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Etiologies of Childhood Hearing Impairment in Schools for the Deaf in Mali.
Yalcouyé A, Traoré O, Taméga A, Maïga AB, Kané F, Oluwole OG, Guinto CO, Kéita M, Timbo SK, DeKock C, Landouré G, Wonkam A. Yalcouyé A, et al. Front Pediatr. 2021 Nov 29;9:726776. doi: 10.3389/fped.2021.726776. eCollection 2021. Front Pediatr. 2021. PMID: 34912757 Free PMC article.
Hearing loss and brain disorders: A review of multiple pathologies.
Oluwole OG, James K, Yalcouye A, Wonkam A. Oluwole OG, et al. Among authors: yalcouye a. Open Med (Wars). 2021 Dec 15;17(1):61-69. doi: 10.1515/med-2021-0402. eCollection 2022. Open Med (Wars). 2021. PMID: 34993346 Free PMC article. Review.
GJB1 variants in Charcot-Marie-Tooth disease X-linked type 1 in Mali.
Yalcouyé A, Diallo SH, Cissé L, Karembé M, Diallo S, Coulibaly T, Diarra S, Coulibaly D, Keita M, Guinto CO, Fischbeck KH, Wonkam A, Landouré G; H3Africa Consortium. Yalcouyé A, et al. J Peripher Nerv Syst. 2022 Jun;27(2):113-119. doi: 10.1111/jns.12486. Epub 2022 Apr 5. J Peripher Nerv Syst. 2022. PMID: 35383424 Free PMC article.
Fahr's syndrome with hyperparathyroidism revealed by seizures and proximal weakness.
Dembélé K, Cissé L, Djimdé S, Coulibaly Y, Diarra S, Yalcouyé A, Maiga B, Guinto CO, Landouré G; from The H3Africa Consortium. Dembélé K, et al. Among authors: yalcouye a. eNeurologicalSci. 2019 Apr 25;15:100192. doi: 10.1016/j.ensci.2019.100192. eCollection 2019 Jun. eNeurologicalSci. 2019. PMID: 31080899 Free PMC article. No abstract available.
A novel mutation in the GARS gene in a Malian family with Charcot-Marie-Tooth disease.
Yalcouyé A, Diallo SH, Coulibaly T, Cissé L, Diallo S, Samassékou O, Diarra S, Coulibaly D, Keita M, Guinto CO, Fischbeck K, Landouré G; H3Africa Consortium. Yalcouyé A, et al. Mol Genet Genomic Med. 2019 Jul;7(7):e00782. doi: 10.1002/mgg3.782. Epub 2019 Jun 7. Mol Genet Genomic Med. 2019. PMID: 31173493 Free PMC article.
26 results