作者：
Alessandro,Rossi [1]
;
Irene J,Hoogeveen [2]
;
Vanessa B,Bastek [2]
;
Foekje,de Boer [2]
;
Chiara,Montanari [3]
;
Uta,Meyer [4]
;
Arianna,Maiorana [5]
;
Andrea,Bordugo [6]
;
Alice,Dianin [6]
;
Carmen,Campana [5]
;
Miriam,Rigoldi [7]
;
Priya S,Kishnani [8]
;
Surekha,Pendyal [8]
;
Pietro,Strisciuglio [1]
;
Serena,Gasperini [9]
;
Giancarlo,Parenti [1]
;
Rossella,Parini [9]
;
Sabrina,Paci [3]
;
Daniela,Melis [10]
;
Terry G J,Derks [2]
作者单位：
Department of Translational Medicine, Section of Pediatrics, University of Naples "Federico II", Naples, Italy.
[1]
Section of Metabolic Diseases, Beatrix Children's Hospital, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
[2]
Department of Pediatrics, San Paolo Hospital, ASST Santi Paolo e Carlo, University of Milan, Milan, Italy.
[3]
Department of Pediatrics, Hannover Medical School, Hannover, Germany.
[4]
Division of Metabolic Diseases, Department of Pediatric Specialties, Bambino Gesù Children's Hospital, Rome, Italy.
[5]
Inherited Metabolic Diseases Unit, Department of Paediatrics, Regional Centre for Newborn Screening, Diagnosis and Treatment of Inherited Metabolic Diseases and Congenital Endocrine Diseases, Azienda Ospedaliera Universitaria Integrata, Verona, Italy.
[6]
Rare Diseases Center, ASST Monza, San Gerardo Hospital, Monza, Italy.
[7]
Division of Medical Genetics, Department of Pediatrics, Duke University Medical Center, Durham, North Carolina, USA.
[8]
Rare Metabolic Diseases Pediatric Center, Pediatric Clinic, Fondazione MBBM, San Gerardo Hospital, Monza, Italy.
[9]
Department of Medicine, Surgery and Dentistry "Scuola Medica Salernitana", Section of Pediatrics, University of Salerno, Baronissi (SA), Italy.
[10]
DOI
10.1002/jimd.12224
PMID
32064649
发布时间
2021-08-23
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