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- 2022
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Mark
Insights on Genetic and Environmental Factors in Parkinson's Disease from a Regional Swedish Case-Control Cohort
(
- Contribution to journal › Article
- 2019
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Mark
Low prevalence of known pathogenic mutations in dominant PD genes : A Swedish multicenter study
(
- Contribution to journal › Article
- 2016
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Mark
Wilson disease: Acute dystonia during treatment with SSRI or SNRI
2016) XXI World Congress on Parkinson's Disease and Related Disorders In Parkinsonism and Related Disorders 22(Suppl 2). p.140-141(
- Contribution to journal › Published meeting abstract
- 2012
-
Mark
First neuropathological description of a patient with Parkinson's disease and LRRK2 p.N1437H mutation.
(
- Contribution to journal › Article
- 2010
-
Mark
Hereditary Parkinson's Disease of Unknown Genetic Cause in Two Families from Southern Sweden
2010) 24th Annual Symposium on Etiology, Pathogenesis and Treatment of Parkinsons Disease and Other Movement Disorders In Movement Disorders 25(6).(
- Contribution to journal › Published meeting abstract
- 2009
-
Mark
Herman Lundborg did not describe Unverricht-Lundborg disease: hyperekplexia in a Swedish family with hereditary Parkinson's disease due to alpha-synuclein multiplications
2009) 13th Congress of the European-Federation-of-Neurological-Societies In European Journal of Neurology 16. p.153-153(
- Contribution to journal › Published meeting abstract
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Mark
Alpha-synuclein multiplications with parkinsonism, dementia or progressive myoclonus?
(
- Contribution to journal › Article
-
Mark
A Swedish family with de novo alpha-synuclein A53T mutation: Evidence for early cortical dysfunction.
(
- Contribution to journal › Article