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A novel variant in the GNE gene in a Malian patient presenting with distal myopathy.
Kotioumbe M, Maiga AB, Bamba S, Cissé L, Diarra S, Diallo S, Yalcouyé A, Kané F, Diallo SH, Coulibaly D, Coulibaly T, Dembélé K, Maiga B, Guinto CO, Landouré G. Kotioumbe M, et al. Among authors: yalcouye a. Res Sq [Preprint]. 2024 Mar 7:rs.3.rs-4004982. doi: 10.21203/rs.3.rs-4004982/v1. Res Sq. 2024. PMID: 38496429 Free PMC article. Preprint.
A novel de novo variant in the RUNX2 gene causes cleidocranial dysplasia in a Malian girl.
Cissé L, Yalcouyé A, Touré KO, Coulibaly Y, Maiga AB, Bamba S, Diallo D, Diarra S, Taméga A, Traoré O, Kotioumbé M, Sangaré MA, Ba HO, Simaga A, Koné FI, Samassekou O, Koné A, Guinto CO, Landouré G; H3Africa consortium. Cissé L, et al. Among authors: yalcouye a. Clin Case Rep. 2024 Feb 26;12(2):e8551. doi: 10.1002/ccr3.8551. eCollection 2024 Feb. Clin Case Rep. 2024. PMID: 38415192 Free PMC article.
Novel variant in CADM3 causes Charcot-Marie-Tooth disease.
Yalcouyé A, Rebelo AP, Cissé L, Rives L, Bamba S, Cogan J, Esoh K, Diarra S, Ezell KM, Taméga A, Guinto CO, Dohrn MF, Hamid R, Fischbeck KH, Zuchner S, Landouré G. Yalcouyé A, et al. Brain Commun. 2023 Sep 5;5(5):fcad227. doi: 10.1093/braincomms/fcad227. eCollection 2023. Brain Commun. 2023. PMID: 38074074 Free PMC article.
Pentanucleotide Repeat Insertions in RAI1 Cause Benign Adult Familial Myoclonic Epilepsy Type 8.
Yeetong P, Dembélé ME, Pongpanich M, Cissé L, Srichomthong C, Maiga AB, Dembélé K, Assawapitaksakul A, Bamba S, Yalcouyé A, Diarra S, Mefoung SE, Rakwongkhachon S, Traoré O, Tongkobpetch S, Fischbeck KH, Gahl WA, Guinto CO, Shotelersuk V, Landouré G. Yeetong P, et al. Among authors: yalcouye a. Mov Disord. 2024 Jan;39(1):164-172. doi: 10.1002/mds.29654. Epub 2023 Nov 22. Mov Disord. 2024. PMID: 37994247
Socio-cultural representation of epilepsy at the teaching hospital of point G, Mali.
Coulibaly T, Dicko OA, Sangaré M, Sissoko AS, Cissé L, Landouré G, Djimdé SO, Yalcouyé A, Coulibaly T, Karambé M, Maiga YM, Guinto CO. Coulibaly T, et al. Among authors: yalcouye a. eNeurologicalSci. 2023 Sep 26;33:100477. doi: 10.1016/j.ensci.2023.100477. eCollection 2023 Dec. eNeurologicalSci. 2023. PMID: 37786566 Free PMC article.
Clinical, paraclinical and genetic aspects of autosomal recessive cerebellar ataxias (ARCA) in Mali.
Cissé C, Cissé L, Samassékou O, Ba HO, Coulibaly T, Diallo SH, Diallo S, Taméga A, Diarra S, Maïga AB, Kané F, Yalcouyé A, Bocoum A, Dembélé ME, Traoré O, Simaga A, Traoré SF, Keita M, Fischbeck K, Traoré M, Guinto CO, Landouré G. Cissé C, et al. Among authors: yalcouye a. Mali Med. 2022 Dec 26;37(4):61-65. Mali Med. 2022. PMID: 36919030 Free PMC article.
26 results