Clinical case: cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy
- Authors: Blokhina E.V1, Kozlova K.A1, Iskander E.V2, Soloveva E.Y.2
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Affiliations:
- City clinical hospital №13 of the Department of Health of Moscow
- N.I.Pirogov Russian National Research Medical University of the Ministry of Health of the Russian Federation
- Issue: Vol 20, No 9 (2018)
- Pages: 35-38
- Section: Articles
- URL: https://journal-vniispk.ru/2075-1753/article/view/95071
- DOI: https://doi.org/10.26442/2075-1753_2018.9.35-38
- ID: 95071
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##article.viewOnOriginalSite##About the authors
E. V Blokhina
City clinical hospital №13 of the Department of Health of Moscow
Email: koshak005@gmail.com
врач-невролог 115280, Russian Federation, Moscow, ul. Velozavodskaia, d. 1/1
K. A Kozlova
City clinical hospital №13 of the Department of Health of Moscow
Email: kseniya55555@mail.ru
115280, Russian Federation, Moscow, ul. Velozavodskaia, d. 1/1
E. V Iskander
N.I.Pirogov Russian National Research Medical University of the Ministry of Health of the Russian Federation
Email: local93@yandex.ru
студент V курса 117997, Russian Federation, Moscow, ul. Ostrovitianova, d. 1
E. Yu Soloveva
N.I.Pirogov Russian National Research Medical University of the Ministry of Health of the Russian Federation
Email: ellasolovieva@yandex.ru
д-р мед. наук, проф. каф. неврологии ФДПО 117997, Russian Federation, Moscow, ul. Ostrovitianova, d. 1
References
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- Joutel A et al. Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia. Nature 1996; 383 (66020): 707.
- Meester J.A.N et al. Overlapping but distinct roles for NOTCH receptors in human cardiovascular disease. Clin Genet 2018. doi: 10.1111/cge.13382
- Morroni M et al. Role of electron microscopy in the diagnosis of CADASIL syndrome: a study of 32 patients. PLoS One 2013; 8 (6): e65482.
- Duering M et al. Co-aggregate formation of CADASIL-mutant NOTCH3: a single-particle analysis. Hum Mol Genet 2011; 20 (16): 3256-65.
- Perneczky R et al. Is the time ripe for new diagnostic criteria of cognitive impairment due to cerebrovascular disease? Consensus report of the International Congress on Vascular Dementia working group. BMC Med 2016; 14 (1): 162.
- Carone D.A. CADASIL and multiple sclerosis: A case report of prolonged misdiagnosis. Appl Neuropsychol: Adult 2017; 24 (3): 294-7.
- Yanagawa S et al. Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy. Neurology 2002; 58 (5): 817-20.
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