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Mechanisms underlying chemotherapy-induced neurotoxicity and the potential for neuroprotective strategies

Current medicinal chemistry, 2008-12, Vol.15 (29), p.3081

2008

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Riluzole, neuroprotection and amyotrophic lateral sclerosis

Current medicinal chemistry, 2010-06, Vol.17 (18), p.1942

2010

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Cortical hyperexcitability and disease spread in amyotrophic lateral sclerosis

European journal of neurology, 2017-06, Vol.24 (6), p.816-824

2017

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Amyotrophic lateral sclerosis and motor neuron syndromes in Asia

Journal of Neurology, Neurosurgery and Psychiatry, 2016-08, Vol.87 (8), p.821-830

2016

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Effects of membrane polarization and ischaemia on the excitability properties of human motor axons

Brain (London, England : 1878), 2000-12, Vol.123 (12), p.2542-2551

2000

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Cortical inexcitability defines an adverse clinical profile in amyotrophic lateral sclerosis

European journal of neurology, 2021-01, Vol.28 (1), p.90-97

2021

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Association Between Calcineurin Inhibitor Treatment and Peripheral Nerve Dysfunction in Renal Transplant Recipients

American journal of transplantation, 2013-09, Vol.13 (9), p.2426-2432

2013

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Diagnostic utility of cortical excitability studies in amyotrophic lateral sclerosis

European journal of neurology, 2014-12, Vol.21 (12), p.1451-1457

2014

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Conduction block in immune‐mediated neuropathy: paranodopathy versus axonopathy

European journal of neurology, 2019-08, Vol.26 (8), p.1121-1129

2019

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Quantitative muscle ultrasound as a biomarker in Charcot-Marie-Tooth neuropathy

Clinical neurophysiology, 2017-01, Vol.128 (1), p.227-232

2017

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A Compound Heterozygous Mutation in Calpain 1 Identifies a New Genetic Cause for Spinal Muscular Atrophy Type 4 (SMA4)

Frontiers in genetics, 2022-01, Vol.12, p.801253-801253

2022

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Effects of temperature on the excitability properties of human motor axons

Brain (London, England : 1878), 2001-04, Vol.124 (4), p.816-825

2001

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Importance and challenge of making an early diagnosis in LMNA-related muscular dystrophy

Neurology, 2012-04, Vol.78 (16), p.1258

2012

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Cortical excitability in hereditary motor neuronopathy with pyramidal signs: comparison with ALS

Journal of neurology, neurosurgery and psychiatry, 2010, Vol.81 (1), p.97-100

2010

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What influences patient decision-making in amyotrophic lateral sclerosis multidisciplinary care? A study of patient perspectives

Patient preference and adherence, 2012-01, Vol.6 (default), p.829-838

2012

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What are the roles of carers in decision-making for amyotrophic lateral sclerosis multidisciplinary care?

Patient preference and adherence, 2013-01, Vol.7 (default), p.171-181

2013

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Ion Channel Modulation as a Therapeutic Approach in Multiple Sclerosis

Current medicinal chemistry, 2015-01, Vol.22 (38), p.4366

2015

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Differences in the recovery of excitability in sensory and motor axons of human median nerve

Brain (London, England : 1878), 1996-08, Vol.119 (4), p.1099-1105

1996

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Sensory nerve excitability and neuropathy in end stage kidney disease

Journal of neurology, neurosurgery and psychiatry, 2006-04, Vol.77 (4), p.548-551

2006

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Upregulation of persistent sodium conductances in familial ALS

Journal of neurology, neurosurgery and psychiatry, 2010-02, Vol.81 (2), p.222-227

2010

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Inhibition of HERV-K (HML-2) in amyotrophic lateral sclerosis patients on antiretroviral therapy

Journal of the neurological sciences, 2021-04, Vol.423, p.117358-117358, Article 117358

2021

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FUS mutations in amyotrophic lateral sclerosis: clinical, pathological, neurophysiological and genetic analysis

Journal of neurology, neurosurgery and psychiatry, 2010-06, Vol.81 (6), p.639-645

2010

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Autoantibody responses to nodal and paranodal antigens in chronic inflammatory neuropathies

Journal of neuroimmunology, 2017-08, Vol.309, p.41-46

2017

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Excitability properties of motor axons in patients with spontaneous motor unit activity

Journal of neurology, neurosurgery and psychiatry, 2001-01, Vol.70 (1), p.56-64

2001

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Abnormalities in cortical and peripheral excitability in flail arm variant amyotrophic lateral sclerosis

Journal of neurology, neurosurgery and psychiatry, 2007-08, Vol.78 (8), p.849-852

2007

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Mechanisms underlying chemotherapy-induced neurotoxicity and the potential for neuroprotective strategies

Riluzole, neuroprotection and amyotrophic lateral sclerosis

Cortical hyperexcitability and disease spread in amyotrophic lateral sclerosis

Amyotrophic lateral sclerosis and motor neuron syndromes in Asia

Effects of membrane polarization and ischaemia on the excitability properties of human motor axons

Cortical inexcitability defines an adverse clinical profile in amyotrophic lateral sclerosis

Association Between Calcineurin Inhibitor Treatment and Peripheral Nerve Dysfunction in Renal Transplant Recipients

Diagnostic utility of cortical excitability studies in amyotrophic lateral sclerosis

Conduction block in immune‐mediated neuropathy: paranodopathy versus axonopathy

Quantitative muscle ultrasound as a biomarker in Charcot-Marie-Tooth neuropathy

A Compound Heterozygous Mutation in Calpain 1 Identifies a New Genetic Cause for Spinal Muscular Atrophy Type 4 (SMA4)

Effects of temperature on the excitability properties of human motor axons

Importance and challenge of making an early diagnosis in LMNA-related muscular dystrophy

Cortical excitability in hereditary motor neuronopathy with pyramidal signs: comparison with ALS

What influences patient decision-making in amyotrophic lateral sclerosis multidisciplinary care? A study of patient perspectives

What are the roles of carers in decision-making for amyotrophic lateral sclerosis multidisciplinary care?

Ion Channel Modulation as a Therapeutic Approach in Multiple Sclerosis

Differences in the recovery of excitability in sensory and motor axons of human median nerve

Sensory nerve excitability and neuropathy in end stage kidney disease

Upregulation of persistent sodium conductances in familial ALS

Inhibition of HERV-K (HML-2) in amyotrophic lateral sclerosis patients on antiretroviral therapy

FUS mutations in amyotrophic lateral sclerosis: clinical, pathological, neurophysiological and genetic analysis

Autoantibody responses to nodal and paranodal antigens in chronic inflammatory neuropathies

Excitability properties of motor axons in patients with spontaneous motor unit activity

Abnormalities in cortical and peripheral excitability in flail arm variant amyotrophic lateral sclerosis

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