• 24-Year-Old Patient with Klippel-Trenaunay Syndrome Underwent Cementless Robotic Cruciate-Retaining TKA: A Case Report
• A acute pontine infarction with one-and-a-half syndrome as the manifestation: A case report
• A case report of fifteen-and-a-half syndrome
• A Rare Case of Klippel Trenaunay Syndrome with Von Willebrand Factor Deficiency and Multiple Accessory Spleens: A Case Report and Brief Literature Review
• ACR Appropriateness Criteria® Pulmonary Arteriovenous Malformation (PAVM): 2023 Update
• Acute peripheral facial paralysis caused by tegmental pontine infarction
• Altered static and dynamic cerebellar-cerebral functional connectivity in acute pontine infarction
• Alternative Venous Pathways: A Potential Key Imaging Feature for Early Diagnosis of Sturge-Weber Syndrome Type 1
• An analysis of clinical characteristics of rare bilateral medial medullary infarction: An observational study
• 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
• Anesthetic management of a patient with Sturge-Weber syndrome in sagittal split ramus osteotomy surgery
• Assessing sleep-related breathing disorders among newly diagnosed rheumatoid and psoriatic arthritis patients: a 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
• Blepharophimosis with intellectual disability and Helsmoortel-Van Der Aa Syndrome share episignature and phenotype
• Capillary malformations
• Case report: Febrile infection-related epilepsy syndrome in a 14-year-old girl with multiple organ failure and lethal outcome
• Cerebrofacial venous metameric syndrome mimicking vein of Galen aneurysmal malformation
• Co-Morbidities of Irritable Bowel Syndrome in a Racially and Ethnically Diverse Population
• Comprehensive functional characterization of Complement factor I rare variant genotypes identified in the SCOPE Geographic Atrophy cohort
• Cracking the NLRP3 code: Pioneering precision medicine for inflammation
• Cystic Fibrosis Foundation Evidence-Based Guideline for the Management of CRMS/CFSPID
• De novo brain vascular malformation in an adult with hereditary hemorrhagic telangiectasia and juvenile polyposis overlap syndrome
• Dermato-Radiological Evaluation of Congenital Limb Overgrowth Vascular Syndromes
• Detailed phenotype and long-term follow-up of <em>RAB28-</em>associated cone-rod dystrophy
• Diagnostic pathway and management of first seizures in infants with Sturge-Weber syndrome
• Difficult-to-Treat Nephrotic Syndrome in Childhood-Global Depletion of B-Cells
• Does the distal radioulnar joint orientation influence the outcome of ulnar shortening osteotomy: a retrospective study
• 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
• Early Infantile Diagnosis of Hereditary Hemorrhagic Telangiectasia Complicated by Child Abuse
• Effect of TRPV4 Antagonist GSK2798745 on Chlorine Gas-Induced Acute Lung Injury in a Swine Model
• Efficacy and safety of bendamustine for lymphodepletion before lisocabtagene maraleucel
• Epidemiology of Irritable Bowel Syndrome in a Large Academic Safety-Net Hospital
• 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
• Flow Cytometry-Based Measurement of Antibodies Specific for Cell Surface-Expressed Folded SARS-CoV-2 Receptor-Binding Domains
• Fragile X Syndrome and FMR1 premutation: results from a survey on associated conditions and treatment priorities in Italy
• Harlequin syndrome in a patient with probable hemicrania continua and exertional headache - is there a link? a case report
• Headache in Sturge-Weber syndrome: A systematic review
• Hemispheric surgery in children: perisylvian technique
• Incident HIV-Associated Wasting/Low Weight Is Associated with Nearly Doubled Mortality Risk in the Modern ART Era
• Interdisciplinary, collaborative D-A-CH (Germany, Austria and Switzerland) consensus statement concerning the diagnostic and treatment of myalgic encephalomyelitis/chronic fatigue syndrome
• Iron Deficiency and Sleep/Wake Behaviors: A Scoping Review of Clinical Practice Guidelines-How to Overcome the Current Conundrum?
