Close Follow-Up of Patients with Neurofibromatosis Type 1 Reduces the Incidence of Malignant Peripheral Nerve Sheath Tumour
Neurofibromatosis type 1 (NF1) is an autosomal dominant genetic condition with a birth incidence of one in 2000 to one in 3000 [...].
Authors
- Thomas Decramer (ORCID: https://orcid.org/0000-0002-2585-581X)
- Hilde Brems (ORCID: https://orcid.org/0000-0002-0325-4060)
- Ellen Denayer (ORCID: https://orcid.org/0000-0001-6478-181X)
- Christophe M. Deroose (ORCID: https://orcid.org/0000-0002-6080-1577)
- Dries Ruttens (ORCID: https://orcid.org/0000-0002-1048-1800)
- Vincent Vandecaveye (ORCID: https://orcid.org/0000-0002-0800-3279)
- Eric Legius (ORCID: https://orcid.org/0000-0003-2410-6996)
- Daphne Hompes (ORCID: https://orcid.org/0000-0001-7068-9569)
- Thomas Douchy (ORCID: https://orcid.org/0000-0001-9972-644X)
- Sandra Jacobs (ORCID: https://orcid.org/0000-0002-9455-5394)
- Raf Sciot (ORCID: https://orcid.org/0000-0003-2244-5839)
- Frank Van Calenbergh
- Maria Pia Iasella
Institutions
- Princess Máxima Center (NL)
- KU Leuven (BE)
Publication Details
- Journal
- Cancers
- Published
- 2025-04-12
- DOI
- https://doi.org/10.3390/cancers17081306
- Citations
- 2
- Primary Topic
- Neurofibromatosis and Schwannoma Cases
- Type
- article
- Field-Weighted Citation Impact
- 2.78
Funders
- KU Leuven