• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利：CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法，用中文像聊天一样搜索，搜遍4000万医学文献。AI智能推荐，让科研检索更轻松。

立即免费搜索

文件翻译

保留排版，准确专业，支持PDF/Word/PPT等文件格式，支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述，25分钟生成高质量综述，智能提取关键信息，辅助科研写作。

立即免费体验

基底动脉动脉瘤与安德森-法布里病

Basilar artery aneurysm and Anderson-Fabry disease.

作者信息

Maisey D N, Cosh J A

出版信息

J Neurol Neurosurg Psychiatry. 1980 Jan;43(1):85-7. doi: 10.1136/jnnp.43.1.85.

DOI:10.1136/jnnp.43.1.85
PMID:6766499
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC490469/
Abstract

A case of basilar artery aneurysm is described. The patient had a family history of similar aneurysms and also of a rare spingolipidosis, Anderson-Fabry disease.

摘要

本文描述了一例基底动脉动脉瘤病例。该患者有类似动脉瘤的家族病史，同时还有一种罕见的鞘脂沉积病——安德森-法布里病。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1c6a/490469/5bc7188e2d62/jnnpsyc00069-0094-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1c6a/490469/5bc7188e2d62/jnnpsyc00069-0094-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1c6a/490469/5bc7188e2d62/jnnpsyc00069-0094-a.jpg

相似文献

1
Basilar artery aneurysm and Anderson-Fabry disease.基底动脉动脉瘤与安德森-法布里病
J Neurol Neurosurg Psychiatry. 1980 Jan;43(1):85-7. doi: 10.1136/jnnp.43.1.85.
2
[Biochemical diagnosis of Anderson-Fabry disease in two brothers].[两兄弟中安德森-法布里病的生化诊断]
Vopr Med Khim. 1986 Sep-Oct;32(5):120-3.
3
Specificities of the two genetically distinct beta-galactosidases in human sphingolipidoses.人类鞘脂贮积症中两种基因不同的β-半乳糖苷酶的特异性
Arch Biochem Biophys. 1976 Jul;175(1):332-40. doi: 10.1016/0003-9861(76)90515-4.
4
The biochemistry of sphingolipid storage diseases.鞘脂贮积病的生物化学
Angew Chem Int Ed Engl. 1977 May;16(5):273-85. doi: 10.1002/anie.197702733.
5
[The first diagnosis of Farber's disease in Finland].[芬兰首例法伯病诊断]
Duodecim. 2000;116(15):1555-60.
6
[Vertebro-basilar aneurysms, with special reference to the transpharyngeal approach to basilar artery aneurysm].[椎基底动脉瘤，特别提及经咽入路治疗基底动脉动脉瘤]
No To Shinkei. 1966 Dec;18(12):1197-203.
7
[Fenestrated basilar artery with ruptured cerebral aneurysms: case report].[伴有破裂脑动脉瘤的开窗型基底动脉：病例报告]
No Shinkei Geka. 1990 Dec;18(12):1129-33.
8
Endovascular treatment of basilar aneurysms.基底动脉瘤的血管内治疗
Neurosurg Clin N Am. 2014 Jul;25(3):485-95. doi: 10.1016/j.nec.2014.04.007.
9
Horizontal deployment of an intracranial stent via an antegrade approach for coil embolization of a basilar apex aneurysm: technical note.经顺行途径横向放置颅内支架辅助基底尖动脉瘤线圈栓塞治疗：技术说明。
J Neurointerv Surg. 2011 Dec 1;3(4):355-7. doi: 10.1136/jnis.2010.004481. Epub 2011 Feb 23.
10
[The pneumographic syndrome of basilar aneurysm].[基底动脉瘤的气脑造影综合征]
Rev Otoneuroophtalmol. 1962 Jan-Feb;34:42-5.

