An update on the ophthalmic features in hereditary haemorrhagic telangiectasia (Rendu-Osler-Weber syndrome)
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1573-2630
- Extent
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Online-Ressource
- Language
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Englisch
- Notes
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online resource.
- Bibliographic citation
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An update on the ophthalmic features in hereditary haemorrhagic telangiectasia (Rendu-Osler-Weber syndrome) ; day:16 ; month:1 ; year:2022 ; pages:1-9
International ophthalmology ; (16.1.2022), 1-9
- Creator
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Abdolrahimzadeh, Solmaz
Formisano, Martina
Marani, Carla
Rahimi, Siavash
- Contributor
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SpringerLink (Online service)
- DOI
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10.1007/s10792-021-02197-y
- URN
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urn:nbn:de:101:1-2022042921364485815333
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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15.08.2025, 7:33 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Abdolrahimzadeh, Solmaz
- Formisano, Martina
- Marani, Carla
- Rahimi, Siavash
- SpringerLink (Online service)
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The bleeding diathesis in patients with hereditary haemorrhagic telangiectasia is not due to impaired platelet function
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Specific cancer rates may differ in patients with hereditary haemorrhagic telangiectasia compared to controls
Gastrointestinal bleeding in patients with hereditary haemorrhagic telangiectasia: Long-term results of endoscopic treatment
A long diagnostic delay in patients with Hereditary Haemorrhagic Telangiectasia: a questionnaire-based retrospective study
Reproducibility of right-to-left shunt quantification using transthoracic contrast echocardiography in hereditary haemorrhagic telangiectasia
European Reference Network For Rare Vascular Diseases (VASCERN) Outcome Measures For Hereditary Haemorrhagic Telangiectasia (HHT)
The bleeding diathesis in patients with hereditary haemorrhagic telangiectasia is not due to impaired platelet function
Imaging of Hereditary Hemorrhagic Telangiectasia
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