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- Journal Article
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Long-term safety, tolerability, and efficacy of efgartigimod (ADAPT+) : interim results from a phase 3 open-label extension study in participants with generalized myasthenia gravis
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Potential new autoimmune target in inclusion body myositis
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- Journal Article
- A1
- open access
Comparison of clinical features between patients with anti-synthetase syndrome and dermatomyositis : results from the MYONET registry
(2024) RHEUMATOLOGY. -
- Journal Article
- A1
- open access
Retrospective study shows that serum levels of chemokine CXCL10 and cytokine GDF15 support a diagnosis of sporadic inclusion body myositis and immune-mediated necrotizing myopathy
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Wat zijn de ervaringen van personen met amyotrofische laterale sclerose (ALS) en hun mantelzorgers met vroegtijdige zorgplanning?
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- Journal Article
- A1
- open access
Exome sequencing and multigene panel testing in 1,411 patients with adult-onset neurologic disorders
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- Journal Article
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- open access
C-terminal frameshift variant of TDP-43 with pronounced aggregation-propensity causes rimmed vacuole myopathy but not ALS/FTD
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- Journal Article
- A1
- open access
Identification of novel associations and localization of signals in idiopathic inflammatory myopathies using genome‐wide imputation
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Anoctamin-5 related muscle disease : clinical and genetic findings in a large European cohort
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Low gene copy numbers of complement C4 and complement C4A deficiency are strong and highly significant genetic risk factors for idiopathic inflammatory myopathy and its major subgroups
(2023) CLINICAL AND EXPERIMENTAL RHEUMATOLOGY. In Clinical and Experimental Rheumatology 41(2). p.416-416 -
- Conference Paper
- C3
- open access
Hematological effects of intravenous immunoglobulin therapy in patients with neuromuscular diseases : a retrospective analysis
(2022) JOURNAL OF NEUROMUSCULAR DISEASES. In Journal of Neuromuscular Diseases 9(supplement 1). p.S226-S227 -
HATTR-polyneuropathie : diagnose en behandeling
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Neuromusculaire aandoeningen
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Een ischemische beroerte als presentatie van een occulte maligniteit : typisch beeld op een MRI van de hersenen
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- Journal Article
- A2
- open access
An exploratory study of circulating cytokines and chemokines in patients with muscle disorders proposes CD40L and CCL5 represent general disease markers while CXCL10 differentiates between patients with an autoimmune myositis
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Het ‘three territory sign’ als een merker van occulte maligniteit bij een beroerte
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- Journal Article
- A2
- open access
Inducible heat shock protein 70 levels in patients and the mdx mouse affirm regulation during skeletal muscle regeneration in muscular dystrophy
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- Conference Paper
- C3
- open access
Risk of malignant hyperthermia in patients carrying a variant in the ryanodine receptor 1 gene
(2022) JOURNAL OF NEUROMUSCULAR DISEASES. In Journal of Neuromuscular Diseases 9(supplement 1). p.S296-S296 -
- Conference Paper
- C3
- open access
Expanded phenotyping by microscopic imaging
(2022) JOURNAL OF INHERITED METABOLIC DISEASE. In Journal of Inherited Metabolic Disease 45(Supplement 1). p.69-69 -
Osmotic stress-associated sodium/myo-inositol co-transporter is upregulated in skeletal muscle of the mdx mouse
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- Conference Paper
- C3
