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- Diagnosing Alexander disease in adults
- Gfap Mutation and Astrocyte Dysfunction Lead to a Neurodegenerative Profile with Impaired Synaptic Plasticity and Cognitive Deficits in a Rat Model of Alexander Disease
- Brainstem Chipmunk Sign: A Diagnostic Imaging Clue across All Subtypes of Alexander Disease
- Adult-Onset Alexander Disease: New Causal Sequence Variant in the GFAP Gene
- Teaching NeuroImage: Dorsal Medullary Lesions in Juvenile-Onset Alexander Disease
- Pearls & Oy-sters: Adult-Onset Alexander Disease With Transient Swelling of the Medulla Oblongata
- Antisense therapy in a new rat model of Alexander disease reverses GFAP pathology, white matter deficits, and motor impairment
- A novel mutation in the GFAP gene expands the phenotype of Alexander disease
- Structural basis for the inhibition of translation through eIF2{alpha} phosphorylation
- Brain MR Imaging Findings in Woodhouse-Sakati Syndrome
- CSF and Blood Levels of GFAP in Alexander Disease
- Megalencephalic leucoencephalopathy with subcortical cysts: subcortical diffuse leucoencephalopathy associated with white matter cystic degeneration
- A practical approach to diagnosing adult onset leukodystrophies
- Neuroimaging and clinical features in type II (late-onset) Alexander disease
- Alexander Disease
- GFAP mutations, age at onset, and clinical subtypes in Alexander disease
- Invited Article: An MRI-based approach to the diagnosis of white matter disorders
- Alexander disease: Ventricular garlands and abnormalities of the medulla and spinal cord
- Alexander disease: Not just a leukodystrophy anymore
- The clinicopathological spectrum of Rosenthal fibre encephalopathy and Alexander's disease: a case report and review of the literature
- Molecular findings in symptomatic and pre-symptomatic Alexander disease patients