作者：
Lorenzo,Nanetti [1]
;
Mary,Kearney [2]
;
Sylvia,Boesch [3]
;
Lucie,Stovickova [4]
;
Juan Darío,Ortigoza-Escobar [5]
;
Alfons,Macaya [6]
;
David,Gomez-Andres [7]
;
Emmanuel,Roze [8]
;
Maria-Judit,Molnar [9]
;
Nicole I.,Wolf [10]
;
Alejandra,Darling [11]
;
Gessica,Vasco [12]
;
Enrico,Bertini [13]
;
Elisabetta,Indelicato [14]
;
David,Neubauer ;
Tobias B.,Haack ;
Judit C.,Sagi ;
Federica R.,Danti ;
Deborah,Sival ;
Ginevra,Zanni ;
Anneli,Kolk ;
Odile,Boespflug-Tanguy ;
Ludger,Schols ;
Bart,van de Warrenburg ;
Marie,Vidailhet ;
Michèl A.,Willemsen ;
Annemieke I.,Buizer ;
Enrico,Orzes ;
Sophie,Ripp ;
Carola,Reinhard ;
Isabella,Moroni ;
Caterina,Mariotti
作者单位：
Center for Rare Movement Disorders, Department of NeurologySecond Faculty of Medicine and Motol
[1]
Sorbonne University, INSERM, CNRS, Paris Brain Institute, APHP Salpêtrière Hospital
[2]
Sorbonne University, INSERM, CNRS, Paris Brain Institute, APHP Salpêtrière HospitalSemmelweis
[3]
Center for Rare Movement Disorders, Department of Neurology
[4]
UMCL, Children’s Hospital Ljubljana and University of Ljubljana
[5]
Institute of Medical Genetics and Applied Genomics University of Tübingen
[6]
Institute of Medical Genetics and Applied Genomics University of TübingenSemmelweis University
[7]
Tartu University Hospital Children’s Clinic, Department of Pediatrics and Neurology
[8]
APHP, Université Paris Cité, INSERM UMR1141, H?pital Robert Debré, Service de Neuropédiatrie
[9]
Sorbonne University, INSERM, CNRS, Paris Brain Institute, APHP Salpêtrière HospitalRadboud
[10]
Osservatorio Malattie Rare - Rarelab S.R.L.
[11]
Osservatorio Malattie Rare - Rarelab S.R.L.University Hospital Tübingen Centre for Rare Diseases
[12]
The Doctoral School of the Medical University of SilesiaJagiellonian University Medical College
[13]
Patient Advocate at the European Reference Network Representing Individuals With Ataxia, and
[14]
发布时间
2024-04-04
换一批
