Disease: Osler Rendu Weber syndrome 3
- A <em>GDF2</em> missense mutation potentially involved in the pathogenesis of hereditary hemorrhagic telangiectasia: a case report
- A 37-Year-Old Man with Familial Hereditary Hemorrhagic Telangiectasia and Pulmonary Arteriovenous Malformations Presenting with Seizures and a Diagnosis of Brain Abscesses
- A GDF2 missense mutation potentially involved in the pathogenesis of hereditary hemorrhagic telangiectasia: a case report
- A novel germline SMAD4 variant detected in a Japanese family with juvenile polyposis syndrome and hereditary hemorrhagic telangiectasia
- A rare homozygous missense GDF2 (BMP9) mutation causing PAH in siblings: Does BMP10 status contribute?
- ALK1 controls hepatic vessel formation, angiodiversity, and angiocrine functions in hereditary hemorrhagic telangiectasia of the liver
- An <em>in vitro</em> study on the effect of bevacizumab on endothelial cell proliferation and VEGF concentration level in patients with hereditary hemorrhagic telangiectasia
- An in vitro study on the effect of bevacizumab on endothelial cell proliferation and VEGF concentration level in patients with hereditary hemorrhagic telangiectasia
- ANG2 Blockade Diminishes Proangiogenic Cerebrovascular Defects Associated With Models of Hereditary Hemorrhagic Telangiectasia
- Anticoagulation and antiplatelet therapy in hereditary hemorrhagic telangiectasia: A scoping review
- Antiplatelet and anticoagulant therapies in hereditary hemorrhagic telangiectasia: A large French cohort study (RETROPLACOTEL)
- Application of contrast-enhanced ultrasound in hemothorax of hereditary hemorrhagic telangiectasia: A case report and literature review
- Assessing the Psychometric Validity of the Epistaxis Severity Score: Internal Consistency and Test-Retest Reliability
- Association of socioeconomic status with the management outcome of unruptured intracranial arteriovenous malformation
- Bilateral Lung Transplantation for Congenital Pulmonary Arteriovenous Fistula with Intraoperative Venovenous ECMO Support: The First Case Report in China
- Brain Abscess and Stroke in Children and Adults With Hereditary Hemorrhagic Telangiectasia: Analysis of a Large National Claims Database
- Brain AVM compactness score in children with hereditary hemorrhagic telangiectasia
- Can aura migraine be elicited by isolated pulmonary arteriovenous fistula?-A case report
- Cerebral arterio-venous malformations hemodynamics changes in hereditary hemorrhagic telangiectasia - case report
- Comparative Treatment of Mucocutaneous Lesions in Hereditary Haemorrhagic Telangiectasia Patients With Dual Sequential Pulsed Dye Laser and Neodymium: Yttrium-Aluminium-Garnet Versus Neodymium: Yttrium-Aluminium-Garnet Laser Alone: A Double-Blind Randomiz
- Comparative Treatment of Mucocutaneous Lesions in Hereditary Haemorrhagic Telangiectasia Patients With Dual Sequential Pulsed Dye Laser and Neodymium: Yttrium-Aluminium-Garnet Versus Neodymium: Yttrium-Aluminium-Garnet Laser Alone: A Double-Blind Randomiz
- Comparative treatment of mucocutaneous lesions in hereditary hemorrhagic telangiectasia patients with dual sequential pulsed dye laser and neodymium: yttrium-aluminum-garnet versus neodymium: yttrium-aluminum-garnet laser alone: a double-blind randomized
- Comparison of Transthoracic Contrast Echocardiography with High-Resolution Chest CT after Embolization of Pulmonary Arteriovenous Malformation
- Computational and Experimental Analyses for Pathogenicity Prediction of <em>ACVRL1</em> Missense Variants in Hereditary Hemorrhagic Telangiectasia
- Computational and Experimental Analyses for Pathogenicity Prediction of ACVRL1 Missense Variants in Hereditary Hemorrhagic Telangiectasia
- Conservative management by embolization of a ruptured renal arterio-venous malformation (AVM) in Hereditary Hemorrhagic Telangiectasia (HHT)
- Cost-effectiveness of bevacizumab therapy in the care of patients with hereditary hemorrhagic telangiectasia
- Defining the clinical validity of genes reported to cause pulmonary arterial hypertension
- Development and performance of a hereditary hemorrhagic telangiectasia-specific quality-of-life instrument
- Development and validation of a quality of life measurement scale specific to hereditary hemorrhagic telangiectasia: the QoL-HHT
