Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Brigitte Dussardier-Gilbert"'
Autor:
Thi Thao Truc Le, Guillaume Martinent, Sophie Dupuis-Girod, Antoine Parrot, Anne Contis, Sophie Riviere, Thierry Chinet, Vincent Grobost, Olivier Espitia, Brigitte Dussardier-Gilbert, Laurent Alric, Guillaume Armengol, Hélène Maillard, Vanessa Leguy-Seguin, Sylvie Leroy, Murielle Rondeau-Lutz, Christian Lavigne, Shirine Mohamed, Laurent Chaussavoine, Pascal Magro, Julie Seguier, Mallorie Kerjouan, Sylvie Fourdrinoy
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 17, Iss 1, Pp 1-14 (2022)
Abstract Background Hereditary hemorrhagic telangiectasia (HHT) disease is a rare genetic disorder with symptoms and complications that can significantly affect patients’ daily lives. To date, no scale has been validated to assess the specific symp
Externí odkaz:
https://doaj.org/article/cecf83f4ed6f4dbb8475401e0e67d5cb
Autor:
Le, Thi Thao Truc1 (AUTHOR), Martinent, Guillaume2 (AUTHOR), Dupuis-Girod, Sophie3 (AUTHOR), Parrot, Antoine4 (AUTHOR), Contis, Anne5 (AUTHOR), Riviere, Sophie6 (AUTHOR), Chinet, Thierry7 (AUTHOR), Grobost, Vincent8 (AUTHOR), Espitia, Olivier9 (AUTHOR), Dussardier-Gilbert, Brigitte10 (AUTHOR), Alric, Laurent11 (AUTHOR), Armengol, Guillaume12 (AUTHOR), Maillard, Hélène13 (AUTHOR), Leguy-Seguin, Vanessa14 (AUTHOR), Leroy, Sylvie15 (AUTHOR), Rondeau-Lutz, Murielle16 (AUTHOR), Lavigne, Christian17 (AUTHOR), Mohamed, Shirine18 (AUTHOR), Chaussavoine, Laurent19 (AUTHOR), Magro, Pascal20 (AUTHOR)
Publikováno v:
Orphanet Journal of Rare Diseases. 7/19/2022, Vol. 17 Issue 1, p1-14. 14p.