Advances in Sturge-Weber syndrome
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Clinical Neurology,Neurology
Reference44 articles.
1. Encephalofacial angiomatosis sparing the occipital lobe and without facial nevus: on the spectrum of Sturge-Weber syndrome variants?;Comi;J Child Neurol,2003
2. Evidence of somatic mosaicism in Sturge-Weber syndrome;Huq;Neurology,2002
3. Increased fibronectin expression in Sturge-Weber syndrome fibroblasts and brain tissue;Comi;Pediatr Res,2003
4. Capillary malformation-arteriovenous malformation, a new clinical and genetic disorder caused by RASA1 mutations;Eerola;Am J Hum Genet,2003
5. The ultrastructure of Sturge-Weber disease;Norman;Acta Neuropathol (Berl),1977
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1. Seizure, Motor, and Cognitive Outcomes After Epilepsy Surgery for Patients With Sturge-Weber Syndrome;Neurology;2024-07-09
2. Seizure outcomes in children with Sturge-Weber syndrome undergoing epilepsy surgery: An individual participant data meta-analysis;Seizure: European Journal of Epilepsy;2023-04
3. Sturge-Weber Syndrome: A Review of Pathophysiology, Genetics, Clinical Features, and Current Management Approache;The Application of Clinical Genetics;2023-04
4. Pregnancy and refractory epilepsy in Sturge–Weber syndrome: Challenges and outcomes;Epileptic Disorders;2023-02
5. A deep insight on psychological aspect in patients with Sturge-Weber syndrome;Journal of Education and Health Promotion;2023
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