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Supportive and symptomatic management of amyotrophic lateral sclerosis

Nature reviews. Neurology, 2016-09, Vol.12 (9), p.526-538

2016

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The stage is set for a new trial end point in ALS

Journal of neurology, neurosurgery and psychiatry, 2021-02, Vol.92 (2), p.117-117

McDermott, Christopher J

2021

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Stay at home with the amyotrophic lateral sclerosis functional rating scale

Journal of neurology, neurosurgery and psychiatry, 2020-01, Vol.91 (1), p.7-7

McDermott, Christopher J

2020

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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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Prognosis for patients with amyotrophic lateral sclerosis: development and validation of a personalised prediction model

Lancet neurology, 2018-05, Vol.17 (5), p.423-433

2018

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Supporting people with Motor Neuron Disease (MND) to make decisions about gastrostomy feeding tube placement: a survey of UK healthcare professionals' practice and beliefs

Amyotrophic lateral sclerosis and frontotemporal degeneration, 2024-05, Vol.25 (3-4), p.290-298

2024

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A report of resources used by clinicians in the UK to support motor neuron disease genomic testing

Amyotrophic lateral sclerosis and frontotemporal degeneration, 2024-04, Vol.25 (3-4), p.1-412

2024

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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.510-518

2021

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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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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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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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Analysis of incidence of motor neuron disease in England 1998-2019: use of three linked datasets

Amyotrophic lateral sclerosis and frontotemporal degeneration, 2022-07, Vol.23 (5-6), p.363-371

2022

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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)

European journal of neurology, 2024-06, Vol.31 (6), p.e16264-n/a

2024

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An old friend who has overstayed their welcome: the ALSFRS-R total score as primary endpoint for ALS clinical trials

Amyotrophic lateral sclerosis and frontotemporal degeneration, 2021-04, Vol.22 (3-4), p.300-307

2021

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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.248-255

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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Improving the measurement properties of the Amyotrophic Lateral Sclerosis Functional Rating Scale-Revised (ALSFRS-R): deriving a valid measurement total for the calculation of change

Amyotrophic lateral sclerosis and frontotemporal degeneration, 2024-04, Vol.25 (3-4), p.1-409

2024

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Gastrostomy use in motor neurone disease (MND): A review, meta-analysis and survey of current practice

Amyotrophic lateral sclerosis and frontotemporal degeneration, 2013-03, Vol.14 (2), p.96-104

2013

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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, 2024-08, Vol.31 (8), p.e16317-n/a

2024

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Tensor electrical impedance myography identifies bulbar disease progression in amyotrophic lateral sclerosis

Clinical neurophysiology, 2022-07, Vol.139, p.69-75

2022

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Exploring patient and public involvement in motor neuron disease research

Amyotrophic lateral sclerosis and frontotemporal degeneration, 2019-10, Vol.20 (7-8), p.511-520

2019

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A qualitative evaluation of the revised amyotrophic lateral sclerosis functional rating scale (ALSFRS-R) by the patient community: a web-based cross-sectional survey

Amyotrophic lateral sclerosis and frontotemporal degeneration, 2023-04, Vol.24 (3-4), p.272-280

2023

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The TiM system: developing a novel telehealth service to improve access to specialist care in motor neurone disease using user-centered design

Amyotrophic lateral sclerosis and frontotemporal degeneration, 2018-07, Vol.19 (5-6), p.351-361

2018

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Multi-dimensional electrical impedance myography of the tongue as a potential biomarker for amyotrophic lateral sclerosis

Clinical neurophysiology, 2020-04, Vol.131 (4), p.799-808

2020

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Supportive and symptomatic management of amyotrophic lateral sclerosis

The stage is set for a new trial end point in ALS

Stay at home with the amyotrophic lateral sclerosis functional rating scale

Improving clinical trial outcomes in amyotrophic lateral sclerosis

Prognosis for patients with amyotrophic lateral sclerosis: development and validation of a personalised prediction model

Supporting people with Motor Neuron Disease (MND) to make decisions about gastrostomy feeding tube placement: a survey of UK healthcare professionals' practice and beliefs

A report of resources used by clinicians in the UK to support motor neuron disease genomic testing

Value of systematic genetic screening of patients with amyotrophic lateral sclerosis

A review of Mendelian randomization in amyotrophic lateral sclerosis

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

Magnetic resonance spectroscopy reveals mitochondrial dysfunction in amyotrophic lateral sclerosis

Analysis of incidence of motor neuron disease in England 1998-2019: use of three linked datasets

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)

An old friend who has overstayed their welcome: the ALSFRS-R total score as primary endpoint for ALS clinical trials

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

Improving the measurement properties of the Amyotrophic Lateral Sclerosis Functional Rating Scale-Revised (ALSFRS-R): deriving a valid measurement total for the calculation of change

Gastrostomy use in motor neurone disease (MND): A review, meta-analysis and survey of current practice

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

Tensor electrical impedance myography identifies bulbar disease progression in amyotrophic lateral sclerosis

Exploring patient and public involvement in motor neuron disease research

A qualitative evaluation of the revised amyotrophic lateral sclerosis functional rating scale (ALSFRS-R) by the patient community: a web-based cross-sectional survey

The TiM system: developing a novel telehealth service to improve access to specialist care in motor neurone disease using user-centered design

Multi-dimensional electrical impedance myography of the tongue as a potential biomarker for amyotrophic lateral sclerosis

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