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Page 1
Hereditary spastic paraplegia and amyotrophy associated with a novel locus on chromosome 19.
Meilleur KG, Traoré M, Sangaré M, Britton A, Landouré G, Coulibaly S, Niaré B, Mochel F, La Pean A, Rafferty I, Watts C, Shriner D, Littleton-Kearney MT, Blackstone C, Singleton A, Fischbeck KH. Meilleur KG, et al. Among authors: sangare m. Neurogenetics. 2010 Jul;11(3):313-8. doi: 10.1007/s10048-009-0230-0. Epub 2009 Dec 29. Neurogenetics. 2010. PMID: 20039086 Free PMC article.
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: sangare 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.
Hereditary spastic paraplegia type 43 (SPG43) is caused by mutation in C19orf12.
Landouré G, Zhu PP, Lourenço CM, Johnson JO, Toro C, Bricceno KV, Rinaldi C, Meilleur KG, Sangaré M, Diallo O, Pierson TM, Ishiura H, Tsuji S, Hein N, Fink JK, Stoll M, Nicholson G, Gonzalez MA, Speziani F, Dürr A, Stevanin G, Biesecker LG; NIH Intramural Sequencing Center; Accardi J, Landis DM, Gahl WA, Traynor BJ, Marques W Jr, Züchner S, Blackstone C, Fischbeck KH, Burnett BG. Landouré G, et al. Among authors: sangare m. Hum Mutat. 2013 Oct;34(10):1357-60. doi: 10.1002/humu.22378. Epub 2013 Aug 12. Hum Mutat. 2013. PMID: 23857908 Free PMC article.
Genetics of low spinal muscular atrophy carrier frequency in sub-Saharan Africa.
Sangaré M, Hendrickson B, Sango HA, Chen K, Nofziger J, Amara A, Dutra A, Schindler AB, Guindo A, Traoré M, Harmison G, Pak E, Yaro FN, Bricceno K, Grunseich C, Chen G, Boehm M, Zukosky K, Bocoum N, Meilleur KG, Daou F, Bagayogo K, Coulibaly YI, Diakité M, Fay MP, Lee HS, Saad A, Gribaa M, Singleton AB, Maiga Y, Auh S, Landouré G, Fairhurst RM, Burnett BG, Scholl T, Fischbeck KH. Sangaré M, et al. Ann Neurol. 2014 Apr;75(4):525-32. doi: 10.1002/ana.24114. Epub 2014 Apr 2. Ann Neurol. 2014. PMID: 24515897 Free PMC article.
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. 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.
Clinical and genetic analysis of spinocerebellar ataxia in Mali.
Traoré M, Coulibaly T, Meilleur KG, La Pean A, Sangaré M, Landouré G, Mochel F, Karambé M, Guinto CO, Fischbeck KH. Traoré M, et al. Among authors: sangare m. Eur J Neurol. 2011 Oct;18(10):1269-71. doi: 10.1111/j.1468-1331.2011.03376.x. Epub 2011 Mar 21. Eur J Neurol. 2011. PMID: 21418439 Free PMC article.
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: sangare 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.
Lymphedema in three previously Wuchereria bancrofti-endemic health districts in Mali after cessation of mass drug administration.
Dolo H, Coulibaly YI, Konipo FN, Coulibaly SY, Doumbia SS, Sangare MB, Soumaoro L, Coulibaly ME, Diallo AA, Diarra Y, Sangare M, Doumbia S, Colebunders R, Nutman TB. Dolo H, et al. Among authors: sangare mb, sangare m. BMC Infect Dis. 2020 Jan 15;20(1):48. doi: 10.1186/s12879-020-4777-6. BMC Infect Dis. 2020. PMID: 31941448 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: sangare 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.
91 results