Associated Papers
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
Identification of a novel de novo pathogenic variant in GFAP in an Iranian family with Alexander disease by whole-exome sequencing.
Heshmatzad K et al.
European Journal of Medical Research, 2022
A report of two cases of bulbospinal form Alexander disease and preliminary exploration of the disease.
Song X et al.
Molecular Medicine Reports, 2021
Novel GFAP p. Glu206Ala Mutation in Alexander Disease with Decreased Dopamine Transporter Uptake.
Ogawa T et al.
Movement Disorders Clinical Practice, 2020
Alexander's disease and the story of Louise.
Wilson BA et al.
Neuropsychological Rehabilitation, 2018
An autopsied case of adult-onset bulbospinalform Alexander disease with a novel S393R mutation in the GFAP gene.
Iwasaki Y et al.
Clinical Neuropathology, 0
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