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European Reference Network For Rare Vascular Diseases (VASCERN) Outcome Measures For Hereditary Haemorrhagic Telangiectasia (HHT)

Orphanet journal of rare diseases, 2018-08, Vol.13 (1), p.136-136, Article 136

2018

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Safety of thalidomide and bevacizumab in patients with hereditary hemorrhagic telangiectasia

Orphanet journal of rare diseases, 2019-02, Vol.14 (1), p.28-14, Article 28

2019

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High output cardiac failure in 3 patients with hereditary hemorrhagic telangiectasia and hepatic vascular malformations, evaluation of treatment

Orphanet journal of rare diseases, 2020-11, Vol.15 (1), p.1-334, Article 334

2020

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European Reference Network for Rare Vascular Diseases (VASCERN) position statement on cerebral screening in adults and children with hereditary haemorrhagic telangiectasia (HHT)

Orphanet journal of rare diseases, 2020-06, Vol.15 (1), p.1-165, Article 165

2020

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Long non-coding RNA expression profiles in hereditary haemorrhagic telangiectasia

PloS one, 2014-03, Vol.9 (3), p.e90272-e90272

2014

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Chromosomal translocation disrupting the SMAD4 gene resulting in the combined phenotype of Juvenile polyposis syndrome and Hereditary Hemorrhagic Telangiectasia

Molecular genetics & genomic medicine, 2020-11, Vol.8 (11), p.e1498-n/a

2020

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Complement defects in patients with chronic rhinosinusitis

PloS one, 2012-11, Vol.7 (11), p.e47383-e47383

2012

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Chronic rhinosinusitis and occupational risk factors among 20- to 75-year-old Danes-A GA(2) LEN-based study

American journal of industrial medicine, 2012-11, Vol.55 (11), p.1037-1043

2012

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Prevalence of chronic rhinosinusitis in a population of patients with gastroesophageal reflux disease

American journal of rhinology & allergy, 2015-05, Vol.29 (3), p.e70-e74

2015

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European Reference Network for Rare Vascular Diseases (VASCERN): When and how to use intravenous bevacizumab in Hereditary Haemorrhagic Telangiectasia (HHT)?

European journal of medical genetics, 2022-10, Vol.65 (10), p.104575-104575, Article 104575

2022

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Gastrointestinal bleeding in patients with hereditary hemorrhagic telangiectasia

The American journal of gastroenterology, 2000-02, Vol.95 (2), p.415-418

2000

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Clinical and radiological long-term follow-up after embolization of pulmonary arteriovenous malformations

Cardiovascular and interventional radiology, 2006-02, Vol.29 (1), p.70-74

2006

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ENG mutational mosaicism in a family with hereditary hemorrhagic telangiectasia

Molecular genetics & genomic medicine, 2018-01, Vol.6 (1), p.121-125

2018

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Global gene expression profiling of telangiectasial tissue from patients with hereditary hemorrhagic telangiectasia

Microvascular research, 2015-05, Vol.99, p.118-126

2015

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Do patients with chronic rhinosinusitis benefit from consultation with an ENT-doctor?

Acta oto-laryngologica, 2015-07, Vol.135 (7), p.706-712

2015

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Chronic rhinosinusitis and occupational risk factors among 20- to 75-year-old Danes-A GA2LEN-based study

American journal of industrial medicine, 2012-11, Vol.55 (11), p.1037-1043

2012

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Long-Term Follow-up After Embolization of Pulmonary Arteriovenous Malformations with Detachable Silicone Balloons

Cardiovascular and interventional radiology, 2008-05, Vol.31 (3), p.569-574

2008

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Surfactant Proteins A, B, C and D in the Human Nasal Airway: Associated with Mucosal Glands and Ciliated Epithelium but Absent in Fluid-Phase Secretions and Mucus

O.R.L. Journal for oto-rhino-laryngology and its related specialties, 2014-01, Vol.76 (5), p.288-301

2014

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Post-tonsillectomy hemorrhage: assessment of risk factors with special attention to introduction of coblation technique