• Limitations in next-generation sequencing-based genotyping of breast cancer polygenic risk score loci
• Management of hereditary hemorrhagic telangiectasia-like symptoms induced by trastuzumab emtansine in a breast cancer patient: case report
• Matching proposed clinical and MRI criteria of aggressive multiple sclerosis to serum and cerebrospinal fluid markers of neuroaxonal and glial injury
• Measures of youth e-cigarette use: strengths, weaknesses and recommendations
• Motor cortex stimulation for the treatment of trigeminal neuralgia after brainstem infarction: A case report
• 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
• Neuroimaging and clinical features of bilateral Wallerian degeneration of middle cerebellar peduncles subsequent to pontine infarction
• Oral Sirolimus for Diffuse Choroidal Hemangioma in Sturge-Weber Syndrome
• Orofacial myofunctional and polysomnographic characteristics of children with Down syndrome and obstructive sleep apnea: a pilot study
• Overlapping Spots of Photodynamic Therapy for Treatment of Choroidal Hemangioma in Sturge-Weber Syndrome: A Case Report
• Pediatric Limb Asymmetry: A Unique Presentation of Angioosteohypertrophic Syndrome
• Percutaneous embolization of pulmonary arteriovenous malformation for the treatment of chronic hypoxemia in a patient with Osler-Weber-Rendu syndrome
• Population-based study of rare epilepsy incidence in a US urban population
• Prenatal diagnosis of pulmonary arteriovenous malformations with a postnatal diagnosis of Osler-Weber-Rendu syndrome
• Prevalence of hereditary hemorrhagic telangiectasia in a medical care program organization in Buenos Aires, Argentina
• Protocol and rationale for a randomized controlled SGLT2 inhibitor trial in pediatric and young adult populations with chronic kidney disease: DOUBLE PRO-TECT Alport
• Pulmonary arteriovenous malformations in Rendu-Osler-Weber syndrome
• Pulmonary Embolism in Klippel-Trenaunay-Weber Syndrome With Slipped Capital Femoral Epiphysis
• 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
• Retrospective Analysis of Presymptomatic Treatment In Sturge-Weber Syndrome
• Safety, tolerability, and pharmacokinetics of antisense oligonucleotide BIIB078 in adults with C9orf72-associated amyotrophic lateral sclerosis: a phase 1, randomised, double blinded, placebo-controlled, multiple ascending dose study
• Sagittal balance parameters measurement on cervical spine MR images based on superpixel segmentation
• Segregation, immunohistochemical, molecular and functional analyses classify a novel missense variant in fumarate hydratase (FH) as pathogenic
• Seizure, Motor, and Cognitive Outcomes After Epilepsy Surgery for Patients With Sturge-Weber Syndrome: Results From a Multicenter Study
• Serum Concentrations of Matrix Metalloproteinase-1 and Procollagen Type I Carboxy Terminal Propeptide Discriminate Infarct-Like Myocarditis and Non-ST-Segment-Elevation Myocardial Infarction
• Similarities and differences between brain and skin GNAQ p.R183Q driven capillary malformations
• SOLAMEN syndrome with cardiovascular damage
• Spinal Cord and Brainstem Extensive Infarction: A Case with Rare Complication of COVID-19 Infection
• Spontaneous haemothorax caused by a ruptured pulmonary arterio-venous malformation: A manifestation of hereditary haemorrhagic telangiectasia in pregnancy
• Stasis imaging predicts the risk of cardioembolic events related to acute myocardial infarction
• Stasis imaging predicts the risk of cardioembolic events related to acute myocardial infarction: the ISBITAMI study
• Sturge-Weber syndrome with cemento-ossifying fibroma in the maxilla and giant odontoma in the mandible: A case report
• Sturge-Weber syndrome: an update for the pediatrician
• Surgery of Neoaortic Pseudoaneurysm with Transsternal Penetration in a HLHS Patient
• 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
• Systematic analysis of SCN5A variants associated with inherited cardiac diseases
• Telangiectasias, recurrent epistaxis and a strong family history-a case of Osler- Weber-Rendu Syndrome in Pakistan
• The "Heart Appearance Sign" in Bilateral Medial Medullary Infarction with Unusual Presentation as Incomplete Syndrome
• The profile of epilepsy and its characteristics in children with neurocutaneous syndromes
• The shared decision-making tool for caregivers of children with prenatal opioid exposure: A pilot and acceptability study
• The Spectrum of CAR Cellular Effectors: Modes of Action in Anti-Tumor Immunity
• Time to change our approach to presymptomatic treatment of Sturge-Weber syndrome
• Transverse diameter of brainstem infarction is a strong predictor of miserable outcome after mechanical thrombectomy for acute basilar artery occlusion
• Triheptanoin Did Not Show Benefit versus Placebo for the Treatment of Paroxysmal Movement Disorders in Glut1 Deficiency Syndrome: Results of a Randomized Phase 3 Study
• Uncommon Streptococcus Constellatus Meningitis Leading to Pulmonary Abscess and Brainstem Infarct in an Immunocompetent Patient
• 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
• Variation in neuroimaging and outcomes in patients with Sturge Weber syndrome Type III