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Potential new autoimmune target in inclusion body myositis
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- Journal Article
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- open access
Comparison of clinical features between patients with anti-synthetase syndrome and dermatomyositis : results from the MYONET registry
(2024) RHEUMATOLOGY. -
- Journal Article
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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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- Journal Article
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- open access
Identification of novel associations and localization of signals in idiopathic inflammatory myopathies using genome‐wide imputation
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Mammalian target of rapamycin inhibition enhances delivery and activity of antisense oligonucleotides in uveal melanoma cells
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Diagnose en subtypering van myositis op basis van cytokine profielen : hoe wetenschappelijke inzichten langzaam de weg kunnen vinden naar de kliniek
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De toekomst van innovatief onderzoek naar Duchenne spierdystrofie: Maak kennis met de huidige lichting studenten in het laboratorium voor neuropathologie
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Organic osmolytes and Duchenne muscular dystrophy : from homeostasis, inflammation and skeletal muscle regeneration to therapeutic target
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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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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 -
- Journal Article
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- open access
Neonatal lactic acidosis explained by LARS2 defect
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- Journal Article
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- open access
Urine lactate concentration as a non-invasive screener for metabolic abnormalities : findings in children with autism spectrum disorder and regression
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Osmolyten als ondersteunende therapie voor Duchenne musculaire dystrofie : het potentieel van taurine en ectoïne als voedingssupplement
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- Journal Article
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- 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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- 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 -
- Conference Paper
- C3
- open access
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 -
- 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 -
- Journal Article
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- 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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- Journal Article
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Expanding the TDP-43 proteinopathy pathway from neurons to muscle : physiological and pathophysiological functions
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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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Osmotic stress-associated sodium/myo-inositol co-transporter is upregulated in skeletal muscle of the mdx mouse
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- Journal Article
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The role of taurine in skeletal muscle functioning and its potential as a supportive treatment for Duchenne Muscular Dystrophy
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- Journal Article
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Description of osmolyte pathways in maturing mdx mice reveals altered levels of taurine and sodium/myo-inositol co-transporters
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- Journal Article
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Clinical heterogeneity in MT-ATP6 pathogenic variants : same genotype—different onset
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- Miscellaneous
- open access
The long non-coding RNA SAMMSON is essential for uveal melanoma cell survival (Sept, 10.1038/s41388-021-02006-x, 2021)
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- Journal Article
- A2
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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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- Journal Article
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The long non-coding RNA SAMMSON is essential for uveal melanoma cell survival
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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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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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Pathologie van dunne vezels als link tussen de zeldzame diagnose van dunnevezelneuropathie en de vaak voorkomende aandoening fibromyalgie
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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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Hoe ontstaan chronische klachten bij patiënten met fibromyalgie? De insula, een hersengebied met een mogelijke sleutelrol
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- Journal Article
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The PKA-p38MAPK-NFAT5-organic osmolytes pathway in Duchenne muscular dystrophy : from essential player in osmotic homeostasis, inflammation and skeletal muscle regeneration to therapeutic target
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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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- Conference Paper
- C3
- open access
mTor inhibitor GDC-0349 improves ASO induced SAMMSON knock down resulting in enhanced anti-tumor efficacy in uveal melanoma
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- Conference Paper
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mTor inhibitor GDC-0349 improves ASO induced SAMMSON knock down resulting in enhanced anti-tumor efficacy in uveal melanoma
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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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- Journal Article
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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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- Conference Paper
- C3
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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
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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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- Journal Article
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Progressive skeletal muscle atrophy in muscular dystrophies : a role for toll-like receptor-signaling in disease pathogenesis
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- Journal Article
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Myo-inositol transporter SLC5A3 associates with degenerative changes and inflammation in sporadic inclusion body myositis
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A capital role for the brain’s insula in the diverse fibromyalgia-associated symptoms
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- Journal Article
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Anti-inflammatory and general glucocorticoid physiology in skeletal muscles affected by Duchenne muscular dystrophy : exploration of steroid-sparing agents
