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Page 1
Creutzfeldt-Jakob disease.
de Villemeur TB. de Villemeur TB. Handb Clin Neurol. 2013;112:1191-3. doi: 10.1016/B978-0-444-52910-7.00040-4. Handb Clin Neurol. 2013. PMID: 23622328 Review.
Gaucher disease.
Mignot C, Gelot A, De Villemeur TB. Mignot C, et al. Among authors: de villemeur tb. Handb Clin Neurol. 2013;113:1709-15. doi: 10.1016/B978-0-444-59565-2.00040-X. Handb Clin Neurol. 2013. PMID: 23622393 Review.
Progressive megalencephaly due to specific EIF2Bepsilon mutations in two unrelated families.
Passemard S, Gelot A, Fogli A, N'Guyen S, Barnerias C, Niel F, Doummar D, Arbues AS, Mignot C, de Villemeur TB, Ponsot G, Boespflug-Tanguy O, Rodriguez D. Passemard S, et al. Among authors: de villemeur tb. Neurology. 2007 Jul 24;69(4):400-2. doi: 10.1212/01.wnl.0000266388.02772.f8. Neurology. 2007. PMID: 17646634 No abstract available.
Expanding the clinical and neuroradiologic phenotype of primary microcephaly due to ASPM mutations.
Passemard S, Titomanlio L, Elmaleh M, Afenjar A, Alessandri JL, Andria G, de Villemeur TB, Boespflug-Tanguy O, Burglen L, Del Giudice E, Guimiot F, Hyon C, Isidor B, Mégarbané A, Moog U, Odent S, Hernandez K, Pouvreau N, Scala I, Schaer M, Gressens P, Gerard B, Verloes A. Passemard S, et al. Among authors: de villemeur tb. Neurology. 2009 Sep 22;73(12):962-9. doi: 10.1212/WNL.0b013e3181b8799a. Neurology. 2009. PMID: 19770472
Genotype at codon 129 and susceptibility to Creutzfeldt-Jakob disease.
Deslys JP, Jaegly A, d'Aignaux JH, Mouthon F, de Villemeur TB, Dormont D. Deslys JP, et al. Among authors: de villemeur tb. Lancet. 1998 Apr 25;351(9111):1251. doi: 10.1016/s0140-6736(05)79317-x. Lancet. 1998. PMID: 9643750 No abstract available.
[Management of acute visual loss in children].
Doummar D, Roussat B, Pelosse B, Le Pointe HD, Iba-Zizen M, Roubergue A, Rodriguez D, de Villemeur TB. Doummar D, et al. Among authors: de villemeur tb. Arch Pediatr. 2004 Nov;11(11):1384-8. doi: 10.1016/j.arcped.2004.04.005. Arch Pediatr. 2004. PMID: 15519841 Review. French.
Type 2 Gaucher disease: 15 new cases and review of the literature.
Mignot C, Doummar D, Maire I, De Villemeur TB; French Type 2 Gaucher Disease Study Group. Mignot C, et al. Among authors: de villemeur tb. Brain Dev. 2006 Jan;28(1):39-48. doi: 10.1016/j.braindev.2005.04.005. Brain Dev. 2006. PMID: 16485335 Review.
[Gaucher disease].
Stirnemann J, de Villemeur TB, Heraoui D, Belmatoug N; Comité d'évaluation du traitement de la maladie de Gaucher. Stirnemann J, et al. Among authors: de villemeur tb. Rev Prat. 2011 Feb;61(2):165-8. Rev Prat. 2011. PMID: 21618759 French. No abstract available.
Microcephaly: a radiological review.
Tarrant A, Garel C, Germanaud D, de Villemeur TB, Mignot C, Lenoir M, le Pointe HD. Tarrant A, et al. Among authors: de villemeur tb. Pediatr Radiol. 2009 Aug;39(8):772-80; quiz 888-9. doi: 10.1007/s00247-009-1266-x. Epub 2009 May 13. Pediatr Radiol. 2009. PMID: 19437006 Review.
Unexpected macrophage-independent dyserythropoiesis in Gaucher disease.
Reihani N, Arlet JB, Dussiot M, de Villemeur TB, Belmatoug N, Rose C, Colin-Aronovicz Y, Hermine O, Le Van Kim C, Franco M. Reihani N, et al. Among authors: de villemeur tb. Haematologica. 2016 Dec;101(12):1489-1498. doi: 10.3324/haematol.2016.147546. Epub 2016 Jul 28. Haematologica. 2016. PMID: 27470603 Free PMC article.
51 results