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Familial primary amyloidosis with severe amyloid heart disease.伴有严重淀粉样心脏病的家族性原发性淀粉样变性
Am J Med. 1962 Sep;33:328-48. doi: 10.1016/0002-9343(62)90230-9.
2
Primary systemic amyloidosis: a review and an experimental, genetic, and clinical study of 29 cases with particular emphasis on the familial form.原发性系统性淀粉样变性:一项综述及对29例病例的实验、遗传和临床研究,特别关注家族性形式。
Medicine (Baltimore). 1956 Sep;35(3):239-334.
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Ocular manifestations of hereditary primary systemic amyloidosis.遗传性原发性系统性淀粉样变性的眼部表现。
AMA Arch Ophthalmol. 1955 Nov;54(5):660-4. doi: 10.1001/archopht.1955.00930020666004.
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A peculiar form of peripheral neuropathy; familiar atypical generalized amyloidosis with special involvement of the peripheral nerves.一种特殊形式的周围神经病变;家族性非典型全身性淀粉样变性,周围神经有特殊受累情况。
Brain. 1952 Sep;75(3):408-27. doi: 10.1093/brain/75.3.408.
5
Meningocerebrovascular amyloidosis associated with a novel transthyretin mis-sense mutation at codon 18 (TTRD 18G).与第18密码子处新型转甲状腺素蛋白错义突变(TTR D18G)相关的脑膜脑血管淀粉样变性
Am J Pathol. 1996 Feb;148(2):361-6.
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Type I familial amyloid polyneuropathy and pontine haemorrhage.I型家族性淀粉样多神经病与桥脑出血。
Acta Neuropathol. 1993;86(5):542-5. doi: 10.1007/BF00228595.
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Familial oculoleptomeningeal amyloidosis.
Brain. 1980 Sep;103(3):473-95. doi: 10.1093/brain/103.3.473.
8
Polymorphism of human plasma thyroxine binding prealbumin.人血浆甲状腺素结合前白蛋白的多态性
Biochem Biophys Res Commun. 1983 Jul 29;114(2):657-62. doi: 10.1016/0006-291x(83)90831-8.
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Familial amyloidosis. A histopathological study.家族性淀粉样变性。一项组织病理学研究。
Acta Pathol Jpn. 1984 Mar;34(2):335-44. doi: 10.1111/j.1440-1827.1984.tb07561.x.
10
Unusual cause of vitreous opacities. Primary familial amyloidosis.玻璃体混浊的罕见病因。原发性家族性淀粉样变性。
Ophthalmologica. 1971;162(3):173-7. doi: 10.1159/000306260.

Leptomeningeal amyloid and variant transthyretins.

作者信息

Benson M D

机构信息

Department of Medicine, Indiana University School of Medicine, Indianapolis, USA.

出版信息

Am J Pathol. 1996 Feb;148(2):351-4.

PMID:8579096
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1861679/
Abstract
摘要