Vuillaume I - Search Results

1

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

2

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

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

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.

5

Slowly progressive spinocerebellar ataxia with extrapyramidal signs and mild cognitive impairment (SCA21).

Delplanque J, Devos D, Vuillaume I, De Becdelievre A, Vangelder E, Maurage CA, Dujardin K, Destée A, Sablonnière B. Delplanque J, et al. Among authors: vuillaume i. Cerebellum. 2008;7(2):179-83. doi: 10.1007/s12311-008-0014-3. Cerebellum. 2008. PMID: 18418688

6

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

7

Spinocerebellar ataxia: a rational approach to aetiological diagnosis.

Degardin A, Dobbelaere D, Vuillaume I, Defoort-Dhellemmes S, Hurtevent JF, Sablonnière B, Destée A, Defebvre L, Devos D. Degardin A, et al. Among authors: vuillaume i. Cerebellum. 2012 Mar;11(1):289-99. doi: 10.1007/s12311-011-0310-1. Cerebellum. 2012. PMID: 21892625

8

[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.

9

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

10

Powerhouse failure and oxidative damage in autosomal recessive spastic ataxia of Charlevoix-Saguenay.

Criscuolo C, Procaccini C, Meschini MC, Cianflone A, Carbone R, Doccini S, Devos D, Nesti C, Vuillaume I, Pellegrino M, Filla A, De Michele G, Matarese G, Santorelli FM. Criscuolo C, et al. Among authors: vuillaume i. J Neurol. 2015 Dec;262(12):2755-63. doi: 10.1007/s00415-015-7911-4. Epub 2015 Nov 3. J Neurol. 2015. PMID: 26530509

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