A rare case of thyrotoxic periodic paralysis revealing Graves' disease in a young Malian by Mohamed Emile Dembélé, Abdoulaye Yalcouyé, Mamadou Cissoko, Lassana Cissé, Cheick Oumar Guinto, Guida Landouré

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Epidemiological and clinical aspects of HIV associated dementia at the University Hospital of Point G by Cheick Oumar Guinto, Toumany Coulibaly, S Berthé, Mamadou karembe, S Traoré, Thomas Coulibaly, Adama Sissoko, Guida Landoure, Sounkalo Dao, Moussa Traoré

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Etiologies of Childhood Hearing Impairment in Schools for the Deaf in Mali by Abdoulaye Yalcouyé, Abdoulaye Yalcouyé, Oumou Traoré, Abdoulaye Taméga, Alassane B. Maïga, Fousseyni Kané, Oluwafemi G. Oluwole, Cheick Oumar Guinto, Cheick Oumar Guinto, Mohamed Kéita, Mohamed Kéita, Samba Karim Timbo, Samba Karim Timbo, Carmen DeKock, Guida Landouré, Guida Landouré, Ambroise Wonkam, Ambroise Wonkam

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An unusual case of Dyke–Davidoff–Masson syndrome revealed by status epilepticus in a Malian patient by Samba O. Djimdé, Abdoulaye Yalcouyé, Abdou Koïta, Hassana Samir, Pofinet Kebkiba, Chrystelle Awovi Gueli, Alassane B. Maïga, Adama S. Sissoko, Guida Landouré

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Socio-cultural adaptation and standardization of Dubois' five words testing in a population of normal subject in Mali, West Africa by Cheick O. Guinto, Toumany Coulibaly, Zeinab Koné, Souleymane Coulibaly, Boubacar Maiga, Kekouta Dembélé, Lassana Cissé, Mamadou Konaté, Thomas Coulibaly, Adama S. Sissoko, Mamadou Karambé, Barrington Burnett, Guida Landouré, Moussa Traoré

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A novel mutation in the GARS gene in a Malian family with Charcot‐Marie‐Tooth disease by Abdoulaye Yalcouyé, Seybou H. Diallo, Thomas Coulibaly, Lassana Cissé, Salimata Diallo, Oumar Samassékou, Salimata Diarra, Dramane Coulibaly, Mohamed Keita, Cheick O. Guinto, Kenneth Fischbeck, Guida Landouré, The H3Africa Consortium

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A monoallelic variant in EYA1 is associated with Branchio‐Otic syndrome in a Malian family by Abdoulaye Yalcouyé, Oumou Traoré, Salimata Diarra, Isabelle Schrauwen, Kevin Esoh, Magda Kamila Kadlubowska, Thashi Bharadwaj, Samuel Mawuli Adadey, Mohamed Kéita, Cheick O. Guinto, Suzanne M. Leal, Guida Landouré, Ambroise Wonkam

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Case report: Novel variants cause developmental and epileptic encephalopathy in three unrelated families from Mali by Salia Bamba, Salia Bamba, Lala Sidibé, Lala Sidibé, Seybou H. Diallo, Seybou H. Diallo, Lassana Cissé, Kékouta Dembélé, Abdoulaye Yalcouyé, Weizhen Ji, Mohamed Emile Dembélé, Salimata Diarra, Salimata Diarra, Alassane dit Baneye Maiga, Oumou Traoré, Salimata Diallo, Samuel Ephrata Mefoung, Amadou Touré, Amadou Touré, Adama Koné, Lauren Jeffries, Cheick O. Guinto, Cheick O. Guinto, Emily K. Mis, Kenneth H. Fischbeck, Mustafa K. Khokha, Saquib A. Lakhani, Guida Landouré, Guida Landouré

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Increasing African genomic data generation and sharing to resolve rare and undiagnosed diseases in Africa: a call-to-action by the H3Africa rare diseases working group by Aimé Lumaka, Nadia Carstens, Koenraad Devriendt, Amanda Krause, Benard Kulohoma, Judit Kumuthini, Gerrye Mubungu, John Mukisa, Melissa Nel, Timothy O. Olanrewaju, Zané Lombard, Guida Landouré, as members of the Rare Disease Working Group of the H3Africa Consortium

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Genetic profile of progressive myoclonic epilepsy in Mali reveals novel findings by Lassana Cissé, Lassana Cissé, Salia Bamba, Salia Bamba, Seybou H. Diallo, Seybou H. Diallo, Weizhen Ji, Mohamed Emile Dembélé, Abdoulaye Yalcouyé, Abdoulaye Yalcouyé, Toumany Coulibaly, Ibrahima Traoré, Lauren Jeffries, Salimata Diarra, 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, Cheick Oumar Guinto, Kenneth H. Fischbeck, Mustafa K. Khokha, Saquib A. Lakhani, Guida Landouré, Guida Landouré

