• 24-Year-Old Patient with Klippel-Trenaunay Syndrome Underwent Cementless Robotic Cruciate-Retaining TKA: A Case Report
• A deep insight on psychological aspect in patients with Sturge-Weber syndrome
• A Patient with Klippel-Trenaunay Syndrome and Mild Ophthalmic Manifestations
• A Rare Case of Klippel Trenaunay Syndrome with Von Willebrand Factor Deficiency and Multiple Accessory Spleens: A Case Report and Brief Literature Review
• A rare presentation of asymmetric limb hypertrophy and diffuse capillary malformations in a pediatric patient with Loeys-Dietz syndrome type 3
• Active and passive mechanical characterization of a human descending thoracic aorta with Klippel-Trenaunay syndrome
• Acute pulmonary embolism in a patient with Klippel-Trenaunay-Weber syndrome treated with catheter-directed thrombectomy: a case report
• Alternative Venous Pathways: A Potential Key Imaging Feature for Early Diagnosis of Sturge-Weber Syndrome Type 1
• An Atypical Seizure Onset and Re-Emergence in a Refugee with an Undiagnosed Sturge-Weber Syndrome: A Case Report from a Limited Setting
• An Ultrasound Biomicroscopy Study of Acute Hydrops in Neonatal Glaucoma with Sturge-Weber Syndrome
• An Update on Multimodal Ophthalmological Imaging of Diffuse Choroidal Hemangioma in Sturge-Weber Syndrome
• Analysis of disease composition and primary surgical procedures in pediatric secondary glaucoma inpatients: a single-center study
• Anesthetic management of a patient with Sturge-Weber syndrome in sagittal split ramus osteotomy surgery
• Arterial spin-labeled (ASL) perfusion in children with Sturge-Weber syndrome: a retrospective cross-sectional study
• Assessment of the Corneal Biomechanical Features of Sturge-Weber Syndrome Using Dynamic Ultrahigh-speed Scheimpflug Imaging
• Bevacizumab and External Beam Radiation Therapy for Diffuse Choroidal Hemangioma in Sturge-Weber Syndrome: A Case Report
• Bilateral ocular manifestations of Sturge-Weber syndrome: a rare case report
• Capillary malformations
• Cerebrofacial Venous Metameric Syndrome Mimicking Vein of Galen Aneurysmal Malformation
• Characterization of Patient-Derived GNAQ Mutated Endothelial Cells from Capillary Malformations
• Clinical and pathologic features of Sturge-Weber syndrome in patients with refractory epilepsy
• Correction: Current situation and influencing factors of Disease uncertainty in parents of children with Sturge‒Weber syndrome: a retrospective study
• Dermato-Radiological Evaluation of Congenital Limb Overgrowth Vascular Syndromes
• Determinants of Functional Outcome after Pediatric Hemispherotomy
• Diagnostic pathway and management of first seizures in infants with Sturge-Weber syndrome
• Diffuse choroidal hemangioma in pregnancy: Symptomatic diffuse choroidal hemangioma spontaneously resolving postpartum
• Dyke-Davidoff-Masson Syndrome as a Rare Cause of Cerebral Hemiatrophy: Insights From a Case Series
• Dyke-Davidoff-Masson syndrome secondary to Sturge-Weber syndrome
• Epileptic seizures as an initial symptom for Sturge-Weber syndrome type III: A report of two cases
• Erratum: Sturge-Weber Syndrome: A Review of Pathophysiology, Genetics, Clinical Features, and Current Management Approache [Corrigendum]
• Feasibility and Potential Diagnostic Value of Noncontrast Brain MRI in Nonsedated Children With Sturge-Weber Syndrome and Healthy Siblings
• Fetal Klippel-Trenaunay-Weber Syndrome: Antenatal Diagnosis and Postnatal Management
• Frank's Sign: A Link Between Dermatovenerology, Cardiac Pathology, and Neurology
• Gastrointestinal involvement in Klippel-Trénaunay syndrome: pathophysiology, evaluation, and management
• GNAQ R183Q somatic mutation contributes to aberrant arteriovenous specification in Sturge-Weber syndrome through Notch signaling
• GNAQ/GNA11 Mosaicism Causes Aberrant Calcium Signaling Susceptible to Targeted Therapeutics
• GNAQ/GNA11 mosaicism causes aberrant calcium signalling susceptible to targeted therapeutics
• GNAQ/GNA11 Mosaicism Is Associated with Abnormal Serum Calcium Indices and Microvascular Neurocalcification
• Headache in Sturge-Weber syndrome: A systematic review
• Hemispheric surgery in children: perisylvian technique
• Hypothalamic-pituitary dysfunction in Sturge-Weber syndrome: case report and review of the literature
• Incidence of and Risk Factors for Fellow-Eye Involvement in Sturge-Weber Syndrome Children with Unilateral Glaucoma
• Interhemispheric Vertical Hemispherotomy: Technique, Outcome, and Pitfalls-A Bicentric Retrospective Case Series of 39 Cases
• Kidney transplant and Klippel-Trenaunay-Weber syndrome: an unusual association
• Klippel-Trenaunay syndrome and pregnancy: A Case-Report
• Klippel-Trenaunay syndrome or not? An exploration of atypical presentations
• Klippel-Trenaunay-Weber syndrome: Oro-dental manifestations and management
• KTWS (Klippel-Trenaunay-Weber syndrome): A systematic presentation of a rare disease
• Late-Onset Status Epilepticus Associated With Isolated Leptomeningeal Angioma and Sturge-Weber Syndrome-Related <em>GNA11</em> Pathogenic Variation
