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The impact of Health Information Technology bundles on Hospital performance: An econometric study

Journal of operations management, 2016-01, Vol.41 (1), p.25-41

2016

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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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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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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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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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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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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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Focus as emphasis: Conceptual and performance implications for hospitals

Journal of operations management, 2011-09, Vol.29 (6), p.616-626

2011

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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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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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An exploratory analysis of new competencies: a resource based view perspective

Journal of operations management, 2002-09, Vol.20 (5), p.435-450

2002

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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

Volltextzugriff (PDF)

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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Managing radical product development in large manufacturing firms: a longitudinal study

Journal of operations management, 1999-11, Vol.17 (6), p.631-644

McDermott, Christopher M

1999

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Organizational culture and advanced manufacturing technology implementation

Journal of operations management, 1999-08, Vol.17 (5), p.521-533

1999

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Strategic consensus in operations strategy

Journal of operations management, 1999-03, Vol.17 (3), p.289-305

1999

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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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The impact of Health Information Technology bundles on Hospital performance: An econometric study

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

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

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

Managing radical innovation: an overview of emergent strategy issues

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)

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

Focus as emphasis: Conceptual and performance implications for hospitals

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

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

An exploratory analysis of new competencies: a resource based view perspective

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

Managing radical product development in large manufacturing firms: a longitudinal study

Organizational culture and advanced manufacturing technology implementation

Strategic consensus in operations strategy

Hereditary spastic paraparesis: Disrupted intracellular transport associated with spastin mutation

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

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