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Page 1
Fibrodysplasia ossificans progressiva in a Malian boy of Bamako.
Traore M, Traore Thomas J, Guinto CO, Kane M, Traore S. Traore M, et al. Among authors: traore s, traore thomas j. Clin Rheumatol. 2004 Dec;23(6):527-9. doi: 10.1007/s10067-003-0808-0. Clin Rheumatol. 2004. PMID: 15293086
Does the survival motor neuron copy number variation play a role in the onset and severity of sporadic amyotrophic lateral sclerosis in Malians?
Sangare M, Dicko I, Guinto CO, Sissoko A, Dembele K, Coulibaly Y, Coulibaly SY, Landoure G, Diallo A, Dolo M, Dolo H, Maiga B, Traore M, Karembe M, Traore K, Toure A, Sylla M, Togora A, Coulibaly S, Traore SF, Hendrickson B, Bricceno K, Schindler AB, Kokkinis A, Meilleur KG, Sangho HA, Diakite B, Kassogue Y, Coulibaly YI, Burnett B, Maiga Y, Doumbia S, Fischbeck KH. Sangare M, et al. Among authors: traore sf, traore m, traore k. eNeurologicalSci. 2016 Jan 4;3:17-20. doi: 10.1016/j.ensci.2015.12.001. eCollection 2016 Jun. eNeurologicalSci. 2016. PMID: 29430530 Free PMC article.
Non-motor signs in patients with Parkinson's disease at the University Hospital of Point "G", Mali.
Maïga B, Koné A, Landouré G, Coulibaly T, Sangaré M, Dembélé K, Diop MS, Cissé L, Dadah SML, Konaté M, Coulibaly C, Sissoko AS, Coulibaly T, Karambé M, Guinto CO, Moustapha Ndiaye M, Ndiaye MM, Traoré M. Maïga B, et al. Among authors: traore m. eNeurologicalSci. 2016 Feb 4;3:35-36. doi: 10.1016/j.ensci.2016.02.001. eCollection 2016 Jun. eNeurologicalSci. 2016. PMID: 29430533 Free PMC article.
Socio-cultural adaptation and standardization of Dubois' five words testing in a population of normal subject in Mali, West Africa.
Guinto CO, Coulibaly T, Koné Z, Coulibaly S, Maiga B, Dembélé K, Cissé L, Konaté M, Coulibaly T, Sissoko AS, Karambé M, Burnett B, Landouré G, Traoré M. Guinto CO, et al. Among authors: traore m. eNeurologicalSci. 2016 Feb 10;3:60-63. doi: 10.1016/j.ensci.2016.02.002. eCollection 2016 Jun. eNeurologicalSci. 2016. PMID: 29430538 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: traore m. 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.
Novel mutation in the ATM gene in a Malian family with ataxia telangiectasia.
Landouré G, Mochel F, Meilleur K, Ly M, Sangaré M, Bocoum N, Bagayoko K, Coulibaly T, Sarr AM, Bâ HO, Coulibaly S, Guinto CO, Touré M, Traoré M, Fischbeck KH. Landouré G, et al. Among authors: traore m. J Neurol. 2013 Jan;260(1):324-6. doi: 10.1007/s00415-012-6738-5. Epub 2012 Nov 11. J Neurol. 2013. PMID: 23142947 Free PMC article. No abstract available.
Type 2 Gaucher's disease in a Malian family.
Traoré M, Sylla M, Traoré J, Sidibé T, Oumar GC. Traoré M, et al. Among authors: traore j. Afr J Health Sci. 2004;11(1-2):67-9. Afr J Health Sci. 2004. PMID: 17298119
Genetic testing and counseling for hereditary neurological diseases in Mali.
Meilleur KG, Coulibaly S, Traoré M, Landouré G, La Pean A, Sangaré M, Mochel F, Traoré S, Fischbeck KH, Han HR. Meilleur KG, et al. Among authors: traore s, traore m. J Community Genet. 2011 Mar;2(1):33-42. doi: 10.1007/s12687-011-0038-0. Epub 2011 Feb 22. J Community Genet. 2011. PMID: 22109722 Free PMC article.
480 results