- Distribution of Cerebrovascular Phenotypes According to Variants of the ENG and ACVRL1 Genes in Subjects with Hereditary Hemorrhagic Telangiectasia
- Dysfunction of endothelial BMP-9 signaling in pulmonary vascular disease
- Efficacy and safety of intravenous bevacizumab on severe bleeding associated with hemorrhagic hereditary telangiectasia: A national, randomized multicenter trial
- Efficacy and Safety of Tacrolimus as Treatment for Bleeding Caused by Hereditary Hemorrhagic Telangiectasia: An Open-Label, Pilot Study
- Efficacy and Safety of Venous Sac Embolization With or Without Feeding Artery Embolization Versus Feeding Artery Embolization Alone in the Management of Pulmonary Arteriovenous Malformations: A Systematic Review and Meta-analysis
- Efficacy of Gabapentin For Post-COVID-19 Olfactory Dysfunction: The GRACE Randomized Clinical Trial
- Elevated FVIII levels in hereditary hemorrhagic telangiectasia: Implications for clinical management
- Embolization of De Novo Pulmonary Arteriovenous Malformations Using High-Volume Detachable Non-Fibered Coils: Propensity-Matched Comparison to Traditional Coils
- Embolization of Recurrent Pulmonary Arteriovenous Malformations by Ethylene Vinyl Alcohol Copolymer (Onyx()) in Hereditary Hemorrhagic Telangiectasia: Safety and Efficacy
- Embolization of Recurrent Pulmonary Arteriovenous Malformations by Ethylene Vinyl Alcohol Copolymer (Onyx<sup>®</sup>) in Hereditary Hemorrhagic Telangiectasia: Safety and Efficacy
- Evolution of Pulmonary Arteriovenous Malformations: The Role of Contrast Echocardiography
- Functional filter for whole-genome sequencing data identifies HHT and stress-associated non-coding SMAD4 polyadenylation site variants >5 kb from coding DNA
- Gastrointestinal bleeding in patients with hereditary hemorrhagic telangiectasia: Long-term results of endoscopic treatment
- Generation of a Syngeneic Heterozygous <em>ACVRL1<sup>(wt/mut)</sup></em> Knockout iPS Cell Line for the In Vitro Study of HHT2-Associated Angiogenesis
- Genetic analysis of a family with hereditary hemorrhagic telangiectasia caused by endoglin gene mutation
- Health-Related Quality of Life Outcome Measures in Individuals With Hereditary Hemorrhagic Telangiectasia: A Scoping Review
- Hepatic involvement in hereditary hemorrhagic telangiectasia mimicking focal nodular hyperplasia
- Hereditary haemorrhagic telangiectasia in Danish patients with pathogenic variants in <em>SMAD4:</em> a nationwide study
- Hereditary haemorrhagic telangiectasia in Danish patients with pathogenic variants in SMAD4: a nationwide study
- Hereditary Hemorrhagic Telangiectasia Associating Neuropsychiatric Manifestations with a Significant Impact on Disease Management-Case Report and Literature Review
- Hereditary hemorrhagic telangiectasia may be the most morbid inherited bleeding disorder of women
- Hereditary hemorrhagic telangiectasia with hepatic arteriovenous shunt diagnosed due to liver damage
- Hereditary Hemorrhagic Telangiectasia With Multiple Ear, Nose, and Throat (ENT) Manifestations: A Case Report
- Hereditary hemorrhagic telangiectasia: First demonstration of a founder effect in Italy; the ACVRL1 c.289_294del variant originated in the country of Bergamo 200 years ago
- High risk of ischaemic stroke amongst patients with hereditary haemorrhagic telangiectasia
- Human <em>SMAD4</em> Genomic Variants Identified in Individuals with Heritable and Early-Onset Thoracic Aortic Disease
- Identification of Choroidal Vascular Abnormalities in Patients with Hereditary Hemorrhagic Telangiectasia (HHT)
- Identifying racial disparities in hereditary hemorrhagic telangiectasia
- Impact of SARS-CoV-2 infection in patients with hereditary hemorrhagic telangiectasia: epidemiological and clinical data from the comprehensive Italian retrospective multicenter study
- Improving Hereditary Hemorrhagic Telangiectasia Molecular Diagnosis: A Referral Center Experience
- Infective endocarditis with Osler's nodule in a patient with Osler's disease: a case report and review of the literature
- Iron deficiency responses and integrated compensations in patients according to hereditary hemorrhagic telangiectasia ACVRL1, ENG and SMAD4 genotypes
- Liver imaging and pregnancy: what to expect when your patient is expecting
