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A novel PEX1 mutation in a Moroccan family with Zellweger spectrum disorders.
Bousfiha A, Bakhchane A, Charoute H, Riahi Z, Snoussi K, Rouba H, Bonnet C, Petit C, Barakat A. Bousfiha A, et al. Among authors: snoussi k. Hum Genome Var. 2017 Apr 13;4:17009. doi: 10.1038/hgv.2017.9. eCollection 2017. Hum Genome Var. 2017. PMID: 28446956 Free PMC article.
Novel pathogenic WHRN variant causing hearing loss in a moroccan family.
AitRaise I, Amalou G, Redouane S, Charoute H, Snoussi K, Abdelghaffar H, Bonnet C, Petit C, Barakat A. AitRaise I, et al. Among authors: snoussi k. Mol Biol Rep. 2023 Dec;50(12):10663-10669. doi: 10.1007/s11033-023-08901-8. Epub 2023 Nov 4. Mol Biol Rep. 2023. PMID: 37924449
Atypical Cogan syndrome: a case report.
El Bouhmadi K, Allaoui A, El Khattab M, Youbi M, Anajar S, Essaadi M, Snoussi K, Hajjij A. El Bouhmadi K, et al. Among authors: snoussi k. J Med Case Rep. 2024 Nov 14;18(1):551. doi: 10.1186/s13256-024-04904-6. J Med Case Rep. 2024. PMID: 39543746 Free PMC article.
Intra-Parotid Recurrent Nasopharyngeal Carcinoma Following Intensity-Modulated Radiation Therapy: A Case Report.
Bourial A, Nourallah Laraqui O, Abdillahi Mahamoud C, Elhani H, Elmjabber R, Taali L, Anajar S, Essaadi M, Snoussi K, Dahbi Z, Hajjij A. Bourial A, et al. Among authors: snoussi k. Clin Med Insights Case Rep. 2024 Nov 7;17:11795476241295723. doi: 10.1177/11795476241295723. eCollection 2024. Clin Med Insights Case Rep. 2024. PMID: 39525331 Free PMC article.
The Role of Surgery in the Treatment of Cervical Lymph Node Tuberculosis.
Tahiri I, Yacoubi R, Elhouari O, Anajar S, Loubna T, Hajjij A, Zalagh M, Snoussi K, Essaadi M, Benariba F. Tahiri I, et al. Among authors: snoussi k. Cureus. 2023 May 10;15(5):e38824. doi: 10.7759/cureus.38824. eCollection 2023 May. Cureus. 2023. PMID: 37303344 Free PMC article.
35 results