Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Marina Stavrou"'
Autor:
Marina Stavrou, Kleopas A Kleopa
Publikováno v:
Neural Regeneration Research, Vol 18, Iss 7, Pp 1434-1440 (2023)
Charcot-Marie-Tooth neuropathies (CMT) constitute a group of common but highly heterogeneous, non-syndromic genetic disorders affecting predominantly the peripheral nervous system. CMT type 1A (CMT1A) is the most frequent type and accounts for almost
Externí odkaz:
https://doaj.org/article/f257ad39275b45a2a74999fe3a796c2f
Autor:
Marina Stavrou, Alexia Kagiava, Sarah G. Choudury, Matthew J. Jennings, Lindsay M. Wallace, Allison M. Fowler, Amanda Heslegrave, Jan Richter, Christina Tryfonos, Christina Christodoulou, Henrik Zetterberg, Rita Horvath, Scott Q. Harper, Kleopas A. Kleopa
Publikováno v:
The Journal of Clinical Investigation, Vol 132, Iss 13 (2022)
Charcot-Marie-Tooth disease type 1A (CMT1A), the most common inherited demyelinating peripheral neuropathy, is caused by PMP22 gene duplication. Overexpression of WT PMP22 in Schwann cells destabilizes the myelin sheath, leading to demyelination and
Externí odkaz:
https://doaj.org/article/58c621808db747a4a8de06b28aacae40
Autor:
Jonas Mairhofer, Marina Stavrou
Publikováno v:
Chemie Ingenieur Technik. 95:458-466
Publikováno v:
Chemie Ingenieur Technik. 95:391-404
Publikováno v:
Journal of the Peripheral Nervous System.
Autor:
KleopasA Kleopa, Marina Stavrou
Publikováno v:
Neural regeneration research. 18(7)
Charcot-Marie-Tooth neuropathies (CMT) constitute a group of common but highly heterogeneous, non-syndromic genetic disorders affecting predominantly the peripheral nervous system. CMT type 1A (CMT1A) is the most frequent type and accounts for almost
Autor:
Matthew J Jennings, Alexia Kagiava, Leen Vendredy, Emily L Spaulding, Marina Stavrou, Denisa Hathazi, Anika Grüneboom, Vicky De Winter, Burkhard Gess, Ulrike Schara, Oksana Pogoryelova, Hanns Lochmüller, Christoph H Borchers, Andreas Roos, Robert W Burgess, Vincent Timmerman, Kleopas A Kleopa, Rita Horvath
Publikováno v:
Brain
Molecular markers scalable for clinical use are critical for the development of effective treatments and the design of clinical trials. Here, we identify proteins in sera of patients and mouse models with Charcot-Marie-Tooth disease (CMT) with charac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d4795d8dcae57672a7c0b184c82ccfdb
Publikováno v:
Neuroscience letters. 742
Peripheral neuropathies of genetic etiology are a very diverse group of disorders manifesting either as non-syndromic inherited neuropathies without significant manifestations outside the peripheral nervous system, or as part of a systemic or syndrom
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 6048, p 6048 (2021)
International Journal of Molecular Sciences
International Journal of Molecular Sciences
Inherited neuropathies known as Charcot-Marie-Tooth (CMT) disease are genetically heterogeneous disorders affecting the peripheral nerves, causing significant and slowly progressive disability over the lifespan. The discovery of their diverse molecul
Publikováno v:
Fluid Phase Equilibria. 416:138-149
Statistical Associating Fluid Theory (SAFT) equations of state (EoS) for mixtures require cross-interaction parameters. For real systems, combining rules, such as the Lorenz-Berthelot combining rules, have to be corrected using at least one binary in