Search Results - "Mager, J."
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Second International Guidelines for the Diagnosis and Management of Hereditary Hemorrhagic Telangiectasia
Published in Annals of internal medicine (15-12-2020)“…Hereditary hemorrhagic telangiectasia (HHT) is an autosomal dominant disease with an estimated prevalence of 1 in 5000 that is characterized by the presence of…”
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Pulmonary Vascular Complications in Hereditary Hemorrhagic Telangiectasia and the Underlying Pathophysiology
Published in International journal of molecular sciences (27-03-2021)“…In this review, we discuss the role of transforming growth factor-beta (TGF-β) in the development of pulmonary vascular disease (PVD), both pulmonary…”
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3
Oral itraconazole for epistaxis in hereditary hemorrhagic telangiectasia: a proof of concept study
Published in Angiogenesis (London) (01-05-2021)“…The inhibiting effects of itraconazole, an antifungal drug on vascular endothelial growth factor (VEGF) have recently been discovered. By inhibiting VEGF,…”
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Evolution of Pulmonary Arteriovenous Malformations: The Role of Contrast Echocardiography
Published in Chest (01-03-2023)“…Pulmonary arteriovenous malformations (PAVMs) are direct connections between the pulmonary artery and the pulmonary vein, mostly associated with hereditary…”
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Second International Guidelines for the Diagnosis and Management of Hereditary Hemorrhagic Telangiectasia
Published in Annals of internal medicine (01-07-2021)Get full text
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6
Pulmonary artery pseudoaneurysm after thoracic radiation therapy: A case report and review of the literature
Published in Respirology case reports (01-04-2024)“…Pulmonary artery pseudoaneurysm (PAP) is a rare cause of hemoptysis. Potential causes include trauma, infection, or medical interventions. There is a risk of…”
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Pulmonary Arterial Hypertension and Hereditary Haemorrhagic Telangiectasia
Published in International journal of molecular sciences (17-10-2018)“…Hereditary haemorrhagic telangiectasia (HHT) is an autosomal dominant inherited disease characterised by multisystemic vascular dysplasia. Heritable pulmonary…”
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Safety of direct oral anticoagulants in patients with hereditary hemorrhagic telangiectasia
Published in Orphanet journal of rare diseases (28-08-2019)“…Hereditary hemorrhagic telangiectasia (HHT) is a rare vascular dysplasia resulting in visceral arteriovenous malformations and smaller mucocutaneous…”
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Clinical Implications of Pulmonary Shunting on Saline Contrast Echocardiography
Published in Journal of the American Society of Echocardiography (01-03-2015)“…Pulmonary right-to-left shunting can be encountered using transthoracic contrast echocardiography (TTCE) with agitated saline. Diseases associated with…”
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Thresholds of Endoglin Expression in Endothelial Cells Explains Vascular Etiology in Hereditary Hemorrhagic Telangiectasia Type 1
Published in International journal of molecular sciences (19-08-2021)“…Hereditary Hemorrhagic Telangiectasia type 1 (HHT1) is an autosomal dominant inherited disease characterized by arteriovenous malformations and hemorrhage…”
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Four-year survival rate in pulmonary sarcoidosis with extensive pulmonary hypertension screening
Published in Respiratory medicine (01-04-2022)“…Sarcoidosis is a systemic disease of unknown aetiology with significant morbidity and mortality. The PULSAR study prospectively performed cardiac analysis…”
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12
Intranasal Efudix reduces epistaxis in hereditary hemorrhagic telangiectasia
Published in Angiogenesis (London) (01-08-2020)“…Background Local application of fluorouracil (Efudix, 5-FU) induces sclerosis in patients with sinonasal tumors and superficial basocellular skin carcinoma. As…”
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Decreased Expression of Vascular Endothelial Growth Factor Receptor 1 Contributes to the Pathogenesis of Hereditary Hemorrhagic Telangiectasia Type 2
Published in Circulation (New York, N.Y.) (04-12-2018)“…BACKGROUND:Hereditary Hemorrhagic Telangiectasia type 2 (HHT2) is an inherited genetic disorder characterized by vascular malformations and hemorrhage. HHT2…”
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Follow-up of pulmonary right-to-left shunt in hereditary haemorrhagic telangiectasia
Published in The European respiratory journal (01-06-2016)“…Pulmonary arteriovenous malformations (PAVMs) are associated with severe neurological complications in hereditary haemorrhagic telangiectasia (HHT)…”
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BMP Receptor Inhibition Enhances Tissue Repair in Endoglin Heterozygous Mice
Published in International journal of molecular sciences (18-02-2021)“…Hereditary hemorrhagic telangiectasia type 1 (HHT1) is a severe vascular disorder caused by mutations in the TGFβ/BMP co-receptor . Endoglin haploinsufficiency…”
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Safety and efficacy of balloon pulmonary angioplasty in chronic thromboembolic pulmonary hypertension in the Netherlands
Published in Netherlands heart journal (01-02-2020)“…Background Balloon pulmonary angioplasty (BPA) is an emerging treatment in patients with chronic thromboembolic pulmonary hypertension (CTEPH) and chronic…”
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Long-term real world clinical outcomes of macitentan therapy in chronic thromboembolic pulmonary hypertension
Published in Respiratory medicine (01-06-2020)“…Macitentan treatment for chronic thromboembolic pulmonary hypertension (CTEPH) in the routine clinical setting is increasing. However, ‘real world’ macitentan…”
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Bosentan or Macitentan Therapy in Chronic Thromboembolic Pulmonary Hypertension?
Published in Lung (01-12-2019)“…Objective Research comparing bosentan and macitentan in chronic thromboembolic pulmonary hypertension (CTEPH) is scarce, although macitentan might have…”
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Idiopathic and hereditary haemorrhagic telangiectasia associated pulmonary arteriovenous malformations: comparison of clinical and radiographic characteristics
Published in Clinical radiology (01-05-2021)“…To determine whether there are differences between idiopathic and hereditary haemorrhagic telangiectasia (HHT) associated pulmonary arteriovenous malformations…”
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Life expextancy of parents with Hereditary Haemorrhagic Telangiectasia
Published in Orphanet journal of rare diseases (22-04-2016)“…Hereditary Haemorrhagic Telangiectasia (HHT) is an autosomal dominant disease associated with epistaxis, arteriovenous malformations and telangiectasias…”
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