Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Khaoula Ben-Farhat"'
Autor:
Raif S. Geha, Stefano Maio, Wayne Bainter, Jeff Goldsmith, Erin Janssen, Silvia Parolini, Janet Chou, Yousef R. Badran, Manuela Baronio, Christy Kam, Hazel Wilkie, Paolo Incardona, Abdallah Beano, Georg A. Holländer, Vassilios Lougaris, Mrinmoy Das, Rodrigo Hoyos-Bachiloglu, Birgitta Schmidt, Phammela Abarzua, Alessandro Plebani, Maria Pia Bondioni, Zachary Peters, Giovanna Tabellini, Jacqueline G. Wallace, Antonella Meini, Luisa Bercich, Vincenzo Villanacci, George F. Murphy, Khaoula Ben Farhat
Publikováno v:
Sci Immunol
Inhibitor of nuclear factor kappa B kinase alpha (IKKα) is critical for p100/NF-κB2 phosphorylation and processing into p52 and activation of the noncanonical NF-κB pathway. A patient with recurrent infections, skeletal abnormalities, absent secon
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e44723c58581bfe1ab739559710838be
https://pubmed.ncbi.nlm.nih.gov/34533979
https://pubmed.ncbi.nlm.nih.gov/34533979
Autor:
Khaoula Ben-Farhat, Monia Khemiri, Zohra Fitouri, Sihem Barsaoui, Najla Mekki, Meriem Ben-Ali, Selim Abdelmoula, Mohamed-Neji Guediche, M. R. Barbouche, Samir Boukthir, Saber Hamami, Imen Ben-Mustapha, Amel Ben-Chehida, Jalel Chemli, Karen Rouault, Beya Larguèche
Publikováno v:
Journal of Clinical Immunology
Journal of Clinical Immunology, Springer Verlag, 2016, 36 (6), pp.547-554. ⟨10.1007/s10875-016-0299-9⟩
Journal of Clinical Immunology, Springer Verlag, 2016, 36 (6), pp.547-554. ⟨10.1007/s10875-016-0299-9⟩
International audience; Chronic granulomatous disease (CGD) is the prototypic functional neutrophil disorder caused by genetic defects in one of the five genes encoding the superoxide-generating nicotinamide adenine dinucleotide phosphate (NADPH)-oxi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d93add6bc9843dc959ccce1265808deb
https://doi.org/10.1007/s10875-016-0299-9
https://doi.org/10.1007/s10875-016-0299-9
Autor:
Hanan E. Shamseldin, Hiba Shendi, Jennifer Whangbo, Sultan Albuhairi, Janet Chou, Laila S. Alawdah, Mohammed F. Alosaimi, Jennifer Jones, Khaoula Ben Farhat, Sandra K. Burchett, Suleiman Al-Hammadi, Raif S. Geha, Ansgar Schulz, Neha Kwatra, Fowzan S. Alkuraya, Klaus Schwarz
Publikováno v:
Journal of Allergy and Clinical Immunology. 143:1240-1243.e4
This case demonstrates successful immune reconstitution following hematopoietic stem cell transplantation in NIK deficiency.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c501d0344055666485c4d8cb9d53ebf6
https://doi.org/10.1016/j.jaci.2018.11.003
https://doi.org/10.1016/j.jaci.2018.11.003
Autor:
Monia Khemiri, Mohamed Bejaoui, Khaoula Ben-Farhat, J. Bouguila, Naouel Guirat-Dhouib, Mohamed-Ridha Barbouche, Meriem Ben-Ali, Lamia Sfaihi Ben-Mansour, Beya Larguèche, Imen Ben-Mustapha, Fethi Mellouli, Jalel Chemli, Emna Dhemaied
Publikováno v:
Journal of Clinical Immunology. 33:865-870
Major histocompatibility complex class II (MHC-II) expression deficiency is a combined primary immunodeficiency leading to the impairment of the cellular and humoral immune responses. A majority of affected patients belong to consanguineous families
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::217e08ca055c334d6d99470721f83a1a
https://doi.org/10.1007/s10875-013-9863-8
https://doi.org/10.1007/s10875-013-9863-8