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Description of osmolyte pathways in maturing MDX mice reveals altered taurine and sodium/myo-inositol co-transporter levels
(2022) JOURNAL OF NEUROMUSCULAR DISEASES. In Journal of Neuromuscular Diseases 9(supplement 1). p.S302-S302 -
- Journal Article
- A1
- open access
Expanding the TDP-43 proteinopathy pathway from neurons to muscle : physiological and pathophysiological functions
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- Journal Article
- A1
- open access
Description of osmolyte pathways in maturing mdx mice reveals altered levels of taurine and sodium/myo-inositol co-transporters
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- Conference Paper
- C3
- open access
Belgian retrospective survey of hereditary transthyretin-mediated (hATTR) amyloidosis patients treated with patisiran in real-world practice
(2022) JOURNAL OF NEUROMUSCULAR DISEASES. In Journal of Neuromuscular Diseases 9(supplement 1). p.S273-S274 -
- Journal Article
- A1
- open access
Advance care planning in amyotrophic lateral sclerosis (ALS) : study protocol for a qualitative longitudinal study with persons with ALS and their family carers
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- Journal Article
- A1
- open access
Exploring the therapeutic potential of ectoine in Duchenne Muscular Dystrophy : comparison with taurine, a supplement with known beneficial effects in the mdx mouse
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- Journal Article
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- open access
Unraveling the molecular basis of the dystrophic process in limb-girdle muscular dystrophy LGMD-R12 by differential gene expression profiles in diseased and healthy muscles
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- Conference Paper
- C3
- open access
Efficacy of efgartigimod in generalized myasthenia gravis : myasthenia gravis composite score analysis from ADAPT
(2022) JOURNAL OF NEUROMUSCULAR DISEASES. In Journal of Neuromuscular Diseases 9(supplement 1). p.S82-S83 -
- Conference Paper
- C3
- open access
Two-years prospective natural history study in 24 adult LGMDR12 patients : clinical and radiological outcome measures
(2022) JOURNAL OF NEUROMUSCULAR DISEASES. In Journal of Neuromuscular Diseases 9(supplement 1). p.S170-S171 -
- Conference Paper
- C3
- open access
A structural variant of the C-terminal prion-like domain of TDP-43 causes vacuolar muscle degeneration
(2022) JOURNAL OF NEUROMUSCULAR DISEASES. In Journal of Neuromuscular Diseases 9(supplement 1). p.S119-S119 -
Clinical features of extra-muscular disease in dermatomyositis and anti-synthetase syndrome patients with skin involvement classified by presence of disease-specific autoantibodies : results from the EuroMyositis registry
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- Journal Article
- A1
- open access
Shortcutting the diagnostic odyssey : the multidisciplinary program for undiagnosed rare diseases in adults (UD-PrOZA)
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The heterogeneity of immune-mediated necrotizing myopathy illustrated in a cohort of Belgian patients : consequences for diagnosis and disease management
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Case report : olanzapine post-injection delirium/sedation syndrome mimicking brainstem-thrombosis
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Duchenne muscular dystrophy fibrosis potentially explained by abnormal NFAT5 physiology in Duchenne muscular dystrophy fibroblasts
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Study of NFAT5 physiology in Duchenne muscular dystrophy fibroblasts : provisionary explanation for the permanent fibrosis formation in Duchenne muscular dystrophy
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Studies on anti-inflammatory and general glucocorticoid physiology in skeletal muscles affected by Duchenne muscular dystrophy : an approach towards exploration of steroid-sparing agents
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Diagnostic muscle biopsies in the era of genetics : the added value of myopathology in a selection of limb-girdle muscular dystrophy patients
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Myotonic dystrophy type 1 as a major risk factor for severe COVID-19?
