Canavan disease, a rare early-onset human spongiform leukodystrophy: Insights into its genesis and possible clinical interventions

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Aspartoacylase deficiency and N‐acetylaspartic aciduria in patients with canavan disease

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Glial-conditional deletion of aquaporin-4 ( <i>Aqp4</i> ) reduces blood–brain water uptake and confers barrier function on perivascular astrocyte endfeet

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Direct and fast detection of neuronal activation in the human brain with diffusion MRI

Denis Le Bihan, Shin‐ichi Urayama, Toshihiko Aso et al. · Proceedings of the National Academy of Sciences · 2006 · 280 citations · Full text

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Defective N-acetylaspartate catabolism reduces brain acetate levels and myelin lipid synthesis in Canavan's disease

Chikkathur N. Madhavarao, Peethambaran Arun, John R. Moffett et al. · Proceedings of the National Academy of Sciences · 2005 · 233 citations · Full text

Life Sciences, Neurobiology, Neuroscience +17