European archives of oto-rhino-laryngology, 2009-07, Vol.266 (7), p.1011-1015

2009

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Allelic dropout in the ENG gene, affecting the results of genetic testing in hereditary hemorrhagic telangiectasia

Genetic testing and molecular biomarkers, 2012-12, Vol.16 (12), p.1419

2012

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Mo1191 - Bevacizumab as Treatment of Bleeding in Patients with Hereditary Haemorrhagic Telangiectasia (HHT)

Gastroenterology (New York, N.Y. 1943), 2018-05, Vol.154 (6), p.S-701-S-702

2018

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The Otitis Media-6 questionnaire: psychometric properties with emphasis on factor structure and interpretability

Health and quality of life outcomes, 2013-11, Vol.11 (1), p.201-201

2013

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European Reference Network For Rare Vascular Diseases

Orphanet journal of rare diseases, 2018-08, Vol.13 (1)

2018

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European Reference Network for Rare Vascular Diseases

Orphanet journal of rare diseases, 2020-06, Vol.15 (1)

2020

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Gastrointestinal bleeding in patients with hereditary hemorrhagic telangiectasia

The American journal of gastroenterology, 2000-02, Vol.95 (2), p.415-418

2000

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European Reference Network For Rare Vascular Diseases (VASCERN) Outcome Measures For Hereditary Haemorrhagic Telangiectasia (HHT)

Safety of thalidomide and bevacizumab in patients with hereditary hemorrhagic telangiectasia

High output cardiac failure in 3 patients with hereditary hemorrhagic telangiectasia and hepatic vascular malformations, evaluation of treatment

European Reference Network for Rare Vascular Diseases (VASCERN) position statement on cerebral screening in adults and children with hereditary haemorrhagic telangiectasia (HHT)

Long non-coding RNA expression profiles in hereditary haemorrhagic telangiectasia

Chromosomal translocation disrupting the SMAD4 gene resulting in the combined phenotype of Juvenile polyposis syndrome and Hereditary Hemorrhagic Telangiectasia

Complement defects in patients with chronic rhinosinusitis

Chronic rhinosinusitis and occupational risk factors among 20- to 75-year-old Danes-A GA(2) LEN-based study

Prevalence of chronic rhinosinusitis in a population of patients with gastroesophageal reflux disease

European Reference Network for Rare Vascular Diseases (VASCERN): When and how to use intravenous bevacizumab in Hereditary Haemorrhagic Telangiectasia (HHT)?

Gastrointestinal bleeding in patients with hereditary hemorrhagic telangiectasia

Clinical and radiological long-term follow-up after embolization of pulmonary arteriovenous malformations

ENG mutational mosaicism in a family with hereditary hemorrhagic telangiectasia

Global gene expression profiling of telangiectasial tissue from patients with hereditary hemorrhagic telangiectasia

Do patients with chronic rhinosinusitis benefit from consultation with an ENT-doctor?

Chronic rhinosinusitis and occupational risk factors among 20- to 75-year-old Danes-A GA2LEN-based study

Long-Term Follow-up After Embolization of Pulmonary Arteriovenous Malformations with Detachable Silicone Balloons

Surfactant Proteins A, B, C and D in the Human Nasal Airway: Associated with Mucosal Glands and Ciliated Epithelium but Absent in Fluid-Phase Secretions and Mucus

Post-tonsillectomy hemorrhage: assessment of risk factors with special attention to introduction of coblation technique

Allelic dropout in the ENG gene, affecting the results of genetic testing in hereditary hemorrhagic telangiectasia

Mo1191 - Bevacizumab as Treatment of Bleeding in Patients with Hereditary Haemorrhagic Telangiectasia (HHT)

The Otitis Media-6 questionnaire: psychometric properties with emphasis on factor structure and interpretability

European Reference Network For Rare Vascular Diseases

European Reference Network for Rare Vascular Diseases

Gastrointestinal bleeding in patients with hereditary hemorrhagic telangiectasia

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