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- Journal Article
- A1
- open access
Post-intervention status in patients with refractory myasthenia gravis treated with eculizumab during REGAIN and its open-label extension
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In-depth phenotypic description of TBK1 mutations ; a frequent cause of FTD and ALS in the Flanders-Belgian population
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Extensive genetic and phenotypic description of MAPT p.R406W in the Flanders-Belgian population
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- Journal Article
- A1
- open access
No association of CpG SNP rs9357140 with onset age in Belgian C9orf72 repeat expansion carriers
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- Journal Article
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- open access
Efficacy and safety of rozanolixizumab in moderate to severe generalized myasthenia gravis : a phase 2 randomized control trial
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Contribution of homozygous and compound heterozygous missense mutations in VWA2 to Alzheimer's disease
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- Journal Article
- A2
- open access
High-throughput imaging of ATG9A distribution as a diagnostic functional assay for adaptor protein complex 4-associated hereditary spastic paraplegia
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Genotype-phenotype correlations in VCP disease : results of an international multicentric study (The VCP study group)
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Myositis-specific and myositis-associated autoantibodies predict trajectories of damage over time in idiopathic inflammatory myopathies
(2021) SCANDINAVIAN JOURNAL OF RHEUMATOLOGY. In Scandinavian Journal of Rheumatology 50(Supplement 130). p.49-50 -
Efficacy and safety of Bimagrumab in sporadic inclusion body myositis : long-term extension of RESILIENT
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Safety and efficacy of oral levosimendan in people with amyotrophic lateral sclerosis (the REFALS study) : a randomised, double-blind, placebo-controlled phase 3 trial
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Safety, efficacy, and tolerability of efgartigimod in patients with generalised myasthenia gravis (ADAPT) : a multicentre, randomised, placebo-controlled, phase 3 trial
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Autoantilichamen bij dermatomyositis
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The myokine GDF-15 is a potential biomarker for myositis and associates with the protein aggregates of sporadic inclusion body myositis.
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- Journal Article
- A1
- open access
Description of a novel mechanism possibly explaining the antiproliferative properties of glucocorticoids in Duchenne muscular dystrophy fibroblasts based on glucocorticoid receptor GR and NFAT5
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- Journal Article
- A1
- open access
Abnormal NFAT5 physiology in Duchenne muscular dystrophy fibroblasts as a putative explanation for the permanent fibrosis formation in Duchenne muscular dystrophy
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- Conference Paper
- C3
- open access
Abnormal NFAT5 physiology in Duchenne muscular dystrophy fibroblasts as a putative explanation for continuous fibrotic tissue production and the interaction between NFAT5 and glucocorticoid receptor
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- Journal Article
- A1
- open access
Anti-inflammatory and general glucocorticoid physiology in skeletal muscles affected by Duchenne muscular dystrophy : exploration of steroid-sparing agents
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- Journal Article
- A1
- open access
Myo-inositol transporter SLC5A3 associates with degenerative changes and inflammation in sporadic inclusion body myositis
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Long lasting trigeminal neuropathy, limbic encephalitis and abdominal ganglionitis without primary cancer : an atypical case of Hu-Antibody syndrome
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239th ENMC International Workshop : Classification of dermatomyositis, Amsterdam, the Netherlands, 14-16 December 2018
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- Journal Article
- A1
- open access
Consistent improvement with eculizumab across muscle groups in myasthenia gravis
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- Journal Article
- A1
- open access
‘Minimal symptom expression’ in patients with acetylcholine receptor antibody-positive refractory generalized myasthenia gravis treated with eculizumab
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- Book Chapter
- open access
Localization and expression of nuclear factor of activated T-cells 5 in myoblasts exposed to pro-inflammatory cytokines or hyperosmolar stress and in biopsies from myositis patients
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Pitfalls in the detection of myositis specific antibodies by lineblot in clinically suspected idiopathic inflammatory myopathy
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- Journal Article
- A1
- open access
Multisystem proteinopathy due to a homozygous p.Arg159His VCP mutation : a tale of the unexpected
