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Quantification of facial skeletal shape variation in fibroblast growth factor receptor-related craniosynostosis syndromes.
Heuzé Y, Martínez-Abadías N, Stella JM, Arnaud E, Collet C, García Fructuoso G, Alamar M, Lo LJ, Boyadjiev SA, Di Rocco F, Richtsmeier JT. Heuzé Y, et al. Among authors: arnaud e. Birth Defects Res A Clin Mol Teratol. 2014 Apr;100(4):250-9. doi: 10.1002/bdra.23228. Epub 2014 Feb 27. Birth Defects Res A Clin Mol Teratol. 2014. PMID: 24578066 Free PMC article. Clinical Trial.
Crouzon syndrome with acanthosis nigricans: a case-based update.
Di Rocco F, Collet C, Legeai-Mallet L, Arnaud E, Le Merrer M, Hadj-Rabia S, Renier D. Di Rocco F, et al. Among authors: arnaud e. Childs Nerv Syst. 2011 Mar;27(3):349-54. doi: 10.1007/s00381-010-1347-z. Epub 2010 Dec 7. Childs Nerv Syst. 2011. PMID: 21136065
The growth of the foramen magnum in Crouzon syndrome.
Coll G, Arnaud E, Selek L, Brunelle F, Sainte-Rose C, Collet C, Di Rocco F. Coll G, et al. Among authors: arnaud e. Childs Nerv Syst. 2012 Sep;28(9):1525-35. doi: 10.1007/s00381-012-1805-x. Epub 2012 Aug 8. Childs Nerv Syst. 2012. PMID: 22872269
Mucopolysaccharidosis type I and craniosynostosis.
Ziyadeh J, Le Merrer M, Robert M, Arnaud E, Valayannopoulos V, Di Rocco F. Ziyadeh J, et al. Among authors: arnaud e. Acta Neurochir (Wien). 2013 Oct;155(10):1973-6. doi: 10.1007/s00701-013-1831-9. Epub 2013 Aug 6. Acta Neurochir (Wien). 2013. PMID: 23917744
302 results