Histopathologic features of an autopsied patient with cerebral small vessel disease and a heterozygous HTRA1 mutation-Reference-Cited by-同舟云学术

Histopathologic features of an autopsied patient with cerebral small vessel disease and a heterozygous HTRA1 mutation

Published:2018-05-25 Issue:4 Volume:38 Page:428-432
ISSN:0919-6544
Container-title:Neuropathology
language:en
Short-container-title:Neuropathology

Author:

Ito Junko¹^ORCID,Nozaki Hiroaki²,Toyoshima Yasuko¹,Abe Takashi³,Sato Aki⁴,Hashidate Hideki⁵,Igarashi Shuichi⁴,Onodera Osamu⁶,Takahashi Hitoshi¹,Kakita Akiyoshi¹

Affiliation:

1. Department of Pathology; Brain Research Institute, Niigata University; Niigata Japan

2. Department of Medical Technology, Graduate School of Health Sciences; Niigata University; Niigata Japan

3. Department of Hematology; Niigata City General Hospital; Niigata Japan

4. Department of Neurology; Niigata City General Hospital; Niigata Japan

5. Department of Pathology; Niigata City General Hospital; Niigata Japan

6. Department of Neurology; Brain Research Institute, Niigata University; Niigata Japan

Publisher

Wiley

Subject

Neurology (clinical),General Medicine,Pathology and Forensic Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/neup.12473/fullpdf

Reference13 articles.

1. Association of HTRA1 mutations and familial ischemic cerebral small-vessel disease;Hara;N Engl J Med,2009

2. HtrA1 serine protease inhibits signaling mediated by TGF-β family proteins;Oka;Development,2004

3. Heterozygous HTRA1 mutations are associated with autosomal dominant cerebral small vessel disease;Verdura;Brain,2015

4. Distinct molecular mechanisms of HTRA1 mutants in manifesting heterozygotes with CARASIL;Nozaki;Neurology,2016

5. Histopathologic analysis of cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL): A report of a new genetically confirmed case and comparison to 2 previous cases;Ito;J Neuropathol Exp Neurol,2016

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