Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Ruth Martha, Stassart"'
Autor:
Ruth Martha, Stassart, Gunther, Helms, Enrique, Garea-Rodríguez, Stefan, Nessler, Liat, Hayardeny, Christiane, Wegner, Christina, Schlumbohm, Eberhard, Fuchs, Wolfgang, Brück
Publikováno v:
Brain Pathol
Multiple sclerosis (MS) is the most common cause for sustained disability in young adults, yet treatment options remain very limited. Although numerous therapeutic approaches have been effective in rodent models of experimental autoimmune encephalomy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::db03c6cef3994d0808cbea98abf23d22
https://pubmed.ncbi.nlm.nih.gov/26207848
https://pubmed.ncbi.nlm.nih.gov/26207848
Autor:
Alejandro, Leal, Kathrin, Huehne, Finn, Bauer, Heinrich, Sticht, Philipp, Berger, Ueli, Suter, Bernal, Morera, Gerardo, Del Valle, James R, Lupski, Arif, Ekici, Francesca, Pasutto, Sabine, Endele, Ramiro, Barrantes, Corinna, Berghoff, Martin, Berghoff, Bernhard, Neundörfer, Dieter, Heuss, Thomas, Dorn, Peter, Young, Lisa, Santolin, Thomas, Uhlmann, Michael, Meisterernst, Michael Werner, Sereda, Michael, Sereda, Ruth Martha, Stassart, Gerd, Meyer zu Horste, Klaus-Armin, Nave, André, Reis, Bernd, Rautenstrauss
Publikováno v:
Neurogenetics
Neurogenetics Vol.10 2009
Repositorio UNA
Universidad Nacional de Costa Rica
instacron:UNA
Europe PubMed Central
Neurogenetics Vol.10 2009
Repositorio UNA
Universidad Nacional de Costa Rica
instacron:UNA
Europe PubMed Central
Charcot-Marie-Tooth (CMT) disease is a clinically and genetically heterogeneous disorder. All mendelian patterns of inheritance have been described. We identified a homozygous p.A335V mutation in the MED25 gene in an extended Costa Rican family with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9b23a78f635992e815380fd695a622a7
https://hdl.handle.net/11858/00-001M-0000-002A-2D82-D21.11116/0000-000D-3C26-621.11116/0000-000D-3C27-5
https://hdl.handle.net/11858/00-001M-0000-002A-2D82-D21.11116/0000-000D-3C26-621.11116/0000-000D-3C27-5
Autor:
Fazal, Shaline V., Mutschler, Clara, Chen, Civia Z., Turmaine, Mark, Chiung-Ya Chen, Yi-Ping Hsueh, Ibañez-Grau, Andrea, Loreto, Andrea, Casillas-Bajo, Angeles, Cabedo, Hugo, Franklin, Robin J. M., Barker, Roger A., Monk, Kelly R., Steventon, Benjamin J., Coleman, Michael P., Gomez-Sanchez, Jose A., Arthur-Farraj, Peter
Publikováno v:
Frontiers in Cellular Neuroscience; 4/5/2023, Vol. 17, p1-17, 17p
Autor:
Leal, Alejandro, Huehne, Kathrin, Bauer, Finn, Sticht, Heinrich, Berger, Philipp, Suter, Ueli, Morera, Bernal, Valle, Gerardo, Lupski, James, Ekici, Arif, Pasutto, Francesca, Endele, Sabine, Barrantes, Ramiro, Berghoff, Corinna, Berghoff, Martin, Neundörfer, Bernhard, Heuss, Dieter, Dorn, Thomas, Young, Peter, Santolin, Lisa
Publikováno v:
Neurogenetics; Oct2009, Vol. 10 Issue 4, p375-376, 2p
Autor:
Stassart, Ruth Martha, Helms, Gunther, Garea-Rodríguez, Enrique, Nessler, Stefan, Hayardeny, Liat, Wegner, Christiane, Schlumbohm, Christina, Fuchs, Eberhard, Brück, Wolfgang
Publikováno v:
Brain Pathology; Jul2016, Vol. 26 Issue 4, p452-464, 13p