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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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Nanoscopic X-ray imaging and quantification of the iron cellular architecture within single fibroblasts of Friedreich's ataxia patients
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- Conference Paper
- C3
- open access
Therapeutic applications of SAMMSON lncRNA inhibition in uveal melanoma
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- Conference Paper
- C3
- open access
Therapeutic applications of SAMMSON lncRNA inhibition in uveal melanoma
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How mitochondrial DNA-driven changes to chromosomal DNA methylation add a layer of complexity to mitochondrial disease
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Idiopathic inflammatory myopathy : interrater variability in muscle biopsy reading
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- Journal Article
- A2
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The changed transcriptome of muscular dystrophy and inflammatory myopathy : contributions of non-coding RNAs to muscle damage and recovery
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- Journal Article
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Muscular dystrophy with arrhythmia caused by loss-of-function mutations in BVES
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- Conference Paper
- C3
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Therapeutic applications of SAMMSON lncRNA inhibition in uveal melanoma
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- Journal Article
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Sporadic inclusion body myositis : an acquired mitochondrial disease with extras
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- Conference Paper
- C3
- open access
Therapeutic applications of SAMMSON lncRNA inhibition in uveal melanoma
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Therapeutic applications of SAMMSON lncRNA inhibition in uveal melanoma
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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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BVES loss-of-function mutations in limb-girdle muscular dystrophy 2X with cardiac conduction disorders
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Cyclic vomiting in a subject with homoplasmic m.14674T>C alteration
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The clinical heterogeneity of the NARS2 c.822G>C mutation clearly illustrated in two siblings : epilepsy and myopathy
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Complex III deficiency due to a homozygous mutation in the nuclear encoded subunit UQCRQ
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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
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- 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
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- 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
Nanoscopic X-ray fluorescence imaging and quantification of intracellular key-elements in cryofrozen Friedreich's ataxia fibroblasts
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Near-infrared spectroscopy screening to allow detection of pathogenic mitochondrial DNA variants in individuals with unexplained abnormal fatigue : a preliminary study
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How long noncoding RNAs enforce their will on mitochondrial activity : regulation of mitochondrial respiration, reactive oxygen species production, apoptosis, and metabolic reprogramming in cancer
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- Journal Article
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- open access
The EuroMyositis registry : an international collaborative tool to facilitate myositis research
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- Conference Paper
- C3
- open access
Therapeutic applications of SAMMSON lncRNA inhibition in uveal melanoma
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- Journal Article
- A1
- open access
New insights into the phenotype of FARS2 deficiency
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- Journal Article
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A critical assessment of the therapeutic potential of resveratrol supplements for treating mitochondrial disorders
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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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Cytokines as orchestrators of skeletal muscle tissue maintenance and the inflammation associated with acquired autoimmune and hereditary muscle diseases
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- Journal Article
- A2
- open access
Osmolytes as mediators of the muscle tissue’s responses to inflammation : emerging regulators of myositis with therapeutic potential
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- Journal Article
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A recipe for myositis : nuclear factor κB and nuclear factor of activated T-cells transcription factor pathways spiced up by cytokines
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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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Vascular changes and perifascicular muscle fiber damage in dermatomyositis : another question of the chicken or the egg that is on our mind
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- Journal Article
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- open access
POLG2 deficiency causes adult-onset syndromic sensory neuropathy, ataxia and parkinsonism
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- Journal Article
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Rare variants in SQSTM1 and VCP genes and risk of sporadic inclusion body myositis
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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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Pathogenic mutations in TMEM126b, a recently discovered complex I assembly factor, identified in four siblings from two Belgian families
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Pathogenic mutations in FARS2 in a patient with motor regression and epilepsy as first signs, later evolving to spastic paraplegia associated with autonomic disturbances
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Mild early epileptic encephalopathy evolving to spastic paraplegia, neurogenic bladder and generalized slow colon transit in an 18-year old patient with pathogenic mutations in FARS2
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- Conference Paper
- C3
- open access
Inflammatory mediators in inflammatory myopathies
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- Journal Article
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Biallelic mutations in TMEM126B cause severe complex I deficiency with a variable clinical phenotype
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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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The core protein to myogenesis NFAT5 forms aggresomes in normal and Duchenne muscular dystrophy myotubes exposed to cell stressors
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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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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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Does perinatal infection affect the capacity of umbilical vein endothelial cells to produce adenosine triphosphate?
