Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Mariusz W. Mucha"'
Autor:
Olga M. Koper-Lenkiewicz, Anna J. Milewska, Joanna Kamińska, Karol Sawicki, Robert Chrzanowski, Justyna Zińczuk, Joanna Reszeć, Marzena Tylicka, Ewa Matuszczak, Joanna Matowicka-Karna, Zenon Mariak, Mariusz W. Mucha, Robert Pawlak, Violetta Dymicka-Piekarska
Publikováno v:
Annals of Medicine, Vol 53, Iss 1, Pp 1710-1721 (2021)
AbstractIntroduction Taking into account the possibility of myelin-associated proteins having a role in brain tumour development, the study aimed to evaluate the diagnostic usefulness of myelin-associated proteins (Nogo-A, MAG, OMgp) released into ex
Externí odkaz:
https://doaj.org/article/9ed92d9a21d8480c91a0817fdd8d9ed3
Autor:
Gaurav V, Harlalka, Meriel E, McEntagart, Neerja, Gupta, Anna E, Skrzypiec, Mariusz W, Mucha, Barry A, Chioza, Michael A, Simpson, Ajith, Sreekantan-Nair, Anthony, Pereira, Sven, Günther, Amir, Jahic, Hamid, Modarres, Heather, Moore-Barton, Richard C, Trembath, Madhulika, Kabra, Emma L, Baple, Seema, Thakur, Michael A, Patton, Christian, Beetz, Robert, Pawlak, Andrew H, Crosby
Publikováno v:
Human mutation. 37(11)
Hereditary spastic paraplegias (HSPs) are genetically and clinically heterogeneous axonopathies primarily affecting upper motor neurons and, in complex forms, additional neurons. Here, we report two families with distinct recessive mutations in TFG,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5b645abe715f82f28528f5cfdc9aff97
https://pubmed.ncbi.nlm.nih.gov/27492651
https://pubmed.ncbi.nlm.nih.gov/27492651