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The French Gaucher's disease registry: clinical characteristics, complications and treatment of 562 patients.
Stirnemann J, Vigan M, Hamroun D, Heraoui D, Rossi-Semerano L, Berger MG, Rose C, Camou F, de Roux-Serratrice C, Grosbois B, Kaminsky P, Robert A, Caillaud C, Froissart R, Levade T, Masseau A, Mignot C, Sedel F, Dobbelaere D, Vanier MT, Valayanopoulos V, Fain O, Fantin B, de Villemeur TB, Mentré F, Belmatoug N. Stirnemann J, et al. Among authors: de roux serratrice c, de villemeur tb. Orphanet J Rare Dis. 2012 Oct 9;7:77. doi: 10.1186/1750-1172-7-77. Orphanet J Rare Dis. 2012. PMID: 23046562 Free PMC article.
[Organization of Gaucher disease management in France].
Stirnemann J, de Villemeur TB, Belmatoug N. Stirnemann J, et al. Among authors: de villemeur tb. Rev Med Interne. 2007 Oct;28 Suppl 2:S198-201. doi: 10.1016/s0248-8663(07)78882-3. Rev Med Interne. 2007. PMID: 18228688 French.
[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.
Miglustat therapy in the French cohort of paediatric patients with Niemann-Pick disease type C.
Héron B, Valayannopoulos V, Baruteau J, Chabrol B, Ogier H, Latour P, Dobbelaere D, Eyer D, Labarthe F, Maurey H, Cuisset JM, de Villemeur TB, Sedel F, Vanier MT. Héron B, et al. Among authors: de villemeur tb. Orphanet J Rare Dis. 2012 Jun 7;7:36. doi: 10.1186/1750-1172-7-36. Orphanet J Rare Dis. 2012. PMID: 22676771 Free PMC article. Clinical Trial.
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.
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.
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.
Involvement of hepcidin in iron metabolism dysregulation in Gaucher disease.
Lefebvre T, Reihani N, Daher R, de Villemeur TB, Belmatoug N, Rose C, Colin-Aronovicz Y, Puy H, Le Van Kim C, Franco M, Karim Z. Lefebvre T, et al. Among authors: de villemeur tb. Haematologica. 2018 Apr;103(4):587-596. doi: 10.3324/haematol.2017.177816. Epub 2018 Jan 5. Haematologica. 2018. PMID: 29305416 Free PMC article.
Type 3 Gaucher disease, diagnostic in adulthood.
Detollenaere C, Benghergbia M, Brassier A, de Villemeur TB, Amsallem D, Berger M, Stirnemann J, Belmatoug N, Rose C. Detollenaere C, et al. Among authors: de villemeur tb. Mol Genet Metab Rep. 2017 Jul 11;13:1-2. doi: 10.1016/j.ymgmr.2017.07.002. eCollection 2017 Dec. Mol Genet Metab Rep. 2017. PMID: 28736718 Free PMC article. No abstract available.
51 results