Your browser doesn't support javascript.
loading
Correction to: A guide to writing systematic reviews of rare disease treatments to generate FAIRcompliant datasets: building a Treatabolome.
Atalaia, Antonio; Thompson, Rachel; Corvo, Alberto; Carmody, Leigh; Piscia, Davide; Matalonga, Leslie; Macaya, Alfons; Lochmuller, Angela; Fontaine, Bertrand; Zurek, Birte; Hernandez-Ferrer, Carles; Reinhard, Carola; Gómez-Andrés, David; Desaphy, Jean-François; Schon, Katherine; Lohmann, Katja; Jennings, Matthew J; Synofzik, Matthis; Riess, Olaf; Yaou, Rabah Ben; Evangelista, Teresinha; Ratnaike, Thiloka; Bros-Facer, Virginie; Gumus, Gulcin; Horvath, Rita; Chinnery, Patrick; Laurie, Steven; Graessner, Holm; Robinson, Peter; Lochmuller, Hanns; Beltran, Sergi; Bonne, Gisèle.
Afiliação
  • Atalaia A; Sorbonne Universite - Inserm UMRS 974, Center of Research in Myology, Institut de Myologie, G.H. Pitié-Salpêtrière Paris, 47, boulevard de l'Hopital, 75 651, Paris Cedex 13, France. antonio.marques-atalaia@inserm.fr.
  • Thompson R; Children's Hospital of Eastern Ontario Research Institute, Ottawa, Canada.
  • Corvo A; CNAG-CRG, Centre for Genomic Regulation (CRG), Barcelona Institute of Science and Technology (BIST), Barcelona, Spain.
  • Carmody L; The Jackson Laboratory for Genomic Medicine, Farmington, CT, 06032, USA.
  • Piscia D; CNAG-CRG, Centre for Genomic Regulation (CRG), Barcelona Institute of Science and Technology (BIST), Barcelona, Spain.
  • Matalonga L; CNAG-CRG, Centre for Genomic Regulation (CRG), Barcelona Institute of Science and Technology (BIST), Barcelona, Spain.
  • Macaya A; Paediatric Neurology, Vall D'Hebron University Hospital and VHIR (Euro-NMD, ERN-RND), 08035, Barcelona, Spain.
  • Lochmuller A; Department of Clinical Neurosciences, University of Cambridge School of Clinical Medicine, Cambridge Biomedical Campus, Cambridge, UK.
  • Fontaine B; Sorbonne Universite - Inserm UMRS 974, Center of Research in Myology, Institut de Myologie, G.H. Pitié-Salpêtrière Paris, 47, boulevard de l'Hopital, 75 651, Paris Cedex 13, France.
  • Zurek B; Institute of Medical Genetics and Applied Genomics, University of Tuebingen, Tübingen, Germany.
  • Hernandez-Ferrer C; CNAG-CRG, Centre for Genomic Regulation (CRG), Barcelona Institute of Science and Technology (BIST), Barcelona, Spain.
  • Reinhard C; Institute of Medical Genetics and Applied Genomics, University of Tuebingen, Tübingen, Germany.
  • Gómez-Andrés D; Paediatric Neurology, Vall D'Hebron University Hospital and VHIR (Euro-NMD, ERN-RND), 08035, Barcelona, Spain.
  • Desaphy JF; Department of Biomedical Sciences and Human Oncology, School of Medicine, University of Bari Aldo Moro, Bari, Italy.
  • Schon K; Department of Clinical Neurosciences, University of Cambridge School of Clinical Medicine, Cambridge Biomedical Campus, Cambridge, UK.
  • Lohmann K; Institute of Neurogenetics, University of Lübeck, 23538, Lübeck, Germany.
  • Jennings MJ; Department of Clinical Neurosciences, University of Cambridge School of Clinical Medicine, Cambridge Biomedical Campus, Cambridge, UK.
  • Synofzik M; Department of Neurodegenerative Diseases, Hertie-Institute for Clinical Brain Research and Center of Neurology, University of Tübingen, Tübingen, Germany.
  • Riess O; German Center for Neurodegenerative Diseases (DZNE), University of Tübingen, Tübingen, Germany.
  • Yaou RB; Institute of Medical Genetics and Applied Genomics, University of Tuebingen, Tübingen, Germany.
  • Evangelista T; Sorbonne Universite - Inserm UMRS 974, Center of Research in Myology, Institut de Myologie, G.H. Pitié-Salpêtrière Paris, 47, boulevard de l'Hopital, 75 651, Paris Cedex 13, France.
  • Ratnaike T; Unité de Morphologie Neuromusculaire, Institut de Myologie, GHU Pitié-Salpêtrière, Paris, France.
  • Bros-Facer V; Sorbonne Université, AP-HP, INSERM, Centre de Référence Des Maladies Neuromusculaires Nord/Est, Ile de France, Paris, France.
  • Gumus G; Department of Paediatrics, Cambridge University Hospitals NHS Foundation Trust, Cambridge, England.
  • Horvath R; Department of Clinical Neurosciences, University of Cambridge, Cambridge, UK.
  • Chinnery P; EURORDIS - Rare Diseases Europe, Paris, France.
  • Laurie S; EURORDIS - Rare Diseases Europe, Paris, France.
  • Graessner H; Department of Clinical Neurosciences, University of Cambridge School of Clinical Medicine, Cambridge Biomedical Campus, Cambridge, UK.
  • Robinson P; Department of Clinical Neurosciences, School of Clinical Medicine, University of Cambridge and MRC Mitochondrial Biology Unit, Cambridge Biomedical Campus, Cambridge, UK.
  • Lochmuller H; CNAG-CRG, Centre for Genomic Regulation (CRG), Barcelona Institute of Science and Technology (BIST), Barcelona, Spain.
  • Beltran S; Institute of Medical Genetics and Applied Genomics, University of Tuebingen, Tübingen, Germany.
  • Bonne G; The Jackson Laboratory for Genomic Medicine, Farmington, CT, 06032, USA.
Orphanet J Rare Dis ; 16(1): 145, 2021 Mar 22.
Article em En | MEDLINE | ID: mdl-33752678
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Orphanet J Rare Dis Ano de publicação: 2021 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Orphanet J Rare Dis Ano de publicação: 2021 Tipo de documento: Article