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Muscle strength and motor function throughout life in a cross‐sectional cohort of 180 patients with spinal muscular atrophy types 1c–4

European journal of neurology, 2018-03, Vol.25 (3), p.512-518

2018

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A comparative study of brachial plexus sonography and magnetic resonance imaging in chronic inflammatory demyelinating neuropathy and multifocal motor neuropathy

European journal of neurology, 2017-10, Vol.24 (10), p.1307-1313

2017

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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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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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Cardiac pathology in spinal muscular atrophy: a systematic review

Orphanet journal of rare diseases, 2017-04, Vol.12 (1), p.67-67, Article 67

2017

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Multidisciplinary ALS care improves quality of life in patients with ALS

Neurology, 2005-10, Vol.65 (8), p.1264-1267

2005

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A natural history study of late onset spinal muscular atrophy types 3b and 4

Journal of neurology, 2008-09, Vol.255 (9), p.1400-1404

2008

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Arabic and its Alternatives: Religious Minorities and their Languages in the Emerging Nation States of the Middle East (1920-1950)

1, 2020

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Ultrasonography shows extensive nerve enlargements in multifocal motor neuropathy

Neurology, 2005-07, Vol.65 (2), p.305-307

2005

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Prose memory impairment in amyotrophic lateral sclerosis patients is related to hippocampus volume

European journal of neurology, 2015-03, Vol.22 (3), p.547-554

2015

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Diagnostic value of high-resolution sonography in ulnar neuropathy at the elbow

Neurology, 2004-03, Vol.62 (5), p.767-773

2004

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Correlation of the patient's reported outcome Inflammatory-RODS with an objective metric in immune-mediated neuropathies

European journal of neurology, 2016-07, Vol.23 (7), p.1248-1253

2016

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Composite endpoint for ALS clinical trials based on patient preference: Patient-Ranked Order of Function (PROOF)

Journal of neurology, neurosurgery and psychiatry, 2022-05, Vol.93 (5), p.539-546

2022

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Diagnostic accuracy of nerve excitability and compound muscle action potential scan derived biomarkers in amyotrophic lateral sclerosis

European journal of neurology, 2023-10, Vol.30 (10), p.3068-3078

2023

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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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No association between Borrelia burgdorferi antibodies and amyotrophic lateral sclerosis in a case–control study

European journal of neurology, 2017-01, Vol.24 (1), p.227-230

2017

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Multifocal motor neuropathy: long‐term clinical and electrophysiological assessment of intravenous immunoglobulin maintenance treatment

Brain (London, England : 1878), 2002-08, Vol.125 (8), p.1875-1886

2002

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Paraplegin mutations in sporadic adult-onset upper motor neuron syndromes

Neurology, 2008-11, Vol.71 (19), p.1500-1505

2008

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Presence of Enteric Viruses in Source Waters for Drinking Water Production in the Netherlands

Applied and Environmental Microbiology, 2010-09, Vol.76 (17), p.5965-5971

2010

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Lifetime occupation, education, smoking, and risk of ALS

Neurology, 2007-10, Vol.69 (15), p.1508-1514

2007

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Trends and determinants of end-of-life practices in ALS in the Netherlands

Neurology, 2009-09, Vol.73 (12), p.954-961

2009

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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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Intake of polyunsaturated fatty acids and vitamin E reduces the risk of developing amyotrophic lateral sclerosis

Journal of neurology, neurosurgery and psychiatry, 2007-04, Vol.78 (4), p.367-371

2007

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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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Progranulin genetic variability contributes to amyotrophic lateral sclerosis

Neurology, 2008-07, Vol.71 (4), p.253-259

2008

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Muscle strength and motor function throughout life in a cross‐sectional cohort of 180 patients with spinal muscular atrophy types 1c–4

A comparative study of brachial plexus sonography and magnetic resonance imaging in chronic inflammatory demyelinating neuropathy and multifocal motor neuropathy

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

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

Cardiac pathology in spinal muscular atrophy: a systematic review

Multidisciplinary ALS care improves quality of life in patients with ALS

A natural history study of late onset spinal muscular atrophy types 3b and 4

Arabic and its Alternatives: Religious Minorities and their Languages in the Emerging Nation States of the Middle East (1920-1950)

Ultrasonography shows extensive nerve enlargements in multifocal motor neuropathy

Prose memory impairment in amyotrophic lateral sclerosis patients is related to hippocampus volume

Diagnostic value of high-resolution sonography in ulnar neuropathy at the elbow

Correlation of the patient's reported outcome Inflammatory-RODS with an objective metric in immune-mediated neuropathies

Composite endpoint for ALS clinical trials based on patient preference: Patient-Ranked Order of Function (PROOF)

Diagnostic accuracy of nerve excitability and compound muscle action potential scan derived biomarkers in amyotrophic lateral sclerosis

SMN1 gene duplications are associated with sporadic ALS

No association between Borrelia burgdorferi antibodies and amyotrophic lateral sclerosis in a case–control study

Multifocal motor neuropathy: long‐term clinical and electrophysiological assessment of intravenous immunoglobulin maintenance treatment

Paraplegin mutations in sporadic adult-onset upper motor neuron syndromes

Presence of Enteric Viruses in Source Waters for Drinking Water Production in the Netherlands

Lifetime occupation, education, smoking, and risk of ALS

Trends and determinants of end-of-life practices in ALS in the Netherlands

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

Intake of polyunsaturated fatty acids and vitamin E reduces the risk of developing amyotrophic lateral sclerosis

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

Progranulin genetic variability contributes to amyotrophic lateral sclerosis

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