Charles André AbstrAct Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is the most common genetic cause of ischemic

MEDICAL POLICY - GENETIC TESTING OF CADASIL SYNDROMEMedical Policy Joint Medical Policies are a source for BCBSM and BCN medical policy information only. These documents

SHORT REPORT Retinal abnormalities in CADASIL: a retrospective study of 18 patients R Cumurciuc, P Massin, M Paques, V Krisovic, A Gaudric, M G Bousser, H Chabriat . . .

Redalyc.CADASIL. Case reportComportamento Brasil Vasconcelos da Silva, Julio Cesar; Gasparetto, Emerson L.; Engelhardt, Eliasz CADASIL. Case report Dementia & Neuropsychologia,

Modeling CADASIL vascular pathologies with patient-derived induced pluripotent stem cellsChen Ling1,2,3, Zunpeng Liu4,6, Moshi Song5,6,8, Weiqi Zhang1,3,6,8, Si Wang1,3,6,8,

INTRODUCTION Cerebral autosomal dominant arteriopathy with subcorti- cal infarcts and leukoencephalopathy (CADASIL) is an auto- somal dominantly inherited condition characterized

177 ©Copyright 2019 by the Bezmiâlem Vakf University Bezmiâlem Science published by Galenos Publishing House. Received: 09.06.2017 Accepted: 08.01.2018 Cite

DOI: 10.1159/000507542 Published online: December 14, 2020 © 2020 The Author(s) Published by S. Karger AG, Basel www.karger.com/crn This article is licensed under the

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) in Argentina Arteropatia cerebral autosomal dominante com infartos subcorticais

Review began 05/20/2021 Review ended 05/24/2021 Published 05/31/2021 © Copyright 2021 Ameer et al. This is an open access article distributed under the terms of the