Works matching DE "HEREDITARY hemorrhagic telangiectasia"
Results: 740
Quantifying the burden of hereditary hemorrhagic telangiectasia on quality of life and psychological health: a cross-sectional study.
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- Orphanet Journal of Rare Diseases, 2025, v. 20, n. 1, p. 1, doi. 10.1186/s13023-025-03620-8
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- Article
Pulmonary arteriovenous malformations in Rendu-Osler-Weber syndrome.
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- Jornal Vascular Brasileiro, 2024, v. 23, p. 1, doi. 10.1590/1677-5449.202301332
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- Article
Health outcomes following COVID-19 infection and vaccination in hereditary hemorrhagic telangiectasia.
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- Orphanet Journal of Rare Diseases, 2025, v. 20, n. 1, p. 1, doi. 10.1186/s13023-025-03561-2
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- Article
Diagnosing rashes, part 12: lip lesions.
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- Practice Nursing, 2014, v. 25, n. 11, p. 557, doi. 10.12968/pnur.2014.25.11.557
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- Article
BMP9 and BMP10: Two close vascular quiescence partners that stand out.
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- Developmental Dynamics, 2022, v. 251, n. 1, p. 178, doi. 10.1002/dvdy.395
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- Article
Stereotactic radiosurgery for brain arteriovenous malformations in patients with hereditary hemorrhagic telangiectasia.
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- Acta Neurochirurgica, 2024, v. 166, n. 1, p. 1, doi. 10.1007/s00701-024-05923-4
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- Article
Recurrence of brain arteriovenous malformations in pediatric patients: a long-term follow-up study.
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- Acta Neurochirurgica, 2023, v. 165, n. 6, p. 1565, doi. 10.1007/s00701-023-05612-8
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- Article
Intractable bleeding from the renal pelvis in a patient with hereditary haemorrhagic telangiectasia (Rendu-Osler-Weber disease).
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- Scandinavian Journal of Urology, 2020, v. 54, n. 5, p. 449, doi. 10.1080/21681805.2020.1798505
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- Article
Preliminary experience with the micro vascular plug for the treatment of pulmonary arteriovenous malformation: case series of four patients.
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- CVIR Endovascular, 2018, v. 1, n. 1, p. N.PAG, doi. 10.1186/s42155-018-0027-z
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- Article
Rhinoscleroma in a 9-year old boy: Rare case report.
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- Global Pediatric Health, 2023, p. 1, doi. 10.1177/2333794X231210673
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- Article
Cerebrovascular and cardiovascular disease burden in patients with hereditary hemorrhagic telangiectasia.
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- Neurological Sciences, 2021, v. 42, n. 12, p. 5117, doi. 10.1007/s10072-021-05135-z
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- Article
A case report of hereditary hemorrhagic telangiectasia in a family with initial presentation of cerebral abscess and pulmonary arteriovenous malformation in the proband.
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- 2020
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- Publication type:
- Letter
Juvenile stroke in combined syndrome of hereditary hemorrhagic telangiectasia and juvenile polyposis.
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- 2014
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- Publication type:
- Letter
Hereditary hemorrhagic telangiectasia and health-related quality of life: a qualitative investigation.
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- 2020
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- Publication type:
- journal article
Complications of Pulmonary AVMs in a Patient with Rendu-Osler-Weber Disease.
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- Collegium Antropologicum, 2014, v. 38, n. 3, p. 1071
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- Article
A Teenage Boy with Systemic Lupus Erythematosus Complicated with Acquired von Willebrand Syndrome: A Rare Case and Challenging in Making Diagnosis.
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- 2023
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- Publication type:
- Case Study
OSLER - WEBER - RENDU SYNDROME: A RARE CASE OF UPPER GASTROINTESTINAL BLEEDING.
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- Khyber Medical University Journal, 2022, v. 14, n. 2, p. 138
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- Article
VP32.10: Identification of a de novo mutation of ENG gene in a fetus with pulmonary arteriovenous fistula in a Chinese family.
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- Ultrasound in Obstetrics & Gynecology, 2020, v. 56, p. 190, doi. 10.1002/uog.22813
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- Article
EP10.10: Large fetal pulmonary arteriovenous malformation with severe cardiomegaly and favourable postnatal outcome.
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- Ultrasound in Obstetrics & Gynecology, 2018, v. 52, p. 237, doi. 10.1002/uog.19939
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- Article
von Willebrand disease (VWD) and BATs: How do they connect and why should I care?
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- Haemophilia, 2022, v. 28, n. 3, p. e89, doi. 10.1111/hae.14549
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- Article
Outcomes of long‐term von Willebrand factor prophylaxis use in von Willebrand disease: A systematic literature review.
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- Haemophilia, 2022, v. 28, n. 3, p. 373, doi. 10.1111/hae.14550
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- Article
An international survey to evaluate systemic bevacizumab for chronic bleeding in hereditary haemorrhagic telangiectasia.
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- Haemophilia, 2020, v. 26, n. 6, p. 1038, doi. 10.1111/hae.14034
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- Article
Social support and resilience in persons with severe haemophilia: An interpretative phenomenological analysis.
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- Haemophilia, 2020, v. 26, n. 3, p. e74, doi. 10.1111/hae.13999
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- Article
A Novel SMAD4 Mutation Causing Severe Juvenile Polyposis Syndrome with Protein Losing Enteropathy, Immunodeficiency, and Hereditary Haemorrhagic Telangiectasia.
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- Case Reports in Gastrointestinal Medicine, 2015, v. 2015, p. 1, doi. 10.1155/2015/140616
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- Article
Blood Flow and Shear Stress Allow Monitoring of Progression and Prognosis of Tumor Diseases.
