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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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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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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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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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Tracheostomy in motor neurone disease

Practical neurology, 2019-12, Vol.19 (6), p.467-475

2019

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Non‐negative matrix factorisation of Raman spectra finds common patterns relating to neuromuscular disease across differing equipment configurations, preclinical models and human tissue

Journal of Raman spectroscopy, 2023-03, Vol.54 (3), p.258-268

2023

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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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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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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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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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The nutritional management of people living with amyotrophic lateral sclerosis: A national survey of dietitians

Journal of human nutrition and dietetics, 2021-12, Vol.34 (6), p.1064-1071

2021

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A phase II−III trial of olesoxime in subjects with amyotrophic lateral sclerosis

European journal of neurology, 2014-03, Vol.21 (3), p.529-536

2014

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Health care professionals’ views on psychological factors affecting nutritional behaviour in people with motor neuron disease: A thematic analysis

British journal of health psychology, 2019-11, Vol.24 (4), p.953-969

2019

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Middle Aged
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Motor Neuron Disease
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Motor Neuron Disease - Complications
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Factors influencing decisions people with motor neuron disease make about gastrostomy placement and ventilation: A qualitative evidence synthesis

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)

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

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

Tracheostomy in motor neurone disease

Non‐negative matrix factorisation of Raman spectra finds common patterns relating to neuromuscular disease across differing equipment configurations, preclinical models and human tissue

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

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

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

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

The nutritional management of people living with amyotrophic lateral sclerosis: A national survey of dietitians

A phase II−III trial of olesoxime in subjects with amyotrophic lateral sclerosis

Health care professionals’ views on psychological factors affecting nutritional behaviour in people with motor neuron disease: A thematic analysis

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