Sablonnière B - Search Results

1

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. Among authors: sablonniere b. 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.

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: sablonniere b. Neurosci Lett. 2002 Aug 2;328(1):1-4. doi: 10.1016/s0304-3940(02)00231-8. Neurosci Lett. 2002. PMID: 12123845

3

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. Among authors: sablonniere b. 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.

4

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: sablonniere b. Neurology. 2001 Jan 23;56(2):234-8. doi: 10.1212/wnl.56.2.234. Neurology. 2001. PMID: 11160961

5

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. Among authors: sablonniere b. Ann Neurol. 2002 Nov;52(5):666-70. doi: 10.1002/ana.10344. Ann Neurol. 2002. PMID: 12402269

6

Association between caffeine intake and age at onset in Huntington's disease.

Simonin C, Duru C, Salleron J, Hincker P, Charles P, Delval A, Youssov K, Burnouf S, Azulay JP, Verny C, Scherer C, Tranchant C, Goizet C, Debruxelles S, Defebvre L, Sablonnière B, Romon-Rousseaux M, Buée L, Destée A, Godefroy O, Dürr A, Landwehrmeyer B; REGISTRY Study of the European Huntington's Disease Network; Bachoud-Levi AC, Richard F, Blum D, Krystkowiak P; Huntington French Speaking Network. Simonin C, et al. Among authors: sablonniere b. Neurobiol Dis. 2013 Oct;58:179-82. doi: 10.1016/j.nbd.2013.05.013. Epub 2013 May 31. Neurobiol Dis. 2013. PMID: 23732677

7

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. Among authors: sablonniere b. Diagn Mol Pathol. 1998 Jun;7(3):174-9. doi: 10.1097/00019606-199806000-00009. Diagn Mol Pathol. 1998. PMID: 9836074

8

The first European family with tibial muscular dystrophy outside the Finnish population.

de Seze J, Udd B, Haravuori H, Sablonnière B, Maurage CA, Hurtevent JF, Boutry N, Stojkovic T, Schraen S, Petit H, Vermersch P. de Seze J, et al. Among authors: sablonniere b. Neurology. 1998 Dec;51(6):1746-8. doi: 10.1212/wnl.51.6.1746. Neurology. 1998. PMID: 9855539

9

[Genetic dystonia].

Destée A, Brique S, Sablonnière B. Destée A, et al. Among authors: sablonniere b. Presse Med. 1999 Feb 13;28(6):298-305. Presse Med. 1999. PMID: 10073176 Review. French.

10

Analysis of ERDA1, CTG18.1, and uncloned CAG/CTG repeat sequences in familial Parkinson's disease with anticipation.

Schraen-Maschke S, Brique S, Chartier-Harlin MC, Brique E, Destée A, Sablonnière B. Schraen-Maschke S, et al. Among authors: sablonniere b. Am J Med Genet. 1999 Dec 15;88(6):738-41. Am J Med Genet. 1999. PMID: 10581499

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