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- Journal Article
- A1
- open access
Late-onset Pompe disease (LOPD) in Belgium : clinical characteristics and outcome measures
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- Journal Article
- A1
- open access
Functional characterization of the first missense variant in CEP78, a founder allele associated with cone‐rod dystrophy, hearing loss and reduced male fertility
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New genotype-phenotype correlations in a large European cohort of patients with sarcoglycanopathy
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Current evidence for treatment with nusinersen for spinal muscular atrophy : a systematic review
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Cladribine in myasthenia gravis : a case urging for prudence
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Two successfully completed pregnancies in adult onset Pompe disease, under continued treatment with alglucosidase alfa
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Effect of methylprednisolone on NFAT5 in Duchenne muscular dystrophy fibroblasts
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- Conference Paper
- C3
- open access
The proliferation of Duchenne muscular dystrophy fibroblasts cultured under inflammatory conditions is reduced by methylprednisolone through modulation of NFAT5 localization in the cell
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Exertional rhabdomyolysis : relevance of clinical and laboratory findings, and clues for investigation
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- Journal Article
- A1
- open access
Seronegative patients form a distinctive subgroup of immune-mediated necrotizing myopathy
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Healthcare utilization at the end of life in people dying from amyotrophic lateral sclerosis : a retrospective cohort study using linked administrative data
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- Journal Article
- A1
- open access
Eculizumab improves fatigue in refractory generalized myasthenia gravis
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Nonsense mutations in alpha-II spectrin in three families with juvenile onset hereditary motor neuropathy
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- Journal Article
- A1
- open access
Long-term efficacy and safety of eculizumab in Japanese patients with generalized myasthenia gravis : a subgroup analysis of the REGAIN open-label extension study
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A phase 3 multicenter, prospective, open-label efficacy and safety study of immune globulin (human) 10% caprylate/chromatography purified in patients with myasthenia gravis exacerbations
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Idiopathic inflammatory myopathy : interrater variability in muscle biopsy reading
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- Journal Article
- A1
- open access
Efficacy and safety of IVIG in CIDP : combined data of the PRIMA and PATH studies
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- Journal Article
- A1
- open access
Long-term safety and efficacy of eculizumab in generalized myasthenia gravis
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- Journal Article
- A1
- open access
Muscular dystrophy with arrhythmia caused by loss-of-function mutations in BVES
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Expansion of the role and functional characterization of a missense variant in CEP78 associated with cone-rod dystrophy and hearing loss
(2019) -
FAHN/SPG35 : a narrow phenotypic spectrum across disease classifications
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- Journal Article
- A1
- open access
Focused HLA analysis in Caucasians with myositis identifies significant associations with autoantibody subgroups
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Loss of paraplegin drives spasticity rather than ataxia in a cohort of 241 patients with SPG7
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- Journal Article
- A1
- open access
Loss of DPP6 in neurodegenerative dementia : a genetic player in the dysfunction of neuronal excitability
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Safety and efficacy of intravenous bimagrumab in inclusion body myositis (RESILIENT) : a randomised, double-blind, placebo-controlled phase 2b trial
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Aanpak van familiale amyloïdpolyneuropathie
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Immune checkpoint failures in inflammatory myopathies : an overview
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Single-centre experience on transthyretin familial amyloid polyneuropathy : case series and literature review
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NFAT5 and p38 MAPKs interact in muscle cells responding to osmotic and inflammatory stress and in polymyositis
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- Journal Article
- A1
- open access
Induction of osmolyte pathways in skeletal muscle inflammation : novel biomarkers for myositis
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- Journal Article
- A1
- open access
