Genealogical studies in LRRK2-associated Parkinson’s disease in central Norway
Author:
Publisher
Elsevier BV
Subject
Neurology (clinical),Geriatrics and Gerontology,Neurology
Reference26 articles.
1. A frequent LRRK2 gene mutation associated with autosomal dominant Parkinson’s disease;Di Fonzo;Lancet,2005
2. A common LRRK2 mutation in idiopathic Parkinson’s disease;Gilks;Lancet,2005
3. Genetic screening for a single common LRRK2 mutation in familial Parkinson’s disease;Nichols;Lancet,2005
4. Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson’s disease: a case-control study;Healy;Lancet Neurol,2008
5. Clinical features of LRRK2-associated Parkinson’s disease in central Norway;Aasly;Ann Neurol,2005
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1. Obituary for Jan O. Aasly (1950–2022);Movement Disorders;2022-08-25
2. Inflammatory Diseases Among Norwegian LRRK2 Mutation Carriers. A 15-Years Follow-Up of a Cohort;Frontiers in Neuroscience;2021-01-28
3. Community‐based genetic study of Parkinson's disease in Estonia;Acta Neurologica Scandinavica;2020-08-20
4. Long-Term Outcomes of Genetic Parkinson’s Disease;Journal of Movement Disorders;2020-05-31
5. Clinical and Imaging Markers of Prodromal Parkinson's Disease;Frontiers in Neurology;2020-05-08
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