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Fatigue and daytime sleepiness scale in myotonic dystrophy type 1

Muscle & nerve, 2013-01, Vol.47 (1), p.89-95

2013

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Small fibers, large impact: Quality of life in small-fiber neuropathy

Muscle & nerve, 2014-03, Vol.49 (3), p.329-336

2014

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196th ENMC international workshop: Outcome measures in inflammatory peripheral neuropathies 8–10 February 2013, Naarden, The Netherlands

Neuromuscular disorders : NMD, 2013-11, Vol.23 (11), p.924-933

2013

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Fatigue, Pain, Anxiety and Depression in Guillain-Barré Syndrome and Chronic Inflammatory Demyelinating Polyradiculoneuropathy

European neurology, 2016, Vol.75 (3-4), p.199-206

2016

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Incidence and prevalence of small-fiber neuropathy: a survey in the Netherlands

Neurology, 2013-10, Vol.81 (15), p.1356-1360

2013

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Minimal clinically important difference in myasthenia gravis: Outcomes from a randomized trial

Muscle & nerve, 2014-05, Vol.49 (5), p.661-665

2014

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Rasch analysis to evaluate the motor function measure for patients with facioscapulohumeral muscular dystrophy

International journal of rehabilitation research, 2021-03, Vol.44 (1), p.38-44

2021

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Channelopathies, painful neuropathy, and diabetes: which way does the causal arrow point?

Trends in molecular medicine, 2014-10, Vol.20 (10), p.544-550

2014

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Contact heat evoked potentials: Normal values and use in small-fiber neuropathy

Muscle & nerve, 2015-05, Vol.51 (5), p.743-749

2015

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Small Fiber Neuropathy in Children: Two Case Reports Illustrating the Importance of Recognition

Pediatrics (Evanston), 2016-10, Vol.138 (4)

2016

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Epidermal innervation morphometry by immunofluorescence and bright‐field microscopy

Journal of the peripheral nervous system, 2015-12, Vol.20 (4), p.387-391

2015

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Fatigue in immune-mediated neuropathies

Neuromuscular disorders : NMD, 2012-12, Vol.22, p.S203-S207

2012

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Observations on chronic inflammatory demyelinating polyneuropathy: A plea for a rigorous approach to diagnosis and treatment

Journal of the neurological sciences, 2013-07, Vol.330 (1), p.2-3

2013

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Peripheral neuropathies: Moving closer to mechanism

Neuroscience letters, 2015-06, Vol.596, p.1-2

2015

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Differential effect of D623N variant and wild-type Nav1.7 sodium channels on resting potential and interspike membrane potential of dorsal root ganglion neurons

Brain research, 2013-09, Vol.1529, p.165-177

2013

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Pharmacometric analysis linking immunoglobulin exposure to clinical efficacy outcomes in chronic inflammatory demyelinating polyneuropathy

CPT: pharmacometrics and systems pharmacology, 2021-08, Vol.10 (8), p.839-850

2021

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Electrical spinal cord stimulation in painful diabetic polyneuropathy, a systematic review on treatment efficacy and safety

European journal of pain, 2011-09, Vol.15 (8), p.783-788

2011

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The applicability of the digit wrinkle scan to quantify sympathetic nerve function

Clinical neurophysiology practice, 2022-01, Vol.7, p.115-119

2022

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Rasch-built myotonic dystrophy type 1 activity and participation scale (DM1-Activ)

Neuromuscular disorders : NMD, 2010-05, Vol.20 (5), p.310-318

2010

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Monitoring Clinical Course and Treatment Response in Chronic Inflammatory Demyelinating Polyneuropathy During Routine Care: A Review of Clinical and Laboratory Assessment Measures

JAMA neurology, 2020-09, Vol.77 (9), p.1159

2020

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Proceed with caution: Benefits and drawbacks of modern clinimetric analysis

Developmental medicine and child neurology, 2023-05, Vol.65 (5), p.597-598

2023

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Gain-of-function Naᵥ1.8 mutations in painful neuropathy

Proceedings of the National Academy of Sciences - PNAS, 2012-11, Vol.109 (47), p.19444-19449

2012

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Outcome measures in Duchenne muscular dystrophy: Are we ready for the new therapeutic era?

Neuromuscular disorders : NMD, 2009-06, Vol.19 (6), p.447-447

2009

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Gain-of-function mutations in sodium channel Nav1.9 in painful neuropathy

Brain (London, England : 1878), 2014-06, Vol.137 (6), p.1627-1642

2014

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Small‐fiber neuropathy: Expanding the clinical pain universe

Journal of the peripheral nervous system, 2019-03, Vol.24 (1), p.19-33

2019

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Fatigue and daytime sleepiness scale in myotonic dystrophy type 1

Small fibers, large impact: Quality of life in small-fiber neuropathy

196th ENMC international workshop: Outcome measures in inflammatory peripheral neuropathies 8–10 February 2013, Naarden, The Netherlands

Fatigue, Pain, Anxiety and Depression in Guillain-Barré Syndrome and Chronic Inflammatory Demyelinating Polyradiculoneuropathy

Incidence and prevalence of small-fiber neuropathy: a survey in the Netherlands

Minimal clinically important difference in myasthenia gravis: Outcomes from a randomized trial

Rasch analysis to evaluate the motor function measure for patients with facioscapulohumeral muscular dystrophy

Channelopathies, painful neuropathy, and diabetes: which way does the causal arrow point?

Contact heat evoked potentials: Normal values and use in small-fiber neuropathy

Small Fiber Neuropathy in Children: Two Case Reports Illustrating the Importance of Recognition

Epidermal innervation morphometry by immunofluorescence and bright‐field microscopy

Fatigue in immune-mediated neuropathies

Observations on chronic inflammatory demyelinating polyneuropathy: A plea for a rigorous approach to diagnosis and treatment

Peripheral neuropathies: Moving closer to mechanism

Differential effect of D623N variant and wild-type Nav1.7 sodium channels on resting potential and interspike membrane potential of dorsal root ganglion neurons

Pharmacometric analysis linking immunoglobulin exposure to clinical efficacy outcomes in chronic inflammatory demyelinating polyneuropathy

Electrical spinal cord stimulation in painful diabetic polyneuropathy, a systematic review on treatment efficacy and safety

The applicability of the digit wrinkle scan to quantify sympathetic nerve function

Rasch-built myotonic dystrophy type 1 activity and participation scale (DM1-Activ)

Monitoring Clinical Course and Treatment Response in Chronic Inflammatory Demyelinating Polyneuropathy During Routine Care: A Review of Clinical and Laboratory Assessment Measures

Proceed with caution: Benefits and drawbacks of modern clinimetric analysis

Gain-of-function Naᵥ1.8 mutations in painful neuropathy

Outcome measures in Duchenne muscular dystrophy: Are we ready for the new therapeutic era?

Gain-of-function mutations in sodium channel Nav1.9 in painful neuropathy

Small‐fiber neuropathy: Expanding the clinical pain universe

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