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LETTERS TO THE EDITOR   

Minerva Medica 2021 August;112(4):518-20

DOI: 10.23736/S0026-4806.19.06054-3

Copyright © 2019 EDIZIONI MINERVA MEDICA

lingua: Inglese

Primary ciliary dyskinesia: can we identify patients with the most severe phenotype?

Gioia PIATTI 1, Maria M. DE SANTI 2, Andrea FAROLFI 3, Lucia BARCELLINI 3, Enza D’AURIA 3, Maria F. PATRIA 4, Dario CONSONNI 5, Umberto AMBROSETTI 6

1 Unit of Bronchopneumology, Department of Pathophysiology and Transplantation, Fondazione IRCCS Ca’ Granda, Ospedale Maggiore Policlinico, University of Milan, Milan, Italy; 2 Unit of Pathological Anatomy, Department of Human Pathology and Oncology, Le Scotte Polyclinic Hospital, University of Siena, Siena, Italy; 3 Pediatric Pulmonology, Pediatric Department, Vittore Buzzi Children’s Hospital, University of Milan, Milan, Italy; 4 Pediatric Highly Intensive Care Unit, Fondazione IRCCS Ca’ Granda, Ospedale Maggiore Policlinico, University of Milan, Milan, Italy; 5 Unit of Epidemiology, Fondazione IRCCS Ca’ Granda, Ospedale Maggiore Policlinico, University of Milan, Milan, Italy; 6 Unit of Audiology, Department of Clinical Sciences and Community Health, Fondazione IRCCS Ca’ Granda, Ospedale Maggiore Policlinico, University of Milan, Milan, Italy



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