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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. J Huntingtons Dis. 2022;11(2):195-201. doi: 10.3233/JHD-220529. J Huntingtons Dis. 2022. PMID: 35311712
[Hyperthyroidism in children. Experience in internal medicine in Mali].
Sidibé AT, Dembélé M, Diarra AS, Bocoum AI, Mousseni E, Ag Aboubacrine S, Traoré HA, Ag Rhaly A. Sidibé AT, et al. Among authors: bocoum ai. Ann Endocrinol (Paris). 2007 Jun;68(2-3):177-80. doi: 10.1016/j.ando.2007.05.003. Epub 2007 Jul 10. Ann Endocrinol (Paris). 2007. PMID: 17624293 French.
Hereditary spastic paraplegia type 35 in a family from Mali.
Landouré G, Dembélé K, Cissé L, Samassékou O, Diarra S, Bocoum A, Dembélé ME, Fischbeck KH, Guinto CO; from The H3Africa Consortium. Landouré G, et al. Among authors: bocoum a. Am J Med Genet A. 2019 Jul;179(7):1122-1125. doi: 10.1002/ajmg.a.61179. Epub 2019 May 14. Am J Med Genet A. 2019. PMID: 31087769 Free PMC article.
A novel variant in the spatacsin gene causing SPG11 in a Malian family.
Landouré G, Dembélé K, Diarra S, Cissé L, Samassékou O, Bocoum A, Yalcouyé A, Traoré M, Fischbeck KH, Guinto CO; H3Africa Consortium. Landouré G, et al. Among authors: bocoum a. J Neurol Sci. 2020 Apr 15;411:116675. doi: 10.1016/j.jns.2020.116675. Epub 2020 Jan 7. J Neurol Sci. 2020. PMID: 32007754 Free PMC article. No abstract available.
[Clinical and laboratory features of recessive Limb Girdle Muscular dystrophies in the Department Neurology of University Hospital of Point G].
Coulibaly T, Ouabo AJ, Landouré G, Bah HO, Cissé L, Diallo SH, Diallo S, Samassékou O, Maïga AB, Kané F, Yalcouyé A, Taméga A, Bocoum A, Dembélé ME, Témé A, Sidibé CO, Cissé AK, Traoré O, Traoré M, Guinto CO. Coulibaly T, et al. Among authors: bocoum a. Health Sci Dis. 2021 Nov;22(11):24-28. Health Sci Dis. 2021. PMID: 34824573 Free PMC article. French.
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: bocoum a. Mali Med. 2022 Dec 26;37(4):61-65. Mali Med. 2022. PMID: 36919030 Free PMC article.
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