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Guida Landouré

Showing results (1-10 of 51) with videos related to

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Social Science & Medicine (1982)|June 11, 2020
Stigma in African genomics research: Gendered blame, polygamy, ancestry and disease causal beliefs impact on the risk of harmJantina de Vries, Guida Landouré, Ambroise Wonkam
Med (New York, N.Y.)|February 10, 2024
Rare Disease Day: Amplifying voices, advocating hopeHelene Cederroth, William A Gahl, Guida Landouré, et al.
North African and Middle East Epilepsy Journal|September 29, 2015
Epilepsy genetics in Africa: challenges and future perspectivesGuida Landouré, Youssoufa Maiga, Oumar Samassékou, et al.
Le Mali Medical|January 11, 2024
[A rare case of Horton's disease without inflammatory syndrome in the Department of Neurology of the Teaching Hospital of Point G, Bamako, Mali]Guida Landouré, Abdoulaye Yalcouyé, Sidi Touré, et al.
Clinical Case Reports|February 26, 2024
A rare case of thyrotoxic periodic paralysis revealing Graves' disease in a young MalianMohamed Emile Dembélé, Abdoulaye Yalcouyé, Mamadou Cissoko, et al.
Molecular Cytogenetics|April 4, 2026
Acquired pericentric inversion of der(9) with BCR and ABL1 codeletion in chronic myeloid leukemia: a rare cytogenetic finding from MaliOumar Samassekou, Modibo K Goita, Madani Ly, et al.
Clinical Case Reports|October 6, 2025
Using the Fluorescence In Situ Hybridization in the Diagnosis of Trisomy 13 in a Male Newborn From MaliAlassane Baneye Maiga, Oumar Samassekou, Cheick Oumar Sidibé, et al.
Molecular Genetics & Genomic Medicine|April 12, 2016
Genetics and genomic medicine in Mali: challenges and future perspectivesGuida Landouré, Oumar Samassékou, Mahamadou Traoré, et al.
American Journal of Medical Genetics. Part A|May 16, 2019
Hereditary spastic paraplegia type 35 in a family from MaliGuida Landouré, Kékouta Dembélé, Lassana Cissé, et al.
Clinical Case Reports|October 21, 2022
An unusual case of Dyke-Davidoff-Masson syndrome revealed by status epilepticus in a Malian patientSamba O Djimdé, Abdoulaye Yalcouyé, Abdou Koïta, et al.
Pageof 6

Showing results (1-10 of 51) with videos related to

Sort By:
Pageof 6
Social Science & Medicine (1982)|June 11, 2020
Stigma in African genomics research: Gendered blame, polygamy, ancestry and disease causal beliefs impact on the risk of harmJantina de Vries, Guida Landouré, Ambroise Wonkam
Med (New York, N.Y.)|February 10, 2024
Rare Disease Day: Amplifying voices, advocating hopeHelene Cederroth, William A Gahl, Guida Landouré, et al.
North African and Middle East Epilepsy Journal|September 29, 2015
Epilepsy genetics in Africa: challenges and future perspectivesGuida Landouré, Youssoufa Maiga, Oumar Samassékou, et al.
Le Mali Medical|January 11, 2024
[A rare case of Horton's disease without inflammatory syndrome in the Department of Neurology of the Teaching Hospital of Point G, Bamako, Mali]Guida Landouré, Abdoulaye Yalcouyé, Sidi Touré, et al.
Clinical Case Reports|February 26, 2024
A rare case of thyrotoxic periodic paralysis revealing Graves' disease in a young MalianMohamed Emile Dembélé, Abdoulaye Yalcouyé, Mamadou Cissoko, et al.
Molecular Cytogenetics|April 4, 2026
Acquired pericentric inversion of der(9) with BCR and ABL1 codeletion in chronic myeloid leukemia: a rare cytogenetic finding from MaliOumar Samassekou, Modibo K Goita, Madani Ly, et al.
Clinical Case Reports|October 6, 2025
Using the Fluorescence In Situ Hybridization in the Diagnosis of Trisomy 13 in a Male Newborn From MaliAlassane Baneye Maiga, Oumar Samassekou, Cheick Oumar Sidibé, et al.
Molecular Genetics & Genomic Medicine|April 12, 2016
Genetics and genomic medicine in Mali: challenges and future perspectivesGuida Landouré, Oumar Samassékou, Mahamadou Traoré, et al.
American Journal of Medical Genetics. Part A|May 16, 2019
Hereditary spastic paraplegia type 35 in a family from MaliGuida Landouré, Kékouta Dembélé, Lassana Cissé, et al.
Clinical Case Reports|October 21, 2022
An unusual case of Dyke-Davidoff-Masson syndrome revealed by status epilepticus in a Malian patientSamba O Djimdé, Abdoulaye Yalcouyé, Abdou Koïta, et al.
Pageof 6