Associated Papers
Genotype-phenotype correlations of GFAP variants in type I Alexander disease subtypes.
Bachetti T et al.
Molecular Genetics and Metabolism, 2026
A systematic review and meta-analysis of GFAP gene variants in Alexander disease.
Grossi A et al.
Scientific Reports, 2024
39420046 (PubMed )
Supplement: 41598_2024_75383_MOESM2_ESM.xlsx › Suppl._Table_2
Case report: A novel mutation of glial fibrillary acidic protein gene causing juvenile-onset Alexander disease.
Romano C et al.
Frontiers in Neurology, 2024
A report of two cases of bulbospinal form Alexander disease and preliminary exploration of the disease.
Song X et al.
Molecular Medicine Reports, 2021
An unusual GFAP mutation in a Taiwanese child with infantile Alexander disease.
Liang JS et al.
Pediatrics and Neonatology, 2018
Nationwide survey of Alexander disease in Japan and proposed new guidelines for diagnosis.
Yoshida T et al.
Journal of Neurology, 2011
Neurocognitive decline in Alexander disease.
Restrepo J et al.
The Clinical Neuropsychologist, 2011
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