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Page 1
Clinical and Genetic Aspects of Huntington's Disease in the Malian Population.
Bocoum A, Coulibaly T, Ouologuem M, Cissé L, Diallo SH, Maiga BB, Dembélé K, Diallo S, Coulibaly SDP, Kané F, Coulibaly T, Coulibaly D, Taméga A, Yalcouyé A, Diarra S, Dembélé ME, Maiga AB, Cissé CAK, Traoré O, Fischbeck KH, Guinto CO, Maiga Y, Landouré G; from The H3Africa consortium. Bocoum A, et al. Among authors: cisse cak. J Huntingtons Dis. 2022;11(2):195-201. doi: 10.3233/JHD-220529. J Huntingtons Dis. 2022. PMID: 35311712
Friedreich ataxia in a family from Mali, West Africa/Friedreich ataxia in a Malian family.
Cissé CAK, Cissé L, Ba HO, Samassékou O, Simaga A, Taméga A, Diarra S, Diallo SH, Coulibaly T, Diallo S, Yalcouyé A, Maiga AB, Keita M, Fischbeck KH, Traoré SF, Guinto CO, Landouré G; from the H3Africa Consortium. Cissé CAK, et al. Clin Case Rep. 2021 Mar 24;9(5):e04065. doi: 10.1002/ccr3.4065. eCollection 2021 May. Clin Case Rep. 2021. PMID: 34084490 Free PMC article.
The First Case of Huntington's Disease like 2 in Mali, West Africa.
Bocoum A, Ouologuem M, Cissé L, Essop F, Dit Papa Coulibaly S, Botha N, Cissé CAK, Dit Baneye Maiga A, Krause A, Landouré G; H3Africa consortium. Bocoum A, et al. Among authors: cisse cak. Tremor Other Hyperkinet Mov (N Y). 2024 Apr 2;14:15. doi: 10.5334/tohm.859. eCollection 2024. Tremor Other Hyperkinet Mov (N Y). 2024. PMID: 38617831 Free PMC article.
AP2A2 mutation and defective endocytosis in a Malian family with hereditary spastic paraplegia.
Diarra S, Ghosh S, Cissé L, Coulibaly T, Yalcouyé A, Harmison G, Diallo S, Diallo SH, Coulibaly O, Schindler A, Cissé CAK, Maiga AB, Bamba S, Samassekou O, Khokha MK, Mis EK, Lahkani SA, Donovan FX, Jacobson S, Blackstone C, Guinto CO, Landouré G, Bonifacino JS, Fischbeck KH, Grunseich C. Diarra S, et al. Among authors: cisse cak. Neurobiol Dis. 2024 May 19:106537. doi: 10.1016/j.nbd.2024.106537. Online ahead of print. Neurobiol Dis. 2024. PMID: 38772452