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A misleading presentation of juvenile Tay Sachs disease.
Zouiri G, Rhouda H, Kriouile Y. Zouiri G, et al. Among authors: kriouile y. Rev Neurol (Paris). 2020 Mar;176(3):213-214. doi: 10.1016/j.neurol.2019.06.011. Epub 2019 Sep 19. Rev Neurol (Paris). 2020. PMID: 31543363 No abstract available.
Pathologic Confirmation of Lafora Disease.
Rhouda H, Malihy A, Zouiri G, Kriouile Y. Rhouda H, et al. Among authors: kriouile y. Pediatr Neurol. 2020 Jul;108:128. doi: 10.1016/j.pediatrneurol.2020.02.004. Epub 2020 Feb 28. Pediatr Neurol. 2020. PMID: 32279901 No abstract available.
First characterization of congenital myasthenic syndrome type 5 in North Africa.
Khaoula R, Cerino M, Da Silva N, Delague V, Nahili H, Kriouile Y, Gorokhova S, Bartoli M, Saïle R, Barakat A, Krahn M. Khaoula R, et al. Among authors: kriouile y. Mol Biol Rep. 2021 Oct;48(10):6999-7006. doi: 10.1007/s11033-021-06530-7. Epub 2021 Sep 22. Mol Biol Rep. 2021. PMID: 34553317 Free article.
Omenn syndrome with mutation in RAG1 gene.
Jaouad IC, Ouldim K, Ali Ou Alla S, Kriouile Y, Villa A, Sefiani A. Jaouad IC, et al. Among authors: kriouile y. Indian J Pediatr. 2008 Sep;75(9):944-6. doi: 10.1007/s12098-008-0197-0. Epub 2008 Nov 15. Indian J Pediatr. 2008. PMID: 19011808
Tay-Sachs Disease: Two Novel Rare HEXA Mutations from Pakistan and Morocco.
Bibi F, Ullah A, Bourinaris T, Efthymiou S, Kriouile Y, Sultan T, Haider S, Salpietro V, Houlden H, Kaukab Raja G. Bibi F, et al. Among authors: kriouile y. Klin Padiatr. 2021 Sep;233(5):226-230. doi: 10.1055/a-1371-1561. Epub 2021 Apr 8. Klin Padiatr. 2021. PMID: 33831955 English.
34 results