Zobrazeno 1 - 10
of 956
pro vyhledávání: '"Landouré, A"'
Autor:
Youssoufa Maiga, Leon Samuel Moskatel, Seybou H. Diallo, Oumar Sangho, Housseini Dolo, Fatoumata Konipo, Salimata Diallo, Awa Coulibaly, Mariam Daou, Modibo Sangaré, Thomas Coulibaly, Adama Sissoko, Guida Landouré, Mohamed Albakaye, Zoumana Traoré, Abdoul Karim Dao, Mamadou Togo, Saliou Mahamadou, Souleymane dit papa Coulibaly, Najib Kissani, Karamoko Nimaga, Rokia Sanogo, Fabrice Berna, Madani Ouologem, Callixte Kuaté, Robert Cowan, Julien Nizard
Publikováno v:
BMC Complementary Medicine and Therapies, Vol 24, Iss 1, Pp 1-13 (2024)
Abstract Introduction Neurological disorders (ND) have a high incidence in sub-Saharan Africa (SSA). In this region, systemic challenges of conventional medicine (CM) and cultural beliefs have contributed to a large utilization of traditional medicin
Externí odkaz:
https://doaj.org/article/1ec8c46b5e7745d8b803bf21c43b7457
Autor:
Salia Bamba, Lala Sidibé, Seybou H. Diallo, Lassana Cissé, Kékouta Dembélé, Abdoulaye Yalcouyé, Weizhen Ji, Mohamed Emile Dembélé, Salimata Diarra, Alassane dit Baneye Maiga, Oumou Traoré, Salimata Diallo, Samuel Ephrata Mefoung, Amadou Touré, Adama Koné, Lauren Jeffries, Cheick O. Guinto, Emily K. Mis, Kenneth H. Fischbeck, Mustafa K. Khokha, Saquib A. Lakhani, Guida Landouré
Publikováno v:
Frontiers in Genetics, Vol 15 (2024)
Background and ObjectivesDevelopmental and epileptic encephalopathies (DEEs) are a group of neurological disorders characterized by early-onset seizures that are often resistant to treatment, by electroencephalographic abnormalities, and by developme
Externí odkaz:
https://doaj.org/article/79262882c788440abcc222bde68735db
Autor:
Youssoufa Maiga, Seybou H. Diallo, Oumar Sangho, Leon Samuel Moskatel, Fatoumata Konipo, Abdoulaye Bocoum, Salimata Diallo, Awa Coulibaly, Mariam Daou, Housseini Dolo, Modibo Sangaré, Mohamed Albakaye, Zoumana Traoré, Thomas Coulibaly, Adama Sissoko, Guida Landouré, Boubacar Guindo, Mahamoudou Ahamadou, Mahamane Drahamane Toure, Abibatou Dembele, Habib Sacko, Cheick Abdoul Kadri Sao, Diakalia Coulibaly, Salimata Dembele, Cheick Oumar Coulibaly, Mohamadou Sanogo, Sekou Boiguilé, Julien Nizard, Robert Cowan, Timothy J. Steiner, and Andreas Husøy
Publikováno v:
The Journal of Headache and Pain, Vol 25, Iss 1, Pp 1-11 (2024)
Abstract Background Our recent studies have shown headache disorders to be very common in the central and western sub-Saharan countries of Benin and Cameroon. Here we report headache in nearby Mali, a strife-torn country that differs topographically,
Externí odkaz:
https://doaj.org/article/2071fd77d2c74a2089eb972717116708
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:
Salimata Diarra, Saikat Ghosh, Lassana Cissé, Thomas Coulibaly, Abdoulaye Yalcouyé, George Harmison, Salimata Diallo, Seybou H. Diallo, Oumar Coulibaly, Alice Schindler, Cheick A.K. Cissé, Alassane B. Maiga, Salia Bamba, Oumar Samassekou, Mustafa K. Khokha, Emily K. Mis, Saquib A. Lakhani, Frank X. Donovan, Steve Jacobson, Craig Blackstone, Cheick O. Guinto, Guida Landouré, Juan S. Bonifacino, Kenneth H. Fischbeck, Christopher Grunseich
Publikováno v:
Neurobiology of Disease, Vol 198, Iss , Pp 106537- (2024)
Hereditary spastic paraplegia (HSP) comprises a large group of neurogenetic disorders characterized by progressive lower extremity spasticity. Neurological evaluation and genetic testing were completed in a Malian family with early-onset HSP. Three c
Externí odkaz:
https://doaj.org/article/ae7527cfc144494db6ca02e0b1ec3625
Autor:
Diarra, Salimata, Ghosh, Saikat, Cissé, Lassana, Coulibaly, Thomas, Yalcouyé, Abdoulaye, Harmison, George, Diallo, Salimata, Diallo, Seybou H., Coulibaly, Oumar, Schindler, Alice, Cissé, Cheick A.K., Maiga, Alassane B., Bamba, Salia, Samassekou, Oumar, Khokha, Mustafa K., Mis, Emily K., Lakhani, Saquib A., Donovan, Frank X., Jacobson, Steve, Blackstone, Craig, Guinto, Cheick O., Landouré, Guida, Bonifacino, Juan S., Fischbeck, Kenneth H., Grunseich, Christopher
Publikováno v:
In Neurobiology of Disease August 2024 198
Autor:
Yalcouyé, Abdoulaye, Schrauwen, Isabelle, Traoré, Oumou, Bamba, Salia, Aboagye, Elvis Twumasi, Acharya, Anushree, Bharadwaj, Thashi, Latanich, Rachel, Esoh, Kevin, Fortes-Lima, Cesar A., de Kock, Carmen, Jonas, Mario, Maiga, Alassane dit Baneye, Cissé, Cheick A.K., Sangaré, Moussa A., Guinto, Cheick O., Landouré, Guida, Leal, Suzanne M., Wonkam, Ambroise
Publikováno v:
In Human Genetics and Genomics Advances December 2024
Autor:
Mohamed Emile Dembélé, Abdoulaye Yalcouyé, Mamadou Cissoko, Lassana Cissé, Cheick Oumar Guinto, Guida Landouré
Publikováno v:
Clinical Case Reports, Vol 12, Iss 2, Pp n/a-n/a (2024)
Abstract Sporadic thyrotoxic periodic paralysis (TPP) is a rare muscle disorder that manifests with abrupt muscle weakness and hypokalemia associated with hyperthyroidism. It is mostly reported in the Asian population, and rare in Caucasians. Only fe
Externí odkaz:
https://doaj.org/article/464c3ad4a90342708839e5d15e6e1605
Autor:
Lassana Cissé, Abdoulaye Yalcouyé, Kadidia Oumar Touré, Youlouza Coulibaly, Alassane Baneye Maiga, Salia Bamba, Dramane Diallo, Salimata Diarra, Abdoulaye Taméga, Oumou Traoré, Mahamadou Kotioumbé, Moussa Aly Sangaré, Hamidou Oumar Ba, Assiatou Simaga, Fatogoma Issa Koné, Oumar Samassekou, Amadou Koné, Cheick Oumar Guinto, Guida Landouré, the H3Africa consortium
Publikováno v:
Clinical Case Reports, Vol 12, Iss 2, Pp n/a-n/a (2024)
Key Clinical Message Cleidocranial dysplasia (CCD) is a rare genetic skeletal disorder with only few cases reported in Africa, mostly based on clinical and radiological findings. We report the first case in Mali, caused by a novel de novo variant in
Externí odkaz:
https://doaj.org/article/3d1bcdfff01a4e70b7d6c92ffddb67c7
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