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Breach rhythm related to a solitary skull lesion caused by multiple myeloma

Journal of neurology, neurosurgery and psychiatry, 2008-07, Vol.79 (7), p.819-819

2008

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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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Distinguishing acute-onset CIDP from fluctuating Guillain-Barre syndrome: a prospective study

Neurology, 2010-05, Vol.74 (21), p.1680-1686

2010

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Discontinuation of enzyme replacement therapy in adults with Pompe disease: Evaluating the European POmpe Consortium stop criteria

Neuromuscular disorders : NMD, 2020-01, Vol.30 (1), p.59-66

2020

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Prediction of respiratory insufficiency in Guillain-Barré syndrome

Annals of neurology, 2010-06, Vol.67 (6), p.781-787

2010

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Intravenous immune globulin (10% caprylate-chromatography purified) for the treatment of chronic inflammatory demyelinating polyradiculoneuropathy (ICE study): a randomised placebo-controlled trial

Lancet neurology, 2008-02, Vol.7 (2), p.136-144

2008

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Clinimetric evaluation of a new overall disability scale in immune mediated polyneuropathies

Journal of neurology, neurosurgery and psychiatry, 2002-05, Vol.72 (5), p.596-601

2002

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Epidemiology of inclusion body myositis in the Netherlands: a nationwide study

Neurology, 2000-11, Vol.55 (9), p.1385-1388

2000

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Disease severity in children and adults with Pompe disease related to age and disease duration

Neurology, 2005-06, Vol.64 (12), p.2139-2141

2005

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Epstein-Barr virus and disease activity in multiple sclerosis

Journal of neurology, neurosurgery and psychiatry, 2005-10, Vol.76 (10), p.1377-1381

2005

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Cardiac evaluation in children and adults with Pompe disease sharing the common c.−32-13T>G genotype rarely reveals abnormalities

Journal of the neurological sciences, 2008-12, Vol.275 (1), p.46-50

2008

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Derivation and validation of diagnostic criteria for chronic inflammatory demyelinating polyneuropathy

Journal of the neurological sciences, 2009-02, Vol.277 (1), p.1-8

2009

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Course of disability and respiratory function in untreated late-onset Pompe disease

Neurology, 2006-02, Vol.66 (4), p.581-583

2006

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TDP-43 pathology in familial frontotemporal dementia and motor neuron disease without Progranulin mutations

Brain (London, England : 1878), 2007-05, Vol.130 (5), p.1375-1385

2007

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Revising two-point discrimination assessment in normal aging and in patients with polyneuropathies

Journal of neurology, neurosurgery and psychiatry, 2008-07, Vol.79 (7), p.832-834

2008

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Amantadine for treatment of fatigue in Guillain-Barré syndrome: a randomised, double blind, placebo controlled, crossover trial

Journal of neurology, neurosurgery and psychiatry, 2006-01, Vol.77 (1), p.61-65

2006

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ANO5 mutations in the Dutch limb girdle muscular dystrophy population

Neuromuscular disorders : NMD, 2013-06, Vol.23 (6), p.456-460

2013

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Late-onset Pompe disease primarily affects quality of life in physical health domains

Neurology, 2004-11, Vol.63 (9), p.1688-1692

2004

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Extension of the clinical spectrum of Danon disease

Neurology, 2008-04, Vol.70 (16), p.1358-1359

2008

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Connecting impairment, disability, and handicap in immune mediated polyneuropathies

Journal of neurology, neurosurgery and psychiatry, 2003-01, Vol.74 (1), p.99-104

2003

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Quality of life complements traditional outcome measures in immune-mediated polyneuropathies

Neurology, 2002-07, Vol.59 (1), p.84-91

2002

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Health-related quality-of-life improvements in CIDP with immune globulin IV 10%: the ICE Study

Neurology, 2009-04, Vol.72 (15), p.1337-1344

2009

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Diagnostic value of anti-GM1 ganglioside serology and validation of the INCAT-ELISA

Journal of the neurological sciences, 2005-12, Vol.239 (1), p.37-44

2005

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Ptosis as a feature of late-onset glycogenosis type II

Neurology, 2006-12, Vol.67 (12), p.2261-2262

2006

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Infections and course of disease in mild forms of Guillain-Barré syndrome

Neurology, 2002-02, Vol.58 (4), p.610-614

2002

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Breach rhythm related to a solitary skull lesion caused by multiple myeloma

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

Distinguishing acute-onset CIDP from fluctuating Guillain-Barre syndrome: a prospective study

Discontinuation of enzyme replacement therapy in adults with Pompe disease: Evaluating the European POmpe Consortium stop criteria

Prediction of respiratory insufficiency in Guillain-Barré syndrome

Intravenous immune globulin (10% caprylate-chromatography purified) for the treatment of chronic inflammatory demyelinating polyradiculoneuropathy (ICE study): a randomised placebo-controlled trial

Clinimetric evaluation of a new overall disability scale in immune mediated polyneuropathies

Epidemiology of inclusion body myositis in the Netherlands: a nationwide study

Disease severity in children and adults with Pompe disease related to age and disease duration

Epstein-Barr virus and disease activity in multiple sclerosis

Cardiac evaluation in children and adults with Pompe disease sharing the common c.−32-13T>G genotype rarely reveals abnormalities

Derivation and validation of diagnostic criteria for chronic inflammatory demyelinating polyneuropathy

Course of disability and respiratory function in untreated late-onset Pompe disease

TDP-43 pathology in familial frontotemporal dementia and motor neuron disease without Progranulin mutations

Revising two-point discrimination assessment in normal aging and in patients with polyneuropathies

Amantadine for treatment of fatigue in Guillain-Barré syndrome: a randomised, double blind, placebo controlled, crossover trial

ANO5 mutations in the Dutch limb girdle muscular dystrophy population

Late-onset Pompe disease primarily affects quality of life in physical health domains

Extension of the clinical spectrum of Danon disease

Connecting impairment, disability, and handicap in immune mediated polyneuropathies

Quality of life complements traditional outcome measures in immune-mediated polyneuropathies

Health-related quality-of-life improvements in CIDP with immune globulin IV 10%: the ICE Study

Diagnostic value of anti-GM1 ganglioside serology and validation of the INCAT-ELISA

Ptosis as a feature of late-onset glycogenosis type II

Infections and course of disease in mild forms of Guillain-Barré syndrome

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