Search for dissertations about: "Jan Hillert"
Showing result 1 - 5 of 6 swedish dissertations containing the words Jan Hillert.
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1. Studies on T cells and cytokines in Guillain-Barré syndrome and experimental allergic neuritis
Abstract : Guillain-Barrésyndrome (GBS) is an inflammatory disease of peripheral nerves, characterised by muscle weakness. The nerves are attacked and destroyed by the immune system. The symptoms usually progress over a few weeks and many patients become severely disabled. READ MORE
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2. Genetic Studies of Alzheimer's Disease
Abstract : Patients with Alzheimer's disease (AD) often have a family history of the disease, implicating genetics as a major risk factor. Three genes are currently known to cause familial early-onset AD (65 years), only the APOE gene has repeatedly been associated to AD, where the ε4 allele increases disease risk and decreases age at onset. READ MORE
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3. Mechanisms in inflammatory demyelinating diseases of the nervous system : immunological and methodological aspects
Abstract : The diseases studied in this thesis, Guillain-Barré Syndrome (GBS), Multiple Sclerosis (MS) and Polyneuropathy associated with monoclonal gammopathy of uncertain significance (PNMGUS), are of autoimmune origin with myelin components as putative auto antigens. T cells are important for the pathogenesis, as well as the cytokine network and autoantibodies. READ MORE
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4. Functional Role of Genetic Polymorphisms Associated with Systemic Lupus Erythematosus
Abstract : Systemic lupus erythematosus (SLE) is a chronic and complex autoimmune disorder characterized by a failure in the mechanism of self-tolerance and production of autoantibodies, potentially affecting any organ in the body. The genetic factors behind the disease have been extensively studied in the past years and to date a list of more than 30 loci have been associated with SLE. READ MORE
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5. Genetic studies of stroke in Northern Sweden
Abstract : Stroke is a common disorder of later life with a complex etiology, including both environmental and genetic risk factors. The inherited predisposition is challenging to study due to the complexity of the stroke phenotype. READ MORE