Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

Search Results

26 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Results By Year timeline is not available.
Page 1
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: yalcouye a. 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.
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. 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.
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: yalcouye a. 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.
Friedreich ataxia in a family from Mali, West Africa/Friedreich ataxia in a Malian family.
Cissé CAK, Cissé L, Ba HO, Samassékou O, Simaga A, Taméga A, Diarra S, Diallo SH, Coulibaly T, Diallo S, Yalcouyé A, Maiga AB, Keita M, Fischbeck KH, Traoré SF, Guinto CO, Landouré G; from the H3Africa Consortium. Cissé CAK, et al. Among authors: yalcouye a. Clin Case Rep. 2021 Mar 24;9(5):e04065. doi: 10.1002/ccr3.4065. eCollection 2021 May. Clin Case Rep. 2021. PMID: 34084490 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: yalcouye a. 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. Front Pediatr. 2021 Nov 29;9:726776. doi: 10.3389/fped.2021.726776. eCollection 2021. Front Pediatr. 2021. PMID: 34912757 Free PMC article.
26 results