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Minerva Medica 2019 Jun 25

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 Margherita DE SANTI 2, Andrea FAROLFI 3, Lucia BARCELLINI 3, Enza C. D'AURIA 3, Maria Francesca 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, Policlinico Le Scotte, University of Siena, Siena, Italy; 3 Department of Pediatric Pulmonology, Vittore Buzzi Children’s Hospital, University of Milan, Milan, Italy; 4 Paediatric Highly Intensive Care Unit, Department of Pathophysiology and Transplantation, Fondazione IRCCS Ca’ Granda, Ospedale Maggiore Policlinico, University of Milan, Milan, Italy; 5 Epidemiology Unit, Fondazione IRCCS Ca’ Granda, Ospedale Maggiore Policlinico, Milan, Italy; 6 Audiology Unit, Department of Clinical Sciences and Community Health, Fondazione IRCCS Ca’ Granda, Ospedale Maggiore Policlinico, University of Milan Milan, Italy


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