : 1878), 2022-04, Vol.145 (3), p.832-842

2022

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Enteral feeding in neurological disorders

Practical Neurology, 2016-10, Vol.16 (5), p.352-361

2016

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Magnetic resonance spectroscopy reveals mitochondrial dysfunction in amyotrophic lateral sclerosis

Brain (London, England : 1878), 2020-12, Vol.143 (12), p.3603-3618

2020

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Efficacy of the Head Up collar in facilitating functional head movements in patients with Amyotrophic Lateral Sclerosis

Clinical biomechanics (Bristol), 2018-08, Vol.57, p.114-120

2018

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Do pain, anxiety and depression influence quality of life for people with amyotrophic lateral sclerosis/motor neuron disease? A national study reconciling previous conflicting literature

Journal of neurology, 2020-03, Vol.267 (3), p.607-615

2020

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Imaging muscle as a potential biomarker of denervation in motor neuron disease

Journal of neurology, neurosurgery and psychiatry, 2018-03, Vol.89 (3), p.248

2018

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Reinnervation as measured by the motor unit size index is associated with preservation of muscle strength in amyotrophic lateral sclerosis, but not all muscles reinnervate

Muscle & nerve, 2022-02, Vol.65 (2), p.203-210

2022

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Cost-effectiveness of acceptance and commitment therapy for people living with motor neuron disease, and their health-related quality of life

European journal of neurology, 2024-04, p.e16317-e16317

2024

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Non-invasive ventilation in motor neuron disease: an update of current UK practice

Journal of neurology, neurosurgery and psychiatry, 2012-04, Vol.83 (4), p.371-376

2012

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Management of oral secretions in neurological disease

Practical neurology, 2017-04, Vol.17 (2), p.96

2017

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Loss of nuclear TDP-43 in amyotrophic lateral sclerosis (ALS) causes altered expression of splicing machinery and widespread dysregulation of RNA splicing in motor neurones

Neuropathology and applied neurobiology, 2014-10, Vol.40 (6), p.670-685

2014

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Longitudinal multi-modal muscle-based biomarker assessment in motor neuron disease

Journal of neurology, 2020-01, Vol.267 (1), p.244-256

2020

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Developing the evidence base for the management of drooling

Developmental medicine and child neurology, 2020-03, Vol.62 (3), p.270-270

Mcdermott, Christopher

2020

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Tracheostomy in motor neurone disease

Practical neurology, 2019-12, Vol.19 (6), p.467

2019

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Withdrawal of tracheostomy ventilation in motor neurone disease: implementing advance directives

Practical neurology, 2017-10, Vol.17 (5), p.339

2017

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Gene expression signatures in motor neurone disease fibroblasts reveal dysregulation of metabolism, hypoxia-response and RNA processing functions

Neuropathology and applied neurobiology, 2015-02, Vol.41 (2), p.201-226

2015

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Concurrence of multiple sclerosis and amyotrophic lateral sclerosis in patients with hexanucleotide repeat expansions of C9ORF72

Journal of neurology, neurosurgery and psychiatry, 2013-01, Vol.84 (1), p.79-87

2013

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Use of coping strategies in MND/ALS: Association with demographic and disease‐related characteristics

Acta neurologica Scandinavica, 2019-08, Vol.140 (2), p.131-139

2019

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Supportive and symptomatic management of amyotrophic lateral sclerosis

Factors influencing decisions people with motor neuron disease make about gastrostomy placement and ventilation: A qualitative evidence synthesis

Improving clinical trial outcomes in amyotrophic lateral sclerosis

Value of systematic genetic screening of patients with amyotrophic lateral sclerosis

Diagnosis and management of motor neurone disease

Clinico-pathological features in amyotrophic lateral sclerosis with expansions in C9ORF72

A review of Mendelian randomization in amyotrophic lateral sclerosis

Enteral feeding in neurological disorders

Magnetic resonance spectroscopy reveals mitochondrial dysfunction in amyotrophic lateral sclerosis

Efficacy of the Head Up collar in facilitating functional head movements in patients with Amyotrophic Lateral Sclerosis

Do pain, anxiety and depression influence quality of life for people with amyotrophic lateral sclerosis/motor neuron disease? A national study reconciling previous conflicting literature

Imaging muscle as a potential biomarker of denervation in motor neuron disease

Reinnervation as measured by the motor unit size index is associated with preservation of muscle strength in amyotrophic lateral sclerosis, but not all muscles reinnervate

Cost-effectiveness of acceptance and commitment therapy for people living with motor neuron disease, and their health-related quality of life

Non-invasive ventilation in motor neuron disease: an update of current UK practice

Management of oral secretions in neurological disease

European Academy of Neurology (EAN) guideline on the management of amyotrophic lateral sclerosis in collaboration with European Reference Network for Neuromuscular Diseases (ERN EURO‐NMD)

Loss of nuclear TDP-43 in amyotrophic lateral sclerosis (ALS) causes altered expression of splicing machinery and widespread dysregulation of RNA splicing in motor neurones

Longitudinal multi-modal muscle-based biomarker assessment in motor neuron disease

Developing the evidence base for the management of drooling

Tracheostomy in motor neurone disease

Withdrawal of tracheostomy ventilation in motor neurone disease: implementing advance directives

Gene expression signatures in motor neurone disease fibroblasts reveal dysregulation of metabolism, hypoxia-response and RNA processing functions

Concurrence of multiple sclerosis and amyotrophic lateral sclerosis in patients with hexanucleotide repeat expansions of C9ORF72

Use of coping strategies in MND/ALS: Association with demographic and disease‐related characteristics

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