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Implementation of genomics research in Africa: challenges and recommendations by Sally N. Adebamowo, Veronica Francis, Ernest Tambo, Seybou H. Diallo, Guida Landouré, Victoria Nembaware, Eileen Dareng, Babu Muhamed, Michael Odutola, Teniola Akeredolu, Barbara Nerima, Petronilla J. Ozumba, Slee Mbhele, Anita Ghanash, Ablo P. Wachinou, Nicholas Ngomi

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A Novel Splice Site Variant in COL6A1 Causes Ullrich Congenital Muscular Dystrophy in a Consanguineous Malian Family by Alassane Baneye Maiga, Ibrahim Pamanta, Salia Bamba, Lassana Cissé, Salimata Diarra, Sidi Touré, Abdoulaye Yalcouyé, Seydou Diallo, Salimata Diallo, Fousseyni Kané, Seybou Hassane Diallo, Hamidou Oumar Ba, Cheick Oumar Guinto, Kenneth Fischbeck, Guida Landoure, Idrissa Ahmadou Cissé, The H3Africa Consortium

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Non-motor signs in patients with Parkinson's disease at the University Hospital of Point “G”, Mali by Boubacar Maïga, Aïssata Koné, Guida Landouré, Toumany Coulibaly, Modibo Sangaré, Kekouta Dembélé, Marième Soda Diop, Lassana Cissé, Sami Mohamed Lemine Dadah, Mamadou Konaté, Catherine Coulibaly, Adama Seydou Sissoko, Thomas Coulibaly, Mamadou Karambé, Cheick Oumar Guinto, M. Moustapha Ndiaye, Mouhamadou Mansour Ndiaye, Moussa Traoré

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Friedreich ataxia in a family from Mali, West Africa/Friedreich ataxia in a Malian family by Cheick A. K. Cissé, Lassana Cissé, Hamidou O. Ba, Oumar Samassékou, Assiatou Simaga, Abdoulaye Taméga, Salimata Diarra, Seybou H. Diallo, Thomas Coulibaly, Salimata Diallo, Abdoulaye Yalcouyé, Alassane B. Maiga, Mohamed Keita, Kenneth H. Fischbeck, Sékou F. Traoré, Cheick O. Guinto, Guida Landouré, from the H3Africa Consortium

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A novel de novo variant in the RUNX2 gene causes cleidocranial dysplasia in a Malian girl by 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

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Whole-exome sequencing reveals known and candidate genes for hearing impairment in Mali by Abdoulaye Yalcouyé, Isabelle Schrauwen, Oumou Traoré, Salia Bamba, Elvis Twumasi Aboagye, Anushree Acharya, Thashi Bharadwaj, Rachel Latanich, Kevin Esoh, Cesar A. Fortes-Lima, Carmen de Kock, Mario Jonas, Alassane dit Baneye Maiga, Cheick A.K. Cissé, Moussa A. Sangaré, Cheick O. Guinto, Guida Landouré, Suzanne M. Leal, Ambroise Wonkam

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Assessing traditional medicine in the treatment of neurological disorders in Mali: prelude to efficient collaboration by 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

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AP2A2 mutation and defective endocytosis in a Malian family with hereditary spastic paraplegia by 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

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The burden of headache and a health-care needs assessment in the adult population of Mali: a cross-sectional population-based study by 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

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Does the survival motor neuron copy number variation play a role in the onset and severity of sporadic amyotrophic lateral sclerosis in Malians? by Modibo Sangare, Ilo Dicko, Cheick Oumar Guinto, Adama Sissoko, Kekouta Dembele, Youlouza Coulibaly, Siaka Y. Coulibaly, Guida Landoure, Abdallah Diallo, Mamadou Dolo, Housseini Dolo, Boubacar Maiga, Moussa Traore, Mamadou Karembe, Kadiatou Traore, Amadou Toure, Mariam Sylla, Arouna Togora, Souleymane Coulibaly, Sékou Fantamady Traore, Brant Hendrickson, Katherine Bricceno, Alice B. Schindler, Angela Kokkinis, Katherine G. Meilleur, Hammadoun Ali Sangho, Brehima Diakite, Yaya Kassogue, Yaya Ibrahim Coulibaly, Barrington Burnett, Youssoufa Maiga, Seydou Doumbia, Kenneth H. Fischbeck

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