Genetic background may contribute to the latitude-dependent prevalence of dermatomyositis and anti-TIF1-γ autoantibodies in adult patients with myositis
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- Journal Article
- A1
- open access
Localization and expression of nuclear factor of activated T-cells 5 in myoblasts exposed to pro-inflammatory cytokines or hyperosmolar stress and in biopsies from myositis patients
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- Journal Article
- A1
- open access
An intronic VNTR affects splicing of ABCA7 and increases risk of Alzheimer's disease
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- Journal Article
- A1
- open access
Truncating SLC5A7 mutations underlie a spectrum of dominant hereditary motor neuropathies
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BVES loss-of-function mutations in limb-girdle muscular dystrophy 2X with cardiac conduction disorders
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- Journal Article
- A1
- open access
Clinical variability and onset age modifiers in an extended Belgian GRN founder family
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- Journal Article
- A1
- open access
The EuroMyositis registry : an international collaborative tool to facilitate myositis research
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- Journal Article
- A1
- open access
Common and rare TBK1 variants in early-onset Alzheimer disease in a European cohort
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Interpreting genetic variants in titin in patients with muscle disorders
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- Journal Article
- A1
- open access
No supportive evidence for TIA1 gene mutations in a European cohort of ALS-FTD spectrum patients
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Osmolyte transporters of Betaine GABA (SLC6Al2) and taurine (SLC5A3) are expressed in muscle-infiltrating mononuclear cells in inflammatory myopathies
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Osmolyte accumulator expression is induced in muscle cells in response to inflammation
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- Journal Article
- A2
- open access
Exertional rhabdomyolysis and heat stroke : beware of volatile anesthetic sedation
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Immunemediated necrotizing autoimmune myopathy : Dutch and Belgian experience
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Beyond ALS and FTD : the phenotypic spectrum of TBK1 mutations includes PSP-like and cerebellar phenotypes
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Investigating the role of ALS genes CHCHD10 and TUBA4A in Belgian FTD-ALS spectrum patients
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Targeted next-generation sequencing reveals novel TTN mutations causing recessive distal titinopathy
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Clinical evidence of disease anticipation in families segregating a C9orf72 repeat expansion
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Immune-array analysis in sporadic inclusion body myositis reveals HLA-DRB1 amino acid heterogeneity across the myositis spectrum
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- Journal Article
- A1
- open access
TBK1 mutation spectrum in an extended European patient cohort with frontotemporal dementia and amyotrophic lateral sclerosis
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- Conference Paper
- C3
- open access
Osmoregulatory pathways are activated in polymyositis: increased expression of osmolyte accumulators in muscle fibers and immune cells
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213th ENMC international workshop: Outcome measures and clinical trial readiness in idiopathic inflammatory myopathies, Heemskerk, The Netherlands, 18-20 September 2015
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En de 'khat' komt weer...: recidief van een ischemisch cerebraal infarct bij een jongeman
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Myopathy mimicking an acute coronary syndrome
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NFAT5 in inflammatory myopathies and Duchenne muscular dystrophy
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The core protein to myogenesis NFAT5 forms aggresomes in normal and Duchenne muscular dystrophy myotubes exposed to cell stressors
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Activation of osmolyte pathways in inflammatory myopathy and Duchenne muscular dystrophy points to osmoregulation as a contributing pathogenic mechanism
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NFAT5 in Duchenne muscular dystrophy cultured myoblasts after exposure to hyperosmolar salt conditions
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Comprehensive analysis of TTN coding regions in myopathic patients: challenges and opportunities
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How robust is ACTIVLIM for the follow-up of activity limitations in patients with neuromuscular diseases?
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The core protein to myogenesis NFAT5 forms aggresomes in normal and Duchenne muscular dystrophy myotubes exposed to cell stressors
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PSP and small vessel disease : more than occasional co-occurence?
