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Antecedents of Service Innovation in SMEs: Comparing the Effects of External and Internal Factors

Journal of small business management, 2014-07, Vol.52 (3), p.521-540

2014

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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, 2024-05, Vol.25 (3-4), p.410-3

2024

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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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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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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, 2024-05, Vol.25 (3-4), p.400-409

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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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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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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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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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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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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Impact of the covid-19 pandemic on amyotrophic lateral sclerosis care in the UK

Amyotrophic lateral sclerosis and frontotemporal degeneration, 2023-02, Vol.24 (1-2), p.91-99

2023

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

Amyotrophic lateral sclerosis and frontotemporal degeneration, 2024-03, p.1-11

2024

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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 preliminary randomized trial of the mechanical insufflator-exsufflator versus breath-stacking technique in patients with amyotrophic lateral sclerosis

Amyotrophic lateral sclerosis and frontotemporal degeneration, 2015-11, Vol.16 (7-8), p.448-455

2015

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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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TRICALS: creating a highway toward a cure

Amyotrophic lateral sclerosis and frontotemporal degeneration, 2020-10, Vol.21 (7-8), p.496-501

2020

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Measuring disability in amyotrophic lateral sclerosis/motor neuron disease: the WHODAS 2.0-36, WHODAS 2.0-32, and WHODAS 2.0-12

Amyotrophic lateral sclerosis and frontotemporal degeneration, 2023-02, Vol.24 (1-2), p.63-70

2023

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The natural history of motor neuron disease: Assessing the impact of specialist care

Amyotrophic lateral sclerosis and frontotemporal degeneration, 2013-01, Vol.14 (1), p.13-19

2013

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Using technology to improve access to specialist care in amyotrophic lateral sclerosis: A systematic review

Amyotrophic lateral sclerosis and frontotemporal degeneration, 2016-08, Vol.17 (5-6), p.313-324

2016

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Measuring quality of life in ALS/MND: validation of the WHOQOL-BREF

Amyotrophic lateral sclerosis and frontotemporal degeneration, 2020-07, Vol.21 (5-6), p.364-372

2020

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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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Antecedents of Service Innovation in SMEs: Comparing the Effects of External and Internal Factors

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

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

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

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

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

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

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

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

Exploring patient and public involvement in motor neuron disease research

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

Impact of the covid-19 pandemic on amyotrophic lateral sclerosis care in the UK

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

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

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

A preliminary randomized trial of the mechanical insufflator-exsufflator versus breath-stacking technique in patients with amyotrophic lateral sclerosis

A comfort assessment of existing cervical orthoses

TRICALS: creating a highway toward a cure

Measuring disability in amyotrophic lateral sclerosis/motor neuron disease: the WHODAS 2.0-36, WHODAS 2.0-32, and WHODAS 2.0-12

The natural history of motor neuron disease: Assessing the impact of specialist care

Using technology to improve access to specialist care in amyotrophic lateral sclerosis: A systematic review

Measuring quality of life in ALS/MND: validation of the WHOQOL-BREF

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

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