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- 2012
-
Mark
Kognitiv medicin
(
- Contribution to specialist publication or newspaper › Specialist publication article
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Mark
Creation of an Open-Access, Mutation-Defined Fibroblast Resource for Neurological Disease Research
(
- Contribution to journal › Article
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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
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
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Mark
A Novel Blood Test for the Early Detection of Alzheimer's Disease
(
- Contribution to journal › Article
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Mark
Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case-control study
(
- Contribution to journal › Article
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Mark
Morphometric analysis of subcortical structures in progressive supranuclear palsy: In vivo evidence of neostriatal and mesencephalic atrophy
(
- Contribution to journal › Article
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Mark
Selective frontal neurodegeneration of the inferior fronto-occipital fasciculus in progressive supranuclear palsy (PSP) demonstrated by diffusion tensor tractography
(
- 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