Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Maha Denguir"'
Autor:
Mehdi Hage-Sleiman, Jaja Zhu, Hippolyte Guérineau, Emily Ronez, Katayoun Jondeau, Olivier Kosmider, Véronique Picard, Maha Denguir, Agathe Maillon, Sylvain Clauser, Valérie Bardet
Publikováno v:
HemaSphere, Vol 5, Iss 2, p e517 (2021)
Externí odkaz:
https://doaj.org/article/7a704cb317de4cf48fa5e5a8758d552d
Autor:
Véronique Picard, Corinne Guitton, Lamisse Mansour-Hendili, Bernard Jondeau, Laurence Bendélac, Maha Denguir, Julien Demagny, Valérie Proulle, Frédéric Galactéros, Loic Garçon
Publikováno v:
Frontiers in Physiology, Vol 11 (2021)
Gardos channelopathy (Gardos-HX) or type 2 stomatocytosis/xerocytosis is a hereditary hemolytic anemia due to mutations in the KCNN4 gene. It is rarer than inherited type 1 xerocytosis due to PIEZO1 mutations (Piezo1-HX) and its diagnosis is difficul
Externí odkaz:
https://doaj.org/article/31491852c95e4e7a8d8a25a25a90446b
Autor:
Maha Denguir, Valérie Bardet, Hippolyte Guérineau, Katayoun Jondeau, Mehdi Hage-Sleiman, Véronique Picard, Jaja Zhu, Emily Ronez, Sylvain Clauser, Olivier Kosmider, Agathe Maillon
Publikováno v:
HemaSphere, Vol 5, Iss 2, p e517 (2021)
HemaSphere
HemaSphere
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b8b5efd9088976afd27f70d74fefdb83
http://journals.lww.com/10.1097/HS9.0000000000000517
http://journals.lww.com/10.1097/HS9.0000000000000517