Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Francesca Castelli"'
Autor:
Emanuele Maria Giusti, Barbara Papazian, Chiara Manna, Valentina Giussani, Milena Perotti, Francesca Castelli, Silvia Battaglia, Pietro Galli, Agnese Rossi, Valentina Re, Karine Goulene, Gianluca Castelnuovo, Marco Stramba-Badiale
Publikováno v:
Frontiers in Psychology, Vol 14 (2023)
Externí odkaz:
https://doaj.org/article/d611d41938d34cfc8c7768a25638a0c0
Autor:
Emanuele Maria Giusti, Barbara Papazian, Chiara Manna, Valentina Giussani, Milena Perotti, Francesca Castelli, Silvia Battaglia, Pietro Galli, Agnese Rossi, Valentina Re, Karine Goulene, Gianluca Castelnuovo, Marco Stramba-Badiale
Publikováno v:
Frontiers in Psychology, Vol 12 (2022)
BackgroundChronic airway diseases are prevalent and costly conditions. Interdisciplinary rehabilitation programs that include Acceptance and Commitment-based (ACT) components could be important to tackle the vicious circle linking progression of the
Externí odkaz:
https://doaj.org/article/ff99c7b4035b41cbb7f7b86566266d3e
Autor:
Francesca Castelli
Publikováno v:
Italiano LinguaDue, Vol 2, Iss 1 (2010)
Lo sviluppo di competenze disciplinari e competenze linguistiche procedeparallelamente nell'apprendimento della storia e avviene in una situazione didattica che è, innanzitutto, una situazione comunicativa. Partendo dall'analisi della proposta di un
Externí odkaz:
https://doaj.org/article/641671ed9631413f859ee9aab8e5f6d4
Autor:
Alice Bonuccelli, Andrea Santangelo, Francesca Castelli, Giulia Magherini, Elena Volpi, Elisa Costa, Elena Alesci, Gabriele Massimetti, Francesca Felicia Operto, Diego Giampiero Peroni, Alessandro Orsini
Publikováno v:
International Journal of Environmental Research and Public Health; Volume 20; Issue 1; Pages: 552
Electroencephalography (EEG) is pivotal in the clinical assessment of epilepsy, and sleep is known to improve the diagnostic yield of its recording. Sleep-EEG recording is generally reached by either partial deprivation or by administration of sleep-
Autor:
Paola Santalucia, Giacomo Fraternale, Alessandro Squizzato, Irene Caridi, Fabrizio Fabris, Stefania Antoniazzi, Luigina Guasti, Francesca Castelli, Paola Contaldi, Ilaria Ardoino, Anna Valenti, Marco Proietti, Marilena Durazzo, Tiziana Tognin, Francesca Minonzio, Francesco Baffa Bellucci, Giorgio Annoni, Carlo Sabbà, Francesca Mete, Patrizia Suppressa, Graziana Lupattelli, Alessandro Nobili, Valter Monzani, Pietro Castellino, Hu Cinzia, Maurizio Muscaritoli, Chiara Mussi, Raffaella Rossio, Roberto Manfredini, Miriam Gino, Vanessa Bianconi, Silvano Bosari, Antonio Brucato, V. Beccati, Giovanni Murialdo, Luciano Ottonello, Marco Mazzeo, Donatella Padula, Tiziano Lucchi, Francesco Bandiera, G. Colombo, Franco Dallegri, Nicola Altamura, Carlo Usai, Mario Barbagallo, Maria Perticone, Giovanna Di Bella, Luca Zanoli, L. Burdick, Fabio Fabbian, Maurizio Gabrielli, Kassem Salam, G. Ceriani, Adriana Bruni, Andrea Maria Maresca, Maura Marcucci, Luigi Fenoglio, Francesca Fezza, Gino Roberto Corazza, Armando Napolitano, Enrico Strocchi, Patrizio Odetti, Renzo Rozzini, Michela Zanetti, Remo Melchio, Alessio Marra, Antonella Tufano, Enrico Petrillo, Carlotta Franchi, Francesco Franceschi, Barbara Brignolo, Flora Peyvandi, Nicola Lucio Liberato, Paolo Fornengo, Emanuela Miceli, Francesco Perticone, Marco Bertolotti, Lara Caserza, Alfredo De Giorgi, Dario Manfellotto, Enrico Nicolis, Domenica Cappellini, Claudio Borghi, Pier Mannuccio Mannucci, Alessio Molfino, Maurizio Dore, Paolo Francione, Alessio Nencioni, Gianni Biolo, Silvia Fargion, Federico Cattaneo, Maria Teresa Sartori, Fiammetta Monacelli, Giovanni Di Minno
