Sökning: "Huntington disease"
Visar resultat 1 - 5 av 11 avhandlingar innehållade orden Huntington disease.
1. On neural transplantation in a rat model of Huntington’s disease : a graft survival study
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2. Molecular genetic studies on Huntington disease
Sammanfattning : Huntington disease (HD) is an autosomal dominant neurodegenerative disorder associated with an expanded trinucleotide repeat (CAG). Prior to the gene identification in 1993, linkage analysis was used for predictive testing for at-risk individuals. LÄS MER
3. Mitochondrial dysfunction and metabolic intervention
Sammanfattning : .... LÄS MER
4. Pericytes in Neurodegeneration
Sammanfattning : .... LÄS MER
5. Energy metabolism as a target for new treatment strategies in Huntington’s disease
Sammanfattning : Huntington´s disease (HD) is a fatal inherited neurodegenerative disorder caused by a CAG triplet repeat expansion in the huntingtin (HTT) gene and characterized by cognitive and motoric dysfunctions as well as psychiatric problems. Accumulating evidence, however, suggests altered energy metabolism and a hyper-catabolic state as key features of HD pathology. LÄS MER