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Role, function and challenges of multidisciplinary centres for rare diseases exemplified for neurofibromatosis type 1 syndrome
PURPOSE: Neurofibromatosis type 1 (NF1) syndrome is a common rare/orphan disease that manifests itself early in the paediatric age. It imposes a considerable burden upon patients as well as on caregivers. Decisions regarding optimal care often rely on several medical instances working together as a...
Autores principales: | Toledano-Alhadef, Hagit, Mautner, Victor-Felix, Gugel, Isabel, Zipfel, Julian, Haas-Lude, Karin, Constantini, Shlomi, Schuhmann, Martin U. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7276654/ https://www.ncbi.nlm.nih.gov/pubmed/32514759 http://dx.doi.org/10.1007/s00381-020-04708-1 |
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