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194 results

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Page 1
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: traore o. 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.
[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: traore o, traore m. Health Sci Dis. 2021 Nov;22(11):24-28. Health Sci Dis. 2021. PMID: 34824573 Free PMC article. French.
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. Among authors: traore o. Front Pediatr. 2021 Nov 29;9:726776. doi: 10.3389/fped.2021.726776. eCollection 2021. Front Pediatr. 2021. PMID: 34912757 Free PMC article.
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: traore o. J Huntingtons Dis. 2022;11(2):195-201. doi: 10.3233/JHD-220529. J Huntingtons Dis. 2022. PMID: 35311712
A monoallelic variant in EYA1 is associated with Branchio-Otic syndrome in a Malian family.
Yalcouyé A, Traoré O, Diarra S, Schrauwen I, Esoh K, Kadlubowska MK, Bharadwaj T, Adadey SM, Kéita M, Guinto CO, Leal SM, Landouré G, Wonkam A. Yalcouyé A, et al. Among authors: traore o. Mol Genet Genomic Med. 2022 Jul;10(7):e1995. doi: 10.1002/mgg3.1995. Epub 2022 Jun 14. Mol Genet Genomic Med. 2022. PMID: 35698919 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: traore o. Mov Disord. 2024 Jan;39(1):164-172. doi: 10.1002/mds.29654. Epub 2023 Nov 22. Mov Disord. 2024. PMID: 37994247
Genetic profile of progressive myoclonic epilepsy in Mali reveals novel findings.
Cissé L, Bamba S, Diallo SH, Ji W, Dembélé ME, Yalcouyé A, Coulibaly T, Traoré I, Jeffries L, Diarra S, Maiga ADB, Diallo S, Nimaga K, Touré A, Traoré O, Kotioumbé M, Mis EK, Cissé CAK, Guinto CO, Fischbeck KH, Khokha MK, Lakhani SA, Landouré G. Cissé L, et al. Among authors: traore o. Front Neurol. 2024 Sep 25;15:1455467. doi: 10.3389/fneur.2024.1455467. eCollection 2024. Front Neurol. 2024. PMID: 39385815 Free PMC article.
Efficacy of the oral pentavalent rotavirus vaccine in Mali.
Sow SO, Tapia M, Haidara FC, Ciarlet M, Diallo F, Kodio M, Doumbia M, Dembélé RD, Traoré O, Onwuchekwa UU, Lewis KD, Victor JC, Steele AD, Neuzil KM, Kotloff KL, Levine MM. Sow SO, et al. Among authors: traore o. Vaccine. 2012 Apr 27;30 Suppl 1:A71-8. doi: 10.1016/j.vaccine.2011.11.094. Vaccine. 2012. PMID: 22520140 Clinical Trial.
194 results