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- 2011
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Mark
Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case-control study
(
- Contribution to journal › Article
- 2010
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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
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Mark
Presentation, Diagnosis, and Management of Multiple System Atrophy in Europe: Final Analysis of the European Multiple System Atrophy Registry
(
- Contribution to journal › Article
- 2009
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Mark
Alpha-synuclein multiplications with parkinsonism, dementia or progressive myoclonus?
(
- Contribution to journal › Article
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Mark
A 76-year-old man with cognitive and neurological symptoms
(
- Contribution to journal › Article
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Mark
Reduced CSF CART in dementia with Lewy bodies.
(
- Contribution to journal › Article
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Mark
A Swedish family with de novo alpha-synuclein A53T mutation: Evidence for early cortical dysfunction.
(
- Contribution to journal › Article
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Mark
ABC om demenssjukdomar
(
- Contribution to journal › Article
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Mark
Multidisciplinärt fokus på kognitiv svikt och demens.
(
- Contribution to journal › Article
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Mark
Frontotemporal demens heterogen sjukdomsgrupp.
(
- Contribution to journal › Article