Disease: Weber syndrome
- 24-Year-Old Patient with Klippel-Trenaunay Syndrome Underwent Cementless Robotic Cruciate-Retaining TKA: A Case Report
- 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
- 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
- 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
- Bosworth ankle dislocation fracture - current concept review
- 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
- Diagnostic test accuracy in longitudinal study settings: theoretical approaches with use cases from clinical practice
- Dietary macronutrient composition impacts gene regulation in adipose tissue
- Dupilumab for atopic dermatitis in children with idiopathic nephrotic syndrome treated with cyclosporin: a report of two cases
- 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
- 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
- Healthcare Provider N95 Respirator Contamination Worn Behind Face Shields With SARS-CoV-2 During Routine Clinical Care of Patients With COVID-19
- 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
- Klippel-Trenaunay syndrome or not? An exploration of atypical presentations
- KTWS (Klippel-Trenaunay-Weber syndrome): A systematic presentation of a rare disease
- 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
- Mitigating healthcare worker risk during the COVID-19 pandemic - experience from a large tertiary maternity centre in the United Arab Emirates
- 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
- Neutrophilic Panniculitides
- Olsler Weber Rendu Syndrome
- 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
- Osler Weber Rendu Syndrome
- Overlapping Spots of Photodynamic Therapy for Treatment of Choroidal Hemangioma in Sturge-Weber Syndrome: A Case Report
- Pediatric Central Nervous System Vascular Malformation : Pathological Review with Diagram
- 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
- Pulmonary arteriovenous malformations in Rendu-Osler-Weber syndrome
- 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
- 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
- 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 with massive macroglossia and anterior neck space infection- a case report and review of literature
- 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
- 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 empty pelvis syndrome: a core data set from the PelvEx collaborative
- 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
- Time to change our approach to presymptomatic treatment of Sturge-Weber syndrome
- 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
- Two-dimensional speckle tracking echocardiography in fetuses with critical aortic stenosis before and after fetal aortic valvuloplasty
- 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