P189: Identifying PTPN14-Dependent Mechanisms That Influence Clinical Manifestations of Hereditary Hemorrhagic Telangiectasia
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- Extent
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1 Online-Ressource.
- Language
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Englisch
- Bibliographic citation
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P189: Identifying PTPN14-Dependent Mechanisms That Influence Clinical Manifestations of Hereditary Hemorrhagic Telangiectasia ; volume:20 ; number:1 ; day:7 ; month:12 ; year:2019 ; pages:108 ; date:12.2017
Artery research ; 20, Heft 1 (7.12.2019), 108, 12.2017
- Creator
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Mamai, Ons
- Contributor
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SpringerLink (Online service)
- DOI
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10.1016/j.artres.2017.10.190
- URN
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urn:nbn:de:101:1-2405021308499.039034111133
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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14.08.2025, 10:55 AM CEST
Data provider
This object is provided by:
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Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Mamai, Ons
- SpringerLink (Online service)
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Angiogenesis, hereditary hemorrhagic telangiectasia and COVID-19
Hemorrhagic pericardial effusion resulting in constriction in hereditary hemorrhagic telangiectasia
Pazopanib may reduce bleeding in hereditary hemorrhagic telangiectasia
5'UTR mutations of ENG cause hereditary hemorrhagic telangiectasia
Hereditary hemorrhagic telangiectasia with liver cirrhosis: a case report
Cardiac and Hemodynamic Manifestations of Hereditary Hemorrhagic Telangiectasia
Imaging of Hereditary Hemorrhagic Telangiectasia
Future treatments for hereditary hemorrhagic telangiectasia
Severity score for hereditary hemorrhagic telangiectasia
Brain abscess and hereditary hemorrhagic telangiectasia
Gender differences in hereditary hemorrhagic telangiectasia severity
Hypercoagulability in hereditary hemorrhagic telangiectasia with epilepsy
Angiogenesis, hereditary hemorrhagic telangiectasia and COVID-19
Hemorrhagic pericardial effusion resulting in constriction in hereditary hemorrhagic telangiectasia
Pazopanib may reduce bleeding in hereditary hemorrhagic telangiectasia
5'UTR mutations of ENG cause hereditary hemorrhagic telangiectasia