scholarly journals Retinal capillary perfusion in autosomal dominant Alzheimer’s disease

2020 ◽  
Vol 16 (S4) ◽  
Author(s):  
Maxwell Singer ◽  
John M Ringman ◽  
Alice Laughlin ◽  
Zhongi Chu ◽  
Ruikang Wang ◽  
...  
Keyword(s):  
Alzheimer’S Disease ◽  
Alzheimer's Disease ◽  
Autosomal Dominant ◽  
Capillary Perfusion ◽  
Autosomal Dominant Alzheimer’S Disease ◽  
Retinal Capillary

scholarly journals [P2-372]: UTILITY OF PERFUSION PET MODELS AS MEASURES OF NEURODEGENERATION IN AN AUTOSOMAL DOMINANT ALZHEIMER's DISEASE POPULATION: REPORT FROM THE DIAN STUDY

2017 ◽  
Vol 13 (7S_Part_15) ◽  
pp. P768-P769
Author(s):  
Nelly Joseph-Mathurin ◽  
Yi Su ◽  
Tyler Blazey ◽  
Mateusz S. Jasielec ◽  
Andrei G. Vlassenko ◽  
...  
Keyword(s):  
Alzheimer’S Disease ◽  
Alzheimer's Disease ◽  
Autosomal Dominant ◽  
Autosomal Dominant Alzheimer’S Disease

O2-12-01: LYSOSOMAL DYSFUNCTION AND ALTERED TAU METABOLISM IN STEM CELL MODELS OF AUTOSOMAL DOMINANT ALZHEIMER'S DISEASE

2006 ◽  
Vol 14 (7S_Part_12) ◽  
pp. P650-P650
Author(s):  
Sidhartha Mahali ◽  
Simon Hsu ◽  
Bruno Benitez ◽  
Rita Martinez ◽  
Alison M. Goate ◽  
...  
Keyword(s):  
Alzheimer’S Disease ◽  
Alzheimer's Disease ◽  
Stem Cell ◽  
Autosomal Dominant ◽  
Cell Models ◽  
Lysosomal Dysfunction ◽  
Autosomal Dominant Alzheimer’S Disease ◽  
Stem Cell Models

scholarly journals The Clinical and Neuropathological Features of Sporadic (Late-Onset) and Genetic Forms of Alzheimer’s Disease

2021 ◽  
Vol 10 (19) ◽  
pp. 4582
Author(s):  
Tanzil Rujeedawa ◽  
Eva Carrillo Félez ◽  
Isabel C. H. Clare ◽  
Juan Fortea ◽  
Andre Strydom ◽  
...  
Keyword(s):  
Alzheimer’S Disease ◽  
Alzheimer's Disease ◽  
Down Syndrome ◽  
Autosomal Dominant ◽  
Late Onset ◽  
Prodromal Phase ◽  
Phenotypic Differences ◽  
Autosomal Dominant Alzheimer’S Disease ◽  
Neurological Features

The purpose of this review is to compare and highlight the clinical and pathological aspects of genetic versus acquired Alzheimer’s disease: Down syndrome-associated Alzheimer’s disease in (DSAD) and Autosomal Dominant Alzheimer’s disease (ADAD) are compared with the late-onset form of the disease (LOAD). DSAD and ADAD present in a younger population and are more likely to manifest with non-amnestic (such as dysexecutive function features) in the prodromal phase or neurological features (such as seizures and paralysis) especially in ADAD. The very large variety of mutations associated with ADAD explains the wider range of phenotypes. In the LOAD, age-associated comorbidities explain many of the phenotypic differences.

P4-074: ITALIAN NETWORK FOR AUTOSOMAL DOMINANT ALZHEIMER'S DISEASE AND FRONTOTEMPORAL LOBAR DEGENERATION (ITALIANDIAFN)

2014 ◽  
Vol 10 ◽  
pp. P810-P810
Author(s):  
Martina Bocchetta ◽  
Michela Pievani ◽  
Claudio Babiloni ◽  
Amalia C. Bruni ◽  
Elio Scarpini ◽  
...  
Keyword(s):  
Alzheimer’S Disease ◽  
Alzheimer's Disease ◽  
Frontotemporal Lobar Degeneration ◽  
Autosomal Dominant ◽  
Autosomal Dominant Alzheimer’S Disease
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