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Page 1
Mendelian Susceptibility to Mycobacterial Disease (MSMD): Clinical, Immunological, and Genetic Features of 22 Patients from 15 Moroccan Kindreds.
Errami A, Baghdadi JE, Ailal F, Benhsaien I, Bakkouri JE, Jeddane L, Rada N, Benajiba N, Mokhantar K, Ouazahrou K, Zaidi S, Abel L, Casanova JL, Boisson-Dupuis S, Bustamante J, Bousfiha AA. Errami A, et al. Among authors: bousfiha aa. J Clin Immunol. 2023 May;43(4):728-740. doi: 10.1007/s10875-022-01419-x. Epub 2023 Jan 11. J Clin Immunol. 2023. PMID: 36630059 Free PMC article.
Three new BLM gene mutations associated with Bloom syndrome.
Amor-Guéret M, Dubois-d'Enghien C, Laugé A, Onclercq-Delic R, Barakat A, Chadli E, Bousfiha AA, Benjelloun M, Flori E, Doray B, Laugel V, Lourenço MT, Gonçalves R, Sousa S, Couturier J, Stoppa-Lyonnet D. Amor-Guéret M, et al. Among authors: bousfiha aa. Genet Test. 2008 Jun;12(2):257-61. doi: 10.1089/gte.2007.0119. Genet Test. 2008. PMID: 18471088
[Post-vaccination bullous pemphigoid in infants].
Benslimane Kamal I, Elfetoiki FZ, Hali F, Dahbi Skalli H, Marnissi F, Bousfiha A, Chiheb S. Benslimane Kamal I, et al. Ann Dermatol Venereol. 2020 Nov;147(11):787-789. doi: 10.1016/j.annder.2020.07.003. Epub 2020 Aug 6. Ann Dermatol Venereol. 2020. PMID: 32773143 French. No abstract available.
[Forty-one pediatric cases of non-typhoidal salmonellosis].
Ailal F, Bousfiha AA, Jouhadi Z, Adnane F, Abid A. Ailal F, et al. Among authors: bousfiha aa. Med Mal Infect. 2004 May;34(5):206-9. doi: 10.1016/j.medmal.2004.02.004. Med Mal Infect. 2004. PMID: 16235596 French.
Revisiting human IL-12Rβ1 deficiency: a survey of 141 patients from 30 countries.
de Beaucoudrey L, Samarina A, Bustamante J, Cobat A, Boisson-Dupuis S, Feinberg J, Al-Muhsen S, Jannière L, Rose Y, de Suremain M, Kong XF, Filipe-Santos O, Chapgier A, Picard C, Fischer A, Dogu F, Ikinciogullari A, Tanir G, Al-Hajjar S, Al-Jumaah S, Frayha HH, AlSum Z, Al-Ajaji S, Alangari A, Al-Ghonaium A, Adimi P, Mansouri D, Ben-Mustapha I, Yancoski J, Garty BZ, Rodriguez-Gallego C, Caragol I, Kutukculer N, Kumararatne DS, Patel S, Doffinger R, Exley A, Jeppsson O, Reichenbach J, Nadal D, Boyko Y, Pietrucha B, Anderson S, Levin M, Schandené L, Schepers K, Efira A, Mascart F, Matsuoka M, Sakai T, Siegrist CA, Frecerova K, Blüetters-Sawatzki R, Bernhöft J, Freihorst J, Baumann U, Richter D, Haerynck F, De Baets F, Novelli V, Lammas D, Vermylen C, Tuerlinckx D, Nieuwhof C, Pac M, Haas WH, Müller-Fleckenstein I, Fleckenstein B, Levy J, Raj R, Cohen AC, Lewis DB, Holland SM, Yang KD, Wang X, Wang X, Jiang L, Yang X, Zhu C, Xie Y, Lee PPW, Chan KW, Chen TX, Castro G, Natera I, Codoceo A, King A, Bezrodnik L, Di Giovani D, Gaillard MI, de Moraes-Vasconcelos D, Grumach AS, da Silva Duarte AJ, Aldana R, Espinosa-Rosales FJ, Bejaoui M, Bousfiha AA, Baghdadi JE, Özbek N, Aksu G, K… See abstract for full author list ➔ de Beaucoudrey L, et al. Among authors: bousfiha aa. Medicine (Baltimore). 2010 Nov;89(6):381-402. doi: 10.1097/MD.0b013e3181fdd832. Medicine (Baltimore). 2010. PMID: 21057261 Free PMC article.
Molecular defects in Moroccan patients with ataxia-telangiectasia.
Jeddane L, Ailal F, Dubois-d'Enghien C, Abidi O, Benhsaien I, Kili A, Chaouki S, Kriouile Y, El Hafidi N, Fadil H, Abilkassem R, Rada N, Bousfiha AA, Barakat A, Stoppa-Lyonnet D, Bellaoui H. Jeddane L, et al. Among authors: bousfiha aa. Neuromolecular Med. 2013 Jun;15(2):288-94. doi: 10.1007/s12017-013-8218-1. Epub 2013 Jan 16. Neuromolecular Med. 2013. PMID: 23322442
A phenotypic approach for IUIS PID classification and diagnosis: guidelines for clinicians at the bedside.
Bousfiha AA, Jeddane L, Ailal F, Al Herz W, Conley ME, Cunningham-Rundles C, Etzioni A, Fischer A, Franco JL, Geha RS, Hammarström L, Nonoyama S, Ochs HD, Roifman CM, Seger R, Tang ML, Puck JM, Chapel H, Notarangelo LD, Casanova JL. Bousfiha AA, et al. J Clin Immunol. 2013 Aug;33(6):1078-87. doi: 10.1007/s10875-013-9901-6. Epub 2013 May 9. J Clin Immunol. 2013. PMID: 23657403 Free PMC article.
98 results