Your browser doesn't support javascript.
loading
An Integrated clinical pathway for diagnosis, treatment and care of rare diseases: model, operating procedures, and results of the project TRANSLATE-NAMSE funded by the German Federal Joint Committee.
Choukair, Daniela; Hauck, Fabian; Bettendorf, Markus; Krude, Heiko; Klein, Christoph; Bäumer, Tobias; Berner, Reinhard; Lee-Kirsch, Min Ae; Grasemann, Corinna; Burgard, Peter; Hoffmann, Georg F.
Affiliation
  • Choukair D; Center for Child and Adolescent Medicine and Center for Rare Diseases, University Hospital Heidelberg, 69120, Heidelberg, Germany.
  • Hauck F; Department of Pediatrics, Dr Von Hauner Children's Hospital, University Hospital and Munich Centre for Rare Diseases, LMU Munich, 80337, Munich, Germany.
  • Bettendorf M; Center for Child and Adolescent Medicine and Center for Rare Diseases, University Hospital Heidelberg, 69120, Heidelberg, Germany.
  • Krude H; Institute for Experimental Pediatric Endocrinology, and Berlin Center for Rare Diseases, Charité - Universitätsmedizin Berlin, 13353, Berlin, Germany.
  • Klein C; Department of Pediatrics, Dr Von Hauner Children's Hospital, University Hospital and Munich Centre for Rare Diseases, LMU Munich, 80337, Munich, Germany.
  • Bäumer T; Institute of Systems Motorscience and Center for Rare Diseases, University of Lübeck, 23562, Lübeck, Germany.
  • Berner R; Department of Pediatrics and University Center for Rare Diseases, University Hospital Carl Gustav Carus, Technische Universität Dresden, 01307, Dresden, Germany.
  • Lee-Kirsch MA; Department of Pediatrics and University Center for Rare Diseases, University Hospital Carl Gustav Carus, Technische Universität Dresden, 01307, Dresden, Germany.
  • Grasemann C; Department of Pediatrics, St-Josef Hospital Bochum and and Center for Rare Diseases, Ruhr-University Bochum, 44791, Bochum, Germany.
  • Burgard P; Center for Child and Adolescent Medicine and Center for Rare Diseases, University Hospital Heidelberg, 69120, Heidelberg, Germany. peter.burgard@t-online.de.
  • Hoffmann GF; Center for Child and Adolescent Medicine and Center for Rare Diseases, University Hospital Heidelberg, 69120, Heidelberg, Germany.
Orphanet J Rare Dis ; 16(1): 474, 2021 11 12.
Article in En | MEDLINE | ID: mdl-34772435

Full text: 1 Database: MEDLINE Therapeutic Methods and Therapies TCIM: Plantas_medicinales Main subject: Critical Pathways / Rare Diseases Type of study: Diagnostic_studies / Guideline / Prognostic_studies Language: En Journal: Orphanet J Rare Dis Year: 2021 Type: Article Affiliation country: Germany

Full text: 1 Database: MEDLINE Therapeutic Methods and Therapies TCIM: Plantas_medicinales Main subject: Critical Pathways / Rare Diseases Type of study: Diagnostic_studies / Guideline / Prognostic_studies Language: En Journal: Orphanet J Rare Dis Year: 2021 Type: Article Affiliation country: Germany