Legius Syndrome and its Relationship with Neurofibromatosis Type 1

por DENAYER, Ellen, LEGIUS, Eric
Publicado 2020

Optical Coherence Tomography Angiography of Retinal Microvascular Changes Overlying Choroidal Nodules in Neurofibromatosis Type 1

por Cassiman, Catherine, Casteels, Ingele, Stalmans, Peter, Legius, Eric, Jacob, Julie
Publicado 2017

Nevus anemicus and RASopathies

por Bulteel, Charlotte, Morren, Marie-Anne, De Haes, Petra, Denayer, Ellen, Legius, Eric, Brems, Hilde
Publicado 2018

Challenges in Treating Genodermatoses: New Therapies at the Horizon

por Morren, Marie-Anne, Legius, Eric, Giuliano, Fabienne, Hadj-Rabia, Smail, Hohl, Daniel, Bodemer, Christine
Publicado 2022

SREBP modulates the NADP(+)/NADPH cycle to control night sleep in Drosophila

por Mariano, Vittoria, Kanellopoulos, Alexandros K., Aiello, Giuseppe, Lo, Adrian C., Legius, Eric, Achsel, Tilmann, Bagni, Claudia
Publicado 2023

What the neurosurgeon should know about hemangioblastoma, both sporadic and in Von Hippel-Lindau disease: A literature review

por Bamps, Sven, Calenbergh, Frank Van, Vleeschouwer, Steven De, Loon, Johannes Van, Sciot, Raf, Legius, Eric, Goffin, Jan
Publicado 2013

Keratinocytic epidermal nevus syndrome with Schwann cell proliferation, lipomatous tumour and mosaic KRAS mutation

por Farschtschi, Said, Mautner, Victor-Felix, Hollants, Silke, Hagel, Christian, Spaepen, Marijke, Schulte, Christoph, Legius, Eric, Brems, Hilde
Publicado 2015

Mutation in NRAS in familial Noonan syndrome – case report and review of the literature

por Ekvall, Sara, Wilbe, Maria, Dahlgren, Jovanna, Legius, Eric, van Haeringen, Arie, Westphal, Otto, Annerén, Göran, Bondeson, Marie-Louise
Publicado 2015

A Patient with Neonatal Cholestasis

por Claeys, Kristl G., Breysem, Luc, Legius, Eric, Brems, Hilde, Cassiman, David, Moisse, Matthieu, Vermeersch, Pieter, Levtchenko, Elena, Jaeken, Jaak
Publicado 2021

MEK inhibition ameliorates social behavior phenotypes in a Spred1 knockout mouse model for RASopathy disorders

por Borrie, Sarah C., Plasschaert, Ellen, Callaerts-Vegh, Zsuzsanna, Yoshimura, Akihiko, D’Hooge, Rudi, Elgersma, Ype, Kushner, Steven A., Legius, Eric, Brems, Hilde
Publicado 2021

Comparative Oncogenomic Analysis of Copy Number Alterations in Human and Zebrafish Tumors Enables Cancer Driver Discovery

por Zhang, GuangJun, Hoersch, Sebastian, Amsterdam, Adam, Whittaker, Charles A., Beert, Eline, Catchen, Julian M., Farrington, Sarah, Postlethwait, John H., Legius, Eric, Hopkins, Nancy, Lees, Jacqueline A.
Publicado 2013

An incidental finding of maternal multiple myeloma by non invasive prenatal testing

por Imbert‐Bouteille, Marion, Chiesa, Jean, Gaillard, Jean‐Baptiste, Dorvaux, Véronique, Altounian, Lucille, Gatinois, Vincent, Mousty, Eve, Finge, Sanae, Bourquard, Pascal, Vermeesch, Joris Robert, Legius, Eric, Vandenberghe, Peter
Publicado 2017

Identifying challenges in neurofibromatosis: a modified Delphi procedure

por Dhaenens, Britt A. E., Ferner, Rosalie E., Bakker, Annette, Nievo, Marco, Evans, D. Gareth, Wolkenstein, Pierre, Potratz, Cornelia, Plotkin, Scott R., Heimann, Guenter, Legius, Eric, Oostenbrink, Rianne
Publicado 2021

Pathogenesis of vestibular schwannoma in ring chromosome 22

por Denayer, Ellen, Brems, Hilde, de Cock, Paul, Evans, Gareth D, Van Calenbergh, Frank, Bowers, Naomi, Sciot, Raf, Debiec-Rychter, Maria, Vermeesch, Joris V, Fryns, Jean-Pierre, Legius, Eric
Publicado 2009

The biology of cutaneous neurofibromas: Consensus recommendations for setting research priorities

por Brosseau, Jean-Philippe, Pichard, Dominique C., Legius, Eric H., Wolkenstein, Pierre, Lavker, Robert M., Blakeley, Jaishri O., Riccardi, Vincent M., Verma, Sharad K., Brownell, Isaac, Le, Lu Q.
Publicado 2018

Characterizing the microstructural basis of “unidentified bright objects” in neurofibromatosis type 1: A combined in vivo multicomponent T2 relaxation and multi-shell diffusion MRI...

por Billiet, Thibo, Mädler, Burkhard, D'Arco, Felice, Peeters, Ronald, Deprez, Sabine, Plasschaert, Ellen, Leemans, Alexander, Zhang, Hui, den Bergh, Bea Van, Vandenbulcke, Mathieu, Legius, Eric, Sunaert, Stefan, Emsell, Louise
Publicado 2014

Methylation Defect in Imprinted Genes Detected in Patients with an Albright's Hereditary Osteodystrophy Like Phenotype and Platelet Gs Hypofunction

por Izzi, Benedetta, Francois, Inge, Labarque, Veerle, Thys, Chantal, Wittevrongel, Christine, Devriendt, Koen, Legius, Eric, Van den Bruel, Annick, D'Hooghe, Marc, Lambrechts, Diether, de Zegher, Francis, Van Geet, Chris, Freson, Kathleen
Publicado 2012

Examination of the genetic factors underlying the cognitive variability associated with neurofibromatosis type 1

por Ottenhoff, Myrthe J., Rietman, André B., Mous, Sabine E., Plasschaert, Ellen, Gawehns, Daniela, Brems, Hilde, Oostenbrink, Rianne, van Minkelen, Rick, Nellist, Mark, Schorry, Elizabeth, Legius, Eric, Moll, Henriette A., Elgersma, Ype
Publicado 2020

ERN GENTURIS tumour surveillance guidelines for individuals with neurofibromatosis type 1

por Carton, Charlotte, Evans, D. Gareth, Blanco, Ignacio, Friedrich, Reinhard E., Ferner, Rosalie E., Farschtschi, Said, Salvador, Hector, Azizi, Amedeo A., Mautner, Victor, Röhl, Claas, Peltonen, Sirkku, Stivaros, Stavros, Legius, Eric, Oostenbrink, Rianne
Publicado 2023

Genome-wide haplotyping embryos developing from 0PN and 1PN zygotes increases transferrable embryos in PGT-M

por Destouni, Aspasia, Dimitriadou, Eftychia, Masset, Heleen, Debrock, Sophie, Melotte, Cindy, Van Den Bogaert, Kris, Zamani Esteki, Masoud, Ding, Jia, Voet, Thiery, Denayer, Ellen, de Ravel, Thomy, Legius, Eric, Meuleman, Christel, Peeraer, Karen, Vermeesch, Joris R
Publicado 2018