Vuillaume I - Search Results

1

Absence of unidentified CAG repeat expansion in patients with Huntington's disease-like phenotype.

Vuillaume I, Meynieu P, Schraen-Maschke S, Destée A, Sablonnière B. Vuillaume I, et al. J Neurol Neurosurg Psychiatry. 2000 May;68(5):672-5. doi: 10.1136/jnnp.68.5.672. J Neurol Neurosurg Psychiatry. 2000. PMID: 10766906 Free PMC article.

2

Mutation analysis and association studies of the ubiquitin carboxy-terminal hydrolase L1 gene in Huntington's disease.

Nazé P, Vuillaume I, Destée A, Pasquier F, Sablonnière B. Nazé P, et al. Among authors: vuillaume i. Neurosci Lett. 2002 Aug 2;328(1):1-4. doi: 10.1016/s0304-3940(02)00231-8. Neurosci Lett. 2002. PMID: 12123845

3

Genetic polymorphisms adjacent to the CAG repeat influence clinical features at onset in Huntington's disease.

Vuillaume I, Vermersch P, Destée A, Petit H, Sablonnière B. Vuillaume I, et al. J Neurol Neurosurg Psychiatry. 1998 Jun;64(6):758-62. doi: 10.1136/jnnp.64.6.758. J Neurol Neurosurg Psychiatry. 1998. PMID: 9647305 Free PMC article.

4

Simple nonisotopic assays for detection of (CAG)n repeats expansions associated with seven neurodegenerative disorders.

Vuillaume I, Schraen S, Rousseaux J, Sablonnière B. Vuillaume I, et al. Diagn Mol Pathol. 1998 Jun;7(3):174-9. doi: 10.1097/00019606-199806000-00009. Diagn Mol Pathol. 1998. PMID: 9836074

5

[Triplet expansion diseases].

Sablonnière B, Vuillaume I, Schraen-Maschke S. Sablonnière B, et al. Among authors: vuillaume i. Ann Biol Clin (Paris). 2000 May-Jun;58(3):356-60. Ann Biol Clin (Paris). 2000. PMID: 10846241 Free article. Review. French. No abstract available.

6

The first identified French family with dentatorubral-pallidoluysian atrophy.

Destée A, Delalande I, Vuillaume I, Schraen-Maschke S, Defebvre L, Sablonnière B. Destée A, et al. Among authors: vuillaume i. Mov Disord. 2000 Sep;15(5):996-9. doi: 10.1002/1531-8257(200009)15:5<996::aid-mds1036>3.0.co;2-9. Mov Disord. 2000. PMID: 11009212

7

Clinical features and genetic analysis of a new form of spinocerebellar ataxia.

Devos D, Schraen-Maschke S, Vuillaume I, Dujardin K, Nazé P, Willoteaux C, Destée A, Sablonnière B. Devos D, et al. Among authors: vuillaume i. Neurology. 2001 Jan 23;56(2):234-8. doi: 10.1212/wnl.56.2.234. Neurology. 2001. PMID: 11160961

8

A new locus for spinocerebellar ataxia (SCA21) maps to chromosome 7p21.3-p15.1.

Vuillaume I, Devos D, Schraen-Maschke S, Dina C, Lemainque A, Vasseur F, Bocquillon G, Devos P, Kocinski C, Marzys C, Destée A, Sablonnière B. Vuillaume I, et al. Ann Neurol. 2002 Nov;52(5):666-70. doi: 10.1002/ana.10344. Ann Neurol. 2002. PMID: 12402269

9

Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study.

Moss DJH, Pardiñas AF, Langbehn D, Lo K, Leavitt BR, Roos R, Durr A, Mead S; TRACK-HD investigators; REGISTRY investigators; Holmans P, Jones L, Tabrizi SJ. Moss DJH, et al. Lancet Neurol. 2017 Sep;16(9):701-711. doi: 10.1016/S1474-4422(17)30161-8. Epub 2017 Jun 20. Lancet Neurol. 2017. PMID: 28642124

10

Real time RT-PCR shows correlation between retinoid-induced apoptosis and NGF-R mRNA levels.

Vuillaume I, Schraen-Maschke S, Formstecher P, Sablonnière B. Vuillaume I, et al. Biochem Biophys Res Commun. 2001 Dec 7;289(3):647-52. doi: 10.1006/bbrc.2001.6028. Biochem Biophys Res Commun. 2001. PMID: 11726196

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