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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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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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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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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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Identifying key signs of motor neurone disease in primary care: a nested case–control study using the QResearch database

BMJ open, 2022-06, Vol.12 (6), p.e058383-e058383

2022

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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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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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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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"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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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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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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A comfort assessment of existing cervical orthoses

Ergonomics, 2018-02, Vol.61 (2), p.329-338

2018

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United Kingdom recommendations for obstetric venous thromboembolism prophylaxis: Evidence and rationale

Seminars in perinatology, 2019-06, Vol.43 (4), p.222-228

2019

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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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Evaluating a novel cervical orthosis, the Sheffield Support Snood, in patients with amyotrophic lateral sclerosis/motor neuron disease with neck weakness

Amyotrophic lateral sclerosis and frontotemporal degeneration, 2016-08, Vol.17 (5-6), p.436-442

2016

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Assessment of the Sheffield Support Snood, an innovative cervical orthosis designed for people affected by neck muscle weakness

Clinical biomechanics (Bristol), 2016-02, Vol.32, p.201-206

2016

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The role of cranial and thoracic electromyography within diagnostic criteria for amyotrophic lateral sclerosis

Muscle & nerve, 2016-09, Vol.54 (3), p.378-385

2016

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The impact of gastrostomy in motor neurone disease: challenges and benefits from a patient and carer perspective

BMJ supportive & palliative care, 2016-03, Vol.6 (1), p.52-59

2016

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Oligogenic inheritance of optineurin (OPTN) and C9ORF72 mutations in ALS highlights localisation of OPTN in the TDP-43-negative inclusions of C9ORF72-ALS

Neuropathology, 2016-04, Vol.36 (2), p.125-134

2016

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Factors influencing decision-making in relation to timing of gastrostomy insertion in patients with motor neurone disease

BMJ supportive & palliative care, 2014-03, Vol.4 (1), p.57-63

2014

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DiPALS: Diaphragm Pacing in patients with Amyotrophic Lateral Sclerosis - a randomised controlled trial

Health technology assessment (Winchester, England), 2016-06, Vol.20 (45), p.1-186

2016

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Value of systematic genetic screening of patients with amyotrophic lateral sclerosis

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

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

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

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

Identifying key signs of motor neurone disease in primary care: a nested case–control study using the QResearch database

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

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

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

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

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

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

A comfort assessment of existing cervical orthoses

United Kingdom recommendations for obstetric venous thromboembolism prophylaxis: Evidence and rationale

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

Evaluating a novel cervical orthosis, the Sheffield Support Snood, in patients with amyotrophic lateral sclerosis/motor neuron disease with neck weakness

Assessment of the Sheffield Support Snood, an innovative cervical orthosis designed for people affected by neck muscle weakness

The role of cranial and thoracic electromyography within diagnostic criteria for amyotrophic lateral sclerosis

The impact of gastrostomy in motor neurone disease: challenges and benefits from a patient and carer perspective

Oligogenic inheritance of optineurin (OPTN) and C9ORF72 mutations in ALS highlights localisation of OPTN in the TDP-43-negative inclusions of C9ORF72-ALS

Factors influencing decision-making in relation to timing of gastrostomy insertion in patients with motor neurone disease

DiPALS: Diaphragm Pacing in patients with Amyotrophic Lateral Sclerosis - a randomised controlled trial

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