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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1988 1
1993 1
1998 1
1999 1
2001 2
2002 1
2004 4
2006 3
2007 4
2008 3
2009 3
2011 5
2012 5
2013 2
2014 1
2016 1
2017 1
2018 2
2019 1
2020 2
2021 1
2022 3
2023 5
2024 1

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51 results

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Page 1
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.
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.
Polyhandicap and aging.
Rousseau MC, de Villemeur TB, Khaldi-Cherif S, Brisse C, Felce A, Loundou A, Baumstarck K, Auquier P; French Polyhandicap Group. Electronic address: eval.plh@gmail.com; French Polyhandicap Group. Rousseau MC, et al. Among authors: de villemeur tb. Disabil Health J. 2019 Oct;12(4):657-664. doi: 10.1016/j.dhjo.2019.01.013. Epub 2019 Feb 26. Disabil Health J. 2019. PMID: 30842063
DNA methylation episignature and comparative epigenomic profiling of HNRNPU-related neurodevelopmental disorder.
Rooney K, van der Laan L, Trajkova S, Haghshenas S, Relator R, Lauffer P, Vos N, Levy MA, Brunetti-Pierri N, Terrone G, Mignot C, Keren B, de Villemeur TB, Volker-Touw CML, Verbeek N, van der Smagt JJ, Oegema R, Brusco A, Ferrero GB, Misra-Isrie M, Hochstenbach R, Alders M, Mannens MMAM, Sadikovic B, van Haelst MM, Henneman P. Rooney K, et al. Among authors: de villemeur tb. Genet Med. 2023 Aug;25(8):100871. doi: 10.1016/j.gim.2023.100871. Epub 2023 Apr 28. Genet Med. 2023. PMID: 37120726 Free article.
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.
Prospective Multicenter Validation of a Simple Blood Test for the Diagnosis of Glut1 Deficiency Syndrome.
Mochel F, Gras D, Luton MP, Nizou M, Giovannini D, Delattre C, Aubart M, Barth M, De Saint-Martin A, Doummar D, Essid N, Garros A, Le Camus CH, Hoebeke C, The Tich SN, Perivier M, Rivera S, Rolland A, Roubertie A, Sarret C, Sevin C, Ville D, Sitbon M, Costa JM, Pons R, Garcia-Cazorla A, Vuillaumier S, Petit V, Boespflug-Tanguy O, De Vivo DC; MetaGlut1 Study Group. Mochel F, et al. Neurology. 2023 Jun 6;100(23):e2360-e2373. doi: 10.1212/WNL.0000000000207296. Epub 2023 Apr 19. Neurology. 2023. PMID: 37076312 Free PMC article.
The French EVAL-PLH cohort of persons with polyhandicap.
Hamouda I, Rousseau MC, Beltran Anzola A, Aim MA, de Villemeur TB, Auquier P, Baumstarck K; EVAL-PLH group. Hamouda I, et al. Among authors: de villemeur tb. Sci Rep. 2022 Jul 22;12(1):12512. doi: 10.1038/s41598-022-16596-3. Sci Rep. 2022. PMID: 35869128 Free PMC article.
Management of neuronopathic Gaucher disease: a European consensus.
Vellodi A, Bembi B, de Villemeur TB, Collin-Histed T, Erikson A, Mengel E, Rolfs A, Tylki-Szymanska A; Neuronopathic Gaucher Disease Task Force of the European Working Group on Gaucher Disease. Vellodi A, et al. Among authors: de villemeur tb. J Inherit Metab Dis. 2001 Jun;24(3):319-27. doi: 10.1023/a:1010514614570. J Inherit Metab Dis. 2001. PMID: 11486896 Review. No abstract available.
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.
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