Mild malformation of cortical development with oligodendroglial hyperplasia in epilepsy (MOGHE): genetics, mechanisms and precision therapy.

Spyrou J, Lockhart PJ, Maljevic S, Howell KB, Reid CA.

DOI: 10.1007/s00401-026-03059-6
Published: 2026-08-02
Container: Acta Neuropathol
Publisher: Not recorded
Open access: yes

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Cite this work

BibTeX

@article{allodium:10.1007/s00401-026-03059-6,
  title = {Mild malformation of cortical development with oligodendroglial hyperplasia in epilepsy (MOGHE): genetics, mechanisms and precision therapy.},
  author = {Spyrou J and  Lockhart PJ and  Maljevic S and  Howell KB and  Reid CA.},
  year = {2026},
  journal = {Acta Neuropathol},
  doi = {10.1007/s00401-026-03059-6},
  url = {https://doi.org/10.1007/s00401-026-03059-6}
}

RIS

TY  - JOUR
TI  - Mild malformation of cortical development with oligodendroglial hyperplasia in epilepsy (MOGHE): genetics, mechanisms and precision therapy.
AU  - Spyrou J
AU  -  Lockhart PJ
AU  -  Maljevic S
AU  -  Howell KB
AU  -  Reid CA.
PY  - 2026
JO  - Acta Neuropathol
DO  - 10.1007/s00401-026-03059-6
UR  - https://doi.org/10.1007/s00401-026-03059-6
ER  -

APA

J, S., PJ, L., S, M., KB, H., & CA., R. (2026). Mild malformation of cortical development with oligodendroglial hyperplasia in epilepsy (MOGHE): genetics, mechanisms and precision therapy.. Acta Neuropathol. https://doi.org/10.1007/s00401-026-03059-6

Source records

europe-pmc · retrieved 2026-09-26T16:24:48.426Z