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Literature DB >> 31257920

A case of cerebral amyloid angiopathy-type hereditary ATTR amyloidosis with Y69H (p.Y89H) variant displaying transient focal neurological episodes as the main symptom.

Yumi Yamada¹, Takao Fukushima¹, Satoshi Kodama², Hiroshi Shimizu³, Akiyoshi Kakita³, Kunihiko Makino¹, Yoshiki Sekijima².

Abstract

Entities: Disease Gene Mutation

Mesh：

Substances：

Year: 2019 PMID： 31257920 DOI： 10.1080/13506129.2019.1632829

Source DB: PubMed Journal: Amyloid ISSN： 1350-6129 Impact factor: 7.141

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1 in total

1. Cerebellar and Cerebral Amyloid Visualized by [¹⁸F]flutemetamol PET in Long-Term Hereditary V30M (p.V50M) Transthyretin Amyloidosis Survivors.

Authors: Erica Irene Uneus; Christer Wilhelmsson; David Bäckström; Intissar Anan; Jonas Wixner; Björn Pilebro; Katrine Riklund; Mattias Ögren; Margareta Ögreen; Jan Axelsson; Ole B Suhr; Torbjörn Sundström
Journal: Front Neurol Date: 2022-03-04 Impact factor: 4.003

1 in total

A case of cerebral amyloid angiopathy-type hereditary ATTR amyloidosis with Y69H (p.Y89H) variant displaying transient focal neurological episodes as the main symptom.

1. Cerebellar and Cerebral Amyloid Visualized by [18F]flutemetamol PET in Long-Term Hereditary V30M (p.V50M) Transthyretin Amyloidosis Survivors.

1. Cerebellar and Cerebral Amyloid Visualized by [¹⁸F]flutemetamol PET in Long-Term Hereditary V30M (p.V50M) Transthyretin Amyloidosis Survivors.