Literature DB >> 11889251

Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy.

Sohei Yanagawa1, Nobuo Ito, Kunimasa Arima, Shu-ichi Ikeda.   

Abstract

The clinicopathologic features of two Japanese sisters with cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL) are described. Neither patient had a history of hypertension, and both experienced cerebrovascular events before reaching their forties. Severe degenerative changes in the lumbar spine and knee joints were seen on radiographs. MRI showed extensive cerebral white matter lesions, which revealed remarkable arteriosclerotic changes on autopsy.

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Year:  2002        PMID: 11889251     DOI: 10.1212/wnl.58.5.817

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  16 in total

Review 1.  [HERNS. A rare, hereditary, multisystemic disease with cerebral microangiopathy].

Authors:  C Seifried; M Sitzer; J Jen; G Auburger
Journal:  Nervenarzt       Date:  2005-10       Impact factor: 1.214

Review 2.  Monogenic causes of stroke: now and the future.

Authors:  Rhea Y Y Tan; Hugh S Markus
Journal:  J Neurol       Date:  2015-06-03       Impact factor: 4.849

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

Authors:  Ilaria Di Donato; Silvia Bianchi; Gian Nicola Gallus; Alfonso Cerase; Ilaria Taglia; Francesca Pescini; Serena Nannucci; Carla Battisti; Domenico Inzitari; Leonardo Pantoni; Andrea Zini; Antonio Federico; Maria Teresa Dotti
Journal:  CNS Neurosci Ther       Date:  2017-08-06       Impact factor: 5.243

4.  Genetics of Vascular Dementia.

Authors:  Melissa E Murray; James F Meschia; Dennis W Dickson; Owen A Ross
Journal:  Minerva Psichiatr       Date:  2010-03

5.  Single gene disorders associated with stroke: a review and update on treatment options.

Authors:  Hurmina Muqtadar; Fernando D Testai
Journal:  Curr Treat Options Cardiovasc Med       Date:  2012-06

6.  A frameshift mutation in HTRA1 expands CARASIL syndrome and peripheral small arterial disease to the Chinese population.

Authors:  Bin Cai; Jiabin Zeng; Yi Lin; Yu Lin; WenPing Lin; Wei Lin; Zhiwen Li; Ning Wang
Journal:  Neurol Sci       Date:  2015-03-13       Impact factor: 3.307

7.  Candesartan prevents arteriopathy progression in cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy model.

Authors:  Taisuke Kato; Ri-Ichiroh Manabe; Hironaka Igarashi; Fuyuki Kametani; Sachiko Hirokawa; Yumi Sekine; Natsumi Fujita; Satoshi Saito; Yusuke Kawashima; Yuya Hatano; Shoichiro Ando; Hiroaki Nozaki; Akihiro Sugai; Masahiro Uemura; Masaki Fukunaga; Toshiya Sato; Akihide Koyama; Rie Saito; Atsushi Sugie; Yasuko Toyoshima; Hirotoshi Kawata; Shigeo Murayama; Masaki Matsumoto; Akiyoshi Kakita; Masato Hasegawa; Masafumi Ihara; Masato Kanazawa; Masatoyo Nishizawa; Shoji Tsuji; Osamu Onodera
Journal:  J Clin Invest       Date:  2021-11-15       Impact factor: 14.808

8.  Adult-Onset Leukoencephalopathy with Axonal Spheroids and Pigmented Glia Caused by a Novel R782G Mutation in CSF1R.

Authors:  Nicola Foulds; Reuben J Pengelly; Simon R Hammans; James A R Nicoll; David W Ellison; Adam Ditchfield; Sarah Beck; Sarah Ennis
Journal:  Sci Rep       Date:  2015-05-15       Impact factor: 4.379

Review 9.  Microvascular pathology and morphometrics of sporadic and hereditary small vessel diseases of the brain.

Authors:  Lucinda J L Craggs; Yumi Yamamoto; Vincent Deramecourt; Raj N Kalaria
Journal:  Brain Pathol       Date:  2014-09       Impact factor: 6.508

10.  Hereditary systemic angiopathy (HSA) with cerebral calcifications, retinopathy, progressive nephropathy, and hepatopathy.

Authors:  D T Winkler; P Lyrer; A Probst; D Devys; T Haufschild; S Haller; N Willi; M J Mihatsch; A J Steck; M Tolnay
Journal:  J Neurol       Date:  2008-01-22       Impact factor: 6.682

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