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- Frontiers in Physiology, 2021, v. 12, p. 1, doi. 10.3389/fphys.2021.693052
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- Article
V‐Y advancement flap for the repair of localized cutaneous defects following nasal closure in severe hereditary hemorrhagic telangiectasia.
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- International Forum of Allergy & Rhinology, 2024, v. 14, n. 12, p. 1961, doi. 10.1002/alr.23415
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- Article
Reply to: "Intralesional cidofovir injections for the treatment of multifocal exophytic sinonasal papilloma": The utility of topical cidofovir.
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- International Forum of Allergy & Rhinology, 2024, v. 14, n. 9, p. 1543, doi. 10.1002/alr.23436
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- Article
Severe epistaxis after posterior nasal nerve ablation requiring surgical intervention: A multi‐center case series.
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- International Forum of Allergy & Rhinology, 2024, v. 14, n. 7, p. 1269, doi. 10.1002/alr.23339
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- Article
Severe unilateral refractory epistaxis arising from the septal branch of the anterior ethmoid artery.
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- International Forum of Allergy & Rhinology, 2024, v. 14, n. 6, p. 1135, doi. 10.1002/alr.23330
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- Article
Exploring effects of atmospheric conditions in hereditary hemorrhagic telangiectasia.
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- International Forum of Allergy & Rhinology, 2023, v. 13, n. 12, p. 2172, doi. 10.1002/alr.23183
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- Article
Injection of cyanoacrylate glue for hereditary hemorrhagic telangiectasia.
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- International Forum of Allergy & Rhinology, 2022, v. 12, n. 11, p. 1439, doi. 10.1002/alr.23017
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- Article
Randomized, controlled, double‐blinded clinical trial of effect of bevacizumab injection in management of epistaxis in hereditary hemorrhagic telangiectasia patients undergoing surgical cauterization.
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- International Forum of Allergy & Rhinology, 2022, v. 12, n. 8, p. 1034, doi. 10.1002/alr.22961
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- Article
Angiomatous Antrochoanal Polyp: A Diagnostic Dilemma.
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- 2024
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- Case Study
Red Papules on the Tongue of a Patient With Hemiparesis.
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- JAMA: Journal of the American Medical Association, 2014, v. 312, n. 7, p. 741, doi. 10.1001/jama.2014.1658
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- Article
Recurrent Gastrointestinal Bleeding in a Patient With Pulmonary Arterial Hypertension Treated With Sotatercept.
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- Annals of Internal Medicine, 2024, v. 177, n. 1, p. 115, doi. 10.7326/L23-0387
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- Article
Second International Guidelines for the Diagnosis and Management of Hereditary Hemorrhagic Telangiectasia.
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- 2021
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- Publication type:
- Letter
Second International Guidelines for the Diagnosis and Management of Hereditary Hemorrhagic Telangiectasia.
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- 2021
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- Publication type:
- Letter
Second International Guidelines for the Diagnosis and Management of Hereditary Hemorrhagic Telangiectasia.
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- 2021
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- Publication type:
- Letter
Annals for Educators - 15 December 2020.
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- 2020
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- Publication type:
- journal article
Second International Guidelines for the Diagnosis and Management of Hereditary Hemorrhagic Telangiectasia.
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- 2020
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- Publication type:
- journal article
Epistaxis in hereditary hemorrhagic telangiectasia: an evidence based review of surgical management.
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- Journal of Otolaryngology -- Head & Neck Surgery, 2016, v. 45, p. 1, doi. 10.1186/s40463-016-0116-8
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- Article
Technique modifications for septodermoplasty: an illustrative case.
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- Journal of Otolaryngology -- Head & Neck Surgery, 2015, v. 44, p. 1, doi. 10.1186/s40463-015-0112-4
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- Publication type:
- Article
Early Signs of Cardiovascular Senescence in a Patient with Hereditary Hemorrhagic Telangiectasia.
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- International Journal of Gerontology, 2023, v. 17, n. 2, p. 141, doi. 10.6890/IJGE.202304_17(2).0012
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- Article
Bevacizumab for treating Hereditary Hemorrhagic Telangiectasia patients with severe hepatic involvement or refractory anemia.
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- PLoS ONE, 2020, v. 15, n. 2, p. 1, doi. 10.1371/journal.pone.0228486
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- Article
Higher prevalence of splenic artery aneurysms in hereditary hemorrhagic telangiectasia: Vascular implications and risk factors.
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- PLoS ONE, 2020, v. 15, n. 1, p. 1, doi. 10.1371/journal.pone.0226681
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- Publication type:
- Article
Identification of two distinct hereditary hemorrhagic telangiectasia patient subsets with different hepatic perfusion properties by combination of contrast-enhanced ultrasound (CEUS) with perfusion imaging quantification.
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- PLoS ONE, 2019, v. 14, n. 4, p. 1, doi. 10.1371/journal.pone.0215178
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- Publication type:
- Article
From 78% oxygen saturation to 95% in 60 minutes: Osler-Weber-Rendu syndrome endovascular treatment.
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- Advances in Interventional Cardiology / Postępy w Kardiologii Interwencyjnej, 2020, v. 16, n. 3, p. 354, doi. 10.5114/aic.2020.99277
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- Article
First use of Micro Vascular Plugs in Australia: Endovascular treatment of pulmonary arteriovenous malformation.
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- 2018
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- Publication type:
- journal article
Austrian syndrome.
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- 2020
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- Publication type:
- Letter to the Editor
Lessons of the month 3: Gone but not forgotten - Osler - a reminder of the syndrome not bearing his.
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- Clinical Medicine, 2019, v. 19, n. 6, p. 523
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- Publication type:
- Article