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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2007 1
2009 4
2010 3
2011 2
2012 4
2013 2
2014 4
2016 5
2017 2
2018 1
2019 5
2020 4
2021 1
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34 results
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Page 1
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. 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.
Fahr's syndrome with hyperparathyroidism revealed by seizures and proximal weakness.
Dembélé K, Cissé L, Djimdé S, Coulibaly Y, Diarra S, Yalcouyé A, Maiga B, Guinto CO, Landouré G; from The H3Africa Consortium. Dembélé K, et al. Among authors: landoure g. eNeurologicalSci. 2019 Apr 25;15:100192. doi: 10.1016/j.ensci.2019.100192. eCollection 2019 Jun. eNeurologicalSci. 2019. PMID: 31080899 Free PMC article. No abstract available.
Neuropsychiatric and socio-cultural aspects in a Malian family with spinocerebellar ataxia.
Coulibaly SP, Coulibaly S, Sango HA, Cissé L, Maïga FI, Maïga B, Diarra S, Diallo SH, Coulibaly T, Traoré M, Guinto CO, Koumaré B, Landouré G. Coulibaly SP, et al. Among authors: landoure g. Ann Med Psychol (Paris). 2020 Mar;178(3):278-282. doi: 10.1016/j.amp.2018.02.018. Epub 2019 Mar 18. Ann Med Psychol (Paris). 2020. PMID: 32431322 Free PMC article.
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. 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.
Implementation of genomics research in Africa: challenges and recommendations.
Adebamowo SN, Francis V, Tambo E, Diallo SH, Landouré G, Nembaware V, Dareng E, Muhamed B, Odutola M, Akeredolu T, Nerima B, Ozumba PJ, Mbhele S, Ghanash A, Wachinou AP, Ngomi N. Adebamowo SN, et al. Among authors: landoure g. Glob Health Action. 2018;11(1):1419033. doi: 10.1080/16549716.2017.1419033. Glob Health Action. 2018. PMID: 29336236 Free PMC article.
A novel mutation in the GARS gene in a Malian family with Charcot-Marie-Tooth disease.
Yalcouyé A, Diallo SH, Coulibaly T, Cissé L, Diallo S, Samassékou O, Diarra S, Coulibaly D, Keita M, Guinto CO, Fischbeck K, Landouré G; H3Africa Consortium. Yalcouyé A, et al. Among authors: landoure g. Mol Genet Genomic Med. 2019 Jul;7(7):e00782. doi: 10.1002/mgg3.782. Epub 2019 Jun 7. Mol Genet Genomic Med. 2019. PMID: 31173493 Free PMC article.
Genetics and genomic medicine in Mali: challenges and future perspectives.
Landouré G, Samassékou O, Traoré M, Meilleur KG, Guinto CO, Burnett BG, Sumner CJ, Fischbeck KH. Landouré G, et al. Mol Genet Genomic Med. 2016 Mar 17;4(2):126-34. doi: 10.1002/mgg3.212. eCollection 2016 Mar. Mol Genet Genomic Med. 2016. PMID: 27066513 Free PMC article.
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