Zobrazeno 1 - 6
of 6
pro vyhledávání: '"E M, de Gussem"'
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
Publikováno v:
Rhinology. 47(1)
Free O2- radicals may cause precapillary sphincter abnormalities, resulting in epistaxis in hemizygous knockout mice for Endoglin. The objective of this study was to test if antioxidants, like N-acetylcysteine (NAC), are have a role in the treatment
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::96480d73b7b5b33e0d4a2b66a3a3a2ce
https://pubmed.ncbi.nlm.nih.gov/19382502
https://pubmed.ncbi.nlm.nih.gov/19382502
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:
de Gussem, Els M., Faughnan, Marie E.
Publikováno v:
Orphan Lung Diseases; 2015, p191-200, 10p
Publikováno v:
Oxidative Medicine & Cellular Longevity; Jan2012, Vol. 2012, Special section p1-9, 9p
The second edition comprehensively reviews the wide field of rare pulmonary diseases. Issues such as less common diseases affecting the airways, systematic disorders with lung involvement, interstitial lung diseases, and many other orphan conditions
