Incidental diagnosis of an asymptomatic adult-onset Alexander disease by brain magnetic resonance imaging for preoperative evaluation
Author:
Publisher
Elsevier BV
Subject
Clinical Neurology,Neurology
Reference10 articles.
1. Mutations in GFAP, encoding glial fibrillary acidic protein, are associated with Alexander disease;Brenner;Nat Genet,2001
2. Adult Alexander disease with autosomal dominant transmission: a distinct entity caused by mutation in the glial fibrillary acid protein gene;Stumpf;Arch Neurol,2003
3. Adult-onset Alexander disease: a series of eleven unrelated cases with review of the literature;Pareyson;Brain,2008
4. Alexander disease: diagnosis with MR imaging;van der Knaap;Am J Neuroradiol,2001
5. Can MR imaging diagnose adult-onset Alexander disease?;Farina;AJNR Am J Neuroradiol,2008
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1. Loss of GFAP cause retinal dysplasia and vision impairment;2022-11-15
2. Identification of a novel de novo pathogenic variant in GFAP in an Iranian family with Alexander disease by whole-exome sequencing;European Journal of Medical Research;2022-09-10
3. Activation of a Cryptic Splice Site of GFAP in a Patient With Adult-Onset Alexander Disease;Neurology Genetics;2021-10-01
4. Clinical and radiological characteristics of older‐adult‐onset Alexander disease;European Journal of Neurology;2021-07-19
5. Adult‐onset Alexander disease with imperceptible neurological findings;Neurology and Clinical Neuroscience;2021-06-05
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