Multiple sclerosis or “inflammatory CADASIL?”: Case Report and review of the literature
Author:
Publisher
Elsevier BV
Subject
Clinical Neurology,General Medicine,Surgery
Reference12 articles.
1. The phenotypic spectrum of CADASIL: clinical findings in 102 cases;Dichgans;Ann. Neurol.,1998
2. CADASIL: cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy;Ruchoux;J. Neuropathol. Exp. Neurol.,1997
3. Inflammatory-like presentation of CADASIL: a diagnostic challenge;Collongues;BMC Neurol.,2012
4. Stanford-Binet Intelligence Scales;Roid,2003
5. Strong clustering and stereotyped nature of Notch3 mutations in CADASIL patients;Joutel;Lancet,1997
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1. Cysteine-Altering NOTCH3 Variants Are Associated with an Increased Risk of Autoimmune Diseases;Journal of Clinical Medicine;2023-09-29
2. A novel report of Cys1298Gly mutation in exon 24 of NOTCH3 gene in a Chinese family with CADASIL;Journal of Stroke and Cerebrovascular Diseases;2023-08
3. Acute bilateral multiple subcortical infarcts as manifestation in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy;Neurological Sciences;2023-07-17
4. ER stress induced immunopathology involving complement in CADASIL: implications for therapeutics;Acta Neuropathologica Communications;2023-05-08
5. Multiple Sclerosis in a Patient With Neurogenic Locus Notch Homolog Protein 3 Mutation;Journal of Clinical Neurology;2023
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