Zobrazeno 1 - 10
of 284
pro vyhledávání: '"Vincenzo La, Bella"'
Autor:
Joanna M. Wasielewska, Juliana C. S. Chaves, Mauricio Castro Cabral-da-Silva, Martina Pecoraro, Stephani J. Viljoen, Tam Hong Nguyen, Vincenzo La Bella, Lotta E. Oikari, Lezanne Ooi, Anthony R. White
Publikováno v:
Fluids and Barriers of the CNS, Vol 21, Iss 1, Pp 1-20 (2024)
Abstract Background Amyotrophic lateral sclerosis (ALS) is a rapidly progressing neurodegenerative disorder with minimally effective treatment options. An important hurdle in ALS drug development is the non-invasive therapeutic access to the motor co
Externí odkaz:
https://doaj.org/article/8207c90e135c40859406d7de78f6d21d
Publikováno v:
Cells, Vol 13, Iss 8, p 677 (2024)
The discovery of hexanucleotide repeats expansion (RE) in Chromosome 9 Open Reading frame 72 (C9orf72) as the major genetic cause of amyotrophic lateral sclerosis (ALS) and the association between intermediate repeats in Ataxin-2 (ATXN2) with the dis
Externí odkaz:
https://doaj.org/article/a1839d92063748a1b6a6b45e4f17ed9b
Autor:
Tommaso Piccoli, Francesca Castro, Vincenzo La Bella, Serena Meraviglia, Marta Di Simone, Giuseppe Salemi, Francesco Dieli, Rossella Spataro
Publikováno v:
BMC Neurology, Vol 23, Iss 1, Pp 1-7 (2023)
Abstract Aims Neuroinflammation might be involved in the degeneration and progression of Amyotrophic Lateral Sclerosis (ALS). Here, we studied the role of the circulating lymphocytes in ALS, in particular the NK cells. We focused on the relationship
Externí odkaz:
https://doaj.org/article/51adaf2b65a04afabcac3773c8f9265f
Autor:
Hazel Quek, Carla Cuní-López, Romal Stewart, Tiziana Colletti, Antonietta Notaro, Tam Hong Nguyen, Yifan Sun, Christine C. Guo, Michelle K. Lupton, Tara L. Roberts, Yi Chieh Lim, Lotta E. Oikari, Vincenzo La Bella, Anthony R. White
Publikováno v:
Journal of Neuroinflammation, Vol 19, Iss 1, Pp 1-21 (2022)
Abstract Background Amyotrophic lateral sclerosis (ALS) is a multifactorial neurodegenerative disease characterised by the loss of upper and lower motor neurons. Increasing evidence indicates that neuroinflammation mediated by microglia contributes t
Externí odkaz:
https://doaj.org/article/7daea003c67c4e248bf5ed9070b7e5d3
Autor:
Giovanna Morello, Valentina La Cognata, Maria Guarnaccia, Vincenzo La Bella, Francesca Luisa Conforti, Sebastiano Cavallaro
Publikováno v:
Cells, Vol 12, Iss 14, p 1884 (2023)
Amyotrophic lateral sclerosis (ALS) is a fatal, progressive neurodegenerative disease with limited treatment options. Diagnosis can be difficult due to the heterogeneity and non-specific nature of the initial symptoms, resulting in delays that compro
Externí odkaz:
https://doaj.org/article/de3c624e6a8447b395751b72fc0d7193
Autor:
Rossella Spataro, Yiyan Xu, Ren Xu, Giorgio Mandalà, Brendan Z. Allison, Rupert Ortner, Alexander Heilinger, Vincenzo La Bella, Christoph Guger
Publikováno v:
Frontiers in Neuroscience, Vol 16 (2022)
ObjectiveClinical assessment of consciousness relies on behavioural assessments, which have several limitations. Hence, disorder of consciousness (DOC) patients are often misdiagnosed. In this work, we aimed to compare the repetitive assessment of co
Externí odkaz:
https://doaj.org/article/add48d84a05046a58e25c7ed8a26e449
Autor:
Angela D'Anzi, Elisa Perciballi, Giorgia Ruotolo, Daniela Ferrari, Antonietta Notaro, Ivan Lombardi, Maurizio Gelati, Katia Frezza, Laura Bernardini, Isabella Torrente, Alessandro De Luca, Vincenzo La Bella, Angelo Luigi Vescovi, Jessica Rosati
Publikováno v:
Stem Cell Research, Vol 63, Iss , Pp 102835- (2022)
Amyotrophic Lateral Sclerosis (ALS) is a fatal disease affecting both upper and lower motoneurons. The transactive response DNA binding protein (TARDBP) gene, encoding for TDP-43, is one of the most commonly mutated gene associated with familial case
Externí odkaz:
https://doaj.org/article/71dbdaeeab21417695fd1e91315f940f
Publikováno v:
Biomolecules, Vol 13, Iss 4, p 706 (2023)
TDP-43 intracellular aggregates are a pathogenic sign of most amyotrophic lateral sclerosis (ALS) cases. Familial ALS, brought on by TARDBP gene mutations, emphasizes the relevance of this altered protein in pathophysiology. Growing evidence suggests
Externí odkaz:
https://doaj.org/article/2140b1df40634d61891cd9571df392be
Autor:
VALENTE, ISABELLA
Voce biografica originale del pittore e grafico napoletano del primo Novecento
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3730::550cddad4dd22b78bed02129067a4460
http://hdl.handle.net/11588/424062
http://hdl.handle.net/11588/424062
Publikováno v:
Frontiers in Neuroscience, Vol 15 (2021)
Mutations in Fused-in-Sarcoma (FUS) gene involving the nuclear localization signal (NLS) domain lead to juvenile-onset Amyotrophic Lateral Sclerosis (ALS). The mutant protein mislocalizes to the cytoplasm, incorporating it into Stress Granules (SG).
Externí odkaz:
https://doaj.org/article/135fd3f75a86416b9a54afed8a42f084