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- 2024
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Mark
Genome-wide analyses reveal a potential role for the MAPT, MOBP, and APOE loci in sporadic frontotemporal dementia
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- Contribution to journal › Article
- 2023
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Mark
Cerebellar and subcortical atrophy contribute to psychiatric symptoms in frontotemporal dementia
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- Contribution to journal › Article
- 2018
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Mark
Reduced penetrance of the PSEN1 H163Y autosomal dominant Alzheimer mutation : A 22-year follow-up study
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- Contribution to journal › Article
- 2017
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Mark
REST suppression mediates neural conversion of adult human fibroblasts via microRNA-dependent and -independent pathways
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- Contribution to journal › Article
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Mark
The interactive effect of demographic and clinical factors on hippocampal volume : A multicohort study on 1958 cognitively normal individuals
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- Contribution to journal › Article
- 2016
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Mark
Ethical aspects of a predictive test for Huntington's Disease: A long term perspective.
(
- Contribution to journal › Article
- 2015
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Mark
DNMT3A moderates cognitive decline in subjects with mild cognitive impairment: replicated evidence from two mild cognitive impairment cohorts.
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- Contribution to journal › Article
- 2014
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Mark
Lesion of the subiculum reduces the spread of amyloid beta pathology to interconnected brain regions in a mouse model of Alzheimer's disease.
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- Contribution to journal › Article
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Mark
Frontotemporal dementia and its subtypes: a genome-wide association study.
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- Contribution to journal › Article
- 2013
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Mark
Ethical aspects of undergoing a predictive genetic testing for Huntington's disease.
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- Contribution to journal › Article
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Mark
The influence of APOE and TOMM40 polymorphisms on hippocampal volume and episodic memory in old age
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- Contribution to journal › Article
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Mark
Genetic Effects on Old-Age Cognitive Functioning: A Population-Based Study
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- Contribution to journal › Article
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Mark
The Association Between APOE epsilon 4 and Alzheimer-type Dementia Among Memory Clinic Patients is Confined to those with a Higher Education. The DESCRIPA Study
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- Contribution to journal › Article
- 2010
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Mark
The PSEN1 I143T mutation in a Swedish family with Alzheimer's disease: clinical report and quantification of A beta in different brain regions
(
- Contribution to journal › Article