Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Fulvia Fiorese"'
Autor:
Fulvia Fiorese, Lucilla Nobbio, Antonio De Flora, Angelo Schenone, Matthias U. Kassack, Laura Sturla, Santina Bruzzone, Elena Zocchi, Elena Mannino, Valeria Prada, Davide Visigalli
Publikováno v:
Journal of Cellular Biochemistry. 115:161-167
Charcot-Marie-Tooth 1A (CMT1A) is a demyelinating hereditary neuropathy whose pathogenetic mechanisms are still poorly defined and an etiologic treatment is not yet available. An abnormally high intracellular Ca(2+) concentration ([Ca(2+)]i) occurs i
Autor:
Santina Bruzzone, Giovanna Basile, Elena Zocchi, Antonio De Flora, Laura Sturla, Federica Benvenuto, Iliana Moreschi, Cesare Usai, Angelo Schenone, Fulvia Fiorese, Lucilla Nobbio
Publikováno v:
Journal of Biological Chemistry. 284:23146-23158
Charcot-Marie-Tooth (CMT) is the most frequent inherited neuromuscular disorder, affecting 1 person in 2500. CMT1A, the most common form of CMT, is usually caused by a duplication of chromosome 17p11.2, containing the PMP22 (peripheral myelin protein
Autor:
Martina Bartolucci, Daniela Calzia, Fulvia Fiorese, Gianluigi Mancardi, Silvia Ravera, Lucilla Nobbio, Davide Visigalli, Angelo Schenone, Alessandro Morelli, Isabella Panfoli
Publikováno v:
Web of Science
Publons
Publons
Myelin sheath is the proteolipid membrane wrapping the axons of CNS and PNS. We have shown data suggesting that CNS myelin conducts oxidative phosphorylation (OXPHOS), challenging its role in limiting the axonal energy expenditure. Here, we focused o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::84fcc7e026d800f875d1a75f26f1eac5
https://hdl.handle.net/11567/630774
https://hdl.handle.net/11567/630774
Autor:
Marina Grandis, Gian Luigi Mancardi, Fulvia Fiorese, Lucilla Nobbio, Michele Abbruzzese, Tiziana Vigo, Angelo Schenone, Gianfranco Gherardi, Roberto Cosimo Melcangi, Michele Cilli
We investigated the contribution of Schwann cell-derived ciliary neurotrophic factor (CNTF) to the pathogenesis of Charcot-Marie-Tooth disease type 1A (CMT1A) and addressed the question as to whether it plays a role in the development of axonal damag
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::48a048021d26f8875540da0e4c980757
http://hdl.handle.net/11567/267496
http://hdl.handle.net/11567/267496