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Pentanucleotide Repeat Insertions in RAI1 Cause Benign Adult Familial Myoclonic Epilepsy Type 8.
Mov Disord. 2024 Jan;39(1):164-172. doi: 10.1002/mds.29654. Epub 2023 Nov 22.
Mov Disord. 2024.
PMID: 37994247
[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: dembele me.
Health Sci Dis. 2021 Nov;22(11):24-28.
Health Sci Dis. 2021.
PMID: 34824573
Free PMC article.
French.
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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: dembele me.
J Huntingtons Dis. 2022;11(2):195-201. doi: 10.3233/JHD-220529.
J Huntingtons Dis. 2022.
PMID: 35311712
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A rare case of thyrotoxic periodic paralysis revealing Graves' disease in a young Malian.
Dembélé ME, Yalcouyé A, Cissoko M, Cissé L, Guinto CO, Landouré G.
Dembélé ME, et al.
Clin Case Rep. 2024 Feb 22;12(2):e8527. doi: 10.1002/ccr3.8527. eCollection 2024 Feb.
Clin Case Rep. 2024.
PMID: 38405362
Free PMC article.
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[Progressive myoclonic epilepsy in the department of neurology of the University Teaching hospital Point "G"].
Dembélé ME, Cissé L, Diarra S, Yalcouyé A, Taméga A, Bocoum A, Maïga AB, Diallo SH, Coulibaly T, Diallo S, Simaga A, Grunseich C, Kéita M, Coulibaly MB, Fischbeck KH, Maiga Y, Guinto CO, Landouré G.
Dembélé ME, et al.
Mali Med. 2022 Jul 8;37(2):17-21.
Mali Med. 2022.
PMID: 36945313
Free PMC article.
French.
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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: dembele me.
Mali Med. 2022 Dec 26;37(4):61-65.
Mali Med. 2022.
PMID: 36919030
Free PMC article.
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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: dembele me.
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.
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