Shifting the CARASIL Paradigm-Reference-Cited by-同舟云学术

Shifting the CARASIL Paradigm

Published:2015-04 Issue:4 Volume:46 Page:1110-1112
ISSN:0039-2499
Container-title:Stroke
language:en
Short-container-title:Stroke

Author:

Menezes Cordeiro Inês¹,Nzwalo Hipólito¹,Sá Francisca¹,Ferreira Rita Bastos¹,Alonso Isabel¹,Afonso Luís¹,Basílio Carlos¹

Affiliation:

1. From the Department of Neurology, Centro Hospitalar do Algarve, Hospital de Faro, Portugal (I.M.C., H.N., F.S., L.A., C.B.); Centro de Genética Preditiva e Preventiva, Instituto de Biologia Molecular e Celular, Universidade do Porto, Portugal (R.B.F., I.A.); Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Portugal (R.B.F., I.A.); and UnIGENe, Instituto de Biologia Molecular e Celular, Universidade do Porto, Portugal (I.A.).

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Advanced and Specialised Nursing,Cardiology and Cardiovascular Medicine,Clinical Neurology

Reference14 articles.

1. Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy

2. Association of HTRA1 Mutations and Familial Ischemic Cerebral Small-Vessel Disease

3. A Novel Mutation in theHTRA1Gene Identified in Chinese CARASIL Pedigree

4. A novel mutation of the high-temperature requirement A serine peptidase 1 (HTRA1) gene in a Chinese family with cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL)

5. A missense HTRA1 mutation expands CARASIL syndrome to the Caucasian population

Cited by 30 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Clinical and neuroradiological spectrum of biallelic variants in NOTCH3;eBioMedicine;2024-09

2. Vascular Leukoencephalopathy Associated Chorea Due to A Heterozygous Htra 1 Variant: Novel Presentation of Cadasil Type II;Movement Disorders Clinical Practice;2024-08-06

3. When Recurrent Strokes, Back Pain, and Alopecia Constitute a Hereditary Cause of Small-Vessel Disease, CARASIL in an Arabic Woman;The Neurologist;2022-12-01

4. HeterozygousHTRA1Mutations Cause Cerebral Small Vessel Diseases;Neurology Genetics;2022-12

5. Report of two pedigrees with heterozygous HTRA1 variants‐related cerebral small vessel disease and literature review;Molecular Genetics & Genomic Medicine;2022-08-10