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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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RYR1-related myopathies: a wide spectrum of phenotypes throughout life

European journal of neurology, 2015-07, Vol.22 (7), p.1094-1112

2015

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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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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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Mutations in RYR1 are a common cause of exertional myalgia and rhabdomyolysis

Neuromuscular disorders : NMD, 2013-07, Vol.23 (7), p.540-548

2013

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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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Anaerobic sludge granulation

Water research (Oxford), 2004-03, Vol.38 (6), p.1376-1389

2004

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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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Mastication in Patients with Spinal Muscular Atrophy Types 2 and 3 is Characterized by Abnormal Efficiency, Reduced Endurance, and Fatigue

Dysphagia, 2022-08, Vol.37 (4), p.715-723

2022

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Altered Energetics of Exercise Explain Risk of Rhabdomyolysis in Very Long-Chain Acyl-CoA Dehydrogenase Deficiency

PloS one, 2016-02, Vol.11 (2), p.e0147818-e0147818

2016

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Clinical outcome of CIDP one year after start of treatment: a prospective cohort study

Journal of neurology, 2022-02, Vol.269 (2), p.945-955

2022

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New perspectives in anaerobic digestion

Water science and technology, 2001, Vol.43 (1), p.1-18

2001

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Randomised controlled trial comparing two different intravenous immunoglobulins in chronic inflammatory demyelinating polyradiculoneuropathy

Journal of neurology, neurosurgery and psychiatry, 2010-12, Vol.81 (12), p.1374-1379

2010

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The POWER-tool: Recommendations for involving patient representatives in choosing relevant outcome measures during rare disease clinical trial design

Health policy (Amsterdam), 2018-12, Vol.122 (12), p.1287-1294

2018

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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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Effect of stem cell transplantation for B-cell malignancies on disease course of associated polyneuropathy

Journal of neurology, 2012-10, Vol.259 (10), p.2100-2104

2012

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Effect of NaCl on thermophilic (55°C) methanol degradation in sulfate reducing granular sludge reactors

Water research (Oxford), 2003-05, Vol.37 (10), p.2269-2280

2003

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Feeding and Swallowing Problems in Infants with Spinal Muscular Atrophy Type 1: an Observational Study

Journal of neuromuscular diseases, 2020-01, Vol.7 (3), p.323-330

2020

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The Lambert–Eaton myasthenic syndrome 1988–2008: A clinical picture in 97 patients

Journal of neuroimmunology, 2008-09, Vol.201, p.153-158

2008

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Oral dexamethasone pulse therapy versus daily prednisolone in sub-acute onset myositis, a randomised clinical trial

Neuromuscular disorders : NMD, 2010-06, Vol.20 (6), p.382-389

2010

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Relevance of Fcγ Receptor and Interleukin-10 Polymorphisms for Meningococcal Disease

The Journal of infectious diseases, 2001-12, Vol.184 (12), p.1548-1555

2001

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Impact of contractures on daily functioning in adolescents with spinal muscular atrophy: a qualitative study

Disability and rehabilitation, 2024-06, Vol.ahead-of-print (ahead-of-print), p.1-7

2024

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Swallowing Problems in Spinal Muscular Atrophy Types 2 and 3: A Clinical, Videofluoroscopic and Ultrasound Study

Journal of neuromuscular diseases, 2023-01, Vol.10 (3), p.427-438

2023

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Competition for H2 between sulfate reducers, methanogens and homoacetogens in a gas-lift reactor

Water science and technology, 2002, Vol.45 (10), p.75-80

2002

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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

RYR1-related myopathies: a wide spectrum of phenotypes throughout life

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

Mutations in RYR1 are a common cause of exertional myalgia and rhabdomyolysis

Cardiac pathology in spinal muscular atrophy: a systematic review

Anaerobic sludge granulation

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

Mastication in Patients with Spinal Muscular Atrophy Types 2 and 3 is Characterized by Abnormal Efficiency, Reduced Endurance, and Fatigue

Altered Energetics of Exercise Explain Risk of Rhabdomyolysis in Very Long-Chain Acyl-CoA Dehydrogenase Deficiency

Clinical outcome of CIDP one year after start of treatment: a prospective cohort study

New perspectives in anaerobic digestion

Randomised controlled trial comparing two different intravenous immunoglobulins in chronic inflammatory demyelinating polyradiculoneuropathy

The POWER-tool: Recommendations for involving patient representatives in choosing relevant outcome measures during rare disease clinical trial design

Cytokine profiles in multifocal motor neuropathy and progressive muscular atrophy

Effect of stem cell transplantation for B-cell malignancies on disease course of associated polyneuropathy

Effect of NaCl on thermophilic (55°C) methanol degradation in sulfate reducing granular sludge reactors

Feeding and Swallowing Problems in Infants with Spinal Muscular Atrophy Type 1: an Observational Study

The Lambert–Eaton myasthenic syndrome 1988–2008: A clinical picture in 97 patients

Oral dexamethasone pulse therapy versus daily prednisolone in sub-acute onset myositis, a randomised clinical trial

Relevance of Fcγ Receptor and Interleukin-10 Polymorphisms for Meningococcal Disease

Impact of contractures on daily functioning in adolescents with spinal muscular atrophy: a qualitative study

Swallowing Problems in Spinal Muscular Atrophy Types 2 and 3: A Clinical, Videofluoroscopic and Ultrasound Study

Competition for H2 between sulfate reducers, methanogens and homoacetogens in a gas-lift reactor

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