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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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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, 2024-04, Vol.31 (8), p.e16317

2024

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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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Developing the evidence base for the management of drooling

Developmental medicine and child neurology, 2020-03, Vol.62 (3), p.270-270

Mcdermott, Christopher

2020

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Tracheostomy in motor neurone disease

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

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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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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Hereditary spastic paraparesis: Disrupted intracellular transport associated with spastin mutation

Annals of neurology, 2003-12, Vol.54 (6), p.748-759

2003

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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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A randomized, double-blind, placebo-controlled trial of pridopidine in Huntington's disease

Movement disorders, 2013-09, Vol.28 (10), p.1407-1415

Anon

2013

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Placebo response in Parkinson's disease: Comparisons among 11 trials covering medical and surgical interventions

Movement disorders, 2008-04, Vol.23 (5), p.690-699

2008

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Content validity of symptom‐based measures for diabetic, chemotherapy, and HIV peripheral neuropathy

Muscle & nerve, 2017-03, Vol.55 (3), p.366-372

2017

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Endovascular and surgical treatment of unruptured cerebral aneurysms: Comparison of risks

Annals of neurology, 2000-07, Vol.48 (1), p.11-19

2000

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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

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

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)

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

Developing the evidence base for the management of drooling

Tracheostomy in motor neurone disease

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

Hereditary spastic paraparesis: Disrupted intracellular transport associated with spastin mutation

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

A randomized, double-blind, placebo-controlled trial of pridopidine in Huntington's disease

Placebo response in Parkinson's disease: Comparisons among 11 trials covering medical and surgical interventions

Content validity of symptom‐based measures for diabetic, chemotherapy, and HIV peripheral neuropathy

Endovascular and surgical treatment of unruptured cerebral aneurysms: Comparison of risks

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