A review of the natural history of Sturge–Weber syndrome through adulthood
Author:
Funder
ANR
Fondation de l'Assistance Publique-Hôpitaux de Paris
Publisher
Springer Science and Business Media LLC
Subject
Neurology (clinical),Neurology
Link
https://link.springer.com/content/pdf/10.1007/s00415-022-11132-9.pdf
Reference45 articles.
1. Sudarsanam A, Ardern-Holmes SL (2014) Sturge-Weber syndrome: from the past to the present. Eur J Paediatr Neurol 18(3):257–266. https://doi.org/10.1016/j.ejpn.2013.10.003
2. Shirley MD, Tang H, Gallione CJ et al (2013) Sturge-Weber syndrome and port-wine stains caused by somatic mutation in GNAQ. N Engl J Med 368(21):1971–1979. https://doi.org/10.1056/NEJMoa1213507
3. Comi AM (2003) Pathophysiology of Sturge-Weber syndrome. J Child Neurol 18(8):509–516. https://doi.org/10.1177/08830738030180080701
4. Comi AM (2011) Presentation, diagnosis, pathophysiology, and treatment of the neurological features of Sturge-Weber syndrome. Neurologist 17(4):179–184. https://doi.org/10.1097/NRL.0b013e318220c5b6
5. Nabbout R, Juhász C (2013) Sturge-Weber syndrome. Handb Clin Neurol 111:315–321. https://doi.org/10.1016/B978-0-444-52891-9.00037-3
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