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Shortcutting the diagnostic odyssey: the multidisciplinary Program for Undiagnosed Rare Diseases in adults (UD-PrOZA).
Schuermans, Nika; Hemelsoet, Dimitri; Terryn, Wim; Steyaert, Sanne; Van Coster, Rudy; Coucke, Paul J; Steyaert, Wouter; Callewaert, Bert; Bogaert, Elke; Verloo, Patrick; Vanlander, Arnaud V; Debackere, Elke; Ghijsels, Jody; LeBlanc, Pontus; Verdin, Hannah; Naesens, Leslie; Haerynck, Filomeen; Callens, Steven; Dermaut, Bart; Poppe, Bruce.
Affiliation
  • Schuermans N; Center for Medical Genetics, Ghent University Hospital, Ghent, Belgium. nika.schuermans@ugent.be.
  • Hemelsoet D; Department of Biomolecular Medicine, Faculty of Medicine and Health Sciences, Ghent University, Ghent, Belgium. nika.schuermans@ugent.be.
  • Terryn W; Department of Neurology, Ghent University Hospital, Ghent, Belgium.
  • Steyaert S; Department of Nephrology, Jan Yperman Hospital, Ieper, Belgium.
  • Van Coster R; Department of General Internal Medicine, Ghent University Hospital, Ghent, Belgium.
  • Coucke PJ; Department of Pediatrics, Division of Pediatric Neurology and Metabolic Diseases, Ghent University Hospital, Ghent, Belgium.
  • Steyaert W; Center for Medical Genetics, Ghent University Hospital, Ghent, Belgium.
  • Callewaert B; Department of Biomolecular Medicine, Faculty of Medicine and Health Sciences, Ghent University, Ghent, Belgium.
  • Bogaert E; Department of Human Genetics, Radboud Institute for Molecular Life Sciences, Radboud University Medical Center, Nijmegen, The Netherlands.
  • Verloo P; Center for Medical Genetics, Ghent University Hospital, Ghent, Belgium.
  • Vanlander AV; Department of Biomolecular Medicine, Faculty of Medicine and Health Sciences, Ghent University, Ghent, Belgium.
  • Debackere E; Center for Medical Genetics, Ghent University Hospital, Ghent, Belgium.
  • Ghijsels J; Department of Biomolecular Medicine, Faculty of Medicine and Health Sciences, Ghent University, Ghent, Belgium.
  • LeBlanc P; Department of Pediatrics, Division of Pediatric Neurology and Metabolic Diseases, Ghent University Hospital, Ghent, Belgium.
  • Verdin H; Department of Pediatrics, Division of Pediatric Neurology and Metabolic Diseases, Ghent University Hospital, Ghent, Belgium.
  • Naesens L; Center for Medical Genetics, Ghent University Hospital, Ghent, Belgium.
  • Haerynck F; Department of Biomolecular Medicine, Faculty of Medicine and Health Sciences, Ghent University, Ghent, Belgium.
  • Callens S; Center for Medical Genetics, Ghent University Hospital, Ghent, Belgium.
  • Dermaut B; Department of Biomolecular Medicine, Faculty of Medicine and Health Sciences, Ghent University, Ghent, Belgium.
  • Poppe B; Center for Medical Genetics, Ghent University Hospital, Ghent, Belgium.
Orphanet J Rare Dis ; 17(1): 210, 2022 05 23.
Article de En | MEDLINE | ID: mdl-35606766
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Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Maladies rares / Maladies non diagnostiquées Type d'étude: Diagnostic_studies / Guideline / Prognostic_studies Limites: Humans Langue: En Journal: Orphanet J Rare Dis Sujet du journal: MEDICINA Année: 2022 Type de document: Article Pays d'affiliation: Belgique
Texte intégral
Ajouter à My VHL
Imprimer
XML
PubMed Links
Recherche sur Google

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Maladies rares / Maladies non diagnostiquées Type d'étude: Diagnostic_studies / Guideline / Prognostic_studies Limites: Humans Langue: En Journal: Orphanet J Rare Dis Sujet du journal: MEDICINA Année: 2022 Type de document: Article Pays d'affiliation: Belgique