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Database crossing allows better understanding of neuromuscular disorders epidemiology: the Belgian example
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- Journal Article
- A2
- open access
Complicated spastic paraplegia in patients with AP5Z1 mutations (SPG48)
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- Journal Article
- A1
- open access
Phenotypic characteristics of Alzheimer patients carrying an ABCA7 mutation
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- Journal Article
- A1
- open access
Clinical features of TBKI carriers compared with C9orf72, GRN and non-mutation carriers in a Belgian cohort
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- Journal Article
- A1
- open access
The C9orf72 repeat size correlates with onset age of disease, DNA methylation and transcriptional downregulation of the promoter
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- Journal Article
- A1
- open access
Rare variants in SQSTM1 and VCP genes and risk of sporadic inclusion body myositis
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- Journal Article
- A1
- open access
A comprehensive study of the genetic impact of rare variants in SORL1 in European early-onset Alzheimer's disease
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Dense genotyping of immune-related loci in idiopathic inflammatory myopathies confirms HLA alleles as the strongest genetic risk factor and suggests different genetic background for major clinical subgroups
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The genetic basis of undiagnosed muscular dystrophies and myopathies: results from 504 patients
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Het postpoliosyndroom [antwoord]
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Het postpoliosyndroom
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Cytomegalovirus-induced myeloradiculopathy in an immunocompetent patient
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Hyperacute presentation of encephalomyelitis 10 days after onset of mycoplasma pneumoniae infection
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- Journal Article
- A1
- open access
Necrotizing myopathy as a paraneoplastic syndrome associated with renal cell carcinoma
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Giant arachnoid granulation of the posterior temporal bone wall mimicking a jugular foramen mass
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NFAT5 forms aggregates in normal and Duchenne muscular dystrophy cultured myotubes after exposure to cell stressors
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Neurological involvement in Erdheim–Chester disease
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Forearm deoxyhemoglobin and deoxymyoglobin (deoxy[Hb + Mb]) measured by near-infrared spectroscopy (NIRS) using a handgrip test in mitochondrial myopathy
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- Journal Article
- A1
- open access
Early stages of building a rare disease registry, methods and 2010 data from the Belgian Neuromuscular Disease Registry (BNMDR)
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Activation of the nuclear factor of activated T-cells 5 pathway is characteristic of the perifascicular muscle fiber atrophy observed in dermatomyositis
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Addition of NaCl upregulates NFAT5 expression in Duchenne muscular dystrophy cultured myotubes
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Pro-inflammatory cell stress in muscle cells is directed by NFAT5
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Inflammatory- and NaCl-induced expression of NFAT5 in muscle cells point to common stress response mechanisms
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Systematic protein-protein interaction and pathway analyses in the idiopathic inflammatory myopathies
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- Journal Article
- A1
- open access
Next generation sequencing on patients with LGMD and nonspecific myopathies: findings associated with ANO5 mutations
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- Journal Article
- A1
- open access
A 22-single nucleotide polymorphism Alzheimer's disease risk score correlates with family history, onset age, and cerebrospinal fluid Aβ42
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Huge variability in a huge gene: TTN variants identified in a large NGS-resequencing project
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205th ENMC international workshop: pathology diagnosis of idiopathic inflammatory myopathies part II, 28-30 March 2014, Naarden, The Netherlands
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- Journal Article
- A1
- open access
The effects of an intronic polymorphism in TOMM40 and APOE genotypes in sporadic inclusion body myositis
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- Journal Article
- A1
- open access
Loss of TBK1 is a frequent cause of frontotemporal dementia in a Belgian cohort
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SQSTM1 and VCP mutations in a series of 205 inclusion body myositis cases
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- Journal Article
- A1
- open access
Investigating the role of filamin C in Belgian patients with frontotemporal dementia linked to GRN deficiency in FTLD-TDP brains
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Development of a disease severity scale for Becker muscular dystrophy
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NFAT5 in idiopathic inflammatory myopathies and Duchenne muscular dystrophy
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Forearm muscle oxygenation responses during and following arterial occlusion in patients with mitochondrial myopathy
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Did lightning strike twice?
