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Natural history of adults with KBG syndrome: A physician-reported experience
Allan Bayat*, Hannah Grimes, Elke de Boer, Morten Krogh Herlin, Rebekka Staal Dahl, Ida Charlotte Bay Lund, Michael Bayat, Anneli Clea Skjelmose Bolund, Cathrine Elisabeth Gjerulfsen, Pernille Axél Gregersen, Monica Zilmer, Stefan Juhl, Katarzyna Cebula, Elisa Rahikkala, Isabelle Maystadt, Angela Peron, Aglaia Vignoli, Rosa Maria Alfano, Franco Stanzial, Francesco Benedicenti
*Corresponding author for this work
- University of Copenhagen
- University Hospitals Bristol and Weston NHS Foundation Trust
- Radboud University Medical Center
- Donders Institute for Brain, Cognition and Behaviour
- Erasmus MC Sophia Children's Hospital
- Aarhus University Hospital
- Aarhus University
- Epilepsihospitalet Filadelfia
- Oulu University Hospital
- Institute Pathology And Genetic
- University of Namur, Faculty of Medicine
- San Paolo Hospital
- Meyer Children’s Hospital
- University of Florence
- University of Milan
- Central Hospital of Bolzano
- Hong Kong Children's Hospital
- Laboratoire National de Santé, Luxembourg.
- Hunter Area Health Service
- Leipzig University
- Münster University Hospital
- University Medical Center Groningen
- Grigol Robakidze University
- Catholic University of Louvain
- Bristol Medical School
Research output: Contribution to journal › Journal article › Research › peer-review