Publikováno v:
British Journal of Clinical Pharmacology. 84:2010-2019
Aims Although oral anticoagulants (OACs) are effective in preventing stroke in older people with atrial fibrillation (AF), they are often underused in this particularly high-risk population. The aim of the present study was to assess the appropriaten
Aims We tested the hypothesis that CB1/CB2 receptor double knockout would produce significant increases in infarct size and volume and significant worsening in clinical score, using two mouse models, one of permanent ischemia and one of ischemia/repe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0fdb76afadb3bb9f21eef66c30ab77e6
https://europepmc.org/articles/PMC5810406/
https://europepmc.org/articles/PMC5810406/
Autor:
Francesco Leporati, Francesca Castelli, Gustavo M. Callico, Emanuele Torti, M. Marrero-Martin, Samuel Ortega, Giordana Florimbi, Himar Fabelo
Publikováno v:
Electronics
Volume 7
Issue 11
Electronics, Vol 7, Iss 11, p 283 (2018)
Volume 7
Issue 11
Electronics, Vol 7, Iss 11, p 283 (2018)
The precise delineation of brain cancer is a crucial task during surgery. There are several techniques employed during surgical procedures to guide neurosurgeons in the tumor resection. However, hyperspectral imaging (HSI) is a promising non-invasive
Autor:
Teija Parkkari, Sara Del Carlo, Marco Macchia, Marco Allarà, Alessia Ligresti, Simone Bertini, Clementina Manera, Giuseppe Saccomanni, Juha R. Savinainen, Francesca Castelli, Anna Maria Malfitano, Valentina Lucchesi, Maurizio Bifulco, Chiara Laezza, Vincenzo Di Marzo
Publikováno v:
European journal of medicinal chemistry (Online) (2014).
info:cnr-pdr/source/autori:Lucchesi V, Parkkari T, Savinainen JR, Malfitano AM, Allarà M, Bertini S, Castelli F, Del Carlo S, Laezza C, Ligresti A, Saccomanni G, Bifulco M, Di Marzo V, Macchia M, Manera C./titolo:1,2-Dihydro-2-oxopyridine-3-carboxamides: the C-5 substituent is responsible for functionality switch at CB2 cannabinoid receptor./doi:/rivista:European journal of medicinal chemistry (Online)/anno:2014/pagina_da:/pagina_a:/intervallo_pagine:/volume
info:cnr-pdr/source/autori:Lucchesi V, Parkkari T, Savinainen JR, Malfitano AM, Allarà M, Bertini S, Castelli F, Del Carlo S, Laezza C, Ligresti A, Saccomanni G, Bifulco M, Di Marzo V, Macchia M, Manera C./titolo:1,2-Dihydro-2-oxopyridine-3-carboxamides: The C-5 substituent is responsible for functionality switch at CB2 cannabinoid receptor./doi:/rivista:European journal of medicinal chemistry (Online)/anno:2014/pagina_da:/pagina_a:/intervallo_pagine:/volume
info:cnr-pdr/source/autori:Lucchesi V, Parkkari T, Savinainen JR, Malfitano AM, Allarà M, Bertini S, Castelli F, Del Carlo S, Laezza C, Ligresti A, Saccomanni G, Bifulco M, Di Marzo V, Macchia M, Manera C./titolo:1,2-Dihydro-2-oxopyridine-3-carboxamides: the C-5 substituent is responsible for functionality switch at CB2 cannabinoid receptor./doi:/rivista:European journal of medicinal chemistry (Online)/anno:2014/pagina_da:/pagina_a:/intervallo_pagine:/volume
info:cnr-pdr/source/autori:Lucchesi V, Parkkari T, Savinainen JR, Malfitano AM, Allarà M, Bertini S, Castelli F, Del Carlo S, Laezza C, Ligresti A, Saccomanni G, Bifulco M, Di Marzo V, Macchia M, Manera C./titolo:1,2-Dihydro-2-oxopyridine-3-carboxamides: The C-5 substituent is responsible for functionality switch at CB2 cannabinoid receptor./doi:/rivista:European journal of medicinal chemistry (Online)/anno:2014/pagina_da:/pagina_a:/intervallo_pagine:/volume
