Search for dissertations about: "Amyotrophic lateral sclerosis ALS"
Showing result 1 - 5 of 67 swedish dissertations containing the words Amyotrophic lateral sclerosis ALS.
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1. Superoxide dismutase 1 and amyotrophic lateral sclerosis
Abstract : Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disease affecting motor neurons in the spinal cord, brain stem and motor cortex, leading to paralysis, respiratory failure and death. In about 5% of ALS cases, the disease is associated with mutations in the CuZn-superoxide dismutase (hSOD1) gene. READ MORE
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2. Extraocular Muscles in Amyotrophic Lateral Sclerosis
Abstract : Amyotrophic lateral sclerosis (ALS) is an incurable neurodegenerative disease of motor neurons characterized by muscle paralysis and death within 3-5 years of onset. However, due to unknown mechanisms, the extraocular muscles (EOMs) remain remarkably unaffected. READ MORE
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3. Of mice and men : SOD1 associated human amyotrophic lateral sclerosis and transgenic mouse models
Abstract : Amyotrophic lateral sclerosis, ALS, is a progressive fatal neurodegenerative disorder affecting motor neurones in motor cortex, brain stem and spinal cord. This inevitably leads to paralysis, respiratory failure and death. READ MORE
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4. On the aetiology of ALS : a comprehensive genetic study
Abstract : Introduction: Amyotrophic lateral sclerosis (ALS) is a deadly, progressive neuromuscular disease that affects individuals all over the world. About 10% of the patients have a familial predisposition (FALS) while the remainder of cases are isolated or sporadic (SALS) and of unknown cause. READ MORE
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5. Amyotrophic Lateral Sclerosis – A Study in Transgenic Mice
Abstract : Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease with an incidence of 1.5-2.7/100000 people/year. Today there is no cure for the disease and only symptomatic treatments are available. READ MORE