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Correction to: Consensus guideline for the diagnosis and treatment of tetrahydrobiopterin (BH4) deficiencies.
Opladen, Thomas; López-Laso, Eduardo; Cortès-Saladelafont, Elisenda; Pearson, Toni S; Sivri, H Serap; Yildiz, Yilmaz; Assmann, Birgit; Kurian, Manju A; Leuzzi, Vincenzo; Heales, Simon; Pope, Simon; Porta, Francesco; García-Cazorla, Angeles; Honzík, Tomás; Pons, Roser; Regal, Luc; Goez, Helly; Artuch, Rafael; Hoffmann, Georg F; Horvath, Gabriella; Thöny, Beat; Scholl-Bürgi, Sabine; Burlina, Alberto; Verbeek, Marcel M; Mastrangelo, Mario; Friedman, Jennifer; Wassenberg, Tessa; Jeltsch, Kathrin; Kulhánek, Jan; Kuseyri Hübschmann, Oya.
Afiliação
  • Opladen T; Division of Child Neurology and Metabolic Disorders, University Children's Hospital, Heidelberg, Germany. Thomas.Opladen@med.uni-heidelberg.de.
  • López-Laso E; Pediatric Neurology Unit, Department of Pediatrics, University Hospital Reina Sofía, IMIBIC and CIBERER, Córdoba, Spain.
  • Cortès-Saladelafont E; Inborn errors of metabolism Unit, Institut de Recerca Sant Joan de Déu and CIBERER-ISCIII, Barcelona, Spain.
  • Pearson TS; Unit of Pediatric Neurology and Metabolic Disorders, Department of Pediatrics, Hospital Germans Trias i Pujol, and Faculty of Medicine, Universitat Autònoma de Barcelona, Badalona, Spain.
  • Sivri HS; Department of Neurology, Washington University School of Medicine, St. Louis, USA.
  • Yildiz Y; Department of Pediatrics, Section of Metabolism, Hacettepe University, Faculty of Medicine, 06100, Ankara, Turkey.
  • Assmann B; Department of Pediatrics, Section of Metabolism, Hacettepe University, Faculty of Medicine, 06100, Ankara, Turkey.
  • Kurian MA; Division of Child Neurology and Metabolic Disorders, University Children's Hospital, Heidelberg, Germany.
  • Leuzzi V; Developmental Neurosciences, UCL Great Ormond Street-Institute of Child Health, London, UK.
  • Heales S; Department of Neurology, Great Ormond Street Hospital, London, UK.
  • Pope S; Unit of Child Neurology and Psychiatry, Department of Human Neuroscience, Sapienza University of Rome, Rome, Italy.
  • Porta F; Neurometabolic Unit, National Hospital, Queen Square, London, UK.
  • García-Cazorla A; Neurometabolic Unit, National Hospital, Queen Square, London, UK.
  • Honzík T; Department of Pediatrics, AOU Città della Salute e della Scienza, Torino, Italy.
  • Pons R; Inborn errors of metabolism Unit, Institut de Recerca Sant Joan de Déu and CIBERER-ISCIII, Barcelona, Spain.
  • Regal L; Department of Paediatrics and Adolescent Medicine, First Faculty of Medicine, Charles University and General University Hospital in Prague, Prague, Czech Republic.
  • Goez H; First Department of Pediatrics of the University of Athens, Aghia Sofia Hospital, Athens, Greece.
  • Artuch R; Department of Pediatric, Pediatric Neurology and Metabolism Unit, UZ Brussel, Brussels, Belgium.
  • Hoffmann GF; Department of Pediatrics, University of Alberta Glenrose Rehabilitation Hospital, Edmonton, Canada.
  • Horvath G; Clinical biochemistry department, Institut de Recerca Sant Joan de Déu, CIBERER and MetabERN Hospital Sant Joan de Déu, Barcelona, Spain.
  • Thöny B; Division of Child Neurology and Metabolic Disorders, University Children's Hospital, Heidelberg, Germany.
  • Scholl-Bürgi S; Department of Pediatrics, Division of Biochemical Genetics, BC Children's Hospital, University of British Columbia, Vancouver, BC, Canada.
  • Burlina A; Division of Metabolism, University Children's Hospital Zurich, Zürich, Switzerland.
  • Verbeek MM; Clinic for Pediatrics I, Medical University of Innsbruck, Anichstr 35, Innsbruck, Austria.
  • Mastrangelo M; U.O.C. Malattie Metaboliche Ereditarie, Dipartimento della Salute della Donna e del Bambino, Azienda Ospedaliera Universitaria di Padova - Campus Biomedico Pietro d'Abano, Padova, Italy.
  • Friedman J; Departments of Neurology and Laboratory Medicine, Alzheimer Centre, Radboud University Medical Center, Donders Institute for Brain, Cognition and Behaviour, Nijmegen, The Netherlands.
  • Wassenberg T; Unit of Child Neurology and Psychiatry, Department of Human Neuroscience, Sapienza University of Rome, Rome, Italy.
  • Jeltsch K; UCSD Departments of Neuroscience and Pediatrics, Rady Children's Hospital Division of Neurology, Rady Children's Institute for Genomic Medicine, San Diego, USA.
  • Kulhánek J; Department of Pediatric, Pediatric Neurology and Metabolism Unit, UZ Brussel, Brussels, Belgium.
  • Kuseyri Hübschmann O; Division of Child Neurology and Metabolic Disorders, University Children's Hospital, Heidelberg, Germany.
Orphanet J Rare Dis ; 15(1): 202, 2020 08 05.
Article em En | MEDLINE | ID: mdl-32758270
ABSTRACT
An amendment to this paper has been published and can be accessed via the original article.
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Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies / Guideline Idioma: En Ano de publicação: 2020 Tipo de documento: Article
Texto completo
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XML
PubMed Links
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Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies / Guideline Idioma: En Ano de publicação: 2020 Tipo de documento: Article