Orphanet Journal of Rare Diseases (Aug 2020)
Correction to: Consensus guideline for the diagnosis and treatment of tetrahydrobiopterin (BH4) deficiencies
- Thomas Opladen,
- Eduardo López-Laso,
- Elisenda Cortès-Saladelafont,
- Toni S. Pearson,
- H. Serap Sivri,
- Yilmaz Yildiz,
- Birgit Assmann,
- Manju A. Kurian,
- Vincenzo Leuzzi,
- Simon Heales,
- Simon Pope,
- Francesco Porta,
- Angeles García-Cazorla,
- Tomáš Honzík,
- Roser Pons,
- Luc Regal,
- Helly Goez,
- Rafael Artuch,
- Georg F. Hoffmann,
- Gabriella Horvath,
- Beat Thöny,
- Sabine Scholl-Bürgi,
- Alberto Burlina,
- Marcel M. Verbeek,
- Mario Mastrangelo,
- Jennifer Friedman,
- Tessa Wassenberg,
- Kathrin Jeltsch,
- Jan Kulhánek,
- Oya Kuseyri Hübschmann,
- on behalf of the International Working Group on Neurotransmitter related Disorders (iNTD)
Affiliations
- Thomas Opladen
- Division of Child Neurology and Metabolic Disorders, University Children’s Hospital
- Eduardo López-Laso
- Pediatric Neurology Unit, Department of Pediatrics, University Hospital Reina Sofía, IMIBIC and CIBERER
- Elisenda Cortès-Saladelafont
- Inborn errors of metabolism Unit, Institut de Recerca Sant Joan de Déu and CIBERER-ISCIII
- Toni S. Pearson
- Department of Neurology, Washington University School of Medicine
- H. Serap Sivri
- Department of Pediatrics, Section of Metabolism, Hacettepe University, Faculty of Medicine
- Yilmaz Yildiz
- Department of Pediatrics, Section of Metabolism, Hacettepe University, Faculty of Medicine
- Birgit Assmann
- Division of Child Neurology and Metabolic Disorders, University Children’s Hospital
- Manju A. Kurian
- Developmental Neurosciences, UCL Great Ormond Street-Institute of Child Health
- Vincenzo Leuzzi
- Unit of Child Neurology and Psychiatry, Department of Human Neuroscience, Sapienza University of Rome
- Simon Heales
- Neurometabolic Unit, National Hospital, Queen Square
- Simon Pope
- Neurometabolic Unit, National Hospital, Queen Square
- Francesco Porta
- Department of Pediatrics, AOU Città della Salute e della Scienza
- Angeles García-Cazorla
- Inborn errors of metabolism Unit, Institut de Recerca Sant Joan de Déu and CIBERER-ISCIII
- Tomáš Honzík
- Department of Paediatrics and Adolescent Medicine, First Faculty of Medicine, Charles University and General University Hospital in Prague
- Roser Pons
- First Department of Pediatrics of the University of Athens, Aghia Sofia Hospital
- Luc Regal
- Department of Pediatric, Pediatric Neurology and Metabolism Unit, UZ Brussel
- Helly Goez
- Department of Pediatrics, University of Alberta Glenrose Rehabilitation Hospital
- Rafael Artuch
- Clinical biochemistry department, Institut de Recerca Sant Joan de Déu, CIBERER and MetabERN Hospital Sant Joan de Déu
- Georg F. Hoffmann
- Division of Child Neurology and Metabolic Disorders, University Children’s Hospital
- Gabriella Horvath
- Department of Pediatrics, Division of Biochemical Genetics, BC Children’s Hospital, University of British Columbia
- Beat Thöny
- Division of Metabolism, University Children’s Hospital Zurich
- Sabine Scholl-Bürgi
- Clinic for Pediatrics I, Medical University of Innsbruck
- Alberto Burlina
- U.O.C. Malattie Metaboliche Ereditarie, Dipartimento della Salute della Donna e del Bambino, Azienda Ospedaliera Universitaria di Padova - Campus Biomedico Pietro d’Abano
- Marcel M. Verbeek
- Departments of Neurology and Laboratory Medicine, Alzheimer Centre, Radboud University Medical Center, Donders Institute for Brain, Cognition and Behaviour
- Mario Mastrangelo
- Unit of Child Neurology and Psychiatry, Department of Human Neuroscience, Sapienza University of Rome
- Jennifer Friedman
- UCSD Departments of Neuroscience and Pediatrics, Rady Children’s Hospital Division of Neurology, Rady Children’s Institute for Genomic Medicine
- Tessa Wassenberg
- Department of Pediatric, Pediatric Neurology and Metabolism Unit, UZ Brussel
- Kathrin Jeltsch
- Division of Child Neurology and Metabolic Disorders, University Children’s Hospital
- Jan Kulhánek
- Department of Paediatrics and Adolescent Medicine, First Faculty of Medicine, Charles University and General University Hospital in Prague
- Oya Kuseyri Hübschmann
- Division of Child Neurology and Metabolic Disorders, University Children’s Hospital
- on behalf of the International Working Group on Neurotransmitter related Disorders (iNTD)
- DOI
- https://doi.org/10.1186/s13023-020-01464-y
- Journal volume & issue
-
Vol. 15,
no. 1
pp. 1 – 5
Abstract
An amendment to this paper has been published and can be accessed via the original article.
