• A falcotentorial dural arteriovenous fistula presented as carotid cavernous fistula clinically treated by transarterial embolization: case report
• A fatal case of Harlequin ichthyosis: Experience from low-resource setting
• A Multicenter Study of COPD and Cognitive Impairment: Unraveling the Interplay of Quantitative CT, Lung Function, HIF-1α, and Clinical Variables
• A new variant in the <em>ZCCHC8</em> gene: diverse clinical phenotypes and expression in the lung
• A novel APC mutation associated with Gardner syndrome in a Chinese family
• A novel mutation of SPAST gene in a hereditary spastic paraplegia type 4 family
• A Rare Case of Extrahepatic Portal Venous Obstruction in a Nine-Year-Old Female and Its Management: A Case Report
• A Spinal Cavernous Malformation in Multiple Cerebral Cavernous Venous Malformations Syndrome
• ACR Appropriateness Criteria® Tinnitus: 2023 Update
• Analysis of PKP2 gene variants in a child with Arrhythmogenic right ventricular cardiomyopathy
• Anatomical and physiological diagnostic discrepancies in fetuses with single-ventricle congenital heart disease in a contemporary cohort
• Angioarchitecture and prognosis of pediatric intracranial pial arteriovenous fistula
• Are there differences in clinical presentation, radiologic findings, and outcomes in female patients with cavernous malformation?
• Arteriovenous Malformations: An Update on Models and Therapeutic Targets
• Bilateral Cavernous Sinus Thrombosis in Presumed COVID-19 Infection
• Bilateral superficial temporal vein thrombosis after acute carbon monoxide poisoning and prolonged immobilisation: a case report
• CAROTID CAVERNOUS SINUS FISTULA FINDINGS IN OPTICAL COHERENCE TOMOGRAPHY ANGIOGRAPHY BEFORE AND AFTER PERCUTANEOUS EMBOLIZATION
• Cavernous Venous Malformation
• Cavernous Venous Malformation
• Cerebral cavernous malformations - An overview on genetics, clinical aspects and therapeutic strategies
• Cervical Artery Dissection and Patent Foramen Ovale in Juvenile Stroke: Causality or Casuality? A Familiar Case Report
• Clinical manifestations and genetic analysis of 4 patients with variants of FBN1 gene
• Clinical-radiological-pathological correlation in pulmonary arterial hypertension
• Coil Embolization of a Large Recurrent Pulmonary Arteriovenous Malformation by Retrograde Transseptal Pulmonary Vein Access
• Comprehensive neurosurgical treatment of right occipital arteriovenous malformation with advanced angiographic techniques
• Coronary Sinus Draining Into the Right Superior Vena Cava: A Rare Anomaly
• Cutaneous vasculitis in autoinflammatory diseases
• Decision making in anomalous aortic origin of a coronary artery
• Deletion of cis-regulatory Element in FOXL2 Promoter in a Chinese Family of Type II Blepharophimosis-ptosis-epicanthus Inversus Syndrome with Polydactyly
• Derivation and Validation of Spontaneous Coronary Artery Dissection Prediction Score in Patients With Myocardial Infarction
• Diffuse pulmonary arteriovenous malformation presenting with secondary polycythemia and headaches: a case report
• Distant Recurrence of a Cerebral Cavernous Malformation in the Vicinity of a Developmental Venous Anomaly: Case Report of Local Oxy-Inflammatory Events
• Emerging Insights Into the Pathophysiology of Multisystem Inflammatory Syndrome Associated With COVID-19 in Children
• Endoluminal Biopsy for Vein of Galen Malformation
• Establishment of Cardiac Laterality
• Evaluating the Quality, Readability, and Activity of Online Information on Brain Arteriovenous Malformations
• Executive summary of the 14th HHT international scientific conference
• Extraction of genomic DNA for sequencing from snail <em>Helix lucorum</em>
• Factors Affecting the Early Maturation of Arteriovenous Fistulae Created at a Tertiary Centre in Oman
• Familial CCM Genes Might Not Be Main Drivers for Pathogenesis of Sporadic CCMs-Genetic Similarity between Cancers and Vascular Malformations
• Familial clustering of coronary anomalies identified through the RAC sign
• Fibro-Adipose Vascular Anomaly: A Case Report and Literature Review
• First Description of Fetal Cystic Hygroma Associated With Early Equine Pregnancy Loss
• Five decades of Fontan palliation: What have we learned? What should we expect?