• Letter Regarding "Clinicopathological Analysis of Sturge-Weber Syndrome With Focal Cortical Dysplasia FCD IIIc"
• Lymphatic Malformations in Parkes Weber Syndrome: Retrospective Review of Sixteen Cases in a Vascular Anomalies Center
• Lymphatic Malformations in Parkes Weber's Syndrome: Retrospective Review of 16 Cases in a Vascular Anomalies Center
• Measures of youth e-cigarette use: strengths, weaknesses and recommendations
• Medium-term efficacy and safety analysis of Ex-PRESS shunt implantation for the treatment of secondary glaucoma in Sturge-Weber syndrome
• Moving Beyond Hemangioma: Interactive, Multidisciplinary, Case-Based Teaching in Vascular Anomalies for Pediatric Residents
• MRC1 and LYVE1 expressing macrophages in vascular beds of GNAQ p.R183Q driven capillary malformations in Sturge Weber syndrome
• Multiple Lymphaticovenular Anastomoses for Chyluria in Klippel-Trenaunay Syndrome
• Myelin-oligodendrocyte glycoprotein antibody-positive encephalitis in a patient with Sturge-Weber syndrome
• Neurological function and drug-refractory epilepsy in Sturge-Weber syndrome children: a retrospective analysis
• Oral Sirolimus for Diffuse Choroidal Hemangioma in Sturge-Weber Syndrome
• Overlapping Spots of Photodynamic Therapy for Treatment of Choroidal Hemangioma in Sturge-Weber Syndrome: A Case Report
• Parkes Weber syndrome: a rare cause of foot drop
• Peculiar aetiology for orbital apex syndrome: Wyburn-Mason syndrome as orbital apex lesion
• Pediatric Central Nervous System Vascular Malformation : Pathological Review with Diagram
• Pediatric Limb Asymmetry: A Unique Presentation of Angioosteohypertrophic Syndrome
• Perfusion management during cardiopulmonary bypass in a patient with high cardiac output due to arteriovenous malformations
• Population-based study of rare epilepsy incidence in a US urban population
• Psychosis in a Patient With Sturge-Weber Syndrome: A Case Report and Literature Review
• Pulmonary Embolism in Klippel-Trenaunay-Weber Syndrome With Slipped Capital Femoral Epiphysis
• Quantification of enlarged deep medullary vein volumes in Sturge-Weber syndrome
• Radio-pathologic correlation: no pial angioma-subarachnoid varicose network drainage pathway in Sturge-Weber syndrome
• Rare Presentation of the Vein of Servelle in a Case of Klippel-Trenaunay Syndrome
• Recurrent hematuria involving urinary system with Klippel-Trenaunay syndrome: A case report
• Retrospective Analysis of Presymptomatic Treatment In Sturge-Weber Syndrome
• Seizure, Motor, and Cognitive Outcomes After Epilepsy Surgery for Patients With Sturge-Weber Syndrome: Results From a Multicenter Study
• Similarities and differences between brain and skin <em>GNAQ</em> p.R183Q driven capillary malformations
• Somatic mutation spectrum of a Chinese cohort of pediatrics with vascular malformations
• Sturge Weber Syndrome and Rod Cone Dystrophy
• Sturge-Weber Syndrome and Hippocampal Sclerosis: Two Epileptogenic Conditions in One Patient
• Sturge-Weber syndrome type III: an important stroke mimic
• Sturge-Weber syndrome with cemento-ossifying fibroma in the maxilla and giant odontoma in the mandible: A case report
• Sturge-Weber syndrome with massive macroglossia and anterior neck space infection- a case report and review of literature
• Sturge-Weber Syndrome: A Case Report
• Sturge-Weber Syndrome: A Report of a Rare Case
• Sturge-Weber syndrome: an update for the pediatrician
• Subcutaneous Cavernous Haemangioma in a Patient with Klippel-Trenaunay Syndrome: A Case Report
• Surgical Orthodontic Treatment for Skeletal Maxillary Protrusion in Sturge-Weber Syndrome: A Case Report and Review of the Literature
• Surgical Outcomes of Early Versus Late Onset Glaucoma Associated with Sturge-Weber Syndrome
• Targeted next-generation sequencing for detection of PIK3CA mutations in archival tissues from patients with Klippel-Trenaunay syndrome in an Asian population : List the full names and institutional addresses for all authors
• The profile of epilepsy and its characteristics in children with neurocutaneous syndromes
• Time to change our approach to presymptomatic treatment of Sturge-Weber syndrome
• Total knee arthroplasty in patients with Klippel Trenaunay syndrome and knee osteoarthritis: A case report and a literature review
• Treatment Outcomes of Primary Combined Trabeculotomy and Trabeculectomy in Early Onset Glaucoma with Sturge-Weber Syndrome
• Undiagnosed Epileptic Case Since Childhood of Sturge-Weber Syndrome: First Case Report from Somalia
• Unilateral Glaucoma Without Facial Angioma in a Pediatric Patient: A Suspected Sturge-Weber Syndrome Variant
• Unmasking Sturge-Weber syndrome in adulthood: a case with extrafacial port-wine stain and delayed neurological symptoms
• Upper-Extremity Klippel-Trenaunay Syndrome
• Value of the short time inversion recovery sequence of magnetic resonance imaging in the staging of Klippel-Trenaunay syndrome complicated with lymphedema
• Variation in neuroimaging and outcomes in patients with Sturge Weber syndrome Type III
• Vesical Haemangioma in Klippel-Trenaunay-Weber Syndrome: A Clinical Case Report