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Investigating the role of rare heterozygous TREM2 variants in Alzheimer's disease and frontotemporal dementia
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International immunochip study in the idiopathic inflammatory myopathies identifies novel susceptability loci and confirms HLA as strongest genetic risk factor
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TNF-cytokines in inflammatoire myopathieën: potentiële targets voor behandeling
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Les cytokines TNF dans les myopathies inflammatoires: une cible thérapeutique potentielle
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The nonnecrotic invaded muscle fibers of polymyositis and sporadic inclusion body myositis: on the interplay of chemokines and stress proteins
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- Journal Article
- A1
- open access
Cytokines and chemokines as regulators of skeletal muscle inflammation: presenting the case of Duchenne muscular dystrophy
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193rd ENMC International workshop: Pathology diagnosis of idiopathic inflammatory myopathies, 30 November-2 December 2012, Naarden, The Netherlands
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Time to response for immunoglobulins in the treatment of CIDP
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Diagnostic hallmarks and pitfalls in late-onset progressive transthyretin-related amyloid-neuropathy
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- Journal Article
- A1
- open access
Efficacy and safety of Privigen® in patients with chronic inflammatory demyelinating polyneuropathy: results of a prospective, single-arm, open-label Phase III study (the PRIMA study)
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Dexpramipexole versus placebo for patients with amyotrophic lateral sclerosis (EMPOWER): a randomised, double-blind, phase 3 trial
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Explorative genetic study of UBQLN2 and PFN1 in an extended Flanders-Belgian cohort of frontotemporal lobar degeneration patients
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Edoxaban versus warfarin in patients with atrial fibrillation
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- Journal Article
- A1
- open access
Morphological spectrum and clinical features of myopathies with tubular aggregates
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Distinct clinical characteristics of C9orf72 expansion carriers compared with GRN, MAPT, and nonmutation carriers in a Flanders-Belgian FTLD cohort
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Resolution of abnormal fractional anisotropy of substantia nigra in organophosphate intoxication. C. Swinnen et al., Acta Neurologica Belgica (2011) 111:378
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TNF-cytokines in inflammatoire myopathieën : potentiële targets voor behandeling
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- Journal Article
- A1
- open access
The tumor necrosis factor superfamily of cytokines in the inflammatory myopathies : potential targets for therapy
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Heat shock protein families 70 and 90 in Duchenne muscular dystrophy and inflammatory myopathy: balancing muscle protection and destruction
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- Conference Paper
- C3
- open access
The multifaceted character of the cytokine lymphotoxinβ in inflammatory myopathies
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Lymphotoxin beta : an important cytokine in inflammatory myopathy
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Expression of chemokines and their receptors in muscle tissues from Duchenne muscular dystrophy patients
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Upregulation of chemokines and their receptors in Duchenne muscular dystrophy: potential for attenuation of myofiber necrosis
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Het guillain-barrésyndroom tijdens de zwangerschap: een casus
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Forearm deoxygenation measured by Nirs during a new handgrip exercise protocol in patients with mitochondrial myopathy
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Efficacy of privigen in patients with chronic inflammatory demyelinating polyneuropathy: results from the PRIMA study
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Distinct clinical characteristics of C9orf72 expansion carriers compared to GRN, MAPT and non-mutation carries in a Flanders-Belgian FTLD cohort
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A C9orf72 promoter repeat expansion in a Flanders-Belgian cohort with disorders of the frontotemporal lobar degeneration-amyotrophic lateral sclerosis spectrum : a gene identification study
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MRI findings in giant pontine capillary telangiectasis associated with a developmental venous anomaly
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Localization of chemokines and their receptors in muscle tissues from Duchenne muscular dystrophy patients
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Phenotypic spectrum in myopathies with tubular aggregates
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Expression of heat shock proteins in skeletal muscle from idiopathic inflammatory myopathy and Duchenne muscular dystrophy patients
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Ptosis as an associated finding in maternally inherited diabetes and deafness
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Progressive myoclonic epilepsy as an adult-onset manifestation of Leigh syndrome due to m.14487T > C
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Sneddon's syndrome
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Role of cytokines and chemokines in idiopathic inflammatory myopathies
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Histochemical methods for the diagnosis of mitochondrial diseases
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Idiopathic inflammatory myopathies and the classical NF-kappa B complex: Current insights and implications for therapy
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Expression of HSP90 alpha and HSP90 beta in the idiopathic inflammatory myopathies and Duchenne muscular dystrophy
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A Dual Role for HSP90 and HSP70 in the Inflammatory Myopathies From Muscle Fiber Protection to Active Invasion by Macrophages
