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Fusiform Intracranial Aneurysms in a CADASIL Patient: A Possibly Missed Association.

作者信息

Agarwal Ayush, Mazumdar Pritam, Gupta Pranjal, Garg Ajay, Radhakrishnan Divya M, Das Animesh, Pandit Awadh K, Srivastava Achal K

机构信息

Department of Neurology, All India Institute of Medical Sciences, New Delhi, India.

Department of Neuroradiology, All India Institute of Medical Sciences, New Delhi, India.

出版信息

Ann Indian Acad Neurol. 2022 Jul-Aug;25(4):747-749. doi: 10.4103/aian.aian_903_21. Epub 2022 Sep 9.

DOI:10.4103/aian.aian_903_21
PMID:36211175
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9540923/
Abstract
摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7bad/9540923/e31817395b87/AIAN-25-747-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7bad/9540923/e1e328b64807/AIAN-25-747-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7bad/9540923/e31817395b87/AIAN-25-747-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7bad/9540923/e1e328b64807/AIAN-25-747-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7bad/9540923/e31817395b87/AIAN-25-747-g002.jpg

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Genes (Basel). 2025 Jul 26;16(8):882. doi: 10.3390/genes16080882.

本文引用的文献

1
Intracranial Large Artery Abnormalities and Association With Cerebral Small Vessel Disease in CADASIL.伴有皮质下梗死和白质脑病的常染色体显性遗传性脑动脉病中的颅内大动脉异常及其与脑小血管病的关联
Front Neurol. 2020 Aug 18;11:726. doi: 10.3389/fneur.2020.00726. eCollection 2020.
2
Cadasil.伴有皮质下梗死和白质脑病的常染色体显性遗传性脑动脉病
Lancet Neurol. 2009 Jul;8(7):643-53. doi: 10.1016/S1474-4422(09)70127-9.
3
Electrocardiogram in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy patients without any clinical evidence of coronary artery disease: a case-control study.
伴有皮质下梗死和白质脑病的常染色体显性遗传性脑动脉病患者的心电图表现:一项无冠心病临床证据的病例对照研究
Stroke. 2006 Apr;37(4):1100-2. doi: 10.1161/01.STR.0000209242.68844.20. Epub 2006 Mar 2.
4
Cerebellar arteriovenous malformation and vertebral artery aneurysm in a CADASIL patient.一名伴有大脑常染色体显性遗传性动脉病伴皮质下梗死和白质脑病(CADASIL)患者的小脑动静脉畸形和椎动脉动脉瘤
Acta Neurol Scand. 2006 Jan;113(1):62-3. doi: 10.1111/j.1600-0404.2005.00539.x.
5
Vascular anomalies in Alagille syndrome: a significant cause of morbidity and mortality.阿拉吉耶综合征中的血管异常:发病和死亡的重要原因。
Circulation. 2004 Mar 23;109(11):1354-8. doi: 10.1161/01.CIR.0000121361.01862.A4. Epub 2004 Mar 1.
6
Notch signaling in vascular development.Notch信号通路在血管发育中的作用
Arterioscler Thromb Vasc Biol. 2003 Apr 1;23(4):543-53. doi: 10.1161/01.ATV.0000060892.81529.8F. Epub 2003 Feb 13.
7
CADASIL: a common form of hereditary arteriopathy causing brain infarcts and dementia.大脑常染色体显性动脉病伴皮质下梗死和白质脑病(CADASIL):一种导致脑梗死和痴呆的常见遗传性动脉病形式。
Brain Pathol. 2002 Jul;12(3):371-84. doi: 10.1111/j.1750-3639.2002.tb00451.x.
8
The ectodomain of the Notch3 receptor accumulates within the cerebrovasculature of CADASIL patients.Notch3受体的胞外结构域在CADASIL患者的脑血管系统中蓄积。
J Clin Invest. 2000 Mar;105(5):597-605. doi: 10.1172/JCI8047.
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The phenotypic spectrum of CADASIL: clinical findings in 102 cases.伴有皮质下梗死和白质脑病的常染色体显性遗传性脑动脉病(CADASIL)的表型谱:102例临床发现
Ann Neurol. 1998 Nov;44(5):731-9. doi: 10.1002/ana.410440506.
10
Patterns of MRI lesions in CADASIL.伴有皮质下梗死和白质脑病的常染色体显性遗传性脑动脉病(CADASIL)的磁共振成像(MRI)病变模式
Neurology. 1998 Aug;51(2):452-7. doi: 10.1212/wnl.51.2.452.