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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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Cytokine profiles in multifocal motor neuropathy and progressive muscular atrophy

Journal of neuroimmunology, 2015-09, Vol.286, p.1-4

2015

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Sexual differences in onset of disease and response to exercise in a transgenic model of ALS

Neuromuscular disorders : NMD, 2003-11, Vol.13 (9), p.737-743

2003

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G.P.290

Neuromuscular disorders : NMD, 2014-10, Vol.24 (9), p.909-909

2014

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P12-18 Exercise-induced weakness in demyelinating neuropathies

Clinical neurophysiology, 2010, Vol.121, p.S176-S176

2010

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G.P.98 Dysfunction of the neuromuscular junction in patients with spinal muscular atrophy type 2 and 3

Neuromuscular disorders : NMD, 2012-10, Vol.22 (9), p.871-872

2012

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Variations in ventral root axon morphology and locomotor behavior components across different inbred strains of mice

Neuroscience, 2009-12, Vol.164 (4), p.1477-1483

2009

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Correlates of outcome and response to IVIg in 88 patients with multifocal motor neuropathy

Neurology, 2010-08, Vol.75 (9), p.818-825

2010

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Homozygous deletion of the survival motor neuron 2 gene is a prognostic factor in sporadic ALS

Neurology, 2001-03, Vol.56 (6), p.749-752

2001

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P3.6 Segmental distribution of muscle weakness in Dutch patients with SMA type 2, 3 and 4

Neuromuscular disorders : NMD, 2011-10, Vol.21 (9), p.683-684

2011

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HP19: Preliminary evidence of neurophysiological changes in asymptomatic carriers of the C9orf72 gene mutation using EEG

Clinical neurophysiology, 2022-03, Vol.135, p.e5-e5

2022

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Expanded ATXN2 CAG repeat size in ALS identifies genetic overlap between ALS and SCA2

Neurology, 2011-06, Vol.76 (24), p.2066-2072

2011

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Increased glutamine synthetase but normal EAAT2 expression in platelets of ALS patients

Neurochemistry international, 2006-03, Vol.48 (4), p.306-311

2006

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P12-19 Cold paresis in multifocal motor neuropathy

Clinical neurophysiology, 2010, Vol.121, p.S176-S176

2010

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HP51 : Motor unit integrity in multifocal motor neuropathy: A systematic evaluation with CMAP scans

Clinical neurophysiology, 2022-03, Vol.135, p.e12-e13

2022

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OC07: Monitoring disease progression with electrophysiological markers derived from compound muscle action potential scans in amyotrophic lateral sclerosis

Clinical neurophysiology, 2022-03, Vol.135, p.e16-e17

2022

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Multifocal motor neuropathy: association of anti-GM1 IgM antibodies with clinical features

Neurology, 2010-11, Vol.75 (22), p.1961-1967

2010

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Associations between illness cognitions and health-related quality of life in the first year after diagnosis of amyotrophic lateral sclerosis

Journal of psychosomatic research, 2020-05, Vol.132, p.109974-109974, Article 109974

2020

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Corrigendum to ‘Associations between illness cognitions and health-related quality of life in the first year after diagnosis of amyotrophic lateral sclerosis’ [Journal of Psychosomatic Research 132 (2020) 109974]

Journal of psychosomatic research, 2021-01, Vol.140, p.110325-110325, Article 110325

2021

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Neuro-imaging in amyotrophic lateral sclerosis: Should we shift towards the periphery?

Clinical neurophysiology, 2020-09, Vol.131 (9), p.2286-2288

2020

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Long-term remission of CIDP after pulsed dexamethasone or short-term prednisolone treatment

Neurology, 2012-04, Vol.78 (14), p.1079-1084

2012

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Zinc amplifies mSOD1-mediated toxicity in a transgenic mouse model of amyotrophic lateral sclerosis

Neuroscience letters, 2003-12, Vol.352 (3), p.175-178

2003

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SMN1 gene duplications are associated with sporadic ALS

Neurology, 2012-03, Vol.78 (11), p.776-780

2012

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Pathogenicity of anti-ganglioside antibodies in the Guillain-Barré syndrome

Autoimmunity reviews, 2004-02, Vol.3 (2), p.61-68

2004

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Bulbar Problems Self-Reported by Children and Adults with Spinal Muscular Atrophy

Journal of neuromuscular diseases, 2019-01, Vol.6 (3), p.361-368

2019

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

Cytokine profiles in multifocal motor neuropathy and progressive muscular atrophy

Sexual differences in onset of disease and response to exercise in a transgenic model of ALS

G.P.290

P12-18 Exercise-induced weakness in demyelinating neuropathies

G.P.98 Dysfunction of the neuromuscular junction in patients with spinal muscular atrophy type 2 and 3

Variations in ventral root axon morphology and locomotor behavior components across different inbred strains of mice

Correlates of outcome and response to IVIg in 88 patients with multifocal motor neuropathy

Homozygous deletion of the survival motor neuron 2 gene is a prognostic factor in sporadic ALS

P3.6 Segmental distribution of muscle weakness in Dutch patients with SMA type 2, 3 and 4

HP19: Preliminary evidence of neurophysiological changes in asymptomatic carriers of the C9orf72 gene mutation using EEG

Expanded ATXN2 CAG repeat size in ALS identifies genetic overlap between ALS and SCA2

Increased glutamine synthetase but normal EAAT2 expression in platelets of ALS patients

P12-19 Cold paresis in multifocal motor neuropathy

HP51 : Motor unit integrity in multifocal motor neuropathy: A systematic evaluation with CMAP scans

OC07: Monitoring disease progression with electrophysiological markers derived from compound muscle action potential scans in amyotrophic lateral sclerosis

Multifocal motor neuropathy: association of anti-GM1 IgM antibodies with clinical features

Associations between illness cognitions and health-related quality of life in the first year after diagnosis of amyotrophic lateral sclerosis

Corrigendum to ‘Associations between illness cognitions and health-related quality of life in the first year after diagnosis of amyotrophic lateral sclerosis’ [Journal of Psychosomatic Research 132 (2020) 109974]

Neuro-imaging in amyotrophic lateral sclerosis: Should we shift towards the periphery?

Long-term remission of CIDP after pulsed dexamethasone or short-term prednisolone treatment

Zinc amplifies mSOD1-mediated toxicity in a transgenic mouse model of amyotrophic lateral sclerosis

SMN1 gene duplications are associated with sporadic ALS

Pathogenicity of anti-ganglioside antibodies in the Guillain-Barré syndrome

Bulbar Problems Self-Reported by Children and Adults with Spinal Muscular Atrophy

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