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Impact of ICU-acquired weakness on post-ICU physical functioning: a follow-up study

Critical care (London, England), 2015-04, Vol.19 (1), p.196-196, Article 196

2015

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Serum neurofilament light chain in chronic inflammatory demyelinating polyneuropathy

Journal of the peripheral nervous system, 2019-06, Vol.24 (2), p.187-194

2019

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Intravenous immunoglobulins as first-line treatment in idiopathic inflammatory myopathies: a pilot study

Rheumatology (Oxford, England), 2021-04, Vol.60 (4), p.1784-1792

2021

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Increased Early Systemic Inflammation in ICU-Acquired Weakness; A Prospective Observational Cohort Study

Critical care medicine, 2017-06, Vol.45 (6), p.972-979

2017

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Randomized, controlled trial of miglustat in Gaucher's disease type 3

Annals of neurology, 2008-11, Vol.64 (5), p.514-522

2008

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Is dosing of therapeutic immunoglobulins optimal? A review of a three-decade long debate in europe

Frontiers in immunology, 2014-12, Vol.5, p.629

2014

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Diagnostic accuracy of quantitative neuromuscular ultrasound for the diagnosis of intensive care unit-acquired weakness: a cross-sectional observational study

Annals of intensive care, 2017-04, Vol.7 (1), p.40-40, Article 40

2017

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Pulsed high-dose dexamethasone versus standard prednisolone treatment for chronic inflammatory demyelinating polyradiculoneuropathy (PREDICT study): a double-blind, randomised, controlled trial

Lancet neurology, 2010-03, Vol.9 (3), p.245-253

2010

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Early prediction of intensive care unit-acquired weakness using easily available parameters: a prospective observational study

PloS one, 2014-10, Vol.9 (10), p.e111259-e111259

2014

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Depressive symptoms in Fabry disease: the importance of coping, subjective health perception and pain

Orphanet journal of rare diseases, 2020-01, Vol.15 (1), p.28-28, Article 28

2020

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Intravenous immunoglobulin treatment in chronic inflammatory demyelinating polyradiculoneuropathy, a time to start and a time to stop

Journal of the peripheral nervous system, 2016-09, Vol.21 (3), p.121-127

2016

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Treatment with add-on IVIg in Myositis Early In the diSease course May be sUperior to Steroids alone for reaching CLinical improvEment (TIME IS MUSCLE): study protocol of a phase-2 double-blind placebo-controlled randomised trial

BMJ open, 2023-07, Vol.13 (7), p.e067435-e067435

2023

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Oral high dose ascorbic acid treatment for one year in young CMT1A patients: a randomised, double-blind, placebo-controlled phase II trial

BMC medicine, 2009-11, Vol.7 (1), p.70-70, Article 70

2009

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Predictors of objective cognitive impairment and subjective cognitive complaints in patients with Fabry disease

Scientific reports, 2019-01, Vol.9 (1), p.188-188, Article 188

2019

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Treatments for chronic inflammatory demyelinating polyradiculoneuropathy (CIDP): an overview of systematic reviews

Cochrane database of systematic reviews, 2017-01, Vol.1 (1), p.CD010369

2017

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Chronic inflammatory demyelinating polyneuropathy disease activity status: recommendations for clinical research standards and use in clinical practice

Journal of the peripheral nervous system, 2010-12, Vol.15 (4), p.326-333

2010

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Intravenous immunoglobulin for chronic inflammatory demyelinating polyradiculoneuropathy

Cochrane database of systematic reviews, 2013-12 (12), p.CD001797

2013

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Assessment of intensive care unit-acquired weakness in young and old mice: An E. coli septic peritonitis model

Muscle & nerve, 2016-01, Vol.53 (1), p.127-133

2016

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Intravenous immunoglobulin for chronic inflammatory demyelinating polyradiculoneuropathy

Cochrane database of systematic reviews, 2024-02, Vol.2, p.CD001797

2024

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Combining MRI and muscle biopsy improves diagnostic accuracy in subacute-onset idiopathic inflammatory myopathy

Muscle & nerve, 2015-02, Vol.51 (2), p.253-258

2015

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Feasibility and Diagnostic Accuracy of Early Electrophysiological Recordings for ICU-Acquired Weakness: An Observational Cohort Study

Neurocritical care, 2015-06, Vol.22 (3), p.385-394

2015

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FabryScan: a screening tool for early detection of Fabry disease

Journal of neurology, 2012-11, Vol.259 (11), p.2393-2400

2012

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The cognitive profile of type 1 Gaucher disease patients

Journal of inherited metabolic disease, 2012-11, Vol.35 (6), p.1093-1099

2012

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Diagnostic accuracy of MRI and ultrasound in chronic immune-mediated neuropathies

Neurology, 2020-01, Vol.94 (1), p.e62

2020

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Monitoring disease progression using high-density motor unit number estimation in amyotrophic lateral sclerosis

Muscle & nerve, 2010-08, Vol.42 (2), p.239-244

2010

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Impact of ICU-acquired weakness on post-ICU physical functioning: a follow-up study

Serum neurofilament light chain in chronic inflammatory demyelinating polyneuropathy

Intravenous immunoglobulins as first-line treatment in idiopathic inflammatory myopathies: a pilot study

Increased Early Systemic Inflammation in ICU-Acquired Weakness; A Prospective Observational Cohort Study

Randomized, controlled trial of miglustat in Gaucher's disease type 3

Is dosing of therapeutic immunoglobulins optimal? A review of a three-decade long debate in europe

Diagnostic accuracy of quantitative neuromuscular ultrasound for the diagnosis of intensive care unit-acquired weakness: a cross-sectional observational study

Pulsed high-dose dexamethasone versus standard prednisolone treatment for chronic inflammatory demyelinating polyradiculoneuropathy (PREDICT study): a double-blind, randomised, controlled trial

Early prediction of intensive care unit-acquired weakness using easily available parameters: a prospective observational study

Depressive symptoms in Fabry disease: the importance of coping, subjective health perception and pain

Intravenous immunoglobulin treatment in chronic inflammatory demyelinating polyradiculoneuropathy, a time to start and a time to stop

Treatment with add-on IVIg in Myositis Early In the diSease course May be sUperior to Steroids alone for reaching CLinical improvEment (TIME IS MUSCLE): study protocol of a phase-2 double-blind placebo-controlled randomised trial

Oral high dose ascorbic acid treatment for one year in young CMT1A patients: a randomised, double-blind, placebo-controlled phase II trial

Predictors of objective cognitive impairment and subjective cognitive complaints in patients with Fabry disease

Treatments for chronic inflammatory demyelinating polyradiculoneuropathy (CIDP): an overview of systematic reviews

Chronic inflammatory demyelinating polyneuropathy disease activity status: recommendations for clinical research standards and use in clinical practice

Intravenous immunoglobulin for chronic inflammatory demyelinating polyradiculoneuropathy

Assessment of intensive care unit-acquired weakness in young and old mice: An E. coli septic peritonitis model

Intravenous immunoglobulin for chronic inflammatory demyelinating polyradiculoneuropathy

Combining MRI and muscle biopsy improves diagnostic accuracy in subacute-onset idiopathic inflammatory myopathy

Feasibility and Diagnostic Accuracy of Early Electrophysiological Recordings for ICU-Acquired Weakness: An Observational Cohort Study

FabryScan: a screening tool for early detection of Fabry disease

The cognitive profile of type 1 Gaucher disease patients

Diagnostic accuracy of MRI and ultrasound in chronic immune-mediated neuropathies

Monitoring disease progression using high-density motor unit number estimation in amyotrophic lateral sclerosis

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