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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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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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The Effect of Team Leader Characteristics on Learning, Knowledge Application, and Performance of Cross-Functional New Product Development Teams

Decision sciences, 2003-11, Vol.34 (4), p.707-739

2003

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Enteral feeding in neurological disorders

Practical Neurology, 2016-10, Vol.16 (5), p.352-361

2016

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Management of oral secretions in neurological disease

Practical neurology, 2017-04, Vol.17 (2), p.96-103

2017

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Innovation orientations and their effects on business performance: contrasting small- and medium-sized service firms

R & D management, 2013-11, Vol.43 (5), p.486-500

2013

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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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Direct evidence for axonal transport defects in a novel mouse model of mutant spastin-induced hereditary spastic paraplegia (HSP) and human HSP patients

Journal of neurochemistry, 2009-07, Vol.110 (1), p.34-44

2009

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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, 2024-08, Vol.31 (8), p.e16317-n/a

2024

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Managing radical innovation: an overview of emergent strategy issues

The Journal of product innovation management, 2002-11, Vol.19 (6), p.424-438

2002

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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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The application of Raman spectroscopy to the diagnosis of mitochondrial muscle disease: A preliminary comparison between fibre optic probe and microscope formats

Journal of Raman spectroscopy, 2022-02, Vol.53 (2), p.172-181

2022

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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.467-475

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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Withdrawal of tracheostomy ventilation in motor neurone disease: implementing advance directives

Practical neurology, 2017-10, Vol.17 (5), p.339-340

2017

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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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Rueing the Roux-en-Y

Practical neurology, 2016-06, Vol.16 (3), p.227-230

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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Mechanical cough augmentation techniques in amyotrophic lateral sclerosis/motor neuron disease

Cochrane database of systematic reviews, 2016-12, Vol.2016 (12)

2016

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Mapping the Evidence for Measuring Energy Expenditure and Indicating Hypermetabolism in Motor Neuron Disease: A Scoping Review

Nutrition reviews, 2024-10

2024

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

Factors influencing decisions people with motor neuron disease make about gastrostomy placement and ventilation: A qualitative evidence synthesis

The Effect of Team Leader Characteristics on Learning, Knowledge Application, and Performance of Cross-Functional New Product Development Teams

Enteral feeding in neurological disorders

Management of oral secretions in neurological disease

Innovation orientations and their effects on business performance: contrasting small- and medium-sized service firms

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)

Direct evidence for axonal transport defects in a novel mouse model of mutant spastin-induced hereditary spastic paraplegia (HSP) and human HSP patients

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

Managing radical innovation: an overview of emergent strategy issues

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

The application of Raman spectroscopy to the diagnosis of mitochondrial muscle disease: A preliminary comparison between fibre optic probe and microscope formats

Developing the evidence base for the management of drooling

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

Withdrawal of tracheostomy ventilation in motor neurone disease: implementing advance directives

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

Rueing the Roux-en-Y

Hereditary spastic paraparesis: Disrupted intracellular transport associated with spastin mutation

Mechanical cough augmentation techniques in amyotrophic lateral sclerosis/motor neuron disease

Mapping the Evidence for Measuring Energy Expenditure and Indicating Hypermetabolism in Motor Neuron Disease: A Scoping Review

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