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Phenotypic spectrum in myopathies with tubular aggregates
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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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Immunohistochemical analysis of the oxidative phosphorylation complexes in skeletal muscle from patients with mitochondrial DNA encoded tRNA gene defects
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Distribution of glucocorticoid receptor alpha and beta subtypes in the idiopathic inflammatory myopathies
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Mitochondrial mosaics in the liver of patients with Pearson and Alpers-Huttenlocher syndromes
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Linezolid-induced inhibition of mitochondrial protein synthesis
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A Belgian ancestral haplotype harbours a highly prevalent mutation for 17q21-linked tau-negative FTLD
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Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21
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Alpha-chemokine receptors CXCR1-3 and their ligands 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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Mutant small heat-shock protein 27 causes axonal Charcot-Marie-Tooth disease and distal hereditary motor neuropathy
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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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Case-control study of environmental risk factors for Parkinson's disease in Belgium
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Recessive POLG mutations presenting with sensory and ataxic neuropathy in compound heterozygote patients with progressive external ophthalmoplegia
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Mutated POLG associated with progressive external ophtalmoplegia characterised by multiple mtDNA deletions
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Cerebral amyloid angiopathy is a pathogenic lesion in Alzheimer's disease due to a novel presenilin 1 mutation
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Gly341Arg mutation indicating malignant hyperthermia susceptibility: specific cause of chronically elevated serum creatine kinase activity
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An image analysis study of vastus lateralis muscle fibers in malignant hyperthermia susceptible patients
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Prenatal diagnosis of a constitutional interstitial deletion of chromosome 5 (q15q31.1) presenting with features of congenital contractural arachnodactyly.
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Neurological disorders in members of families with Leber's hereditary optic neuropathy (LHON) caused by different mitochondrial mutations.
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BECKER-TYPE MUSCULAR-DYSTROPHY - REPORT OF A FAMILY WITH ONE POSTMORTEM STUDY.
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Cardiac involvement in juvenile ceroid lipofuscinosis of the Spielmeyer-Vogt-Sjogren type: prospective noninvasive findings in 2 siblings