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Distribution of the NF-kappa B Complex in the Inflammatory Exudates Characterizing the Idiopathic Inflammatory Myopathies
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Immunohistochemical analysis of the oxidative phosphorylation complexes in skeletal muscle from patients with mitochondrial DNA encoded tRNA gene defects
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Effect of atorvastatin in elderly patients with recent stroke or transient ischemic attack
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Progressive myoclonic epilepsy as an adult-onset manifestation of Leigh syndrome due to the m.14487T>C mutation in ND6
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- Journal Article
- A1
- open access
Ataxia with oculomotor apraxia type 2: clinical, biological and genotype/phenotype correlation study of a cohort of 90 patients
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Organophosphate and carbamate poisoning
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Chemokines in idiopathic inflammatory myopathies
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A case of 5-fluorouracil-induced peripheral neuropathy
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Recurrent post-infectious rhabdomyolysis in muscle CPT-II deficiency caused by a novel missense mutation
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Open-label trial of anti-TNF-alpha in dermato- and polymyositis treated concomitantly with methotrexate
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TNF alpha receptor genotype influences smoking-induced muscle-fibre-type shift and atrophy in mice
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Relative effects of statin therapy on stroke and cardiovascular events in men and women - Secondary analysis of the Stroke Prevention by Aggressive Reduction in Cholesterol Levels (SPARCL) study
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Neuromusculaire aspecten van statines
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Post-traumatic spontaneous recurrent hypothermia: a variant of Shapiro's syndrome
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Chemokine profile of different inflammatory myopathies reflects humoral versus cytotoxic immune responses
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TNF alpha receptor signalling influences the expression of myosin heavy chain isoforms in musculus gastrocnemius of the mouse
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Immunohistochemical studies of oxidative phosphorylation in skeletal muscle of patients with mitochondrial tRNA gene mutations
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Distribution of glucocorticoid receptor alpha and beta subtypes in the idiopathic inflammatory myopathies
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Two novel mitochondrial DNA mutations in muscle tissue of a patient with limb-girdle myopathy
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Visualizing oxidative phosphorylation defects in skeletal muscle of patients with mitochondrial tRNA gene mutations using immunohistochemistry
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Intermediate syndrome in organophosphate poisoning
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Intracerebral haemorrhage in CADASIL. A case report
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Potential therapeutic targets for idiopathic inflammatory myopathies
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Effect of genetic modifiers on cerebral lesions in Fabry disease
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Khat chewing can cause stroke
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Expression of inhibitor kappa B-alpha in idiopathic inflammatory myopathies
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The distribution of IkappaBalpha in inflammatory myopathies
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Role of tumour necrosis factor-alpha receptor p75 in cigarette smoke-induced pulmonary inflammation and emphysema
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MFN2 mutation distribution and genotype/phenotype correlation in Charcot-Marie-Tooth type 2
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Bespreking Nederlandse richtlijn 'Polyneuropathie', vanuit Vlaams oogpunt
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How to approach the patient with muscular symptoms in the general neurological practice?
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β-chemokine receptor expression in idiopathic inflammatory myopathies
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Neuro-imaging: uw diagnose?
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Reversible visual deficit and corpus callosum lesions due to metronidazole toxicity
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Multiple neurological syndromes during Hodgkin lymphoma remission
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Alpha-chemokine receptors CXCR1-3 and their ligands in idiopathic inflammatory myopathies
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Localization of glucocorticoid receptor alpha and beta subtypes in inflammatory myopathy
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Distribution of glucocorticoid receptor subtypes in inflammatory myopathy
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The genetic causes of basal ganglia calcification, dementia, and bone cysts DAP12 and TREM2
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Work-up of the patient with a hereditary myopathy
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Potentieel reversibele autoimmune limbische encephalopathie met antilichamen tegen neuronale kaliumkanalen
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The idiopathic inflammatory myopathies
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New mutation in first Belgian cases of Nasu-Hakola disease
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Centrale en perifere neurologische toxiciteit door metronidazol
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Centrale en perifere neurotoxiciteit door metronidazol
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Necrotizing myopathy with microvascular deposition of the complement membrane attack complex
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Reversible orofacial dyskinesia after ofloxacin treatment