Segui
Eric Legius
Eric Legius
Hoogleraar Katholieke Universiteit Leuven
Email verificata su telenet.be
Titolo
Citata da
Citata da
Anno
SOX10 mutations in patients with Waardenburg-Hirschsprung disease
V Pingault, N Bondurand, K Kuhlbrodt, DE Goerich, MO Préhu, A Puliti, ...
Nature genetics 18 (2), 171-173, 1998
9491998
A combined syndrome of juvenile polyposis and hereditary haemorrhagic telangiectasia associated with mutations in MADH4 (SMAD4)
CJ Gallione, GM Repetto, E Legius, AK Rustgi, SL Schelley, S Tejpar, ...
The Lancet 363 (9412), 852-859, 2004
8312004
The NF1 tumor suppressor critically regulates TSC2 and mTOR
CM Johannessen, EE Reczek, MF James, H Brems, E Legius, ...
Proceedings of the National Academy of Sciences 102 (24), 8573-8578, 2005
6582005
Germline loss-of-function mutations in SPRED1 cause a neurofibromatosis 1–like phenotype
H Brems, M Chmara, M Sahbatou, E Denayer, K Taniguchi, R Kato, ...
Nature genetics 39 (9), 1120-1126, 2007
4992007
Somatic deletion of the neurofibromatosis type 1 gene in a neurofibrosarcoma supports a tumour suppressor gene hypothesis
E Legius, DA Marchuk, FS Collins, TW Glover
Nature genetics 3 (2), 122-126, 1993
4701993
Soft tissue and visceral sarcomas: ESMO–EURACAN–GENTURIS Clinical Practice Guidelines for diagnosis, treatment and follow-up☆
A Gronchi, AB Miah, AP Dei Tos, N Abecassis, J Bajpai, S Bauer, ...
Annals of Oncology 32 (11), 1348-1365, 2021
4602021
PRC2 loss amplifies Ras-driven transcription and confers sensitivity to BRD4-based therapies
T De Raedt, E Beert, E Pasmant, A Luscan, H Brems, N Ortonne, K Helin, ...
Nature 514 (7521), 247-251, 2014
4422014
Intelligence and psychosocial adjustment in velocardiofacial syndrome: a study of 37 children and adolescents with VCFS.
A Swillen, K Devriendt, E Legius, B Eyskens, M Dumoulin, M Gewillig, ...
Journal of Medical Genetics 34 (6), 453, 1997
4201997
Mechanisms in the pathogenesis of malignant tumours in neurofibromatosis type 1
H Brems, E Beert, T de Ravel, E Legius
The lancet oncology 10 (5), 508-515, 2009
3932009
Revised diagnostic criteria for neurofibromatosis type 1 and Legius syndrome: an international consensus recommendation
E Legius, L Messiaen, P Wolkenstein, P Pancza, RA Avery, Y Berman, ...
Genetics in Medicine 23 (8), 1506-1513, 2021
3682021
Cognitive function and academic performance in neurofibrornatosis 1: Consensus statement from the NF1 Cognitive Disorders Task Force
KN North, V Riccardi, C Samango-Sprouse, R Ferner, B Moore, E Legius, ...
Neurology 48 (4), 1121-1127, 1997
3381997
Elevated risk for MPNST in NF1 microdeletion patients
T De Raedt, H Brems, P Wolkenstein, D Vidaud, S Pilotti, F Perrone, ...
The American Journal of Human Genetics 72 (5), 1288-1292, 2003
3262003
Mutations in the CCN gene family member WISP3 cause progressive pseudorheumatoid dysplasia
JR Hurvitz, WM Suwairi, W Van Hul, H El-Shanti, A Superti-Furga, ...
Nature genetics 23 (1), 94-98, 1999
3181999
PTPN11 mutations in LEOPARD syndrome
E Legius, C Schrander-Stumpel, E Schollen, C Pulles-Heintzberger, ...
Journal of medical genetics 39 (8), 571-574, 2002
3012002
Communication with close and distant relatives in the context of genetic testing for hereditary breast and ovarian cancer in cancer patients
E Claes, G Evers‐Kiebooms, A Boogaerts, M Decruyenaere, L Denayer, ...
American Journal of Medical Genetics Part A 116 (1), 11-19, 2003
2962003
Molecular pathogenesis of multiple gastrointestinal stromal tumors in NF1 patients
O Maertens, H Prenen, M Debiec-Rychter, A Wozniak, R Sciot, P Pauwels, ...
Human molecular genetics 15 (6), 1015-1023, 2006
2742006
CNGB3 mutations account for 50% of all cases with autosomal recessive achromatopsia
S Kohl, B Varsanyi, GA Antunes, B Baumann, CB Hoyng, H Jägle, ...
European Journal of Human Genetics 13 (3), 302-308, 2005
2632005
Atypical neurofibromas in neurofibromatosis type 1 are premalignant tumors
E Beert, H Brems, B Daniëls, I De Wever, F Van Calenbergh, ...
Genes, Chromosomes and Cancer 50 (12), 1021-1032, 2011
2442011
The behavioural phenotype in velo-cardio-facial syndrome (VCFS): from infancy to adolescence.
A Swillen, K Devriendt, E Legius, P Prinzie, A Vogels, P Ghesquière, ...
Genetic Counseling (Geneva, Switzerland) 10 (1), 79-88, 1999
2391999
Gastrointestinal stromal tumours: ESMO–EURACAN–GENTURIS Clinical Practice Guidelines for diagnosis, treatment and follow-up
PG Casali, JY Blay, N Abecassis, J Bajpai, S Bauer, R Biagini, S Bielack, ...
Annals of oncology 33 (1), 20-33, 2022
2362022
Il sistema al momento non può eseguire l'operazione. Riprova più tardi.
Articoli 1–20