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Page 1
Effect of systematic tuberculosis detection on mortality in young children with severe pneumonia in countries with high incidence of tuberculosis: a stepped-wedge cluster-randomised trial.
Marcy O, Wobudeya E, Font H, Vessière A, Chabala C, Khosa C, Taguebue JV, Moh R, Mwanga-Amumpaire J, Lounnas M, Mulenga V, Mavale S, Chilundo J, Rego D, Nduna B, Shankalala P, Chirwa U, De Lauzanne A, Dim B, Tiogouo Ngouana E, Folquet Amorrissani M, Cisse L, Amon Tanoh Dick F, Komena EA, Kwedi Nolna S, Businge G, Natukunda N, Cumbe S, Mbekeka P, Kim A, Kheang C, Pol S, Maleche-Obimbo E, Seddon JA, Mao TE, Graham SM, Delacourt C, Borand L, Bonnet M; TB-Speed Pneumonia Study Group. Marcy O, et al. Among authors: cisse l. Lancet Infect Dis. 2023 Mar;23(3):341-351. doi: 10.1016/S1473-3099(22)00668-5. Epub 2022 Nov 14. Lancet Infect Dis. 2023. PMID: 36395782 Clinical Trial.
Acceptability of the Kangaroo Mother Care at the University Hospital of Treichville in Côte d'Ivoire.
Doukouré D, Kourouma KR, Agbré Yacé ML, Cissé L, Some Méazieu C, N'Guetta Manouan M, Lasme EA, Bayo S, Aké-Tano SOP, Sackou Kouakou J, Konan Kouakou V. Doukouré D, et al. Among authors: cisse l. J Public Health Afr. 2022 Oct 20;13(3):2165. doi: 10.4081/jphia.2022.2165. eCollection 2022 Sep 7. J Public Health Afr. 2022. PMID: 36337678 Free PMC article.
AP2A2 mutation and defective endocytosis in a Malian family with hereditary spastic paraplegia.
Diarra S, Ghosh S, Cissé L, Coulibaly T, Yalcouyé A, Harmison G, Diallo S, Diallo SH, Coulibaly O, Schindler A, Cissé CAK, Maiga AB, Bamba S, Samassekou O, Khokha MK, Mis EK, Lakhani SA, Donovan FX, Jacobson S, Blackstone C, Guinto CO, Landouré G, Bonifacino JS, Fischbeck KH, Grunseich C. Diarra S, et al. Among authors: cisse l. Neurobiol Dis. 2024 May 19;198:106537. doi: 10.1016/j.nbd.2024.106537. Online ahead of print. Neurobiol Dis. 2024. PMID: 38772452 Free article.
The First Case of Huntington's Disease like 2 in Mali, West Africa.
Bocoum A, Ouologuem M, Cissé L, Essop F, Dit Papa Coulibaly S, Botha N, Cissé CAK, Dit Baneye Maiga A, Krause A, Landouré G; H3Africa consortium. Bocoum A, et al. Among authors: cisse l. Tremor Other Hyperkinet Mov (N Y). 2024 Apr 2;14:15. doi: 10.5334/tohm.859. eCollection 2024. Tremor Other Hyperkinet Mov (N Y). 2024. PMID: 38617831 Free PMC article.
A novel variant in the GNE gene in a Malian patient presenting with distal myopathy.
Kotioumbe M, Maiga AB, Bamba S, Cissé L, Diarra S, Diallo S, Yalcouyé A, Kané F, Diallo SH, Coulibaly D, Coulibaly T, Dembélé K, Maiga B, Guinto CO, Landouré G. Kotioumbe M, et al. Among authors: cisse l. Res Sq [Preprint]. 2024 Mar 7:rs.3.rs-4004982. doi: 10.21203/rs.3.rs-4004982/v1. Res Sq. 2024. PMID: 38496429 Free PMC article. Preprint.
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. 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.
Novel variant in CADM3 causes Charcot-Marie-Tooth disease.
Yalcouyé A, Rebelo AP, Cissé L, Rives L, Bamba S, Cogan J, Esoh K, Diarra S, Ezell KM, Taméga A, Guinto CO, Dohrn MF, Hamid R, Fischbeck KH, Zuchner S, Landouré G. Yalcouyé A, et al. Among authors: cisse l. Brain Commun. 2023 Sep 5;5(5):fcad227. doi: 10.1093/braincomms/fcad227. eCollection 2023. Brain Commun. 2023. PMID: 38074074 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: cisse l. Mov Disord. 2024 Jan;39(1):164-172. doi: 10.1002/mds.29654. Epub 2023 Nov 22. Mov Disord. 2024. PMID: 37994247
84 results