Bevacizumab in hereditary hemorrhagic telangiectasia-associated epistaxis: effectiveness of an injection protocol based on the vascular anatomy of the nose

scientific article

Bevacizumab in hereditary hemorrhagic telangiectasia-associated epistaxis: effectiveness of an injection protocol based on the vascular anatomy of the nose is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1002/LARY.23303
P698PubMed publication ID22565282
P5875ResearchGate publication ID224917718

P2093author name stringTerje Osnes
Amy Østertun Geirdal
Ralph Dollner
Sinan Dheyauldeen
Liv Sofie Vartdal
P2860cites workManagement of epistaxis in hereditary hemorrhagic telangiectasia by Nd:YAG laser and quality of life assessment using the HR-QoL questionnaireQ33212390
The impact of septodermoplasty and potassium-titanyl-phosphate (KTP) laser therapy in the treatment of hereditary hemorrhagic telangiectasia-related epistaxisQ33328736
The effect of bevacizumab (Avastin) treatment on epistaxis in hereditary hemorrhagic telangiectasiaQ33405788
Diagnostic criteria for hereditary hemorrhagic telangiectasia (Rendu-Osler-Weber syndrome).Q33897059
Efficiency of laser treatment in patients with hereditary hemorrhagic telangiectasiaQ33943392
A retrospective analysis of low dose, intranasal injected bevacizumab (Avastin) in hereditary haemorrhagic telangiectasiaQ33976779
Hereditary haemorrhagic telangiectasia: Pathophysiology, diagnosis and treatmentQ34024081
Hereditary haemorrhagic telangiectasia (Osler-Weber-Rendu syndrome): a view from the 21st century.Q35059330
Hereditary hemorrhagic telangiectasia: an update on clinical manifestations and diagnostic measuresQ36480144
Efficacy of intranasal Bevacizumab (Avastin) treatment in patients with hereditary hemorrhagic telangiectasia-associated epistaxisQ37846178
Safety of intranasal Bevacizumab (Avastin) treatment in patients with hereditary hemorrhagic telangiectasia-associated epistaxisQ37846182
Health-related quality of life in hereditary hemorrhagic telangiectasiaQ42619248
Impact of genotype and mutation type on health-related quality of life in patients with hereditary hemorrhagic telangiectasiaQ46316673
Cross-cultural comparisons of the content of SF-36 translations across 10 countries: results from the IQOLA Project. International Quality of Life AssessmentQ47743496
An epistaxis severity score for hereditary hemorrhagic telangiectasiaQ48906632
The natural history of epistaxis in patients with hereditary hemorrhagic telangiectasia in the Norwegian population: a cross-sectional study.Q51429301
Health-related quality of life in a rare disease: hereditary hemorrhagic telangiectasia (HHT) or Rendu-Osler-Weber disease.Q51934035
P433issue6
P407language of work or nameEnglishQ1860
P921main subjectnosebleedQ202013
bevacizumabQ413299
hereditary hemorrhagic telangiectasiaQ776881
P304page(s)1210-1214
P577publication date2012-05-07
P1433published inThe LaryngoscopeQ15755068
P1476titleBevacizumab in hereditary hemorrhagic telangiectasia-associated epistaxis: effectiveness of an injection protocol based on the vascular anatomy of the nose
P478volume122

Reverse relations

cites work (P2860)
Q46283167Bevacizumab in the treatment of hereditary hemorrhagic telangiectasia.
Q38367321Evidence-based management of epistaxis in hereditary haemorrhagic telangiectasia
Q47941894Hereditary haemorrhagic telangiectasia: to transplant or not to transplant - is there a right time for liver transplantation?
Q87403186Intranasal submucosal bevacizumab for epistaxis in hereditary hemorrhagic telangiectasia: a double-blind, randomized, placebo-controlled trial
Q33957962Molecular pathways: can activin-like kinase pathway inhibition enhance the limited efficacy of VEGF inhibitors?
Q48187031Osteonecrosis after intranasal injection with bevacizumab in treating hereditary hemorrhagic telangiectasia: A case report
Q37602295Quality of life in patients with hereditary haemorrhagic telangiectasia (HHT)
Q38354161Successful management of chronic gastrointestinal hemorrhage using bevacizumab in the setting of hereditary hemorrhagic telangiectasia
Q49826259Vascular deficiency of Smad4 causes arteriovenous malformations: a mouse model of Hereditary Hemorrhagic Telangiectasia

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