The relevance of CB2R-mediated therapeutic effects is well-known for the treatment of inflammatory and neuropathic pain and neurodegenerative disorders. In our search for new cannabinoid receptor modulators, we report the optimization of a series of
Autor:
Antonio Marco Maria Osculati, Luisa Andrello, Francesca Castelli, Silvia Damiana Visonà, Francesco Ventura
Publikováno v:
Medicine. 95:e4586
Background: Generally, rheumatic heart disease is, today, sporadic in developed countries, even though it continues to be a major health hazard in the developing ones. It is also a very rare cause of sudden unexpected death. We report a case of a 15-
Autor:
Anna Maria Malfitano, Giuseppe Saccomanni, Adriano Martinelli, Valentina Lucchesi, Tiziano Tuccinardi, Francesca Castelli, Simone Bertini, Antonio Giordano, Alessia Ligresti, Clementina Manera, Maurizio Bifulco, Flavio Rizzolio, Chiara Laezza, Vincenzo Di Marzo, Marco Macchia
Publikováno v:
European journal of medicinal chemistry (Online) (2012).
info:cnr-pdr/source/autori:Manera C, Saccomanni G, Malfitano AM, Bertini S, Castelli F, Laezza C, Ligresti A, Lucchesi V, Tuccinardi T, Rizzolio F, Bifulco M, Di Marzo V, Giordano A, Macchia M, Martinelli A./titolo:Rational design, synthesis and anti-proliferative properties of new CB2 selective cannabinoid receptor ligands: an investigation of the 1,8-naphthyridin-2(1H)-one scaffold./doi:/rivista:European journal of medicinal chemistry (Online)/anno:2012/pagina_da:/pagina_a:/intervallo_pagine:/volume
European journal of medicinal chemistry (2012).
info:cnr-pdr/source/autori:Manera C, Saccomanni G, Malfitano AM, Bertini S, Castelli F, Laezza C, Ligresti A, Lucchesi V, Tuccinardi T, Rizzolio F, Bifulco M, Di Marzo V, Giordano A, Macchia M, Martinelli A./titolo:Rational design, synthesis and anti-proliferative properties of new CB2 selective cannabinoid receptor ligands: an investigation of the 1,8-naphthyridin-2(1H)-one scaffold./doi:/rivista:European journal of medicinal chemistry/anno:2012/pagina_da:/pagina_a:/intervallo_pagine:/volume
info:cnr-pdr/source/autori:Manera C, Saccomanni G, Malfitano AM, Bertini S, Castelli F, Laezza C, Ligresti A, Lucchesi V, Tuccinardi T, Rizzolio F, Bifulco M, Di Marzo V, Giordano A, Macchia M, Martinelli A./titolo:Rational design, synthesis and anti-proliferative properties of new CB2 selective cannabinoid receptor ligands: an investigation of the 1,8-naphthyridin-2(1H)-one scaffold./doi:/rivista:European journal of medicinal chemistry (Online)/anno:2012/pagina_da:/pagina_a:/intervallo_pagine:/volume
European journal of medicinal chemistry (2012).
info:cnr-pdr/source/autori:Manera C, Saccomanni G, Malfitano AM, Bertini S, Castelli F, Laezza C, Ligresti A, Lucchesi V, Tuccinardi T, Rizzolio F, Bifulco M, Di Marzo V, Giordano A, Macchia M, Martinelli A./titolo:Rational design, synthesis and anti-proliferative properties of new CB2 selective cannabinoid receptor ligands: an investigation of the 1,8-naphthyridin-2(1H)-one scaffold./doi:/rivista:European journal of medicinal chemistry/anno:2012/pagina_da:/pagina_a:/intervallo_pagine:/volume
CB2 receptor ligands are becoming increasingly attractive drugs due to the potential role of this receptor in several physiopathological processes. Using our previously described series of 1,8-naphthyridin-2(1H)-on-3-carboxamides as a lead class, sev
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::792b5ba1fa57da3022f3c3fd743f9b0e
http://hdl.handle.net/11588/830241
http://hdl.handle.net/11588/830241