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Systematic protein-protein interaction and pathway analyses in the idiopathic inflammatory myopathies
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- Journal Article
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Scanning for therapeutic targets within the cytokine network of idiopathic inflammatory myopathies
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Inflammatory- and NaCl-induced expression of NFAT5 in muscle cells point to common stress response mechanisms
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SQSTM1 and VCP mutations in a series of 205 inclusion body myositis cases
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Addition of NaCl upregulates NFAT5 expression in Duchenne muscular dystrophy cultured myotubes
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Interferons as components of the complex web of reactions sustaining inflammation in idiopathic inflammatory myopathies
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- Journal Article
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The effects of an intronic polymorphism in TOMM40 and APOE genotypes in sporadic inclusion body myositis
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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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Treatment of idiopathic inflammatory myopathies: targets inside the cytokine network
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Pro-inflammatory cell stress in muscle cells is directed by NFAT5
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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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Two siblings with homozygous pathogenic splice-site variant in mitochondrial asparaginyl-tRNA synthetase (NARS2)
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Possible pathogenic mechanism of propofol infusion syndrome involves coenzyme Q
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Analysis of the whole mitochondrial genome: translation of the Ion Torrent Personal Genome Machine system to the diagnostic bench?
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- Journal Article
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A bumpy ride on the diagnostic bench of massive parallel sequencing, the case of the mitochondrial genome
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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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Did lightning strike twice?
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- Journal Article
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Treating mitochondrial myopathy : can we boost oxidative phosphorylation activities by enhancing mitochondrial biogenesis?
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Two siblings with myopathy, mild mental retardation and combined OXPHOS deficiencies caused by a mutation in the gene encoding asparaginyl tRNA synthetase, NARS2
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Ullrich congenital muscular dystrophy: a new cellular study on cultured skin fibroblasts
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- Journal Article
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- open access
Transcriptomic profiling of TK2 deficient human skeletal muscle suggests a role for the p53 signalling pathway and identifies growth and differentiation factor-15 as a potential novel biomarker for mitochondrial myopathies
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NFAT5 in idiopathic inflammatory myopathies and Duchenne muscular dystrophy
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- Journal Article
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- open access
Clinical variability in neurohepatic syndrome due to combined mitochondrial DNA depletion and Gaucher disease
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Effect of resveratrol on cultured skin fibroblasts from patients with oxidative phosphorylation defects
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A novel compound heterozygous mutation in NFU1 as cause of iron-sulfur cluster biosynthesis
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Mutation of the iron-sulfur cluster assembly IBA57 gene causes lethal myopathy and encephalopathy
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Fatal outcome of iron-sulfur cluster scaffold NFU1 gene mutations in a neonatal patient
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A homozygous mutation in IBA57 involved in intramitochondrial iron-sulfur cluster synthesis causes severe encephalopathy and mypathy in two neonates
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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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- Journal Article
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- open access
Cytokines and chemokines as regulators of skeletal muscle inflammation: presenting the case of Duchenne muscular dystrophy
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Anti-angiogenic therapy for cancer: past, present and future
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- Miscellaneous
- open access
Heat-shock proteins in autoimmunity
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- Journal Article
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Morphological spectrum and clinical features of myopathies with tubular aggregates
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Mutation of the iron-sulfur cluster assembly gene IBA57 causes severe myopathy and encephalopathy
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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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Les cytokines TNF dans les myopathies inflammatoires: une cible thérapeutique potentielle
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TNF-cytokines in inflammatoire myopathieën: potentiële targets voor behandeling
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Unraveling the mechanisms behind the enhanced MTT conversion by irradiated breast cancer cells
