Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Thy Thy Vanem"'
Publikováno v:
Health and Quality of Life Outcomes, Vol 18, Iss 1, Pp 1-8 (2020)
Abstract Background Marfan syndrome, a rare hereditary connective tissue disorder caused by mutations in fibrillin-1, can affect many organ systems, especially the cardiovascular system. Previous research has paid less attention to health-related qua
Externí odkaz:
https://doaj.org/article/abe117e7ef2b4908a273ade6384bf3c1
Publikováno v:
Health and Quality of Life Outcomes, Vol 18, Iss 1, Pp 1-8 (2020)
Health and Quality of Life Outcomes
Health and Quality of Life Outcomes
Background Marfan syndrome, a rare hereditary connective tissue disorder caused by mutations in fibrillin-1, can affect many organ systems, especially the cardiovascular system. Previous research has paid less attention to health-related quality of l
Autor:
Cecilie Røe, Thy Thy Vanem, Benedicte Paus, Svend Rand-Hendriksen, Odd Geiran, Kirsten Krohg-Sørensen
Publikováno v:
Molecular Genetics & Genomic Medicine
Background To explore survival, causes of death, and the prevalence of cardiovascular events in a Norwegian Marfan syndrome (MFS) cohort. MFS is a heritable connective tissue disorder associated with reduced life expectancy–primarily due to aortic
Autor:
Julie De Backer, Anji T. Yetman, Nina Riise, Katharina T I Kornhuber, Laura Muiño Mosquera, Katalin Szöcs, Thy Thy Vanem, Ingmar Staufenbiel, Reed E. Pyeritz, Alexander Rahman, Shaine A. Morris, Leema Robert, Enid Neptune, Evaldas Girdauskas, Svend Rand-Hendriksen, Marina Vogler, Stephan J. Linke, Yskert von Kodolitsch, Harald Kaemmerer, Anthony Demolder
Publikováno v:
Expert Review of Cardiovascular Therapy
Introduction: The revised Ghent nosology presents the classical features of Marfan syndrome. However, behind its familiar face, Marfan syndrome hides less well-known features. Areas covered: The German Marfan Organization listed unusual symptoms and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d3f15aa8ba541c1653253a0ae4d15a77
https://biblio.ugent.be/publication/8640129/file/8641526
https://biblio.ugent.be/publication/8640129/file/8641526
Autor:
Tordis Böker, Rigmor Lundby, Benedicte Paus, Svend Rand-Hendriksen, Are Hugo Pripp, Thy Thy Vanem, Hans-Jørgen Smith
BACKGROUND CONTEXT Dural ectasia is widening of the dural sac often seen in patients with Marfan syndrome and other hereditary connective tissue disorders. Dural ectasia can cause specific symptoms and is associated with surgical complications. The k
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d066c5216386670928a9270f150955b0
http://hdl.handle.net/10852/74341
http://hdl.handle.net/10852/74341
Autor:
Cecilie Røe, Kai Andersen, Svend Rand-Hendriksen, Odd Geiran, Kirsten Krohg-Sørensen, Hans-Jørgen Smith, Eva Kirkhus, Rigmor Lundby, Tordis Böker, Thy Thy Vanem, Benedicte Paus, Gunhild Falleth Sandvik, Liv Drolsum
The age-dependent penetrance of organ manifestations in Marfan syndrome (MFS) is not known. The aims of this follow-up study were to explore how clinical features change over a 10-year period in the same Norwegian MFS cohort. In 2003-2004, we investi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fe4ba1a42f5af1ffd40785ab0231f66e
http://hdl.handle.net/10852/76479
http://hdl.handle.net/10852/76479
Autor:
Marit Sæthre, Symira Cholidis, Liv Drolsum, Svend Rand-Hendriksen, Gunhild Falleth Sandvik, Thy Thy Vanem
Importance Long-term follow-up of Marfan syndrome (MFS) patients. Background Investigate changes in ocular features in MFS patients fulfilling the Ghent-2 criteria following a period of 10 years. Design Repeated cross-sectional study with two observa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::10937da717471729eba0a1db070f015a
http://hdl.handle.net/10852/71660
http://hdl.handle.net/10852/71660
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