- Anesthetic management of a patient with CADASIL syndrome: A case report
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Chon JY, Lee JY
- KMID: 2169150
- Anesth Pain Med.
- 2012 Jan;7(1):59-62.
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is a rare but the most common genetic cause of ischemic strokes. Very little is known about perioperative implications of... -
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- Amyotrophic Lateral Sclerosis Associated With CADASIL
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Lee J, Jang HJ, Kwon B, Lim YM, Kim KK
- KMID: 2184760
- J Korean Neurol Assoc.
- 2013 Aug;31(3):209-210.
No abstract available. -
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- A Case of CADASIL (Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy) Diagnosed by Skin Biopsy
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Rho NK, Choi SJ, Lee ES
- KMID: 2303098
- Korean J Dermatol.
- 2002 Sep;40(9):1136-1138.
CADASIL(cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy) is a rare genetic disease inherited in an autosomal dominant manner, which is characterized by migraine, strokes, mood disorders, and progressive... -
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- Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy: A Genetic Cause of Cerebral Small Vessel Disease
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Choi JC
- KMID: 2135475
- J Clin Neurol.
- 2010 Mar;6(1):1-9.
- doi: 10.3988/jcn.2010.6.1.1
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is a single-gene disorder of the cerebral small blood vessels caused by mutations in the Notch3 gene. The exact prevalence... -
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- Topographical Distribution of Lacunes and Cerebral Microbleeds in CADASIL Affected by Hypertension
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Lee JS, Oh JH, Song SK, Choi JC, Kang SY, Kang JH
- KMID: 2443075
- Dement Neurocogn Disord.
- 2014 Dec;13(4):112-116.
- doi: 10.12779/dnd.2014.13.4.112
BACKGROUND: Cerebral autosomal-dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is an inherited small vessel disease caused by mutations in the Notch3 gene. Lacunes may reflect occlusive type microangiopathy. However,... -
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- The Association Between Hypertension and Cerebral Microbleeds in Patients With CADASIL
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Lee JS, Park SW, Song SK, Choi JC, Kang SY, Kang JH
- KMID: 2191158
- J Korean Neurol Assoc.
- 2014 May;32(2):82-87.
BACKGROUND: Cerebral autosomal-dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is an inherited microangiopathy that is caused by mutations in the Notch3 gene. Typical findings from magnetic resonance imaging (MRI)... -
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- Prosopometamorphopsia and Visual Field Defect Improved by Valproic acid in a CADASIL Patient
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Hwangbo J, Cho JW, Jung SH, Shin JH, Jung NY
- KMID: 2464140
- J Korean Neurol Assoc.
- 2019 Nov;37(4):368-371.
- doi: 10.17340/jkna.2019.4.5
Persistent aura without infarction is defined as an aura persisting for 1 week or more without evidence of infarction on neuroimaging. It is difficult to differentiate persistent visual aura without... -
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- Clinical and MRI Profiles Predicting Clinical Overt Stroke in Patients with CADASIL
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Lee JS, Choi JC, Kang SY, Song SK, Kang JH, Song JK, Na HR
- KMID: 1966503
- J Korean Neurol Assoc.
- 2012 May;30(2):93-99.
BACKGROUND: Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is an inherited arteriopathy caused by mutation in the Notch 3 gene. Cognitive impairment, which is the second most... -
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- Clinical Characteristics of Cerebral Autosomal-Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy Patients with R544C Mutation Aged 90 or Older
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Ko K, Lee J
- KMID: 2449293
- J Korean Neurol Assoc.
- 2019 Feb;37(1):55-58.
- doi: 10.17340/jkna.2019.1.9
Cerebral autosomal-dominant arteriopathy with subcortical infarcts and leukoencephalopathy is an inherited small vessel diseases caused by mutations in the Notch3 gene. In Caucasian patients, the average life expectancy was 65... -
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- Phenotypic Features of Cerebral Autosomal-Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy Subjects with R544C Mutation
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Lee JS, Ko K, Oh JH, Park JH, Lee HK
- KMID: 2442866
- Dement Neurocogn Disord.
- 2016 Mar;15(1):15-19.
