Salivary Cytokines and Airways Disease Severity in Patients with Cystic Fibrosis

Salivary Cytokines and Airways Disease Severity in Patients with Cystic Fibrosis

About 50% of patients with cystic fibrosis (CF) have sinonasal complications, which include inferior turbinate hypertrophy (NTH) and/or nasal polyposis (NP), and different degrees of lung disease, which represents the main cause of mortality. Monitoring of sinonasal disease requires complex instrume...

Täydet tiedot

Bibliografiset tiedot
Päätekijät: Alice Castaldo, Paola Iacotucci, Vincenzo Carnovale, Roberta Cimino, Renato Liguori, Marika Comegna, Valeria Raia, Gaetano Corso, Giuseppe Castaldo, Monica Gelzo
Aineistotyyppi: Artikkeli
Kieli:English
Julkaistu: MDPI AG 2020-04-01
Sarja:Diagnostics
Aiheet:
cystic fibrosis
inferior turbinates hypertrophy
nasal polyposis
salivary cytokines
Linkit:https://www.mdpi.com/2075-4418/10/4/222

Internet

https://www.mdpi.com/2075-4418/10/4/222

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