Global ETD Search

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Showing 1 to 3 of 3 for “"sporadic Parkinson’s disease"”.

  1. A clinical and molecular genetic study into familial and sporadic Parkinson’s Disease

    Parkinson’s disease (PD) is a neurodegenerative disease which causes tremor, muscular rigidity and bradykinesia (slowness of initiation of voluntary movement with progressive reduction in speed and amplitude of repetitive actions). Although the underlying causes remain unknown, there is evidence …

    birmingham Repository record for A clinical and molecular genetic study into familial and sporadic Parkinson’s Disease (opens in a new tab)

  2. Functional study of ubiquitin C-terminal hydrolase-L1 gene promoter haplotypes

    … Alzheimer’s, Huntington’s and particularly Parkinson’s disease.<br/>The main and unique objective of this study was to identify any common Caucasian sequence variants in UCH-L1’s promoter, and to investigate whether they are associated with neurodegenerative symptoms, and any change in …

    soton Repository record for Functional study of ubiquitin C-terminal hydrolase-L1 gene promoter haplotypes (opens in a new tab)

  3. Systems Genetics and Systems Biology Analysis of Paraquat Effects in BXD Recombinant Inbred Mice

    … effects on humans, including increased risk for sporadic Parkinson’s disease (sPD). The etiology of sPD is unclear and the most accepted hypothesis states it is the result of the interaction between environmental factors and genetic susceptibility. Increasing evidence led us to infer a …

    tenn-hsc Repository record for Systems Genetics and Systems Biology Analysis of Paraquat Effects in BXD Recombinant Inbred Mice (opens in a new tab)