Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Koumba, Bagayoko"'
Autor:
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
Publikováno v:
Acta neurologica Belgica.
Hereditary spastic paraplegia (HSP) is a group of neurodegenerative diseases divided into pure and complex forms, with spasticity in lower limbs only, or associated with other neurologic and non-neurologic manifestations, respectively. Although widel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::bb5133bab106a8fcddf19a5d363c642f
https://pubmed.ncbi.nlm.nih.gov/36396882
https://pubmed.ncbi.nlm.nih.gov/36396882
Autor:
Lassana Cissé, Thomas Coulibaly, Alice B. Schindler, Seybou Hassane Diallo, Salimata Diallo, Salimata Diarra, Ke-lian Chen, C.O. Guinto, Kenneth H. Fischbeck, Guida Landouré, Abdoulaye Taméga, Assiatou Simaga, Craig Blackstone, Koumba Bagayoko
Publikováno v:
Annals of Clinical and Translational Neurology
Hereditary spastic paraplegias (HSPs) are well‐characterized disorders but rarely reported in Africa. We evaluated a Malian family in which three individuals had HSP and distal muscle atrophy and sensory loss. HSP panel testing identified a novel h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1517743d9ce83ed01e552f08a843b05d
http://europepmc.org/articles/PMC5376762
http://europepmc.org/articles/PMC5376762
Autor:
Souleymane Coulibaly, Modibo Sangare, Madani Ly, Guida Landouré, Moussa Traoré, Thomas Coulibaly, Hamidou Oumar Bâ, Nouhoum Bocoum, Amadou M. Sarr, Kenneth H. Fischbeck, Mahamadou Touré, C.O. Guinto, Katherine G. Meilleur, Fanny Mochel, Koumba Bagayoko
Dear Sirs, Ataxia telangiectasia (A-T) is a rare, autosomal recessive disorder of childhood characterized by progressive cerebellar ataxia, telangiectasia, and immune defects, and is caused by mutations in the ataxia-telangiectasia mutated (ATM) gene
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dd02cbb6bf33bff5d4bfb724aa95749e
https://europepmc.org/articles/PMC3566581/
https://europepmc.org/articles/PMC3566581/