引用本文的文献

1
Hemorrhagic Cerebrovascular Pathology in the Pediatric Population.儿科人群中的出血性脑血管病变
Front Neurol. 2020 Sep 17;11:1055. doi: 10.3389/fneur.2020.01055. eCollection 2020.
2
Basilar Artery Changes in Fabry Disease.法布里病的基底动脉变化
AJNR Am J Neuroradiol. 2017 Mar;38(3):531-536. doi: 10.3174/ajnr.A5069. Epub 2017 Jan 26.
3
Embolic Strokes of Unknown Source and Cryptogenic Stroke: Implications in Clinical Practice.不明来源的栓塞性卒中与隐源性卒中：对临床实践的启示

本文引用的文献

1
ANGIOKERATOMA CORPORIS DIFFUSUM (FABRY'S DISEASE).弥漫性躯体血管角质瘤（法布里病）
Arch Dermatol. 1965 Mar;91:206-18.
2
FABRY'S DISEASE: CLASSIFICATION AS A SPHINGOLIPIDOSIS AND PARTIAL CHARACTERIZATION OF A NOVEL GLYCOLIPID.法布里病：作为一种鞘脂贮积症的分类及一种新型糖脂的部分特性
J Biol Chem. 1963 Sep;238:3148-50.
3
THE NEUROPATHOLOGY OF HEREDITARY DYSTOPIC LIPIDOSIS.遗传性异位脂质沉积症的神经病理学
Front Neurol. 2016 Mar 21;7:37. doi: 10.3389/fneur.2016.00037. eCollection 2016.
4
Unusual case of subarachnoid haemorrhage in patient with Fabry's disease: case report and literature review.法布里病患者发生蛛网膜下腔出血的罕见病例：病例报告及文献综述
BMJ Case Rep. 2012 Jul 3;2012:bcr0220125727. doi: 10.1136/bcr.02.2012.5727.
5
Association of "top of the basilar" syndrome with megadolichobasilar artery. Clinical and neuroimaging evaluation.基底动脉尖综合征与巨大延长型基底动脉的关联。临床及神经影像学评估。
Ital J Neurol Sci. 1991 Apr;12(2):169-73. doi: 10.1007/BF02337029.
6
Clinical signs associated with megadolichobasilar artery anomaly.与巨长基底动脉异常相关的临床体征。
Neurosurg Rev. 1991;14(4):303-7. doi: 10.1007/BF00383269.
Arch Neurol. 1963 Oct;9:373-85. doi: 10.1001/archneur.1963.00460100061007.
4
Angiokeratoma corporis diffusum. A clinical study of eight affected families.弥漫性躯体血管角质瘤。对八个患病家族的临床研究。
Q J Med. 1962 Apr;31:177-206.
5
The renal lesion in angiokeratoma corporis diffusum.弥漫性躯体血管角化瘤中的肾脏病变。
Br Med J. 1958 May 31;1(5082):1266-8. doi: 10.1136/bmj.1.5082.1266.
6
Angiokeratoma corporis diffusum.弥漫性躯体血管角皮瘤
AMA Arch Derm Syphilol. 1953 Jul;68(1):21-7. doi: 10.1001/archderm.1953.01540070024003.
7
Enzymatic defect in Fabry's disease. Ceramidetrihexosidase deficiency.法布里病的酶缺陷。神经酰胺三己糖苷酶缺乏症。
N Engl J Med. 1967 May 25;276(21):1163-7. doi: 10.1056/NEJM196705252762101.
8
Angiokeratoma corporis diffusum universale (Fabry's disease) in female subjects.女性全身性弥漫性体部血管角质瘤（法布里病）
Am J Med. 1967 Feb;42(2):293-301. doi: 10.1016/0002-9343(67)90027-7.
9
On the pathology of angiokeratoma corporis diffusum (Fabry).弥漫性躯体血管角质瘤（法布里病）的病理学
Acta Pathol Microbiol Scand. 1966;68(3):313-31. doi: 10.1111/apm.1966.68.3.313.
10
Fabry's disease (angiokeratoma corporis diffusum). A report of 5 cases with pain in the extremities as the chief symptom.法布里病（弥漫性躯体血管角质瘤）。5例以肢体疼痛为主要症状的报告。
Pathol Eur. 1968;3(2):377-88.