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1. In vivo base editing of a pathogenic Eif2b5 variant improves vanishing white matter phenotypes in mice.

2. Focal lesions following intracerebral gene therapy for mucopolysaccharidosis IIIA.

3. Therapeutic potential of human stem cell transplantations for Vanishing White Matter: A quest for the Goldilocks graft.

4. In vivo targeting of a variant causing vanishing white matter using CRISPR/Cas9.

5. Glutamate Carrier Involvement in Mitochondrial Dysfunctioning in the Brain White Matter.

6. Astrocyte Subtype Vulnerability in Stem Cell Models of Vanishing White Matter.

7. Cell Replacement Therapy Improves Pathological Hallmarks in a Mouse Model of Leukodystrophy Vanishing White Matter.

8. Cell adhesion and matricellular support by astrocytes of the tripartite synapse.

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