Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Andrea Micaloni"'
Autor:
Enrico Bertini, Elisabetta Bucci, Giovanni Antonini, Luca Leonardi, Marco Salvetti, Bas Uijterwijk, Antonella Stoppacciaro, Martijn Zierikzee, Salvatore Raffa, Fiammetta Vanoli, Tommaso Tartaglione, Laura Fionda, Elena Maria Pennisi, Gioia Merlonghi, Fabiana Fattori, Coen A.C. Ottenheijm, Matteo Garibaldi, Stefania Morino, Andrea Micaloni
Publikováno v:
Garibaldi, M, Fattori, F, Pennisi, E M, Merlonghi, G, Fionda, L, Vanoli, F, Leonardi, L, Bucci, E, Morino, S, Micaloni, A, Tartaglione, T, Uijterwijk, B, Zierikzee, M, Ottenheijm, C, Bertini, E S, Stoppacciaro, A, Raffa, S, Salvetti, M & Antonini, G 2021, ' Novel ACTA1 mutation causes late-presenting nemaline myopathy with unusual dark cores ', Neuromuscular Disorders, vol. 31, no. 2, pp. 139-148 . https://doi.org/10.1016/j.nmd.2020.11.012
Neuromuscular Disorders, 31(2), 139-148. Elsevier Limited
Neuromuscular Disorders, 31(2), 139-148. Elsevier Limited
ACTA1 gene encodes the skeletal muscle alpha-actin, the core of thin filaments of the sarcomere. ACTA1 mutations are responsible of several muscle disorders including nemaline, cores, actin aggregate myopathies and fiber-type disproportion. We report
Autor:
Maurizio Taurino, Tommaso Dezi, Luigi Tritapepe, N. Cifani, F. Del Porto, Maria Proietta, Andrea Micaloni, Salvatore Raffa
Publikováno v:
Clinical and Experimental Medicine. 19:463-468
The aim of this study was to evaluate CD25+ and Lag3+ T regulatory subpopulations in patients with critical carotid artery stenosis (CAS) and Stanford-A acute aortic dissection (AAD). CD25+ and Lag3+ were measured in 36 patients affected by CAS and 2
Objective: The use of a hyaluronic acid-based product has the potential to improve the hydration status of the mucous membranes, especially in the oral cavity. This study has evaluated the in vivo adhesiveness of a product based on hyaluronic acid co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8375c4ea00f861d26229124167b0db9c
https://doi.org/10.21203/rs.2.19263/v1
https://doi.org/10.21203/rs.2.19263/v1
Autor:
Franca Bianchi, Maria Rosaria Torrisi, Leonardo Schirone, Giovanna Gallo, Roberto Violini, Maurizio Forte, Andrea Micaloni, Salvatore Raffa, Giuliano Tocci, Rosita Stanzione, Simona Marchitti, Massimo Volpe, Maria Cotugno, Xiao Lan Diana Chin, Speranza Rubattu
Background Deficiency of NADH dehydrogenase [ubiquinone], the mitochondrial complex I, represents an emerging mechanism of cardiovascular diseases. Ndufc2, a subunit of mitochondrial complex I, is involved in stroke development. We aimed to gain some
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7ca6e13b89da8ceefbe97b196fb85fb9
http://hdl.handle.net/11573/1259776
http://hdl.handle.net/11573/1259776
Autor:
Maria Rosaria Torrisi, Vincenzo Petrozza, Silvia Palmerio, Giacomo Frati, Simona Marchitti, Franca Bianchi, Maria Cotugno, Sebastiano Sciarretta, Maurizio Forte, Andrea Micaloni, Francesca Pagano, Salvatore Raffa, Michela Relucenti, Flavio di Nonno, Massimo Volpe, Rosita Stanzione, Elena De Falco, Michele Madonna, Speranza Rubattu, Isotta Chimenti
Publikováno v:
Autophagy
The identification of the mechanisms predisposing to stroke may improve its preventive and therapeutic strategies in patients with essential hypertension. The role of macroautophagy/autophagy in the development of hypertension-related stroke needs to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5c2e8e2c27fac956a2955e01d712c19a
Autor:
Elena Maria Pennisi, Laura Fionda, Giovanni Antonini, Andrea Micaloni, Luca Leonardi, Elisabetta Bucci, Gioia Merlonghi, Stefania Morino, E. Bertini, Salvatore Raffa, Matteo Garibaldi, Fiammetta Vanoli, Fabiana Fattori
Publikováno v:
Neuromuscular Disorders. 29:S205-S206
Autor:
Aron M. Geurts, Andrea Micaloni, Maria Rosaria Torrisi, Sabatino Valente, Franca Bianchi, Massimo Volpe, Maurizio Forte, Sebastiano Sciarretta, Roberta Coluccia, Cristina Scrofani, Speranza Rubattu, Salvatore Raffa
Publikováno v:
Human Molecular Genetics
Ndufc2, a subunit of the NADH: ubiquinone oxidoreductase, plays a key role in the assembly and activity of complex I within the mitochondrial OXPHOS chain. Its deficiency has been shown to be involved in diabetes, cancer and stroke. To improve our kn
Autor:
Erika Pagannone, Salvatore Raffa, Marco Testa, Cristina Scrofani, Maria Rosaria Torrisi, Andrea Micaloni, Giovanna Gallo, Danilo Ranieri, Sabatino Valente, Massimo Volpe, Gerardo Salerno, Speranza Rubattu, Roberta Coluccia
Publikováno v:
Scopus-Elsevier
Oncotarget
Oncotarget
Oxidative stress is currently viewed as a key factor in the genesis and progression of Heart Failure (HF). The aim of this study was to characterize the mitochondrial changes linked to oxidative stress generation in circulating peripheral blood monon
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::346c7d0948298c1ea3049aa6e24c9027
http://www.scopus.com/inward/record.url?eid=2-s2.0-85054727030&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-85054727030&partnerID=MN8TOARS