Search for dissertations about: "hereditary inclusion-body myopathy"
Found 3 swedish dissertations containing the words hereditary inclusion-body myopathy.
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1. Neuromuscular disorders in childhood. Epidemiology and characterization of a new myopathy
Abstract : Neuromuscular disorders can be subdivided into anterior horn cell disorders, neuropathies, myasthenic disorders and myopathies. Some multisystem disorders, such as myotonic dystrophy and mitochondrial encephalomyopathies, are traditionally also included. READ MORE
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2. Myosin myopathy. A new disease entity
Abstract : By the discovery and characterization of two familial myopathies caused by mutations in myosin heavy chaingenes, we introduce a new entity within the field of neuromuscular disorders: Myosin myopathyThe first myopathy affected a family in western Sweden. Previous linkage analysis had located the gene tochromosome 17p13. READ MORE
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3. Welander distal myopathy : clinical and genetic studies
Abstract : Distal myopathies are a group of muscular disorders described in many countries with different inheritance patterns and variable progression rates. Welander distal myopathy (WDM) is characterised by autosomal dominant inheritance, late onset and distal distribution of muscular weakness. Most cases originate from the middle parts of Sweden. READ MORE