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Heat-shock proteins in autoimmunity
Kamal D Moudgil, Stephen J Thompson, Fabiana Geraci, Boel De Paepe (UGent) and Yehuda Shoenfeld(2012) In Autoimmune Diseases -
Proteomic analysis of cultured skin fibroblasts from UCMD patients reveals the involvement of two new cellular pathways
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Expression of chemokines and their receptors in muscle tissues from Duchenne muscular dystrophy patients
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Lymphotoxin beta : an important cytokine in inflammatory myopathy
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- Journal Article
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- open access
Mitochondrial markers for cancer : relevance to diagnosis, therapy and prognosis, and general understanding of malignant disease mechanisms
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Upregulation of chemokines and their receptors in Duchenne muscular dystrophy: potential for attenuation of myofiber necrosis
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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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TNF-cytokines in inflammatoire myopathieën : potentiële targets voor behandeling
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Fluorescence imaging of mitochondria in cultured skin fibroblasts: a useful method for detection of oxidative phosphorylation defects
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Proteomic analysis in giant axonal neuropathy: new insights into disease mechanisms
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Inborn oxidative phosphorylation defect as risk factor for propofol infusion syndrome
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- Conference Paper
- C3
- open access
The multifaceted character of the cytokine lymphotoxinβ in inflammatory myopathies
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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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JC-1-based fluorescence to evaluate oxidative phosphorylation defects generates both qualitative and quantitative information
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Localization of chemokines and their receptors in muscle tissues from Duchenne muscular dystrophy patients
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ATP synthase deficiency: a diagnostic strategy for not such an uncommon cause of OXPHOS dysfunction
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Analysis of the giant axonal neuropathy fibroblasts proteome
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Hashimoto encephalopathy and antibodies against dimethylargininase-1: a rare cause of cognitive decline in a pediatric Down's syndrome patient
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Complex III staining in blue native polyacrylamide gels
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Anti-NMDA-receptor encephalitis in a 3 year old patient with chromosome 6p21.32 microdeletion including the HLA cluster
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Deleterious mutations in RRM2B result in severe reduction of mtDNA content in skeletal muscle
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Mutations in TMEM70 causes severe encephalocardiomyopathy as well as mild encephalopathy
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Mutations in TMEM70, a gene coding for an assembly factor of complex V, can cause a severe encephalocardiomyopathy in the neonatal period as wel as mild non-progressive encephalopathy in adolescence
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Deleterious mutations in RRM2B, a gene responsible for maintenance of mtDNA, result in severe reduction of mtDNA content in skeletal muscle
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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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Progressive myoclonic epilepsy as an adult-onset manifestation of Leigh syndrome due to m.14487T > C
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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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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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Histochemical methods for the diagnosis of mitochondrial diseases
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Role of cytokines and chemokines in idiopathic inflammatory myopathies
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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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Subcomplexes of mitochondrial complex V reveal mutations in mitochondrial DNA
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MITOCHONDRIAL ABNORMALITIES IN A NEWBORN WITH LACTIC ACIDOSIS AND ADRENAL CALCIFICATIONS
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Lactic Acidosis in a Newborn With Adrenal Calcifications
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- Journal Article
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- open access
Mitochondrial mosaics in the liver of 3 infants with mtDNA defects
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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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Role of BN-page in the diagnosis of mitochondrial DNA depletion
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Chemokines in idiopathic inflammatory myopathies
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Immunostaining technniques in patients with mtDNA depletion
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TNF alpha receptor genotype influences smoking-induced muscle-fibre-type shift and atrophy in mice
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Infantile presentation of the mitochondrial A8344G mutation.
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The presence of complex V subcomplexes in patients with defective intramitochondrial protein translation.
