1. Recurrent multilocular mandibular giant cell granuloma in neurofibromatosis type 1: Evidence for second hit mutation of NF1 gene in the jaw lesion and treatment with curettage and bone substitute materials. Issue 8 (August 2016) Authors: Friedrich, Reinhard E.; Grob, Tobias J.; Hollants, Silke; Zustin, Jozef; Spaepen, Marijke; Mautner, Victor F.; Luebke, Andreas M.; Hagel, Christian; Legius, Eric; Brems, Hilde Journal: Journal of cranio-maxillofacial surgery Issue: Volume 44:Issue 8(2016) Page Start: 1054 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Low mutation burden and frequent loss of CDKN2A/B and SMARCA2, but not PRC2, define premalignant neurofibromatosis type 1–associated atypical neurofibromas. Issue 8 (5th February 2019) Authors: Pemov, Alexander; Hansen, Nancy F; Sindiri, Sivasish; Patidar, Rajesh; Higham, Christine S; Dombi, Eva; Miettinen, Markku M; Fetsch, Patricia; Brems, Hilde; Chandrasekharappa, Settara C; Jones, Kristine; Zhu, Bin; Wei, Jun S; Mullikin, James C; Wallace, Margaret R; Khan, Javed; Legius, Eric; Wide... Journal: Neuro-oncology Issue: Volume 21:Issue 8(2019) Page Start: 981 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. The characteristics of 76 atypical neurofibromas as precursors to neurofibromatosis 1 associated malignant peripheral nerve sheath tumors. Issue 6 (2nd February 2018) Authors: Higham, Christine S; Dombi, Eva; Rogiers, Aljosja; Bhaumik, Sucharita; Pans, Steven; Connor, Steve E J; Miettinen, Markku; Sciot, Raf; Tirabosco, Roberto; Brems, Hilde; Baldwin, Andrea; Legius, Eric; Widemann, Brigitte C; Ferner, Rosalie E Journal: Neuro-oncology Issue: Volume 20:Issue 6(2018) Page Start: 818 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Mutational spectrum by phenotype: panel‐based NGS testing of patients with clinical suspicion of RASopathy and children with multiple café‐au‐lait macules. Issue 2 (12th December 2019) Authors: Castellanos, Elisabeth; Rosas, Inma; Negro, Alex; Gel, Bernat; Alibés, Andreu; Baena, Neus; Pineda, Mercè; Pi, Graciela; Pintos, Guillem; Salvador, Hector; Lázaro, Conxi; Blanco, Ignacio; Vilageliu, Lluïsa; Brems, Hilde; Grinberg, Daniel; Legius, Eric; Serra, Eduard Journal: Clinical genetics Issue: Volume 97:Issue 2(2020) Page Start: 264 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Multidisciplinary approach to neurofibromatosis type 1. (2020) Editors: Tadini, Gianluca; Legius, Eric; Brems, Hilde Record Type: Book Extent: 1 online resource (313 pages) View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Comprehensive targeted next‐generation sequencing approach in the molecular diagnosis of gastrointestinal stromal tumor. Issue 4 (14th December 2020) Authors: Vanden Bempt, Isabelle; Vander Borght, Sara; Sciot, Raf; Spans, Lien; Claerhout, Sofie; Brems, Hilde; Lehnert, Stefan; Dehaspe, Luc; Fransis, Sabine; Neuville, Bart; Topal, Baki; Schöffski, Patrick; Legius, Eric; Debiec‐Rychter, Maria Journal: Genes, chromosomes & cancer Issue: Volume 60:Issue 4(2021) Page Start: 239 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. An update on congenital melanocytic nevus syndrome: A case report and literature review. (2nd August 2021) Authors: Abdulmajid, Lilaf; Bosisio, Francesca Maria; Brems, Hilde; De Vlieger, Greet; Garmyn, Marjan; Segers, Heidi; Demaerel, Philippe; Segers, Katarina; Jansen, Katrien; Lagae, Lieven; Verheecke, Magali Journal: Journal of cutaneous pathology Issue: Volume 48:Number 12(2021) Page Start: 1497 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Genotype-first approach to identify associations between CDH1 germline variants and cancer phenotypes: a multicentre study by the European Reference Network on Genetic Tumour Risk Syndromes. Issue 1 (January 2023) Authors: Garcia-Pelaez, José; Barbosa-Matos, Rita; Lobo, Silvana; Dias, Alexandre; Garrido, Luzia; Castedo, Sérgio; Sousa, Sónia; Pinheiro, Hugo; Sousa, Liliana; Monteiro, Rita; Maqueda, Joaquin J; Fernandes, Susana; Carneiro, Fátima; Pinto, Nádia; Lemos, Carolina; Pinto, Carla; Teixeira, Manuel R; Aretz,... Journal: Lancet oncology Issue: Volume 24:Issue 1(2023) Page Start: 91 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Neurofibromatosis type 1‐related pseudarthrosis: Beyond the pseudarthrosis site. Issue 10 (18th June 2019) Authors: Brekelmans, Carlijn; Hollants, Silke; De Groote, Caroline; Sohier, Natalie; Maréchal, Marina; Geris, Liesbet; Luyten, Frank P.; Ginckels, Lieve; Sciot, Raf; de Ravel, Thomy; De Smet, Luc; Lammens, Johan; Legius, Eric; Brems, Hilde Journal: Human mutation Issue: Volume 40:Issue 10(2019) Page Start: 1760 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Impaired instrumental learning in Spred1−/− mice, a model for a rare RASopathy. (4th March 2021) Authors: Borrie, Sarah C.; Horner, Alexa E.; Yoshimura, Akihiko; Legius, Eric; Kopanitsa, Maksym V.; Brems, Hilde Journal: Genes, brain, and behavior Issue: Volume 20:Number 5(2021) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