Soft tissue and visceral sarcomas: ESMO–EURACAN–GENTURIS Clinical Practice Guidelines for diagnosis, treatment and follow-up von Gronchi, A., Miah, A.B., Dei Tos, A.P., Abecassis, N., Bajpai, J., Bauer, S., Biagini, R., Bielack, S., Blay, J.Y., Bolle, S., Bonvalot, S., Boukovinas, I., Bovee, J.V.M.G., Boye, K., Brennan, B., Brodowicz, T., Buonadonna, A., De Álava, E., Del Muro, X.G., Dufresne, A., Eriksson, M., Fagioli, F., Fedenko, A., Ferraresi, V., Ferrari, A., Frezza, A.M., Gasperoni, S., Gelderblom, H., Gouin, F., Grignani, G., Haas, R., Hassan, A.B., Hecker-Nolting, S., Hindi, N., Hohenberger, P., Joensuu, H., Jones, R.L., Jungels, C., Jutte, P., Kager, L., Kasper, B., Kawai, A., Kopeckova, K., Krákorová, D.A., Le Cesne, A., Le Grange, F., Legius, E., Leithner, A., Lopez-Pousa, A., Martin-Broto, J., Merimsky, O., Messiou, C., Mir, O., Montemurro, M., Morland, B., Morosi, C., Palmerini, E., Pantaleo, M.A., Piana, R., Piperno-Neumann, S., Reichardt, P., Rutkowski, P., Safwat, A.A., Sangalli, C., Sbaraglia, M., Scheipl, S., Schöffski, P., Sleijfer, S., Strauss, D., Strauss, S., Sundby Hall, K., Trama, A., Unk, M., van de Sande, M.A.J., van der Graaf, W.T.A., van Houdt, W.J., Frebourg, T., Casali, P.G., Stacchiotti, S.

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Bone sarcomas: ESMO–EURACAN–GENTURIS–ERN PaedCan Clinical Practice Guideline for diagnosis, treatment and follow-up von Strauss, S.J., Frezza, A.M., Abecassis, N., Bajpai, J., Bauer, S., Biagini, R., Bielack, S., Blay, J.Y., Bolle, S., Bonvalot, S., Boukovinas, I., Bovee, J.V.M.G., Boye, K., Brennan, B., Brodowicz, T., Buonadonna, A., de Álava, E., Dei Tos, A.P., Garcia del Muro, X., Dufresne, A., Eriksson, M., Fagioli, F., Fedenko, A., Ferraresi, V., Ferrari, A., Gaspar, N., Gasperoni, S., Gelderblom, H., Gouin, F., Grignani, G., Gronchi, A., Haas, R., Hassan, A.B., Hecker-Nolting, S., Hindi, N., Hohenberger, P., Joensuu, H., Jones, R.L., Jungels, C., Jutte, P., Kager, L., Kasper, B., Kawai, A., Kopeckova, K., Krákorová, D.A., Le Cesne, A., Le Grange, F., Legius, E., Leithner, A., López Pousa, A., Martin-Broto, J., Merimsky, O., Messiou, C., Miah, A.B., Mir, O., Montemurro, M., Morland, B., Morosi, C., Palmerini, E., Pantaleo, M.A., Piana, R., Piperno-Neumann, S., Reichardt, P., Rutkowski, P., Safwat, A.A., Sangalli, C., Sbaraglia, M., Scheipl, S., Schöffski, P., Sleijfer, S., Strauss, D., Sundby Hall, K., Trama, A., Unk, M., van de Sande, M.A.J., van der Graaf, W.T.A., van Houdt, W.J., Frebourg, T., Ladenstein, R., Casali, P.G., Stacchiotti, S.

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Mutations in LZTR1 drive human disease by dysregulating RAS ubiquitination von Steklov, M, Pandolfi, S, Baietti, M F, Batiuk, A, Carai, P, Najm, P, Zhang, M, Jang, H, Renzi, F, Cai, Y, Abbasi Asbagh, L, Pastor, T, De Troyer, M, Simicek, M, Radaelli, E, Brems, H, Legius, E, Tavernier, J, Gevaert, K, Impens, F, Messiaen, L, Nussinov, R, Heymans, S, Eyckerman, S, Sablina, A A

