Search for dissertations about: "Amyotrophic lateral sclerosis"
Showing result 1 - 5 of 85 swedish dissertations containing the words Amyotrophic lateral sclerosis.
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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. Neurodegeneration in amyotrophic lateral sclerosis : neurotrophic factors and monoamine oxidase B
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3. Autoantibodies in amyotrophic lateral sclerosis
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4. Transmethylation, Polyamines and Apoptosis in Amyotrophic Lateral Sclerosis
Abstract : Amyotrophic lateral sclerosis (ALS) is a relentlessly progressive disorder characterized by degeneration of motor neurons in the cortex, brainstem and spinal cord. The patients usually die within 3-5 years after onset. The full etiology of ALS is unknown and many hypotheses have been proposed to explain the neurodegeneration. READ MORE
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5. 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