Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Cheick Abdel Kader Cissé"'
Autor:
Lassana Cissé, Salia Bamba, Seybou H. Diallo, Weizhen Ji, Mohamed Emile Dembélé, Abdoulaye Yalcouyé, Toumany Coulibaly, Ibrahima Traoré, Lauren Jeffries, Salimata Diarra, Alassane Dit Baneye Maiga, Salimata Diallo, Karamoko Nimaga, Amadou Touré, Oumou Traoré, Mahamadou Kotioumbé, Emily Kathryn Mis, Cheick Abdel Kader Cissé, Cheick Oumar Guinto, Kenneth H. Fischbeck, Mustafa K. Khokha, Saquib A. Lakhani, Guida Landouré
Publikováno v:
Frontiers in Neurology, Vol 15 (2024)
Background and objectivesProgressive myoclonic epilepsy (PME) is a group of neurological disorders characterized by recurrent myoclonic seizures with progressive neurological deterioration. We investigated the genetics of three unrelated patients wit
Externí odkaz:
https://doaj.org/article/2f06178a951d433697e9b4b8e1fc5ee1
Autor:
Lassana Cissé, Cheick Abdel Kader Cissé, Hamidou O Bah, Abdoulaye Taméga, Salimata Diarra, Salimata Diallo, Assiatou Simaga, C.O. Guinto, Alassane B. Maïga, Guida Landouré, Abdoulaye Yalcouyé, Thomas Coulibaly, Seybou Hassane Diallo, Kenneth H. Fischbeck, Sekou F. Traore, Mohamed Amadou Keita, Oumar Samassekou
Friedreich ataxia is the most common inherited ataxia in the world, but yet to be reported in black African. We report the first genetically confirmed case in a West African family. Studying genetic diseases in populations with diverse backgrounds ma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f72914200a6dc40cedfc9407a3b5fc56
https://doi.org/10.22541/au.161414432.28217723/v1
https://doi.org/10.22541/au.161414432.28217723/v1