Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Francesca Giachino"'
Autor:
Fulvio Morello, Marco Santoro, Francesca Giachino, Francesca Caciolli, Elisa Capretti, Matteo Castelli, Emanuele Pivetta, Peiman Nazerian, Enrico Lupia
Publikováno v:
Medicina, Vol 59, Iss 3, p 548 (2023)
Background and Objectives. Acute aortic syndromes (AASs) are emergencies burdened by high morbidity and mortality. Guideline-recommended diagnostic workup is based on pre-test probability assessment (PPA) and d-dimer testing. However, the performance
Externí odkaz:
https://doaj.org/article/9181252c7487441692ed2e2d0d369454
Autor:
Ricciardolo, Barbara Mognetti, Daniela Francesca Giachino, Francesca Bertolini, Vitina Carriero, Andrea Elio Sprio, Fabio Luigi Massimo
Publikováno v:
Applied Sciences; Volume 13; Issue 13; Pages: 7450
Background: Glucocorticoids (GCs) represent the mainstay therapy for asthmatics. A subset of severe asthmatics fails to respond to steroid-based therapies, leading to important healthcare costs. Single nucleotide polymorphisms (SNPs) of glucocorticoi
Autor:
Samuele Sutera, Daniela Francesca Giachino, Alessandra Pelle, Roberta Zuntini, Monica Pentenero
Publikováno v:
Biomedicines; Volume 11; Issue 1; Pages: 81
PTEN hamartoma tumor syndrome (PHTS), is a spectrum of disorders caused by mutations of PTEN, in which non-cancerous growths, called hamartomas, develop in different areas of the body, often including the oral mucosa. PHTS also implies a recognized i
Autor:
Enrico Tagliafico, Isabella Bernardis, Marina Grasso, Maria Rosaria D'Apice, Cristina Lapucci, Annalisa Botta, Daniela Francesca Giachino, Maria Marinelli, Paola Primignani, Silvia Russo, Ilaria Sani, Manuela Seia, Sergio Fini, Paola Rimessi, Elena Tenedini, Anna Ravani, Maurizio Genuardi, Alessandra Ferlini, Molecular Genetics Working Group of the Italian Society of Human Genetics, SIGU
Publikováno v:
PLoS ONE, Vol 13, Iss 11, p e0206855 (2018)
Genetic testing availability in the health care system is rapidly increasing, along with the diffusion of next-generation sequencing (NGS) into diagnostics. These issues make imperative the knowledge-drive optimization of testing in the clinical sett
Externí odkaz:
https://doaj.org/article/e0be3ab1c9574e378228b83edd270268
Autor:
Giorgia Mandrile, Eleonora Di Gregorio, Alessandro Calcia, Alessandro Brussino, Enrico Grosso, Elisa Savin, Daniela Francesca Giachino, Alfredo Brusco
Publikováno v:
Case Reports in Genetics, Vol 2014 (2014)
A recently described genetic disorder has been associated with 13q12.3 microdeletion spanning three genes, namely, KATNAL1, LINC00426, and HMGB1. Here, we report a new case with similar clinical features that we have followed from birth to 5 years ol
Externí odkaz:
https://doaj.org/article/eaaf2417387b4a28a6975a17b4675cf9
Autor:
Cristina Paglieri, Stefania M. Locatelli, Giulio Porrino, Andrea Conterno, Alessia Beux, Maria Avolio, Michela Sozzi, Dario Leone, Pasqualina Visconti, Claudia Sacchi, Ilaria Pia, Silvia Totaro, Astrid Surra, Francesca Risi, Francesca Dellavalle, Federico Grosso, Paolo Baron, Gilberto Calzolari, Fabio Steri, Francesca Basile, Alberto Goffi, Marialessia Capuano, Emanuele Pivetta, Francesca Giachino, Franco Riccardini, Patrizia Ferrera, Andrea Iannaccone, Busso, Alice Bartalucci, Rossana Cavallo, Paolo Fascio Pecetto, Isabel Losano, Lorenzo Richiardi, Paola Del Rizzo, Giulia Silvestri, Marco Ottino, Liliana Chichizola, Arianna Ardito, Matteo Oddi, Paolo Bima, Valentina Beux, Maria Gelardi, Giordano Bianchi, Fulvio Morello, Denise Baricocchi, Irene Cara, Enrico Lupia, Matteo Vesan, Federico Baldassa, Maria Tizzani, Virginia Scategni, Milena Maule, Stefania Dutto, Giulia Labarile
Publikováno v:
Annals of Emergency Medicine
Study objective Accurate diagnostic testing to identify severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection is critical. Although highly specific, SARS-CoV-2 reverse transcriptase–polymerase chain reaction (RT-PCR) has been shown
Autor:
Peiman Nazerian, Christian Mueller, Alexandre de Matos Soeiro, Bernd A. Leidel, Sibilla Anna Teresa Salvadeo, Francesca Giachino, Simone Vanni, Karin Grimm, Múcio Tavares Oliveira, Emanuele Pivetta, Enrico Lupia, Stefano Grifoni, Fulvio Morello, Elisa Capretti, Matteo Castelli, Simona Gualtieri, Federica Trausi, Stefania Battista, Paolo Bima, Federica Carbone, Maria Tizzani, Maria G. Veglio, Patrick Badertscher, Jasper Boeddinghaus, Thomas Nestelberger, Raphael Twerenbold
Publikováno v:
Circulation. 137:250-258
Background: Acute aortic syndromes (AASs) are rare and severe cardiovascular emergencies with unspecific symptoms. For AASs, both misdiagnosis and overtesting are key concerns, and standardized diagnostic strategies may help physicians to balance the
Autor:
Corrado Magnino, Enrico Lupia, Giulia Lucia Massimina Cavalot, Francesca Giachino, Fabio Settanni, Matteo Oddi, Fulvio Morello, Maria Tizzani, Stefania Battista, Peiman Nazerian, Giulio Mengozzi, Alice Ianniello
Publikováno v:
Scientific Reports
Scientific Reports, Vol 8, Iss 1, Pp 1-8 (2018)
Scientific Reports, Vol 8, Iss 1, Pp 1-8 (2018)
Acute aortic syndromes (AAS) are cardiovascular emergencies with unmet diagnostic needs. Copeptin is released upon stress conditions and is approved for rule-out of myocardial infarction (MI). As MI and AAS share presenting symptoms, stress mechanism
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
M. Tavares De Oliveira, S. Gualtieri, Fulvio Morello, Francesca Giachino, Sibilla Anna Teresa Salvadeo, ADvISED Investigators, Enrico Lupia, Simone Vanni, M.G. Veglio, Stefano Grifoni, Alfredo Augusto Vieira Soeiro, Karin Grimm, Peiman Nazerian, Bernd A. Leidel, C Mueller
Publikováno v:
European Heart Journal. 38