• Frequency of Mutations in the TPO Gene in Patients with Congenital Hypothyroidism Due to Dyshormonogenesis in Chile
• Genetic analysis of a Chinese pedigree with Cohen syndrome due to compound heterozygous variants of VPS13B gene
• Genetic and clinical characteristics of ZNF408-related familial exudative vitreoretinopathy
• Genetic characteristic analysis of slight-to-moderate sensorineural hearing loss in children
• Genetic dysregulation of an endothelial Ras signaling network in vein of Galen malformations
• Gestational diabetes mellitus (Update 2023)
• Hereditary hemorrhagic telangiectasia diagnosis: A case report
• Hereditary hemorrhagic telangiectasia in a 42-year-old Ethiopian man presenting with severe anemia and high-output heart failure: A case report with literature review
• Hydrogel-Based Therapies for Ischemic and Hemorrhagic Stroke: A Comprehensive Review
• Immune cell ratio and coagulation markers in assessing prognosis of asthma: a cross-sectional study from Saudi Arabia
• Implications of serial magnetic resonance imaging in the management of a newborn with vein of Galen aneurysmal malformation and a review of the relevant literature
• Influenza vaccination during pregnancy and risk of selected major structural congenital heart defects, National Birth Defects Prevention Study 2006-2011
• Isolated Pulmonary Arteriovenous Malformations Associated With BMPR2 Pathogenic Variants
• Long-Term Outcomes of Unrepaired Isolated Partial Anomalous Pulmonary Venous Connection With an Intact Atrial Septum
• Longitudinal Assessment of Intraretinal Microvascular Abnormalities in Diabetic Retinopathy Using Swept-Source Optical Coherence Tomography Angiography
• Looking at a baby's heart through the lens of the mother's blood
• Lymphatic/blood vessel plasticity: motivation for a future research area based on present and past observations
• Massive hemothorax induced by pulmonary arteriovenous malformation rupture: a case report and literature review
• Metabolomic Differences in Connective Tissue Disease-Associated Versus Idiopathic Pulmonary Arterial Hypertension in the PVDOMICS Cohort
• Migraine Aura-Catch Me If You Can with EEG and MRI-A Narrative Review
• Monogenic Causes in Familial Stroke Across Intracerebral Hemorrhage and Ischemic Stroke Subtypes Identified by Whole-Exome Sequencing
• Mutation of key signaling regulators of cerebrovascular development in vein of Galen malformations
• Myocardial perfusion in cardiac amyloidosis
• Novel <em>PRKAR1A</em> mutation in Carney complex: a case report and literature review
• Opitz GBBB syndrome with total anomalous pulmonary venous connection: A new MID1 gene variant
• Outcomes After Ladd Procedures for Intestinal Malrotation in Newborns with Heterotaxy Syndrome
• Pediatric Cerebral Cavernous Malformation: A Single-Centered Experience of 23 Cases
• Persistent right venous valve as a cause of fetal and neonatal pathology from prenatal to postnatal periods: a case report and review
• Plasma Connective Tissue Growth Factor as a Biomarker of Pulmonary Arterial Hypertension Associated With Congenital Heart Disease in Adults
• Polygenic Risk in Families With Spontaneous Coronary Artery Dissection
• Pouch Transfer for Single Coronary Artery With Nodal Artery Variant in Arterial Switch Operation
• Primary disease of adipose tissue: When to think about and how to evaluate it in clinical practice?
• Pulmonary Arteriovenous Malformation (AVMs)
• Pulmonary Arteriovenous Malformation (AVMs)
• Pulmonary Arteriovenous Malformation (AVMs) (Archived)
• Pulmonary hypertension exacerbated by hereditary hemorrhagic telangiectasia combined with pulmonary arteriovenous fistula and pregnancy status: A case report
• Role of endothelial PDGFB in arterio-venous malformations pathogenesis
• Severe Congenital Neutropenia Type 4: A Rare Disease Harboring a G6pc3 Gene Pathogenic Variant Particular to the Mexican Population
• SMAD4 maintains the fluid shear stress set point to protect against arterial-venous malformations
• Special clinical entity with 15q26 deletion: a novel case report
• Spontaneous haemothorax caused by a ruptured pulmonary arterio-venous malformation: A manifestation of hereditary haemorrhagic telangiectasia in pregnancy
• STIC-HD live flow technology in the antenatal diagnosis of scimitar syndrome: A case report
• Study on The Pedigrees of Three Cases of Whole-Arm Translocation in Hainan China and Literature Review: A Retrospective Study
• Systemic artery to pulmonary artery aneurysm malformations associated with variants at MCF2L
• The choroidal nervous system: a link between mineralocorticoid receptor and pachychoroid
• The contribution of the sinusoidal endothelial cell receptors CLEC4M, stabilin-2, and SCARA5 to VWF-FVIII clearance in thrombosis and hemostasis
• The Prospective Natural History Study of Patients with Intractable Venous Malformation and Klippel-Trenaunay Syndrome to Guide Designing a Proof-of-Concept Clinical Trial for Novel Therapeutic Intervention
• The Shunt of It
• The VASCERN-VASCA Working Group Diagnostic and Management Pathways for Venous Malformations
• Total Anomalous Pulmonary Venous Connections, Human Genetics
• Towards a neurocognitive profile in familial cerebral cavernous malformations
• Two novel homozygous variants of ATP6V0A2 and ALDH18A1 lead to autosomal recessive cutis laxa type 2 and 3 in two Pakistani families
• Two siblings with GAPO syndrome: Ophthalmic presentation and histopathologic findings
• Upregulation of the Four and a Half LIM Domains 1 linked with familial venous dysplasia in a familial genetic examination
• Von Hipple-Lindau disease complicated with central retinal vein occlusion: a case report
• Zonule-Associated Gene Variants in Isolated Ectopia Lentis and Glaucoma