Zobrazeno 1 - 10
of 22
pro vyhledávání: '"M.C. Fadous Khalife"'
Publikováno v:
Trauma Case Reports, Vol 9, Iss , Pp 27-29 (2017)
Isolated gallbladder injury, secondary to a blunt abdominal trauma, is a rare finding in children.The presence of vague symptoms and the unknown dynamic of the trauma may increase the diagnostic challenge especially in pediatrics.A conservative manag
Externí odkaz:
https://doaj.org/article/acc1245f2c10465aa8714857530a22b2
Autor:
G. Abi Fares, Georges Nicolas, Hala Feghali, C. Tayeh, P. Noun, Myriam Amm, A. Farah, Y. Khalife, M.C. Fadous Khalife
Publikováno v:
Open Journal of Pediatrics. :353-358
Introduction: Influenza disease is one of the major health concerns in pediatrics. One of the most recently suggested effects of vitamin D is preventing infectious diseases. The aim of our study was to compare flu vaccine effect to flu vaccine associ
Publikováno v:
THURSDAY, 14 JUNE 2018.
Background “Multicentric Osteolysis with Nodulosis and Arthropathy” (MONA) also known as Winchester-Torg syndrome is a rare chronic skeleton disorder caused by matrix metalloproteinase 2 (MMP2) deficiency. It is characterised by facial dysmorphis
Publikováno v:
Paediatric rheumatology.
Background Familial Mediterranean Fever (FMF) is an autosomal recessive disease affecting mainly eastern Mediterranean populations. Fever and Abdominal pain are the 2 most prevalent features. The most common arthritic manifestation of FMF is acute se
Publikováno v:
THURSDAY, 14 JUNE 2018.
Background IL-10 is defined as an anti-inflammatory cytokine. Its activity is mediated by interaction with a cell surface receptor composed of 2 subunits: alfa (IL-10RA) and beta (IL-10RB). Homozygozous mutations of IL-10RA gene have been linked to V
Autor:
Hala Feghali, Georges Nicolas, Luis Seabra, R. Dagher, Yanick J. Crow, R Ghiye, M.C. Fadous Khalife
Publikováno v:
Poster Presentations.
Background STING-Associated Vasculopathy with onset in Infancy (SAVI) is an auto-inflammatory monogenic disease. SAVI is caused by an upregulation of type I interferon signaling due to sporadic or inherited gain-of-function mutations in the STimulato
Publikováno v:
Archives de Pédiatrie. 21:95-97
Publikováno v:
Archives de Pédiatrie. 21:86-87
Publikováno v:
Archives de Pédiatrie. 22:245
Autor:
J. Menassa Souaiby, R. Chaabane, B. Nasr, P. Abou Jaoude, R. Saba, M.C. Fadous Khalife, I. Issa, Z. Ghorayeb
Publikováno v:
Archives de Pédiatrie. 22:240