Literature DB >> 25116877

Features of cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy.

Hiroaki Nozaki1, Masatoyo Nishizawa1, Osamu Onodera2.   

Abstract

Entities:  

Keywords:  HtrA1 protein, human; TGF-β; cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy; cerebral small vessel diseases; myocytes, smooth muscle

Mesh:

Substances:

Year:  2014        PMID: 25116877     DOI: 10.1161/STROKEAHA.114.004236

Source DB:  PubMed          Journal:  Stroke        ISSN: 0039-2499            Impact factor:   7.914


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  31 in total

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Review 3.  The pathobiology of vascular malformations: insights from human and model organism genetics.

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Review 4.  Cerebrovascular disorders associated with genetic lesions.

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Review 5.  Emerging molecular mechanisms of vascular dementia.

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6.  Heterozygous mutations of HTRA1 gene in patients with familial cerebral small vessel disease.

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Review 7.  Genetic factors in cerebral small vessel disease and their impact on stroke and dementia.

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Journal:  J Cereb Blood Flow Metab       Date:  2016-01       Impact factor: 6.200

Review 8.  Heritable and non-heritable uncommon causes of stroke.

Authors:  A Bersano; M Kraemer; A Burlina; M Mancuso; J Finsterer; S Sacco; C Salvarani; L Caputi; H Chabriat; S Lesnik Oberstein; A Federico; E Tournier Lasserve; D Hunt; M Dichgans; M Arnold; S Debette; H S Markus
Journal:  J Neurol       Date:  2020-04-21       Impact factor: 4.849

Review 9.  Perivascular spaces, glymphatic dysfunction, and small vessel disease.

Authors:  Humberto Mestre; Serhii Kostrikov; Rupal I Mehta; Maiken Nedergaard
Journal:  Clin Sci (Lond)       Date:  2017-08-10       Impact factor: 6.124

Review 10.  Genetic susceptibility to cerebrovascular disease.

Authors:  David Della-Morte; Francesca Pacifici; Tatjana Rundek
Journal:  Curr Opin Lipidol       Date:  2016-04       Impact factor: 4.776

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