Clinical and genetic studies of familial parkinsonism and tremor
- Prosjektnummer
- 911580
- Ansvarlig person
- Kristoffer Haugarvoll
- Institusjon
- Helse Bergen HF
- Prosjektkategori
- Forskerutdanning - postdoc
- Helsekategori
- Neurological
- Forskningsaktivitet
- 2. Aetiology
A woman in her 70s with chronic walking difficulties.
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Severe nigrostriatal degeneration without clinical parkinsonism in patients with polymerase gamma mutations.
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MRI characterisation of adult onset alpha-methylacyl-coA racemase deficiency diagnosed by exome sequencing.
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The role of APOE alleles in incident Parkinson's disease. The Norwegian ParkWest Study.
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A Novel Compound Heterozygous Tyrosine Hydroxylase Mutation (p.R441P) with Complex Phenotype
Journal of Parkinson's Disease, Volume 1, Number 1 / 2011
- Kristoffer Haugarvoll Prosjektleder
- Laurence Bindoff Leder av forskningsgruppe
eRapport er utarbeidet av Sølvi Lerfald og Reidar Thorstensen, Regionalt kompetansesenter for klinisk forskning, Helse Vest RHF, og videreutvikles av de fire RHF-ene i fellesskap, med støtte fra Helse Vest IKT
Alle henvendelser rettes til Faglig rapportering, Helse Vest