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A case of 5-fluorouracil-induced peripheral neuropathy.Chemokine profile of different inflammatory myopathies reflects humoral versus cytotoxic immune responses.The effects of an intronic polymorphism in TOMM40 and APOE genotypes in sporadic inclusion body myositis.The tumor necrosis factor superfamily of cytokines in the inflammatory myopathies: potential targets for therapy.Next generation sequencing on patients with LGMD and nonspecific myopathies: Findings associated with ANO5 mutationsHow to approach the patient with muscular symptoms in the general neurological practice?Disease specificity of autoantibodies to cytosolic 5'-nucleotidase 1A in sporadic inclusion body myositis versus known autoimmune diseases.Potential therapeutic targets for idiopathic inflammatory myopathies.Clinical features of TBK1 carriers compared with C9orf72, GRN and non-mutation carriers in a Belgian cohort.The genetic basis of undiagnosed muscular dystrophies and myopathies: Results from 504 patientsRecurrent post-infectious rhabdomyolysis in muscle CPT-II deficiency caused by a novel missense mutation.Role of cytokines and chemokines in idiopathic inflammatory myopathies.TBK1 Mutation Spectrum in an Extended European Patient Cohort with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis.Cytokines and chemokines as regulators of skeletal muscle inflammation: presenting the case of Duchenne muscular dystrophy.Activation of osmolyte pathways in inflammatory myopathy and Duchenne muscular dystrophy points to osmoregulation as a contributing pathogenic mechanism.Beta-chemokine receptor expression in idiopathic inflammatory myopathies.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.Reversible orofacial dyskinesia after ofloxacin treatment.Distinct clinical characteristics of C9orf72 expansion carriers compared with GRN, MAPT, and nonmutation carriers in a Flanders-Belgian FTLD cohort.Khat chewing can cause stroke.MFN2 mutation distribution and genotype/phenotype correlation in Charcot-Marie-Tooth type 2.Giant arachnoid granulation of the posterior temporal bone wall mimicking a jugular foramen mass.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.Reversible visual deficit and Corpus callosum lesions due to metronidazole toxicity.205th ENMC International Workshop: Pathology diagnosis of idiopathic inflammatory myopathies part II 28-30 March 2014, Naarden, The Netherlands.TNF alpha receptor genotype influences smoking-induced muscle-fibre-type shift and atrophy in mice.Cytomegalovirus-induced myeloradiculopathy in an immunocompetent patient.Myopathy mimicking an acute coronary syndrome.Distribution of glucocorticoid receptor alpha and beta subtypes in the idiopathic inflammatory myopathies.Ptosis as an associated finding in maternally inherited diabetes and deafness.Forearm muscle oxygenation responses during and following arterial occlusion in patients with mitochondrial myopathy.193rd ENMC International workshop Pathology diagnosis of idiopathic inflammatory myopathies 30 November - 2 December 2012, Naarden, The Netherlands.Multiple neurological syndromes during Hodgkin lymphoma remission.A dual role for HSP90 and HSP70 in the inflammatory myopathies: from muscle fiber protection to active invasion by macrophages.Distribution of the NF-kappaB complex in the inflammatory exudates characterizing the idiopathic inflammatory myopathies.The nonnecrotic invaded muscle fibers of polymyositis and sporadic inclusion body myositis: on the interplay of chemokines and stress proteins.Targeted Next-Generation Sequencing Reveals Novel TTN Mutations Causing Recessive Distal Titinopathy.Upregulation of chemokines and their receptors in Duchenne muscular dystrophy: potential for attenuation of myofiber necrosis.Neurological involvement in Erdheim-Chester disease.Forearm deoxyhemoglobin and deoxymyoglobin (deoxy[Hb + Mb]) measured by near-infrared spectroscopy (NIRS) using a handgrip test in mitochondrial myopathy.
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description
hulumtues
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հետազոտող
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Jan L De Bleecker
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Jan L De Bleecker
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Jan L De Bleecker
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Jan L De Bleecker
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Jan L De Bleecker
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Jan L De Bleecker
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Jan L De Bleecker
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Jan L De Bleecker
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Jan L De Bleecker
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Jan De Bleecker
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Jan L De Bleecker
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Jan L De Bleecker
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Jan L De Bleecker
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Jan L De Bleecker
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Jan L De Bleecker
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P21
P31
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0000-0002-1328-1812