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[GLUT-1 deficiency syndrome or De Vivo disease: a case report].
Ticus I, Cano A, Villeneuve N, Milh M, Mancini J, Chabrol B. Ticus I, et al. Among authors: villeneuve n. Arch Pediatr. 2008 Aug;15(8):1296-9. doi: 10.1016/j.arcped.2008.04.024. Epub 2008 Jun 16. Arch Pediatr. 2008. PMID: 18556184 French.
A broad spectrum of clinical presentations in congenital disorders of glycosylation I: a series of 26 cases.
de Lonlay P, Seta N, Barrot S, Chabrol B, Drouin V, Gabriel BM, Journel H, Kretz M, Laurent J, Le Merrer M, Leroy A, Pedespan D, Sarda P, Villeneuve N, Schmitz J, van Schaftingen E, Matthijs G, Jaeken J, Korner C, Munnich A, Saudubray JM, Cormier-Daire V. de Lonlay P, et al. Among authors: villeneuve n. J Med Genet. 2001 Jan;38(1):14-9. doi: 10.1136/jmg.38.1.14. J Med Genet. 2001. PMID: 11134235 Free PMC article.
[Antiepileptics].
Villeneuve N. Villeneuve N. Arch Pediatr. 2002 Aug;9(8):854-61. doi: 10.1016/s0929-693x(02)00016-7. Arch Pediatr. 2002. PMID: 12205797 French.
[Epileptic seizures in childhood: from seizure type to diagnosis].
Milh M, Ticus I, Villeneuve N, Hugonencq C, Mancini J, Chabrol B. Milh M, et al. Among authors: villeneuve n. Arch Pediatr. 2008 Feb;15(2):216-22. doi: 10.1016/j.arcped.2007.11.007. Epub 2008 Jan 14. Arch Pediatr. 2008. PMID: 18248967 French.
[Management of the first nonfebrile seizure in infants and children].
Auvin S, Walls E, Sabouraud P, Bednarek N, Villeneuve N, Vallée L; Commission épilepsie de la Société française de neurologie pédiatrique. Auvin S, et al. Among authors: villeneuve n. Arch Pediatr. 2008 Nov;15(11):1677-84. doi: 10.1016/j.arcped.2008.08.019. Epub 2008 Oct 2. Arch Pediatr. 2008. PMID: 18835140 French.
155 results