- doi: 10.12779/dnd.2016.15.1.15
BACKGROUND AND PURPOSE: Cerebral autosomal-dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is the most-common single gene disorder of cerebral small vessel disease. There is no definite evidence of genotype-phenotype... -
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- Possible Role of a Missense Mutation of p.P167S on NOTCH3 Gene Associated with Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy
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Choi BW, Park S, Kim HJ
- KMID: 2442856
- Dement Neurocogn Disord.
- 2016 Jun;15(2):52-54.
- doi: 10.12779/dnd.2016.15.2.52
BACKGROUND: Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is a single-gene disorder caused by mutations in the NOTCH3 gene, located on chromosome 19p13. NOTCH3 encodes a transmembrane... -
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- Effects of Lacunar Infarctions on Cognitive Impairment in Patients with Cerebral Autosomal-Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy
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Lee JS, Choi JC, Kang SY, Kang JH, Na HR, Park JK
- KMID: 2179006
- J Clin Neurol.
- 2011 Dec;7(4):210-214.
- doi: 10.3988/jcn.2011.7.4.210
BACKGROUND AND PURPOSE: Cerebral autosomal-dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is an inherited microangiopathy caused by mutations in the Notch3 gene. Although previous studies have shown an association... -
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- Small Vessel Disease and Subcortical Vascular Dementia
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Kalaria RN, Erkinjuntti T
- KMID: 2287698
- J Clin Neurol.
- 2006 Mar;2(1):1-11.
- doi: 10.3988/jcn.2006.2.1.1
Atherothromboembolism and intracranial small vessel disease are considered to be the main causes of cerebrovascular injury, which may lead to cognitive impairment and vascular dementia (VaD). VaD appears to be... -
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- Serum Neurofilament Light Chain Levels Are Related to Small Vessel Disease Burden
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Duering M, Konieczny , Tiedt S, Baykara E, Tuladhar A, van Leijsen E, Lyrer P, Engelter S, Gesierich , Achmüller M, Barro C, Adam R, Ewers M, Dichgans M, Kuhle J, de Leeuw F, Peters N
- KMID: 2424426
- J Stroke.
- 2018 May;20(2):228-238.
- doi: 10.5853/jos.2017.02565
BACKGROUND AND PURPOSE: Neurofilament light chain (NfL) is a blood marker for neuroaxonal damage. We assessed the association between serum NfL and cerebral small vessel disease (SVD), which is highly... -
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- Lacunar Infarction and Small Vessel Disease: Pathology and Pathophysiology
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Caplan LR
- KMID: 2223681
- J Stroke.
- 2015 Jan;17(1):2-6.
- doi: 10.5853/jos.2015.17.1.2
Two major vascular pathologies underlie brain damage in patients with disease of small size penetrating brain arteries and arterioles; 1) thickening of the arterial media and 2) obstruction of the... -
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- Genetics of Cerebral Small Vessel Disease
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Choi JC
- KMID: 2223682
- J Stroke.
- 2015 Jan;17(1):7-16.
- doi: 10.5853/jos.2015.17.1.7
Cerebral small vessel disease (SVD) is an important cause of stroke and cognitive impairment among the elderly and is a more frequent cause of stroke in Asia than in the... -
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- Updates on Prevention of Hemorrhagic and Lacunar Strokes
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Tsai HH, Kim JS, Jouvent E, Gurol ME
- KMID: 2424421
- J Stroke.
- 2018 May;20(2):167-179.
- doi: 10.5853/jos.2018.00787
Intracerebral hemorrhage (ICH) and lacunar infarction (LI) are the major acute clinical manifestations of cerebral small vessel diseases (cSVDs). Hypertensive small vessel disease, cerebral amyloid angiopathy, and hereditary causes, such... -
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- Micro-vascular Diseases of White Matter
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Kim W, Yang DW
- KMID: 2222351
- Dement Neurocogn Disord.
- 2012 Sep;11(3):79-86.
- doi: 10.12779/dnd.2012.11.3.79
White matter hyperintensity (WMH) is commonly observed on the brain MRI of elderly subjects. It has been considered as an important biomarker for the micro-vascular damages of white matter of... -
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