Articles with "familial d678h" as a keyword



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Amyloid PET pattern with dementia and amyloid angiopathy in Taiwan familial AD with D678H APP mutation

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Published in 2019 at "Journal of the Neurological Sciences"

DOI: 10.1016/j.jns.2018.12.039

Abstract: INTRODUCTION The novel D678H amyloid precursor protein (APP) gene mutation has been called the "Taiwan mutation". The study aims to identify amyloid deposition patterns and clinical features associated with this mutation. METHODS we analyzed the… read more here.

Keywords: amyloid angiopathy; amyloid; familial d678h; amyloid pet ... See more keywords