Disease: Hereditary hemorrhagic telangiectasia
- A Case of an Splenic Artery Aneurysm and Focal Nodular Hyperplasia Associated with an Abdominal Vascular Abnormality of Hereditary Hemorrhagic Telangiectasia
- A case of hereditary hemorrhagic telangiectasia treated with cryotherapy
- A case report of limitation of transcatheter hepatic arterial embolization for hereditary hemorrhagic telangiectasia type 2 with pulmonary arterial hypertension
- A Microphysiological HHT-on-a-Chip Platform Recapitulates Patient Vascular Lesions
- A Rare Association: Hereditary Hemorrhagic Telangiectasia with Liver Cirrhosis Causing Portal Hypertension
- An integrated docking and molecular dynamics simulation approach to discover potential inhibitors of activin receptor-like kinase 1
- An Uncommon Cause of Hemobilia
- 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
- Blood flow regulates <em>acvrl1</em> transcription via ligand-dependent Alk1 activity
- BMP9 is a key player in endothelial identity and its loss is sufficient to induce arteriovenous malformations
- Bmp9 regulates Notch signaling and the temporal dynamics of angiogenesis via Lunatic Fringe
- Brain AVM compactness score in children with hereditary hemorrhagic telangiectasia
- Comment on Kilian et al. Comparing Characteristics and Treatment of Brain Vascular Malformations in Children and Adults with HHT. <em>J. Clin. Med.</em> 2023, <em>12</em>, 2704
- 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
- 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
- De novo brain vascular malformation in an adult with hereditary hemorrhagic telangiectasia and juvenile polyposis overlap syndrome
- De Novo Brain Vascular Malformations in Hereditary Hemorrhagic Telangiectasia
- Diagnostic Difficulties in Hemorrhagic Hereditary Telangiectasia Presenting With Respiratory Failure and a De Novo Mutation in ENG Gene
- 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
- Endoglin mutants retained in the endoplasmic reticulum exacerbate loss of function in hereditary hemorrhagic telangiectasia type 1 (HHT1) by exerting dominant negative effects on the wild type allele
- Epidemiology of complications among hospitalized children with hereditary hemorrhagic telangiectasia: A kids' inpatient database study
- Essential role of the amino-terminal region of Drosha for the Microprocessor function
- Evaluating the Quality, Readability, and Activity of Online Information on Brain Arteriovenous Malformations
- Functional characterization of variants found in Japanese patients with hereditary hemorrhagic telangiectasia
- Functional filter for whole-genome sequencing data identifies HHT and stress-associated non-coding SMAD4 polyadenylation site variants >5 kb from coding DNA
- Fusion imaging for guidance of pulmonary arteriovenous malformation embolisation with minimal radiation and contrast exposure
- Gastrointestinal bleeding in patients with hereditary hemorrhagic telangiectasia: Long-term results of endoscopic treatment
- Genome sequencing identify chromosome 9 inversions disrupting ENG in 2 unrelated HHT families
- Genomics of iron refractory iron deficiency anemia phenotype reveals a spectrum of novel pathogenic biallelic and monoallelic TMPRSS6 variants and rare overlapping disorders
- Glanzmann's thrombasthenia associated with gastrointestinal angiodysplasias successfully treated with bevacizumab
- Health-Related Quality of Life Outcome Measures in Individuals With Hereditary Hemorrhagic Telangiectasia: A Scoping Review
- Hepatic Vascular Variants in Hereditary Haemorrhagic Telangiectasia: Imaging findings
- Hereditary haemorrhagic telangiectasia and SMAD4 mutation in a patient with complex single ventricle heart disease
- Hereditary hemorrhagic telangiectasia diagnosis: A case report
- Hereditary Hemorrhagic Telangiectasia in a Patient Undergoing Hemodialysis with Anticoagulants and Antiplatelets: A Case Report
- Hereditary hemorrhagic telangiectasia involving portal venous system: A case report and review of the literature
- 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, Clinical Presentations, and Management
- Hereditary hemorrhagic telangiectasia: from signaling insights to therapeutic advances
- High risk of ischaemic stroke amongst patients with hereditary haemorrhagic telangiectasia
- Identification of Choroidal Vascular Abnormalities in Patients with Hereditary Hemorrhagic Telangiectasia (HHT)
- Impact of heterozygous ALK1 mutations on the transcriptomic response to BMP9 and BMP10 in endothelial cells from hereditary hemorrhagic telangiectasia and pulmonary arterial hypertension donors
- Induced Endothelial Cell CycleArrest Prevents Arteriovenous Malformations in Hereditary Hemorrhagic Telangiectasia
- Iron deficiency anemia in a patient with hereditary hemorrhagic telangiectasia. Case report
- Laparoscopic Double Hepatic Artery Banding/Ligation for Patients With Hepatic Hereditary Haemorrhagic Telangiectasia (HHHT)
