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1دورية أكاديمية
المؤلفون: 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
المصدر: Neurobiology of Disease, Vol 198, Iss , Pp 106537- (2024)
مصطلحات موضوعية: Hereditary spastic paraplegia, AP2A2, Endocytosis, Neurosciences. Biological psychiatry. Neuropsychiatry, RC321-571
وصف الملف: electronic resource
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2دورية أكاديمية
المؤلفون: 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
المصدر: Clinical Case Reports, Vol 12, Iss 2, Pp n/a-n/a (2024)
مصطلحات موضوعية: cleidocranial dysplasia, de novo genetic variant, Mali, RUNX2, West Africa, Medicine, Medicine (General), R5-920
وصف الملف: electronic resource
Relation: https://doaj.org/toc/2050-0904
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3دورية أكاديمية
المؤلفون: 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
المصدر: Molecular Genetics & Genomic Medicine, Vol 10, Iss 7, Pp n/a-n/a (2022)
مصطلحات موضوعية: Africa, Branchio‐otic syndrome, EYA1, Mali, syndromic hearing impairment, Genetics, QH426-470
وصف الملف: electronic resource
Relation: https://doaj.org/toc/2324-9269
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4دورية أكاديمية
المؤلفون: 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
المصدر: Clinical Case Reports, Vol 9, Iss 5, Pp n/a-n/a (2021)
مصطلحات موضوعية: Friedreich ataxia, FXN gene, genetic epidemiology, Mali, West Africa, Medicine, Medicine (General), R5-920
وصف الملف: electronic resource
Relation: https://doaj.org/toc/2050-0904
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5
المؤلفون: Abdoulaye, Bocoum, Toumany, Coulibaly, Madani, Ouologuem, Lassana, Cissé, Seybou H, Diallo, Boubacar B, Maiga, Kékouta, Dembélé, Salimata, Diallo, Souleymane Dit Papa, Coulibaly, Fousseyni, Kané, Thomas, Coulibaly, Dramane, Coulibaly, Abdoulaye, Taméga, Abdoulaye, Yalcouyé, Salimata, Diarra, Mohamed E, Dembélé, Alassane B, Maiga, Cheick A K, Cissé, Oumou, Traoré, Kenneth H, Fischbeck, Cheick O, Guinto, Youssoufa, Maiga, Guida, Landouré
المصدر: Journal of Huntington's Disease. 11:195-201
مصطلحات موضوعية: Huntingtin Protein, Cellular and Molecular Neuroscience, Huntington Disease, Phenotype, Mutation, Brain, Humans, Genetic Testing, Neurology (clinical), Mali
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::25a93946c0da89ba8ee564abeb982a89
https://doi.org/10.3233/jhd-220529 -
6دورية أكاديمية
المؤلفون: 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
المصدر: Molecular Genetics & Genomic Medicine, Vol 7, Iss 7, Pp n/a-n/a (2019)
وصف الملف: electronic resource
Relation: https://doaj.org/toc/2324-9269
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7
المؤلفون: 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
المصدر: Molecular Genetics & Genomic Medicine. 10
مصطلحات موضوعية: Adult, Adolescent, Intracellular Signaling Peptides and Proteins, Nuclear Proteins, Middle Aged, Pedigree, Young Adult, Genetics, Humans, Protein Tyrosine Phosphatases, Child, Hearing Loss, Molecular Biology, Branchio-Oto-Renal Syndrome, Genetics (clinical)
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8
المؤلفون: Salimata, Diarra, Thomas, Coulibaly, Kékouta, Dembélé, Nyater, Ngouth, Lassana, Cissé, Seybou H, Diallo, Madani, Ouologuem, Salimata, Diallo, Oumar, Coulibaly, Koumba, Bagayoko, Dramane, Coulibaly, Assiatou, Simaga, Hammadoun A, Sango, Mahamadou, Traoré, Steve, Jacobson, Kenneth H, Fischbeck, Guida, Landouré, Cheick O, Guinto
المصدر: Acta neurologica Belgica.
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9
المؤلفون: B Koumare, Souleymane Coulibaly, Seybou Hassane Diallo, Salimata Diarra, C.O. Guinto, Hammadoun Ali Sango, Guida Landouré, Mahamadou Traoré, Lassana Cissé, B Maiga, Thomas Coulibaly, S Coulibaly, Fatoumata I. Maïga
المصدر: Annales Médico-psychologiques, revue psychiatrique. 178:278-282
مصطلحات موضوعية: 0301 basic medicine, 03 medical and health sciences, Psychiatry and Mental health, 0302 clinical medicine, Arts and Humanities (miscellaneous), 030105 genetics & heredity, 030217 neurology & neurosurgery, Applied Psychology
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10
المؤلفون: Lassana Cissé, Salimata Diarra, Abdoulaye Yalcouyé, Youlouza Coulibaly, Abdoulaye Tamega, Alassane Baneye Maiga, Oumou Traoré, Mahamadou Kotioumbé, Moussa Sangaré, Seybou Hassane Diallo, Salimata Diallo, Hamidou O Bah, Assiatou Simaga, Koné Fatogoma Issa, Thomas Coulibaly, Oumar Samassékou, Cheick Guinto, Guida Landouré
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::b30371b6fe9e6fc15dfc13cd077ce0d1
https://doi.org/10.22541/au.163577941.11511652/v1