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Gastrointestinal stromal tumours: ESMO–EURACAN–GENTURIS Clinical Practice Guidelines for diagnosis, treatment and follow-up von Casali, P.G., Blay, J.Y., Abecassis, N., Bajpai, J., Bauer, S., Biagini, R., Bielack, S., Bonvalot, S., Boukovinas, I., Bovee, J.V.M.G., Boye, K., Brodowicz, T., Buonadonna, A., De Álava, E., Dei Tos, A.P., Del Muro, X.G., Dufresne, A., Eriksson, M., Fedenko, A., Ferraresi, V., Ferrari, A., Frezza, A.M., Gasperoni, S., Gelderblom, H., Gouin, F., Grignani, G., Haas, R., Hassan, A.B., Hindi, N., Hohenberger, P., Joensuu, H., Jones, R.L., Jungels, C., Jutte, P., Kasper, B., Kawai, A., Kopeckova, K., Krákorová, D.A., Le Cesne, A., Le Grange, F., Legius, E., Leithner, A., Lopez-Pousa, A., Martin-Broto, J., Merimsky, O., Messiou, C., Miah, A.B., Mir, O., Montemurro, M., Morosi, C., Palmerini, E., Pantaleo, M.A., Piana, R., Piperno-Neumann, S., Reichardt, P., Rutkowski, P., Safwat, A.A., Sangalli, C., Sbaraglia, M., Scheipl, S., Schöffski, P., Sleijfer, S., Strauss, D., Strauss, S.J., Hall, K Sundby, Trama, A., Unk, M., van de Sande, M.A.J., van der Graaf, W.T.A., van Houdt, W.J., Frebourg, T., Gronchi, A., Stacchiotti, S.

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Clinical and molecular aspects of RAS related disorders von Denayer, E, de Ravel, Th, Legius, E

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Patients with High-Grade Gliomas and Café-au-Lait Macules: Is Neurofibromatosis Type 1 the Only Diagnosis? von Guerrini-Rousseau, L, Suerink, M, Grill, J, Legius, E, Wimmer, K, Brugières, L

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Clinical implementation of NIPT - technical and biological challenges von Brady, P., Brison, N., Van Den Bogaert, K., de Ravel, T., Peeters, H., Van Esch, H., Devriendt, K., Legius, E., Vermeesch, J.R.

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Risk-reducing mastectomy in BRCA carriers: survival is not the issue von Neven, P., Punie, K., Wildiers, H., Willers, N., Van Ongeval, C., Van Buggenhout, G., Legius, E.

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Choroidal abnormalities in café‐au‐lait syndromes: a new differential diagnostic tool? von Cassiman, C., Casteels, I., Jacob, J., Plasschaert, E., Brems, H., Dubron, K., Keer, K.V., Legius, E.

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PGD for a complex chromosomal rearrangement by array comparative genomic hybridization von Vanneste, E., Melotte, C., Voet, T., Robberecht, C., Debrock, S., Pexsters, A., Staessen, C., Tomassetti, C., Legius, E., D'Hooghe, T., Vermeesch, J.R.

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Hypotrichosis-lymphedema-telangiectasia-renal defect associated with a truncating mutation in the SOX18 gene von Moalem, S., Brouillard, P., Kuypers, D., Legius, E., Harvey, E., Taylor, G., Francois, M., Vikkula, M., Chitayat, D.

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Comparative study of the ophthalmological examinations in neurofibromatosis type 1. Proposal for a new screening algorithm von Caen, S, Cassiman, C, Legius, E, Casteels, I

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Elevated Risk for MPNST in NF1 Microdeletion Patients von De Raedt, T., Brems, H., Wolkenstein, P., Vidaud, D., Pilotti, S., Perrone, F., Mautner, V., Frahm, S., Sciot, R., Legius, E.

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Capturing the wide variety of impaired fracture healing phenotypes in Neurofibromatosis Type 1 with eight key factors: a computational study von Carlier, A., Brems, H., Ashbourn, J. M. A., Nica, I., Legius, E., Geris, L.

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Mutation in NRAS in familial Noonan syndrome--case report and review of the literature von Ekvall, Sara, Wilbe, Maria, Dahlgren, Jovanna, Legius, Eric, van Haeringen, Arie, Westphal, Otto, Annerén, Göran, Bondeson, Marie-Louise

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Neuropsychological profile in adults with neurofibromatosis type 1 compared to a control group von Descheemaeker, M.-J., Plasschaert, E., Frijns, J.-P., Legius, E.

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Mutation analysis of RAD51D in non-BRCA1/2 ovarian and breast cancer families von Osher, D J, De Leeneer, K, Michils, G, Hamel, N, Tomiak, E, Poppe, B, Leunen, K, Legius, E, Shuen, A, Smith, E, Arseneau, J, Tonin, P, Matthijs, G, Claes, K, Tischkowitz, M D, Foulkes, W D

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Erratum: Capturing the wide variety of impaired fracture healing phenotypes in Neurofibromatosis Type 1 with eight key factors: a computational study von Carlier, A., Brems, H., Ashbourn, J. M. A., Nica, I., Legius, E., Geris, L.

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Spectrum of single- and multiexon NF1 copy number changes in a cohort of 1,100 unselected NF1 patients von Wimmer, K., Yao, S., Claes, K., Kehrer-Sawatzki, H., Tinschert, S., De Raedt, T., Legius, E., Callens, T., Beiglböck, H., Maertens, O., Messiaen, L.

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NRAS Mutations in Noonan Syndrome von Denayer, E., Peeters, H., Sevenants, L., Derbent, M., Fryns, J.P., Legius, E.

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