Zobrazeno 1 - 10
of 39
pro vyhledávání: '"Oumar Samassekou"'
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:
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
Autor:
Oumar Samassekou
Publikováno v:
Cancers, Vol 5, Iss 3, Pp 1086-1102 (2013)
Chronic myeloid leukemia (CML) is a myeloproliferative neoplasm characterized by the t(9;22) translocation. As in most cancers, short telomeres are one of the features of CML cells, and telomere shortening accentuates as the disease progresses from t
Externí odkaz:
https://doaj.org/article/f8e329bafb384b329c80d7102e49450e
Autor:
Karine Michaud, Marie de Tayrac, Myreille D'Astous, Céline Duval, Claudie Paquet, Oumar Samassekou, Peter Vincent Gould, Stéphan Saikali
Publikováno v:
PLoS ONE, Vol 11, Iss 12, p e0168728 (2016)
To study the feasibility and the diagnostic and prognostic interest of automated analysis of 1p, 19q, 9p and 10q status by FISH technique in oligodendroglial tumors.We analyzed a retrospective series of 33 consecutive gliomas with oligodendroglial hi
Externí odkaz:
https://doaj.org/article/248570a212a8423ab474025c48d5f9bc
Autor:
Oumar Samassekou, Huiyu Li, Josée Hébert, Aimé Ntwari, Haixia Wang, Catherine Grenier Cliché, Eric Bouchard, Shiang Huang, Ju Yan
Publikováno v:
Neoplasia: An International Journal for Oncology Research, Vol 13, Iss 6, Pp 550-560 (2011)
Previous studies demonstrated that critically shortened telomere lengths correlate with the chromosome instability in carcinogenesis. However, little has been noticed regarding the correlation of long telomeres at specific chromosomes with malignant
Externí odkaz:
https://doaj.org/article/bffe01a3fae44e73b6fd0aab33a26a0b
Publikováno v:
Neoplasia: An International Journal for Oncology Research, Vol 11, Iss 11, Pp 1146-1154 (2009)
Chronic myeloid leukemia (CML) is a neoplasia characterized by proliferation of a myeloid cell lineage and chromosome translocation t(9;22) (q34;q11.2). As in the case of most cancers, the average telomere length in CML cells is shorter than that in
Externí odkaz:
https://doaj.org/article/f9997ac4b2824831bb619f05d72abfb3
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
Autor:
Abdoulaye Bocoum, Oumar Samassekou, C.O. Guinto, Kenneth H. Fischbeck, Lassana Cissé, Salimata Diarra, Guida Landouré, K. Dembele, Abdoulaye Yalcouyé, Moussa Traoré
Publikováno v:
J Neurol Sci
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c6cdd88dd465d924ba19e430d2f4a53c
https://europepmc.org/articles/PMC8312886/
https://europepmc.org/articles/PMC8312886/
Autor:
Lassana Cissé, K. Dembele, Salimata Diarra, C.O. Guinto, Kenneth H. Fischbeck, Guida Landouré, Abdoulaye Bocoum, Mohamede E Dembélé, Oumar Samassekou
Publikováno v:
Am J Med Genet A
Variants in FA2H have been associated with a wide range of phenotypes including hereditary spastic paraplegia type 35 (SPG35); however, genetically confirmed cases have not been reported in Africa. We report here the first African family with a varia
Autor:
Oumar Samassekou, Kenneth H. Fischbeck, Katherine G. Meilleur, C.O. Guinto, Barrington G. Burnett, Charlotte J. Sumner, Mahamadou Traoré, Guida Landouré
Publikováno v:
Molecular Genetics & Genomic Medicine
Mali is a landlocked country located in the center of West Africa and is surrounded by seven other countries (Fig. 1). With a territory of 1,220,190 sq km and a population of 15,302,000, the country has a young population; 47% are under 15 years of a