Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Cees J. J. Westermann"'
Autor:
Marco C. Post, Anna E Hosman, Repke J. Snijder, Johannes J. Mager, Els M. de Gussem, Cees J. J. Westermann, Andreanne Gauthier, Walter A. F. Balemans
Publikováno v:
Pediatric Pulmonology. 52:1206-1211
Background Hereditary Hemorrhagic Telangiectasia (HHT) is an autosomal dominant disease with multi-systemic vascular dysplasia. Early diagnosis through screening is important to prevent serious complications. How best to screen children of affected p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aa4cba311bb8c456a7d8ddedf93d48d1
https://doi.org/10.1002/ppul.23704
https://doi.org/10.1002/ppul.23704
Autor:
Cees J. J. Westermann, Anna E Hosman, Repke J. Snijder, Marie E. Faughnan, E. M. de Gussem, Johannes J. Mager, Christine Edwards
Publikováno v:
Orphanet Journal of Rare Diseases
Background Hereditary Haemorrhagic Telangiectasia (HHT) is an autosomal dominant disease associated with epistaxis, arteriovenous malformations and telangiectasias. Disease complications may result in premature death. Method We investigated life-expe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5232d9c22410af063362bab95cec6aca
https://pubmed.ncbi.nlm.nih.gov/27102204
https://pubmed.ncbi.nlm.nih.gov/27102204
Autor:
E. M. de Gussem, Christine P. Edwards, Marie E. Faughnan, Johannes J. Mager, Cees J. J. Westermann
Publikováno v:
C65. PULMONARY HYPERTENSION ASSOCIATED WITH LUNG DISEASES OR OTHER ILLNESSES: PATHOGENESIS, DIAGNOSIS, AND CLINICAL OUTCOMES.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2c61deb8af747292ec4a9090956aef6b
https://doi.org/10.1164/ajrccm-conference.2009.179.1_meetingabstracts.a4912
https://doi.org/10.1164/ajrccm-conference.2009.179.1_meetingabstracts.a4912
Autor:
Mark F.J. Stolk, Cees J. J. Westermann, Sebastiaan A.C. van Tuyl, Repke J. Snijder, Tom G.W. Letteboer, Ernst J. Kuipers, Claudia Rogge-Wolf
Publikováno v:
European Journal of Gastroenterology & Hepatology, 19, 153-158. Lippincott Williams & Wilkins
Introduction Hereditary hemorrhagic teleangiectasia (HHT) is an autosomal dominant disorder with mucocutaneous teleangiectasia and visceral arteriovenous malformations. Mutations of endoglin and Activin A receptor like kinase-1 have different phenoty
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ce2f4e37019b5c59892bc3fb06a3e00a
https://pure.eur.nl/en/publications/41d56fe6-9b0f-417d-932a-75827481025f
https://pure.eur.nl/en/publications/41d56fe6-9b0f-417d-932a-75827481025f
Autor:
Tom G.W. Letteboer, Sebastiaan A.C. van Tuyl, Repke J. Snijder, Claudia Rogge-Wolf, Cees J. J. Westermann, Ernst J. Kuipers, Mark F.J. Stolk
Publikováno v:
Gastrointestinal Endoscopy. 63:AB159
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1b46d56e8dff13fc1ee1dc769639f69f
https://doi.org/10.1016/j.gie.2006.03.318
https://doi.org/10.1016/j.gie.2006.03.318