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Page 1
Craniosynostosis: A rare complication of pycnodysostosis.
Osimani S, Husson I, Passemard S, Elmaleh M, Perrin L, Quelin C, Marey I, Delalande O, Filocamo M, Verloes A. Osimani S, et al. Among authors: delalande o. Eur J Med Genet. 2010 Mar-Apr;53(2):89-92. doi: 10.1016/j.ejmg.2009.12.001. Epub 2010 Jan 5. Eur J Med Genet. 2010. PMID: 20044043
Becker muscular dystrophy severity is linked to the structure of dystrophin.
Nicolas A, Raguénès-Nicol C, Ben Yaou R, Ameziane-Le Hir S, Chéron A, Vié V, Claustres M, Leturcq F, Delalande O, Hubert JF, Tuffery-Giraud S, Giudice E, Le Rumeur E; French Network of Clinical Reference Centres for Neuromuscular Diseases (CORNEMUS). Nicolas A, et al. Among authors: delalande o. Hum Mol Genet. 2015 Mar 1;24(5):1267-79. doi: 10.1093/hmg/ddu537. Epub 2014 Oct 27. Hum Mol Genet. 2015. PMID: 25348330 Free article.
[Disability and epilepsy].
Bordonne C, Delalande O, Heran F. Bordonne C, et al. Among authors: delalande o. J Radiol. 2010 Dec;91(12 Pt 2):1398-405. doi: 10.1016/s0221-0363(10)70219-5. J Radiol. 2010. PMID: 21242937 French.
[Epilepsy surgery in children].
Delalande O, Fohlen M, Dorfmuller G, Bulteau C, Jalin C. Delalande O, et al. Arch Pediatr. 2007 Jun;14(6):579-82. doi: 10.1016/j.arcped.2007.02.021. Epub 2007 Apr 9. Arch Pediatr. 2007. PMID: 17416491 French. No abstract available.
139 results