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Survey of service needs to embed genome sequencing for motor neuron disease in neurology in the English National Health Service

Journal of medical genetics, 2024-07, Vol.61 (7), p.661-665

2024

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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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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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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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An Objective Functional Characterisation of Head Movement Impairment in Individuals with Neck Muscle Weakness Due to Amyotrophic Lateral Sclerosis

PloS one, 2017-01, Vol.12 (1), p.e0169019-e0169019

2017

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Decision-making and referral processes for patients with motor neurone disease: a qualitative study of GP experiences and evaluation of a new decision-support tool

BMC health services research, 2017-05, Vol.17 (1), p.339-339, Article 339

2017

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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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Mutations in the Glycosyltransferase Domain of GLT8D1 Are Associated with Familial Amyotrophic Lateral Sclerosis

Cell reports (Cambridge), 2019-02, Vol.26 (9), p.2298-2306.e5

2019

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Gastrostomy in amyotrophic lateral sclerosis: effects of non-invasive ventilation – Authors' reply

Lancet neurology, 2015-12, Vol.14 (12), p.1153-1153

2015

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Communication change in ALS: engaging people living with ALS and their partners in future research

Disability and rehabilitation: Assistive technology, 2019-10, Vol.14 (7), p.675-681

2019

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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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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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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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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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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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Process evaluation and exploration of telehealth in motor neuron disease in a UK specialist centre

BMJ open, 2019-10, Vol.9 (10), p.e028526-e028526

2019

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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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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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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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Dyspnea (breathlessness) in amyotrophic lateral sclerosis/motor neuron disease: prevalence, progression, severity, and correlates

Amyotrophic lateral sclerosis and frontotemporal degeneration, 2024-08, Vol.25 (5-6), p.475-485

2024

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Physicians' attitudes toward end-of-life decisions in amyotrophic lateral sclerosis

Amyotrophic lateral sclerosis and frontotemporal degeneration, 2019-01, Vol.20 (1-2), p.74-81

2019

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"Anything that makes life's journey better." Exploring the use of digital technology by people living with motor neurone disease

Amyotrophic lateral sclerosis and frontotemporal degeneration, 2017-07, Vol.18 (5-6), p.378-387

2017

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Effect of lipid profile on prognosis in the patients with amyotrophic lateral sclerosis: Insights from the olesoxime clinical trial

Amyotrophic lateral sclerosis and frontotemporal degeneration, 2015-11, Vol.16 (7-8), p.478-484

2015

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Long-term physical activity: an exogenous risk factor for sporadic amyotrophic lateral sclerosis?

Amyotrophic lateral sclerosis and frontotemporal degeneration, 2016-08, Vol.17 (5-6), p.377-384

2016

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Using telehealth in motor neuron disease to increase access to specialist multidisciplinary care: a UK-based pilot and feasibility study

BMJ open, 2019-10, Vol.9 (10), p.e028525

2019

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Survey of service needs to embed genome sequencing for motor neuron disease in neurology in the English National Health Service

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

Value of systematic genetic screening of patients with amyotrophic lateral sclerosis

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

An Objective Functional Characterisation of Head Movement Impairment in Individuals with Neck Muscle Weakness Due to Amyotrophic Lateral Sclerosis

Decision-making and referral processes for patients with motor neurone disease: a qualitative study of GP experiences and evaluation of a new decision-support tool

Magnetic resonance spectroscopy reveals mitochondrial dysfunction in amyotrophic lateral sclerosis

Mutations in the Glycosyltransferase Domain of GLT8D1 Are Associated with Familial Amyotrophic Lateral Sclerosis

Gastrostomy in amyotrophic lateral sclerosis: effects of non-invasive ventilation – Authors' reply

Communication change in ALS: engaging people living with ALS and their partners in future research

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

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

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

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

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

Process evaluation and exploration of telehealth in motor neuron disease in a UK specialist centre

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

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

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

Dyspnea (breathlessness) in amyotrophic lateral sclerosis/motor neuron disease: prevalence, progression, severity, and correlates

Physicians' attitudes toward end-of-life decisions in amyotrophic lateral sclerosis

"Anything that makes life's journey better." Exploring the use of digital technology by people living with motor neurone disease

Effect of lipid profile on prognosis in the patients with amyotrophic lateral sclerosis: Insights from the olesoxime clinical trial

Long-term physical activity: an exogenous risk factor for sporadic amyotrophic lateral sclerosis?

Using telehealth in motor neuron disease to increase access to specialist multidisciplinary care: a UK-based pilot and feasibility study

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