Oculoleptomeningeal amyloidosis in 3 individuals with the transthyretin variant Tyr69His
Author:
Publisher
Elsevier BV
Subject
Ophthalmology,General Medicine
Reference9 articles.
1. Massive leptomeningeal amyloidosis associated with a Val30Met transthyretin gene;Herrick;Neurology,1996
2. Familial oculoleptomeningeal amyloidosis. Report of a new family with unusual features;Uitti;Arch Neurol,1988
3. Oculoleptomeningeal amyloidosis in a large kindred with a new transthyretin variant Tyr69His;Blevins;Neurology,2003
4. Familial oculo-leptomeningeal amyloidosis associated with primary angiitis of the CNS;Dowell;Neurology,2007
5. Oculoleptomeningeal amyloidosis associated with a new trans-thyretin variant Ser64;Uemichi;Arch Neurol,1999
Cited by 21 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. 転倒発作と反復する一過性の言語障害を呈したY69H (p.Y89H)変異型遺伝性トランスサイレチン髄膜アミロイドーシスの1例;Rinsho Shinkeigaku;2023
2. Vitreous amyloidosis caused by a Lys55Asn variant in transthyretin: A case report;World Journal of Clinical Cases;2022-11-16
3. Distribution and progression of cerebral amyloid angiopathy in early-onset V30M (p.V50M) hereditary ATTR amyloidosis;Amyloid;2022-09-30
4. CSF/plasma levels, transthyretin stabilisation and safety of multiple doses of tolcapone in subjects with hereditary ATTR amyloidosis;Amyloid;2022-03-30
5. Current Review of Leptomeningeal Amyloidosis Associated With Transthyretin Mutations;The Neurologist;2021-09
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