Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Laetitia Daou"'
Autor:
Kevin H. Toomer, Gloria F. Gerber, Yifan Zhang, Laetitia Daou, Michael Tushek, Jody E. Hooper, Ivo M. B. Francischetti
Publikováno v:
eJHaem, Vol 4, Iss 2, Pp 324-338 (2023)
Abstract Severe acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2) infection results in coagulation activation although it is usually not associated with consumption coagulopathy. D‐dimers are also commonly elevated despite systemic hypofibr
Externí odkaz:
https://doaj.org/article/6df57bfbd0cd4ecfaec3563339a660f5
Autor:
Shuvro Roy, Nicolas Mercure-Corriveau, Danielle Obando, Yujie Wang, Laetitia Daou, Aaron Tobian, Evan Bloch, Scott Newsome
Publikováno v:
Neurology. 99:S28.2-S29
ObjectiveTo describe the safety, tolerability, and response to TPE in patients with SPSD.BackgroundStiff person syndrome spectrum disorders (SPSD) are a rare group of disabling neuroimmunological disorders. SPSD often require immune therapies especia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1be8b646f10e69fec054fac6356faa98
https://doi.org/10.1212/01.wnl.0000903248.75997.47
https://doi.org/10.1212/01.wnl.0000903248.75997.47
Autor:
Paul M. Ness, Laetitia Daou
Publikováno v:
Annals of Blood. 5:32-32
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::535155e45efa1e099c960ffc4324fbd2
https://doi.org/10.21037/aob-2020-pt-02
https://doi.org/10.21037/aob-2020-pt-02
Autor:
Ryota Hayashi, Mazen Kurban, Laetitia Daou, Georges Nemer, Dana Saadeh, Yutaka Shimomura, Ossama Abbas, Samar Khalil
Publikováno v:
Journal of the European Academy of Dermatology and Venereology. 31:e142-e144
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::af9938b9669659e3380321d88a46f46f
https://doi.org/10.1111/jdv.13882
https://doi.org/10.1111/jdv.13882
Autor:
Humam Kadara, Mazen Kurban, Nelly Rebeiz, Waed Btadini, Abdul-Ghani Kibbi, Diana Delbani, Rémi Safi, Yutaka Shimomura, Ossama Abbas, Mona Tofaili, Fadi Bitar, Georges Nemer, Laetitia Daou
Publikováno v:
Clinical genetics. 92(5)
Erythropoietic protoporphyria (EPP) is a rare cutaneous and systemic disease caused by mutations in the ferrochelatase gene (FECH). The molecular underpinnings of EPP in Middle Eastern populations and relative to other ethnic groups secondary to incr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::41cfed99a8b997bba7dbe828c00ff170
https://pubmed.ncbi.nlm.nih.gov/28075030
https://pubmed.ncbi.nlm.nih.gov/28075030
Autor:
Ryota Hayashi, Christina Bergqvist, Georges Nemer, S. A. Staiteieh, Laetitia Daou, Mazen Kurban, Samar Khalil, Yutaka Shimomura, Ossama Abbas
Publikováno v:
Clinical and experimental dermatology. 42(3)
The Wnt signalling pathway is a major pathway involved in the embryogenic development of the various organs of the body. Appropriate signalling in this pathway relies on the proper functioning of several proteins including the R-spondin family of pro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4df204ec75d70e6680b481a0f41d936e
https://pubmed.ncbi.nlm.nih.gov/28247548
https://pubmed.ncbi.nlm.nih.gov/28247548
Autor:
Fadi Bitar, Ryota Hayashi, Yohya Shigehara, Mazen Kurban, Laetitia Daou, Shujiro Okuda, Adele Chedraoui, Georges Nemer, Yutaka Shimomura, Ossama Abbas, Hiroyuki Nakai, Riichiro Abe, Abdul Ghani Kibbi, Maria Bou Sleiman
Publikováno v:
Human Molecular Genetics. :ddw277
Autosomal recessive congenital ichthyosis (ARCI) is a heterogeneous group of hereditary skin disorder characterized by an aberrant cornification of the epidermis. ARCI is classified into a total of 11 subtypes (ARCI1-ARCI11) based on their causative
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bf35fcf877cad41890934153f8cfea5b
https://doi.org/10.1093/hmg/ddw277
https://doi.org/10.1093/hmg/ddw277