作者：
Ha,Trang [1]
;
Martin,Samuels [2]
;
Isabella,Ceccherini [3]
;
Matthias,Frerick [4]
;
Maria Angeles,Garcia-Teresa [5]
;
Jochen,Peters [4]
;
Johannes,Schoeber [4]
;
Marek,Migdal [6]
;
Agneta,Markstrom [7]
;
Giancarlo,Ottonello [8]
;
Raffaele,Piumelli [9]
;
Maria Helena,Estevao [10]
;
Irena,Senecic-Cala [11]
;
Barbara,Gnidovec-Strazisar [12]
;
Andreas,Pfleger [13]
;
Raquel,Porto-Abal [14]
;
Miriam,Katz-Salamon [7]
作者单位：
Hôpital Universitaire Robert Debré, Centre de référence des maladies respiratoires rares, and Université de Paris, Paris, France. ha.trang@aphp.fr.
[1]
Staffordshire Children's Hospital, Stoke-on-Trent, Staffs and Great Ormond Street Hospital, London, UK.
[2]
Istituto Giannina Gaslini, UOSD Laboratory of Genetics and Genomics of Rare Diseases, Genoa, Italy.
[3]
Department of Pediatrics, Klinikum Dritter Orden, Munich, Germany.
[4]
Niño Jesús University Children's Hospital, Pediatric Intensive Care Unit, Madrid, Spain.
[5]
Department of Anaesthesiology and Intensive care, Children's Memorial Health Institute, Warsaw, Poland.
[6]
Karolinska University Hospital, Stockholm, Sweden.
[7]
Pediatric Primary Care, ASL3, Genoa, Liguria, Italy.
[8]
Sleep Disordered Breathing and SIDS Center, Meyer Children's Hospital, Florence, Italy.
[9]
Pneumology Department, Pediatric Hospital of Coimbra, Coimbra, Portugal.
[10]
University Hospital Centre, Department of Pediatrics, Zagreb and School of Medicine, Zagreb, Croatia.
[11]
University Children's Hospital, Department of child, adolescent & developmental neurology, University Clinical Centre Ljubljana, Ljubljana, Slovenia.
[12]
Medical University of Graz, Paediatric Pulmonology and Allergology, Graz, Austria.
[13]
Department of Pediatrics, Puerta de Hierro Hospital, Madrid, Spain.
[14]
DOI
10.1186/s13023-020-01460-2
PMID
32958024
发布时间
2024-08-02
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