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 Microphysiological HHT-on-a-Chip Platform Recapitulates Patient Vascular Lesions
- A Rare Association: Hereditary Hemorrhagic Telangiectasia with Liver Cirrhosis Causing Portal Hypertension
- A rare case of spinal involvement in hereditary hemorrhagic telangiectasia
- A rare cause of hepatic arteriovenous fistula: Hereditary hemorrhagic telangiectasia
- ACR Appropriateness Criteria® Pulmonary Arteriovenous Malformation (PAVM): 2023 Update
- Acute exacerbation of recurrent epistaxis and anemia in hereditary hemorrhagic telangiectasia: A case report
- An Uncommon Cause of Hemobilia
- Arterial Spin-Labeling MR Imaging in the Detection of Intracranial Arteriovenous Malformations in Patients with Hereditary Hemorrhagic Telangiectasia
- 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
- Blood flow regulates acvrl1 transcription via ligand-dependent Alk1 activity
- BMP9 is a key player in endothelial identity and its loss is sufficient to induce arteriovenous malformations
- Brain AVM compactness score in children with hereditary hemorrhagic telangiectasia
- Can Hemorrhagic Stroke Genetics Help Forensic Diagnosis in Pediatric Age (<5 Years Old)?
- Chronic traumatic encephalopathy pathognomonic lesions occurring in isolation adjacent to infiltrative and non-infiltrative white matter lesions
- 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
- 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
- Current Practice: Rationale for Screening Children with Hereditary Hemorrhagic Telangiectasia for Brain Vascular Malformations
- 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
- Diffuse pulmonary arteriovenous malformation presenting with secondary polycythemia and headaches: a case report
- Early Infantile Diagnosis of Hereditary Hemorrhagic Telangiectasia Complicated by Child Abuse
- 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
- Employment of diverse in vitro systems for analyzing multiple aspects of disease, hereditary hemorrhagic telangiectasia (HHT)
- 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
- Endothelial-to-Mesenchymal Transition in an Hereditary Hemorrhagic Telangiectasia-like Pediatric Case of Multiple Pulmonary Arteriovenous Malformations
- Epidemiology of complications among hospitalized children with hereditary hemorrhagic telangiectasia: A kids' inpatient database study
- Evaluation of Aav Capsids and Delivery Approaches for Hereditary Hemorrhagic Telangiectasia Gene Therapy
- Evaluation of AAV Capsids and Delivery Approaches for Hereditary Hemorrhagic Telangiectasia Gene Therapy
- Functional characterization of variants found in Japanese patients with hereditary hemorrhagic telangiectasia
- Fusion imaging for guidance of pulmonary arteriovenous malformation embolisation with minimal radiation and contrast exposure
- Genetic analysis of a child with Hereditary hemorrhagic telangiectasia type I in conjunct with Splenic sinus shore cell hemangioma
- Genetic analysis of a family with hereditary hemorrhagic telangiectasia caused by a novel frameshift deletion mutation of the endoglin (ENG) gene
- Genome sequencing identify chromosome 9 inversions disrupting ENG in 2 unrelated HHT families
- Hepatic manifestations of hereditary haemorrhagic telangiectasia
- Hereditary Hemorrhagic Telangiectasia (Osler's Disease): Systemic, Interdisciplinary, Relatively Common-and Often Missed
- Hereditary hemorrhagic telangiectasia diagnosis: A case report
- 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 Recurrent Epistaxis, Telangiectasia, Hepatic Arteriovenous Malformation, and a Poorly Developed Middle Cerebral Artery in a Patient with a Novel Mutation in the ACVRL1 Gene
- Hereditary hemorrhagic telangiectasia: from signaling insights to therapeutic advances
- How I Treat Bleeding in Hereditary Hemorrhagic Telangiectasia
- 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
- Increased Risk for Infections and Allergic Disease in Hereditary Hemorrhagic Telangiectasia
- Integration of genotypic data into clinical trial design and reporting in hereditary hemorrhagic telangiectasia could help personalize treatment
- Investigation of the Genetic Determinants of Telangiectasia and Solid Organ Arteriovenous Malformation Formation in Hereditary Hemorrhagic Telangiectasia (HHT)
- Iron deficiency anemia in a patient with hereditary hemorrhagic telangiectasia. Case report
- Ischemic cholangitis: Lethal complication of Osler-Weber-Rendu disease
- Large pulmonary arteriovenous malformation lost to follow-up with 10 years of asymptomatic interval growth: A case report
- Large- and medium-sized arterial aneurysms in two patients with SMAD4-related juvenile polyposis syndrome
- 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
- 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
- Long Term Survival of Heritable Pulmonary Arterial Hypertension Associated with Hereditary Hemorrhagic Telangiectasia: A Case Series
- Management of hereditary hemorrhagic telangiectasia-like symptoms induced by trastuzumab emtansine in a breast cancer patient: case report
- Massive hemothorax induced by pulmonary arteriovenous malformation rupture: a case report and literature review
- Meta-analysis of efficacy and safety of bevacizumab in the treatment of hereditary hemorrhagic telangiectasia epistaxis
- Molecular mechanisms and clinical manifestations of hereditary hemorrhagic telangiectasia
- 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
- Personalised stroke evaluation and management: tailoring individualised patient care for hereditary haemorrhagic telangiectasia
- Phenotypic characterisation of <em>SMAD4</em> variant carriers
- Pioneering the future: CRISPR-Cas9 gene therapy for hereditary hemorrhagic telangiectasia
- Pioneering the future: CRISPR-Cas9 gene therapy for hereditary hemorrhagic telangiectasia. Author's reply
- Preliminary Experience With Novel Straight 3-Fr Guiding Sheath for Transradial Access in Endovascular Treatment: Feasibility and Safety
- 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
- 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 in Rendu-Osler-Weber syndrome
- Pulmonary hypertension exacerbated by hereditary hemorrhagic telangiectasia combined with pulmonary arteriovenous fistula and pregnancy status: A case report
- 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
- Recurrence of Pulmonary Arteriovenous Malformation after Embolization in Patients with Pulmonary Hypertension
- Ruptured pulmonary arteriovenous fistula causing hemothorax in a patient with hereditary hemorrhagic telangiectasia: A case report
- Shear Stress and Sub-Femtomolar Levels of Ligand Synergize to Activate ALK1 Signaling in Endothelial Cells
- Spontaneous haemothorax caused by a ruptured pulmonary arterio-venous malformation: A manifestation of hereditary haemorrhagic telangiectasia in pregnancy
- Stereotactic radiosurgery for brain arteriovenous malformations in patients with hereditary hemorrhagic telangiectasia
- Sudden pediatric death unveiling pulmonary arteriovenous malformations
- Surgery or No Surgery? Exploring the Dilemma of Epistaxis Management in Patients with HHT
- Surgical treatment of brain arteriovenous malformations in patients with hereditary hemorrhagic telangiectasia: a single-center experience
- Telangiectasias, recurrent epistaxis and a strong family history-a case of Osler- Weber-Rendu Syndrome in Pakistan
- 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
- Thyroid Arteriovenous Malformation in Hereditary Hemorrhagic Telangiectasia: Insights on Successful Noninvasive Imaging
- 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?
- Ultra-low dose chest CT for the diagnosis of pulmonary arteriovenous malformation in patients with hereditary hemorrhagic telangiectasia
- 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
- V-Y advancement flap for the repair of localized cutaneous defects following nasal closure in severe hereditary hemorrhagic telangiectasia