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Year | Number of Results |
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2010 | 2 |
2011 | 2 |
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Page 1
HLA-C Genotyping Reveals Haplotype C*07 as a Potential Biomarker of Late Psoriasis Onset in Moroccan Patients.
Curr Issues Mol Biol. 2023 Jan 25;45(2):1012-1023. doi: 10.3390/cimb45020066.
Curr Issues Mol Biol. 2023.
PMID: 36826011
Free PMC article.
HLA-B*27 allele associated to Behçet's disease and to anterior uveitis in Moroccan patients.
Radouane A, Oudghiri M, Chakib A, Naya A, Belhouari A, El Malki A, Bennani S.
Radouane A, et al. Among authors: bennani s.
Ann Biol Clin (Paris). 2011 Jul-Aug;69(4):419-24. doi: 10.1684/abc.2011.0591.
Ann Biol Clin (Paris). 2011.
PMID: 21896406
Free article.
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Design and implementation of the European-Mediterranean Postgraduate Programme on Organ Donation and Transplantation (EMPODaT) for Middle East/North Africa countries.
Ballesté C, Valero R, Istrate M, Peralta P, Mosharafa AA, Morsy AA, Bakr MA, Kamal Abdelkader AI, Sheashaa H, Juvelekian GS, Khachab M, Ahdab R, Faour W, Tahiri Jouti N, Benghanem Gharbi M, Bayahia R, Dakka T, Desatnik P, Jambou P, Pisarski P, Samson-Himmelstjerna P, Lücking KM, Manyalich M; EMPODaT Consortium.
Ballesté C, et al.
Transpl Int. 2021 Aug;34(8):1553-1565. doi: 10.1111/tri.13918. Epub 2021 Jun 22.
Transpl Int. 2021.
PMID: 33993570
Free article.
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SNPs in the TNF-α gene promoter associated with Behcet's disease in Moroccan patients.
Radouane A, Oudghiri M, Chakib A, Bennani S, Touitou I, Barat-Houari M.
Radouane A, et al. Among authors: bennani s.
Rheumatology (Oxford). 2012 Sep;51(9):1595-9. doi: 10.1093/rheumatology/kes141. Epub 2012 Jun 17.
Rheumatology (Oxford). 2012.
PMID: 22711844
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Polymorphism of human leukocyte antigen-A, -B, and -DRB1 in a Moroccan population from Casablanca: study of the allelic and the haplotypic frequencies.
Kabbaj M, Oudghiri M, Naya A, Naamane H, Bennani S.
Kabbaj M, et al. Among authors: bennani s.
Ann Biol Clin (Paris). 2011 May-Jun;69(3):295-301. doi: 10.1684/abc.2011.0581.
Ann Biol Clin (Paris). 2011.
PMID: 21659045
Free article.
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HLA-A, -B, -DRB1 alleles and haplotypes frequencies in Moroccan patients with leukemia.
Kabbaj M, Oudghiri M, Naya A, Naamane H, El Turk J, Bennani S, Hassar M.
Kabbaj M, et al. Among authors: bennani s.
Ann Biol Clin (Paris). 2010 May-Jun;68(3):291-6. doi: 10.1684/abc.2010.0430.
Ann Biol Clin (Paris). 2010.
PMID: 20478772
Free article.
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The 752delG26 mutation in the RFXANK gene associated with major histocompatibility complex class II deficiency: evidence for a founder effect in the Moroccan population.
Naamane H, El Maataoui O, Ailal F, Barakat A, Bennani S, Najib J, Hassar M, Saile R, Bousfiha AA.
Naamane H, et al. Among authors: bennani s.
Eur J Pediatr. 2010 Sep;169(9):1069-74. doi: 10.1007/s00431-010-1179-6. Epub 2010 Apr 23.
Eur J Pediatr. 2010.
PMID: 20414676
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