An unusual presentation of late-onset Alexander’s disease with slow orthostatic tremor and a novel GFAP variant
Author:
Affiliation:
1. Department of Neurology, Mayo Clinic, Rochester, MN, USA
2. Department of Medical Genetics, Mayo Clinic, Rochester, MN, USA
3. Division of Neuroradiology, Mayo Clinic, Rochester, MN, USA
Publisher
Informa UK Limited
Subject
Clinical Neurology,Arts and Humanities (miscellaneous)
Link
https://www.tandfonline.com/doi/pdf/10.1080/13554794.2019.1580749
Reference9 articles.
1. PROGRESSIVE FIBRINOID DEGENERATION OF FIBRILLARY ASTROCYTES ASSOCIATED WITH MENTAL RETARDATION IN A HYDROCEPHALIC INFANT
2. The clinical spectrum of late-onset Alexander disease: a systematic literature review
3. Adult-onset Alexander disease
4. Early Mitochondrial Dysfunction in an Infant With Alexander Disease
5. Neuroimaging and clinical features in type II (late-onset) Alexander disease
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1. Orthostatic Tremor;Contemporary Clinical Neuroscience;2023
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. Type II Alexander disease with fragile X mental retardation 1 gene mutation;Clinical Neurology and Neurosurgery;2021-12
4. Clinical and radiological characteristics of older‐adult‐onset Alexander disease;European Journal of Neurology;2021-07-19
5. Slow Orthostatic Tremor: Review of the Current Evidence;TREMOR OTHER HYPERK;2019
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