Search for dissertations about: "Genetic inventory"
Showing result 1 - 5 of 9 swedish dissertations containing the words Genetic inventory.
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1. Transforming and Strengthening the Links Between Industrial Design, Engineering Design and Production
Abstract : The current form-giving activity in industrial design is characterized by explorations that depend on the individual capability to mentally manipulate a solution space from which to select and express the intended result. Designers often rely on artistic experimentation, aesthetic inspiration, or product specifications. READ MORE
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2. Omega-3 fatty acid treatment in mild to moderate Alzheimer's disease : results from the OmegAD study
Abstract : Alzheimer's disease (AD) is a major public health concern in all countries with an increasing prevalence. It is expected to quadruple by the year 2047. READ MORE
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3. Distal risk factors, interpersonal functioning & family skills training in attempted suicide
Abstract : Background Suicidal behavior is an important global health problem affecting also significant others. Both genetic and environmental influences play an important role in the development of suicidal behavior. There is a need of interventions for family and friends after a suicide attempt. READ MORE
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4. Black Truffles of Sweden : Systematics, Population Studies, Ecology and Cultivation of Tuber aestivum syn. T. uncinatum
Abstract : Tuber aestivum is an ectomycorrhizal ascomycete with underground fruit bodies. It is an economically important species, but has been regarded as endangered in Sweden. My inventory has increased the number of reported localities from 3 to 31. It has long been debated whether T. READ MORE
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5. Long QT syndrome in Sweden : founder effects and associated cardiac phenotypes
Abstract : Background: We aimed to increase the knowledge regarding the familial arrhythmogenic disorder Long QT Syndrome (LQTS) and its recessive variant Jervell and Lange-Nielsen Syndrome (JLNS) in Sweden, including prevalences and clinical phenotypes. A specific focus was directed towards two KCNQ1 mutations –p.Y111C and p. READ MORE