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Investigating and managing neonatal seizures in the UK: an explanatory sequential mixed methods approach

BMC pediatrics, 2020-01, Vol.20 (1), p.36-36, Article 36

2020

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Extensive phenotypic characterisation of a human TDP-43Q331K transgenic mouse model of amyotrophic lateral sclerosis (ALS)

Scientific reports, 2021-08, Vol.11 (1), p.16659-16659, Article 16659

2021

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The GLP-1 receptor agonist, liraglutide, fails to slow disease progression in SOD1G93A and TDP-43Q331K transgenic mouse models of ALS

Scientific reports, 2021-08, Vol.11 (1), p.17027-17027, Article 17027

2021

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Author Correction: Female sex mitigates motor and behavioural phenotypes in TDP-43Q331K knock-in mice

Scientific reports, 2021-05, Vol.11 (1), p.11058-11058, Article 11058

2021

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Conformational fingerprinting with Raman spectroscopy reveals protein structure as a translational biomarker of muscle pathology

Analyst (London), 2024-04, Vol.149 (9), p.2738-2746

2024

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Rapid identification of human muscle disease with fibre optic Raman spectroscopy

Analyst (London), 2022-05, Vol.147 (11), p.2533-254

2022

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Biomarkers in Motor Neuron Disease: A State of the Art Review

Frontiers in neurology, 2019-04, Vol.10, p.291-291

2019

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Label-free fibre optic Raman spectroscopy with bounded simplex-structured matrix factorization for the serial study of serum in amyotrophic lateral sclerosis

Analyst (London), 2022-11, Vol.147 (22), p.5113-512

2022

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Longitudinal multi-modal muscle-based biomarker assessment in motor neuron disease

Journal of neurology, 2020-01, Vol.267 (1), p.244-256

2020

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Vesicular apparatus, including functional calcium channels, are present in developing rodent optic nerve axons and are required for normal node of Ranvier formation

The Journal of physiology, 2008-09, Vol.586 (17), p.4069-4089

2008

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Female sex mitigates motor and behavioural phenotypes in TDP-43Q331K knock-in mice

Scientific reports, 2020-11, Vol.10 (1), p.19220-19220, Article 19220

2020

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Glutamate receptor-mediated ischemic injury of premyelinated central axons

Annals of neurology, 2009-11, Vol.66 (5), p.682-693

2009

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In Vivo Fiber Optic Raman Spectroscopy of Muscle in Preclinical Models of Amyotrophic Lateral Sclerosis and Duchenne Muscular Dystrophy

ACS chemical neuroscience, 2021-05, Vol.12 (10), p.1768-1776

2021

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Central axons preparing to myelinate are highly sensitivity to ischemic injury

Annals of neurology, 2012-12, Vol.72 (6), p.936-951

2012

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White matter synapses: form, function, and dysfunction

Neurology, 2011-01, Vol.76 (4), p.397-404

2011

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Correction to: Longitudinal multi-modal muscle-based biomarker assessment in motor neuron disease

Journal of neurology, 2020, Vol.267 (1), p.257-258

2020

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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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Variable sensory nerve conduction parameters in late onset Friedreich ataxia

Muscle & nerve, 2017-02, Vol.55 (2), p.E7-E8

2017

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Hyperexcitability of the asymptomatic motor cortex in a case of Mills' syndrome

Muscle & nerve, 2024-06, Vol.69 (6), p.733-734

2024

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Anti‐myelin‐associated glycoprotein–negative distal acquired demyelinating symmetric neuropathy in association with a neuroendocrine tumor

Muscle & nerve, 2017-02, Vol.55 (2), p.E6-E7

2017

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In Vivo Raman Spectroscopy of Muscle Is Highly Sensitive for Detection of Healthy Muscle and Highly Specific for Detection of Disease

Analytical chemistry (Washington), 2024-10, Vol.96 (40), p.15991-15997

2024

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Sensory ganglionopathy with livedoid vasculopathy controlled by immunotherapy

Muscle & nerve, 2015-02, Vol.51 (2), p.296-301

2015

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Combining electromyography and Raman spectroscopy: optical EMG

Muscle & nerve, 2023-10, Vol.68 (4), p.464-470

2023

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Autologous hematopoietic stem cell transplantation following pulsed cyclophosphamide in a severely disabled patient with malignant multiple sclerosis

Journal of neurology, 2013-03, Vol.260 (3), p.914-916

2013

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Imaging muscle as a potential biomarker of denervation in motor neuron disease

Journal of neurology, neurosurgery and psychiatry, 2018-03, Vol.89 (3), p.248-255

2018

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Investigating and managing neonatal seizures in the UK: an explanatory sequential mixed methods approach

Extensive phenotypic characterisation of a human TDP-43Q331K transgenic mouse model of amyotrophic lateral sclerosis (ALS)

The GLP-1 receptor agonist, liraglutide, fails to slow disease progression in SOD1G93A and TDP-43Q331K transgenic mouse models of ALS

Author Correction: Female sex mitigates motor and behavioural phenotypes in TDP-43Q331K knock-in mice

Conformational fingerprinting with Raman spectroscopy reveals protein structure as a translational biomarker of muscle pathology

Rapid identification of human muscle disease with fibre optic Raman spectroscopy

Biomarkers in Motor Neuron Disease: A State of the Art Review

Label-free fibre optic Raman spectroscopy with bounded simplex-structured matrix factorization for the serial study of serum in amyotrophic lateral sclerosis

Longitudinal multi-modal muscle-based biomarker assessment in motor neuron disease

Vesicular apparatus, including functional calcium channels, are present in developing rodent optic nerve axons and are required for normal node of Ranvier formation

Female sex mitigates motor and behavioural phenotypes in TDP-43Q331K knock-in mice

Glutamate receptor-mediated ischemic injury of premyelinated central axons

In Vivo Fiber Optic Raman Spectroscopy of Muscle in Preclinical Models of Amyotrophic Lateral Sclerosis and Duchenne Muscular Dystrophy

Central axons preparing to myelinate are highly sensitivity to ischemic injury

White matter synapses: form, function, and dysfunction

Correction to: Longitudinal multi-modal muscle-based biomarker assessment in motor neuron disease

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

Variable sensory nerve conduction parameters in late onset Friedreich ataxia

Hyperexcitability of the asymptomatic motor cortex in a case of Mills' syndrome

Anti‐myelin‐associated glycoprotein–negative distal acquired demyelinating symmetric neuropathy in association with a neuroendocrine tumor

In Vivo Raman Spectroscopy of Muscle Is Highly Sensitive for Detection of Healthy Muscle and Highly Specific for Detection of Disease

Sensory ganglionopathy with livedoid vasculopathy controlled by immunotherapy

Combining electromyography and Raman spectroscopy: optical EMG

Autologous hematopoietic stem cell transplantation following pulsed cyclophosphamide in a severely disabled patient with malignant multiple sclerosis

Imaging muscle as a potential biomarker of denervation in motor neuron disease

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