Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Martina TASSONE"'
Autor:
Martina TASSONE
Publikováno v:
Diacronie. Studi di Storia Contemporanea, Vol 16, Iss 3, Pp 40-59 (2024)
Since the middle of the last century, and especially in the contemporary era, dominated by the image, the power of a historical fact is not only political, social and archival, but also cinematographic: from its very beginnings, cinema possesses a st
Externí odkaz:
https://doaj.org/article/438f6274b41448639b95aa3ae560ae53
Autor:
Annalisa Boscolo, Tommaso Pettenuzzo, Nicolò Sella, Matteo Zatta, Michele Salvagno, Martina Tassone, Chiara Pretto, Arianna Peralta, Luisa Muraro, Francesco Zarantonello, Andrea Bruni, Federico Geraldini, Alessandro De Cassai, Paolo Navalesi
Publikováno v:
European Respiratory Review, Vol 32, Iss 168 (2023)
Background The effect of noninvasive respiratory support (NRS), including high-flow nasal oxygen, bi-level positive airway pressure and continuous positive airway pressure (noninvasive ventilation (NIV)), for preventing and treating post-extubation r
Externí odkaz:
https://doaj.org/article/77e153489f1a468784d1528ecaba5964
Autor:
Alessandro De Cassai, Martina Tassone, Federico Geraldini, Massimo Sergi, Nicolò Sella, Annalisa Boscolo, Marina Munari
Publikováno v:
Korean Journal of Anesthesiology, Vol 74, Iss 5, Pp 383-393 (2021)
Background Trial sequential analysis (TSA) is a recent cumulative meta-analysis method used to weigh type I and II errors and to estimate when the effect is large enough to be unaffected by further studies. The aim of this study was to illustrate pos
Externí odkaz:
https://doaj.org/article/86a77df3d4a247f5a21268ba78184178
Autor:
Annamaria Perri, Francesca Romana Lepri, Martina Tassone, Giulia Severi, Dino Gibertoni, Laura Mazzanti, Maria Gnazzo, Claudio Graziano, Emanuela Scarano, Federica Tamburrino
Publikováno v:
Molecular Syndromology. 10:130-138
KBG syndrome is an autosomal dominant disorder caused by pathogenic variants within ANKRD11 or deletions of 16q24.3 which include ANKRD11. It is characterized by distinctive facial features, developmental delay, short stature, and skeletal anomalies.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::27c2030df07e6b1b14cb799683328fcd
https://doi.org/10.1159/000496172
https://doi.org/10.1159/000496172