Sturge–Weber syndrome
- 1 January 2015
- book chapter
- review article
- Published by Elsevier BV in Handbook of Clinical Neurology
- Vol. 132, 157-168
- https://doi.org/10.1016/b978-0-444-62702-5.00011-1
Abstract
No abstract availableThis publication has 72 references indexed in Scilit:
- Urine vascular biomarkers in Sturge–Weber syndromeVascular Medicine, 2013
- Sturge–Weber Syndrome and Port-Wine Stains Caused by Somatic Mutation inGNAQThe New England Journal of Medicine, 2013
- Aspirin Use in Sturge-Weber SyndromeJournal of Child Neurology, 2012
- Importance of Utilizing a Sensitive Free Thyroxine Assay in Sturge-Weber SyndromeJournal of Child Neurology, 2012
- Cortical calcification in sturge–weber syndrome on MRI‐SWI: Relation to brain perfusion status and seizure severityJournal of Magnetic Resonance Imaging, 2011
- Regulators of G-Protein Signaling and Their Gα Substrates: Promises and Challenges in Their Use as Drug Discovery TargetsPharmacological Reviews, 2011
- Use of quantitative EEG in infants with port-wine birthmark to assess for Sturge–Weber brain involvementClinical Neurophysiology, 2009
- MR susceptibility weighted imaging (SWI) complements conventional contrast enhanced T1 weighted MRI in characterizing brain abnormalities of Sturge-Weber SyndromeJournal of Magnetic Resonance Imaging, 2008
- Role of mTOR in anticancer drug resistance: Perspectives for improved drug treatmentDrug Resistance Updates, 2008
- Port-wine stains: A new hypothesisJournal of the American Academy of Dermatology, 1987