LRRK2 mutations are not common in Alzheimer's disease

This publication has 23 references indexed in Scilit:

• Clinical features of LRRK2‐associated Parkinson's disease in central Norway
  Annals of Neurology, 2005
• Identification of a Novel LRRK2 Mutation Linked to Autosomal Dominant Parkinsonism: Evidence of a Common Founder across European Populations
  American Journal of Human Genetics, 2005
• A frequent LRRK2 gene mutation associated with autosomal dominant Parkinson's disease
  The Lancet, 2005
• Mixed Dementia
  JAMA, 2004
• Neurodegenerative diseases: a decade of discoveries paves the way for therapeutic breakthroughs
  Nature Medicine, 2004
• Dementia with Lewy bodies
  The Lancet Neurology, 2004
• Research evaluation and diagnosis of probable Alzheimer’s disease over the last two decades: I
  Neurology, 2000
• THE CLOCK DRAWING TEST FOR DEMENTIA OF THE ALZHEIMER'S TYPE: A COMPARISON OF THREE SCORING METHODS IN A MEMORY DISORDERS CLINIC
  International Journal of Geriatric Psychiatry, 1997
• Gene Dose of Apolipoprotein E Type 4 Allele and the Risk of Alzheimer's Disease in Late Onset Families
  Science, 1993
• The Informant Questionnaire on Cognitive Decline in the Elderly (IQCODE): socio-demographic correlates, reliability, validity and some norms
  Psychological Medicine, 1989