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- 2020
-
Mark
Plasma neurofilament light protein correlates with diffusion tensor imaging metrics in frontotemporal dementia
(
- Contribution to journal › Article
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Mark
Mendelian randomization implies no direct causal association between leukocyte telomere length and amyotrophic lateral sclerosis
(
- Contribution to journal › Article
- 2019
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Mark
Swedish Version of the Hayling Test : Clinical Utility in Frontotemporal Dementia Syndromes
(
- Contribution to journal › Article
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Mark
Genetic variation across RNA metabolism and cell death gene networks is implicated in the semantic variant of primary progressive aphasia
(
- Contribution to journal › Article
-
Mark
CSF placental growth factor – a novel candidate biomarker of frontotemporal dementia
(
- Contribution to journal › Article
- 2018
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Mark
Slowly progressive dementia caused by MAPT R406W mutations : Longitudinal report on a new kindred and systematic review
(
- Contribution to journal › Article
- 2014
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Mark
Age-related incidence and family history in frontotemporal dementia: data from the Swedish dementia registry.
(
- Contribution to journal › Article
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Mark
A Swedish version of the Hayling Test – clinical validity in patients with a FTD complex disorder
2014) 9th International Conference on Frontotemporal Dementias 2014 In American Journal of Neurodegenerative Disease 3(Supplementary Issues 1). p.77-77(
- Contribution to journal › Published meeting abstract
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Mark
Frontotemporal dementia and its subtypes: a genome-wide association study.
(
- Contribution to journal › Article
- 2012
-
Mark
Diagnosis of frontotemporal dementia in Sweden. Data from the Swedish Dementia Registry.
2012) International Conference on Frontotemporal Dementias, 2012(
- Contribution to conference › Abstract
- 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
A Swedish family with de novo alpha-synuclein A53T mutation: Evidence for early cortical dysfunction.
(
- Contribution to journal › Article
-
Mark
Reduced CSF CART in dementia with Lewy bodies.
(
- Contribution to journal › Article