- Localized conditional induction of brain arteriovenous malformations in a mouse model of hereditary hemorrhagic telangiectasia
- Long-term use of somatostatin analogs for chronic gastrointestinal bleeding in hereditary hemorrhagic telangiectasia
- Longitudinal Assessment of Curacao Criteria in Children with Hereditary Hemorrhagic Telangiectasia
- Management outcomes of peripontine arteriovenous malformation patients presenting with trigeminal neuralgia
- Meta-analysis of efficacy and safety of bevacizumab in the treatment of hereditary hemorrhagic telangiectasia epistaxis
- Most-Cited Patient-Reported Outcome Measures Within Otolaryngology-Revisiting the Minimal Clinically Important Difference: A Review
- Multi-organ hereditary hemorrhagic telangiectasia: A case report
- Multiple brain arteriovenous malformations: systematic review and individual patient data meta-analysis
- Myocardial Infarction in a 29-Year-Old Woman Leads to Diagnosis and Treatment of a Rare Disease
- Not Just Another "Bloody" Case of Right Heart Failure
- Obstetrical and neonatal complications in hereditary haemorrhagic telangiectasia: A retrospective study
- Preliminary Experience with a Low-Profile High-Density Braid Occluder for Transcatheter Embolization of Pulmonary Arteriovenous Malformations
- Prevalence and Characteristics of Intracranial Aneurysms in Hereditary Hemorrhagic Telangiectasia
- Prevalence and Predictors of Hereditary Hemorrhagic Telangiectasia and Capillary-Malformation Arteriovenous Malformation Syndrome Among Children with Neurovascular Malformations
- Prevalence and risk factors for bleeding in hereditary hemorrhagic telangiectasia: a National Inpatient Sample study
- Pro-angiogenic changes of T-helper lymphocytes in hereditary hemorrhagic telangiectasia
- Prognostic Factors for Survival Using a Clinical Severity Staging System Among Patients With Acute Invasive Fungal Sinusitis
- Pulmonary Arteriovenous Malformations: What the Interventional Radiologist Should Know
- Pulmonary vascular phenotype identified in patients with <em>GDF2</em> (<em>BMP9</em>) or <em>BMP10</em> variants: an international multicentre study
- Risk factors and clinical features associated with basal ganglia manganese deposition in patients with hereditary hemorrhagic telangiectasia
- Safety, tolerability, and effectiveness of anticoagulation and antiplatelet therapy in hereditary hemorrhagic telangiectasia
- Schizencephaly in Hereditary Hemorrhagic Telangiectasia
- Shear Stress and Sub-Femtomolar Levels of Ligand Synergize to Activate ALK1 Signaling in Endothelial Cells
- Significance of transesophageal contrast echocardiography with the agitated saline test for diagnosing pulmonary arteriovenous malformations
- SMAD4 maintains the fluid shear stress set point to protect against arterial-venous malformations
- Stereotactic radiosurgery for brain arteriovenous malformations in patients with hereditary hemorrhagic telangiectasia
- Targeted Diode Laser Therapy for Oral and Perioral Capillary-Venous Malformation in Pediatric Patients: A Prospective Study
- The ENG/VEGFalpha Pathway Is Likely Affected by a Nonsense Variant of Endoglin (ENG)/CD105, Causing Hereditary Hemorrhagic Telangiectasia Type 1 (HHT1) in a Chinese Family
- The Use of Beta-Blockers in Hereditary Hemorrhagic Telangiectasia-Related Epistaxis: A Systematic Review
- Thromboembolic hazard in hereditary hemorrhagic telangiectasia
- TIMolol Nasal Spray as a Treatment for Epistaxis in Hereditary Hemorrhagic Telangiectasia (TIM-HHT)-A Prospective, Randomized, Double-Blind, Controlled, Cross-Over Trial
- Treatments of Epistaxis in Hereditary Hemorrhagic Telangiectasia: Systematic Review and Network Meta-Analysis
- Ultra-low dose chest CT for the diagnosis of pulmonary arteriovenous malformation in patients with hereditary hemorrhagic telangiectasia
- Update on pulmonary arteriovenous malformations
- Use of Polyurethane-Covered Stents for Exclusion of Pulmonary Arteriovenous Malformations
- Usefulness of endoscopic endonasal underwater surgery using a combination of coblation and a lens-cleaning system for hemostasis in hereditary hemorrhagic telangiectasia
- VEGFR2 Expression Correlates with Postnatal Development of Brain Arteriovenous Malformations in a Mouse Model of Type I Hereditary Hemorrhagic Telangiectasia