Giulio Cesare Passali

Dr. Giulio Cesare Passali

Institute of Otolaryngology, Catholic University of the Sacred Heart, Agostino Gemelli Polyclinic, Rome, Italy
orcid

Research Focus & Metrics

Academic Career Length

28Years (1999-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

View All Publications
1 August 2003 in Annals of Otology, Rhinology & Laryngology
Verified
Journal Article
Closed access
Desiderio PassàliDesiderio Passàli
Desiderio Passàli
FPFrancesco Maria Passàli
Francesco Maria Passàli
Giulio Cesare PassaliGiulio Cesare Passali
Giulio Cesare Passali
VDValerio Damiani
Valerio Damiani
LBLuisa Bellussi
Luisa Bellussi
In the past 130 years, many surgical procedures for turbinate reduction have been developed. We analyzed the long-term efficacy of 6 of these surgical techniques (turbinectomy, laser cautery, electrocautery, cryotherapy, submucosal resection, and submucosal resection with lateral displacement) over a 6-year follow-up period. We randomly divided 382 patients into 6 therapeutic groups and surgically treated them at the Department of Otorhinolaryngology of the University of Siena. After 6 years, only submucosal resection resulted in optimal long-term normalization of nasal patency and in restoration of mucociliary clearance and local secretory IgA production to a physiological level with few postoperative complications (p < .001). The addition of lateral displacement of the inferior turbinate improved the long-term results. We recommend, in spite of the greater surgical skill required, submucosal resection combined with lateral displacement as the first-choice technique for the treatment of nasal obstruction due to hypertrophy of the inferior turbinates.

1 May 2012 in International Journal of Pediatric Otorhinolaryngology
Verified
Journal Article
Closed access
FFFrancesca Foltran
Francesca Foltran
SBSimonetta Ballali
Simonetta Ballali
FPFrancesco Maria Passali
Francesco Maria Passali
EKEugene Kern
Eugene Kern
BMBruno Morra
Bruno Morra
Dario GregoriDario Gregori
Dario Gregori

1 April 2017 in Acta Otorhinolaryngologica Italica
Verified
Journal Article
Open access
MCMassimo Castagnola
Massimo Castagnola
ESE. Scarano
E. Scarano
Giulio Cesare PassaliGiulio Cesare Passali
Giulio Cesare Passali
IMIrene Messana
Irene Messana
TCTiziana Cabras
Tiziana Cabras
GPG. Paludetti
G. Paludetti
Lo studio della proteomica salivare, test economico e non invasivo, rappresenta una fonte di numerose informazioni, ed è utile per la diagnosi di svariate malattie. Da quando siamo entrati nell’era della tecnologia genomica e delle scienze “omiche”, la raccolta di campioni salivari è aumentata esponenzialmente. Recenti piattaforme proteomiche hanno analizzato il proteoma salivare umano, caratterizzando circa 3000 peptidi e proteine, espressi in maniera differente: più del 90% in peso deriva dalla secrezione delle tre ghiandole salivari maggiori, mentre la restante parte proviene dalle ghiandole salivari minori, dal fluido crevicolare gengivale, da essudati mucosi e dalla microflora orale. L’obiettivo principale dell’analisi proteomica è discriminare tra condizioni fisiologiche e patologiche. Ad oggi, tuttavia, non esiste un preciso protocollo che permetta di analizzare l’intero proteoma salivare, pertanto sono state realizzate svariate strategie. Innanzitutto, è possibile distinguere due tipologie di piattaforme proteomiche: l’approccio “top-down” prevede l’analisi delle proteine sotto esame come entità intatte; nell’approccio “bottom-up” la caratterizzazione della proteina avviene mediante lo studio dei peptidi ottenuti dopo digestione enzimatica (con tripsina tipicamente). A causa di questa eterogeneità, per una stessa patologia sono stati proposti differenti biomarkers. Il proteoma salivare è stato caratterizzato in numerose malattie: carcinoma squamoso e leucoplachie orali, malattia del trapianto contro l’ospite (GVHD) cronica, sindrome di Sjögren e altri disordini autoimmuni come la sindrome SAPHO (sinovite, acne, pustolosi, iperostosi e osteite), schizofrenia e disordine bipolare, malattie genetiche come la sindrome di Down o la malattia di Wilson. In conclusione, i risultati delle ricerche riportate in questa review suggeriscono che nel prossimo futuro la saliva diverrà un fluido di indubbia rilevanza diagnostica utile per fini clinici, sia diagnostici, sia prognostici.

1 May 2012 in International Journal of Pediatric Otorhinolaryngology
Verified
Journal Article
Closed access
HRHugo Rodríguez
Hugo Rodríguez
Giulio Cesare PassaliGiulio Cesare Passali
Giulio Cesare Passali
Dario GregoriDario Gregori
Dario Gregori
ACAlberto Chinski
Alberto Chinski
CTCarlos Tiscornia
Carlos Tiscornia
GCGiselle Cuestas
Giselle Cuestas

7 May 2020 in European Archives of Oto-Rhino-Laryngology
Verified
Journal Article
Open access
PDF file
Giulio Cesare PassaliGiulio Cesare Passali
Giulio Cesare Passali
ABAnna Rita Bentivoglio
Anna Rita Bentivoglio

Verified
Journal Article
Open access
PDF file
Eugenio De CorsoEugenio De Corso
Eugenio De Corso
Stefano SettimiStefano Settimi
Stefano Settimi
CMClaudio Montuori
Claudio Montuori
MCMarco Corbò
Marco Corbò
Giulio Cesare PassaliGiulio Cesare Passali
Giulio Cesare Passali
JGJacopo Galli
Jacopo Galli
The aim of this study was to evaluate the efficacy of dupilumab in the treatment of severe uncontrolled Chronic Rhinosinusitis with Nasal Polyps (CRSwNP), with or without asthma as add-on therapy with intra-nasal corticosteroids in a real-life setting over the first year of treatment. Our data demonstrated that subcutaneous 300 mg dupilumab administered at home via a pre-filled auto-injector every two weeks, based on indications set by the Italian Medicines Agency, was rapidly effective in reducing the size of polyps, decreasing symptoms of disease, improving quality of life, and recovering olfaction. Significant improvement was observed after only 15 days of treatment, and it progressively increased at 6 and 12 months. Dupilumab was also effective in reducing the local nasal eosinophilic infiltrate, in decreasing the need for surgery and/or oral corticosteroids, and in improving control of associated comorbidities such as chronic eosinophilic otitis media and bronchial asthma. After 12 months of treatment, 96.5% of patients had a moderate/excellent response. From our data, it was evident that there was a group of patients that showed a very early response within one month of therapy, another group with early response within six months from baseline, and a last group that improved later within 12 months. The results of this study support the use of dupilumab as an effective option in the current standard of care for patients affected by severe uncontrolled CRSwNP.