Legius E - Search Results

1

Multiple granular cell tumors in a child with Noonan syndrome.

Bamps S, Oyen T, Legius E, Vandenoord J, Stas M. Bamps S, et al. Among authors: legius e. Eur J Pediatr Surg. 2013 Jun;23(3):257-9. doi: 10.1055/s-0032-1322537. Epub 2012 Aug 22. Eur J Pediatr Surg. 2013. PMID: 22915371 No abstract available.

2

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

Bamps S, Calenbergh FV, Vleeschouwer SD, Loon JV, Sciot R, Legius E, Goffin J. Bamps S, et al. Among authors: legius e. Surg Neurol Int. 2013 Nov 8;4:145. doi: 10.4103/2152-7806.121110. Surg Neurol Int. 2013. PMID: 24340227 Free PMC article. Review.

3

Noonan syndrome-like disorder with loose anagen hair: a second case with neuroblastoma.

Garavelli L, Cordeddu V, Errico S, Bertolini P, Street ME, Rosato S, Pollazzon M, Wischmeijer A, Ivanovski I, Daniele P, Bacchini E, Lombardi AA, Izzi G, Biasucci G, Del Rossi C, Corradi D, Cazzaniga G, Dominici C, Rossi C, De Luca A, Bernasconi S, Riccardi R, Legius E, Tartaglia M. Garavelli L, et al. Among authors: legius e. Am J Med Genet A. 2015 Aug;167A(8):1902-7. doi: 10.1002/ajmg.a.37082. Epub 2015 Apr 5. Am J Med Genet A. 2015. PMID: 25846317

4

Holzgreve-Wagner-Rehder syndrome: Potter sequence associated with persistent buccopharyngeal membrane. A second observation.

Legius E, Moerman P, Fryns JP, Vandenberghe K, Eggermont E. Legius E, et al. Am J Med Genet. 1988 Oct;31(2):269-72. doi: 10.1002/ajmg.1320310203. Am J Med Genet. 1988. PMID: 3232694

5

Consecutive glioblastoma and B cell non-Hodgkin's lymphoma in a young child with von Recklinghausen's Neurofibromatosis.

Uyttebroeck A, Legius E, Brock P, Van de Cassey W, Casaer P, Casteels-Van Daele M. Uyttebroeck A, et al. Among authors: legius e. Med Pediatr Oncol. 1995 Jan;24(1):46-9. doi: 10.1002/mpo.2950240110. Med Pediatr Oncol. 1995. PMID: 7968792

6

Fine mapping of Noonan/cardio-facio cutaneous syndrome in a large family.

Legius E, Schollen E, Matthijs G, Fryns JP. Legius E, et al. Eur J Hum Genet. 1998 Jan;6(1):32-7. doi: 10.1038/sj.ejhg.5200150. Eur J Hum Genet. 1998. PMID: 9781012

7

PTPN11 mutation in a large family with Noonan syndrome and dizygous twinning.

Schollen E, Matthijs G, Gewillig M, Fryns JP, Legius E. Schollen E, et al. Among authors: legius e. Eur J Hum Genet. 2003 Jan;11(1):85-8. doi: 10.1038/sj.ejhg.5200915. Eur J Hum Genet. 2003. PMID: 12529711

8

Chantrain CF, Jijon P, De Raedt T, Vermylen C, Poirel HA, Legius E, Brichard B. Chantrain CF, et al. Among authors: legius e. Pediatr Blood Cancer. 2007 Jan;48(1):101-4. doi: 10.1002/pbc.20527. Pediatr Blood Cancer. 2007. PMID: 16078230

9

Tumor spectrum in children with Noonan syndrome and SOS1 or RAF1 mutations.

Denayer E, Devriendt K, de Ravel T, Van Buggenhout G, Smeets E, Francois I, Sznajer Y, Craen M, Leventopoulos G, Mutesa L, Vandecasseye W, Massa G, Kayserili H, Sciot R, Fryns JP, Legius E. Denayer E, et al. Among authors: legius e. Genes Chromosomes Cancer. 2010 Mar;49(3):242-52. doi: 10.1002/gcc.20735. Genes Chromosomes Cancer. 2010. PMID: 19953625

10

NRAS Mutations in Noonan Syndrome.

Denayer E, Peeters H, Sevenants L, Derbent M, Fryns JP, Legius E. Denayer E, et al. Among authors: legius e. Mol Syndromol. 2012 Jun;3(1):34-38. doi: 10.1159/000338467. Epub 2012 May 3. Mol Syndromol. 2012. PMID: 22855653 Free PMC article.

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