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The presence of complex V subcomplexes in patients with defective intramitochondrial protein translation
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ATP synthase subcomplexes are the hallmark of a defective intramitochondrial protein translation
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The evaluation of complex III activity using a novel in-gel activity staining method
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Detection of complex III deficient patients using a novel activity staining method in the BN-page gel
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Two novel mitochondrial DNA mutations in muscle tissue of a patient with limb-girdle myopathy
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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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Visualizing oxidative phosphorylation defects in skeletal muscle of patients with mitochondrial tRNA gene mutations using immunohistochemistry
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Chemokine profile of different inflammatory myopathies reflects humoral versus cytotoxic immune responses
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Distribution of glucocorticoid receptor alpha and beta subtypes in the idiopathic inflammatory myopathies
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A new family with the mitochondrial tRNAGLU gene mutation m.14709T > C presenting with hydrops fetalis
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Complex V subcomplexes detected by BN PAGE are a sign of a defective intramitochondrial protein translation
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Complex V subcomplexes suggestive of a defective intramitochondrial protein translation
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Complex V subcomplexes suggestive of a defective intramitochondrial protein translation.
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A novel mitochondrial tRNA Asn mutation causing multi-organ failure
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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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Potential therapeutic targets for idiopathic inflammatory myopathies
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A novel mitochondrial transfer RNA(Asn) mutation causing multiorgan failure
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Diagnostic value of immunostaining in cultured skin fibroblasts from patients with oxidative phosphorylation defects
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High dose statins and skeletal muscle metabolism in man: A randomized controlled trial.
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Immunocytochemiscal staining of cultured fibroblasts is available first line screening test for oxidative phosphorylation.
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Denaturating high performance liquid chromatography, a rapid mutation screening technique for the entire mitochondrial genome.
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High dose statins and skeletal muscle metabolism in man: A randomized controlled trial.
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Immunocytochemical staining of cultured fibroblasts is a valuable first line screening test for oxidative phosphorylation defects.
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High-dose statins and skeletal muscle metabolism in humans: A randomized, controlled trial
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Distribution of glucocorticoid receptor subtypes in inflammatory myopathy
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Localization of glucocorticoid receptor alpha and beta subtypes in inflammatory myopathy
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Alpha-chemokine receptors CXCR1-3 and their ligands in idiopathic inflammatory myopathies
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β-chemokine receptor expression in idiopathic inflammatory myopathies
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Expression and distribution of the nitric oxide synthases in idiopathic inflammatory myopathies
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Localization of the alpha-chemokine SDF-1 and its receptor CXCR4 in idiopathic inflammatory myopathies
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Localization of Th1 associated chemokines in inflammatory myopathies
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Alpha-chemokines and Th1 mediated inflammation in polymyositis and inclusion body myositis
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Localization of Th1 associated chemokines in inflammatory myopathies
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The idiopathic inflammatory myopathies
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Combination of proteomic techniques as powerful tool in the search for the underlying defect in OXPROS complex deficiencies
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CXCR4 chemokine receptor density in inflammatory myopathies
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Differential expression of chemokines in inflammatory myopathies
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Beta chemokines and their receptors in inflammatory myopathies
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Expression of MCP-1 and its receptors CCR2 and CCR4 in the inflammatory myopathies
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Immunolocalization of the chemokine CXCL12 and its receptor CXCR4 in the inflammatory myopathies
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Chemokine receptors in inflammatory myopathy
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Increased angiotensin II type-2 receptor density in hyperplasia, DCIS and invasive carcinoma of the breast is paralleled with increased iNOS expression
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- Conference Paper
- C3
- open access
Differential organ involvement in peroxisomal disorders
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Chemokines in inflammatory myopathies
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Differential expression of beta-chemokines in inflammatory myopathies
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Growth stimulatory angiotensin II type-1 receptor is upregulated in breast hyperplasia and in situ carcinoma but not in invasive carcinoma
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Distribution of type-1 and type-2 angiotensin receptors in the normal human lung and in lungs from patients with chronic obstructive pulmonary disease.
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Properties of the ventricular adrenergic signal transduction system during ontogeny of spontaneous hypertension in rats.