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- 2013
-
Mark
Population-specific Frequencies for LRRK2 Susceptibility Variants in the Genetic Epidemiology of Parkinson's Disease (GEO-PD) Consortium
(
- Contribution to journal › Article
-
Mark
The natural history of multiple system atrophy: a prospective European cohort study
(
- Contribution to journal › Article
- 2012
-
Mark
Factitious disorder by proxy in the diagnosis of frontotemporal dementia
2012) International Conference on Frontotemporal Dementias, 2012 In Dementia and Geriatric Cognitive Disorders 33(Supplement 1). p.209-209(
- Contribution to journal › Published meeting abstract
-
Mark
First neuropathological description of a patient with Parkinson's disease and LRRK2 p.N1437H mutation.
(
- Contribution to journal › Article
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Mark
Diagnosis of frontotemporal dementia in Sweden. Data from the Swedish Dementia Registry.
2012) International Conference on Frontotemporal Dementias, 2012(
- Contribution to conference › Abstract
- 2011
-
Mark
Independent and Joint Effects of the MAPT and SNCA Genes in Parkinson Disease
(
- Contribution to journal › Article
-
Mark
Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case-control study
(
- 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
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