- Large-scale phosphoproteomics reveals activation of the MAPK/GADD45β/P38 axis and cell cycle inhibition in response to BMP9 and BMP10 stimulation in endothelial cells
- Late-Onset Ovarian Bleeding After Transvaginal Oocyte Retrieval in a Patient With Suspected Hereditary Hemorrhagic Telangiectasia
- Liver failure caused by recurrent biliary bleeding associated with Osler's disease: a case report
- Liver imaging and pregnancy: what to expect when your patient is expecting
- Lobectomy for Pulmonary Arteriovenous Fistula in a Patient With Rendu-Osler-Weber Disease: A Case Report
- Long Term Survival of Heritable Pulmonary Arterial Hypertension Associated with Hereditary Hemorrhagic Telangiectasia: A Case Series
- MEK 1 inhibition and bleeding in hereditary haemorrhagic telangiectasia
- Meta-analysis of efficacy and safety of bevacizumab in the treatment of hereditary hemorrhagic telangiectasia epistaxis
- Multi-organ hereditary hemorrhagic telangiectasia: A case report
- Mutations causing premature termination codons discriminate and generate cellular and clinical variability in HHT
- Outcomes of patients with Juvenile Polyposis-Hereditary Haemorrhagic Telangiectasia caused by pathogenic SMAD4 variants in a pan-Scotland cohort
- Pathogenic Variant Frequencies in Hereditary Haemorrhagic Telangiectasia Support Clinical Evidence of Protection from Myocardial Infarction
- Pediatric Lung Transplantations: New Possibilities and Challenges in Treatment of Children With End-Stage Respiratory Failure
- Percutaneous embolization of pulmonary arteriovenous malformations in adult patient with Rendu-Osler-Weber: a case report
- Personalised stroke evaluation and management: tailoring individualised patient care for hereditary haemorrhagic telangiectasia
- Pharmacogenomic Considerations for Anticoagulant Prescription in Patients with Hereditary Haemorrhagic Telangiectasia
- Phenotypic characterisation of <em>SMAD4</em> variant carriers
- Prenatal diagnosis of pulmonary arteriovenous malformations with a postnatal diagnosis of Osler-Weber-Rendu syndrome
- Prevalence and Characteristics of Intracranial Aneurysms in Hereditary Hemorrhagic Telangiectasia
- Prevalence of hereditary hemorrhagic telangiectasia in a medical care program organization in Buenos Aires, Argentina
- Prevalencia de la Telangiectasia Hemorrágica Hereditaria: estudio de base poblacional en la Comunitat Valenciana (España).
- 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
- Progressive Dyspnea on Exertion in an 82-Year-Old
- Pulmonary arteriovenous malformations in patients with previous brain abscess: a cross-sectional population-based study
- Pulmonary arteriovenous malformations in Rendu-Osler-Weber syndrome
- Pulmonary Hypertension Due to High-Output Heart Failure: Hereditary Hemorrhagic Telangiectasia
- Pulmonary hypertension in hereditary hemorrhagic telangiectasia: A clinical review
- Pulmonary vascular phenotype identified in patients with <em>GDF2 (BMP9)</em> or <em>BMP10</em> variants: An international multicentre study
- Pulmonary vascular phenotype identified in patients with <em>GDF2</em> (<em>BMP9</em>) or <em>BMP10</em> variants: an international multicentre study
- Rare bleeding disorders: Advances in management
- Shear Stress and Sub-Femtomolar Levels of Ligand Synergize to Activate ALK1 Signaling in Endothelial Cells
- SMAD4 variants and its genotype-phenotype correlations to juvenile polyposis syndrome
- Stereotactic radiosurgery for brain arteriovenous malformations in patients with hereditary hemorrhagic telangiectasia
- Surgery or No Surgery? Exploring the Dilemma of Epistaxis Management in Patients with HHT
- Tacrolimus as a Promising Drug for Epistaxis and Gastrointestinal Bleeding in HHT
- The bleeding diathesis in patients with hereditary haemorrhagic telangiectasia is not due to impaired platelet function
- 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 VASCERN PPL working group patient pathway for primary and paediatric lymphoedema
- To Test or Not to Test: A Case Report on Hereditary Hemorrhagic Telangiectasia
- Treatment of Hereditary Haemorrhagic Telangiectasia with Bevacizumab - What More Needs to be Known?
- Treatments of Epistaxis in Hereditary Hemorrhagic Telangiectasia: Systematic Review and Network Meta-Analysis
- uAUG creating variants in the 5'UTR of ENG causing Hereditary Hemorrhagic Telangiectasia
- Ultra-low dose chest CT for the diagnosis of pulmonary arteriovenous malformation in patients with hereditary hemorrhagic telangiectasia
- Understanding hereditary hemorrhagic telangiectasia: From genetic anomalies to systemic manifestations, quality of life, and epistaxis management-Exploring the otolaryngologist's integral role
- 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
- Utility of bevacizumab in chronic gastrointestinal bleeding in hereditary hemorrhagic telangiectasia
- VEGFR2 Expression Correlates with Postnatal Development of Brain Arteriovenous Malformations in a Mouse Model of Type I Hereditary Hemorrhagic Telangiectasia