Cerebrospinal Fluid Biomarkers in Alzheimer’s Disease Families with PSEN1 Mutations
Author:
Publisher
S. Karger AG
Subject
Neurology (clinical),Neurology
Reference27 articles.
1. Clinicopathological features of familial Alzheimer's disease associated with the M139V mutation in the presenilin 1 gene. Pedigree but not mutation specific age at onset provides evidence for a further genetic factor
2. Neuropathology of older persons without cognitive impairment from two community-based studies
3. Cerebrospinal fluid biomarker signature in Alzheimer's disease neuroimaging initiative subjects
4. CSF Biomarkers and Incipient Alzheimer Disease in Patients With Mild Cognitive Impairment
5. Cerebrospinal Fluid Biomarkers and Rate of Cognitive Decline in Very Mild Dementia of the Alzheimer Type
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1. Serum neurofilament light levels correlate with severity measures and neurodegeneration markers in autosomal dominant Alzheimer’s disease;Alzheimer's Research & Therapy;2018-11-03
2. Findings from the Swedish Study on Familial Alzheimer’s Disease Including the APP Swedish Double Mutation;Journal of Alzheimer's Disease;2018-06-12
3. Findings from the Swedish Study on Familial Alzheimer's Disease Including the APP Swedish Double Mutation;ADV ALZH DIS;2018
4. Cerebrospinal fluid Presenilin-1 increases at asymptomatic stage in genetically determined Alzheimer’s disease;Molecular Neurodegeneration;2016-09-29
5. Changes in the plasma proteome at asymptomatic and symptomatic stages of autosomal dominant Alzheimer’s disease;Scientific Reports;2016-07-06
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