Claustres M - Search Results

1

[Treatment of early-onset generalized dystonia by chronic bilateral stimulation of the internal globus pallidus. Apropos of a case].

Coubes P, Echenne B, Roubertie A, Vayssière N, Tuffery S, Humbertclaude V, Cambonie G, Claustres M, Frerebeau P. Coubes P, et al. Among authors: claustres m. Neurochirurgie. 1999 May;45(2):139-44. Neurochirurgie. 1999. PMID: 10448655 French.

2

Electrical stimulation of the globus pallidus internus in patients with primary generalized dystonia: long-term results.

Coubes P, Cif L, El Fertit H, Hemm S, Vayssiere N, Serrat S, Picot MC, Tuffery S, Claustres M, Echenne B, Frerebeau P. Coubes P, et al. Among authors: claustres m. J Neurosurg. 2004 Aug;101(2):189-94. doi: 10.3171/jns.2004.101.2.0189. J Neurosurg. 2004. PMID: 15309907

3

Long-term follow-up of DYT1 dystonia patients treated by deep brain stimulation: an open-label study.

Cif L, Vasques X, Gonzalez V, Ravel P, Biolsi B, Collod-Beroud G, Tuffery-Giraud S, Elfertit H, Claustres M, Coubes P. Cif L, et al. Among authors: claustres m. Mov Disord. 2010 Feb 15;25(3):289-99. doi: 10.1002/mds.22802. Mov Disord. 2010. PMID: 20063427 Free article.

4

No evidence of allelic heterogeneity in the DYT1 gene of European patients with early onset torsion dystonia.

Tuffery-Giraud S, Cavalier L, Roubertie A, Guittard C, Carles S, Calvas P, Echenne B, Coubes P, Claustres M. Tuffery-Giraud S, et al. Among authors: claustres m. J Med Genet. 2001 Oct;38(10):E35. doi: 10.1136/jmg.38.10.e35. J Med Genet. 2001. PMID: 11584049 Free PMC article. No abstract available.

5

Is the early-onset torsion dystonia (EOTD) linked to TOR1A gene as frequent as expected in France?

Frédéric MY, Clot F, Cif L, Blanchard A, Dürr A, Vuillaume I, Lesca G, Kreisler A, Davin C, Besnard T, Rousset F, Thorel D, Saquet C, Mechin D, Ozelius L, Agid Y, Barroso B, Chabrol B, Chan V, Clanet M, Coubes C, Destee A, Nguyen K, Vial C, Vidailhet M, Xie J, Sablonniere B, Calender A, Brice A, Roubertie A, Coubes P, Claustres M, Tuffery-Giraud S, Collod-Beroud G. Frédéric MY, et al. Among authors: claustres m. Neurogenetics. 2008 May;9(2):143-50. doi: 10.1007/s10048-008-0123-7. Epub 2008 Mar 6. Neurogenetics. 2008. PMID: 18322712 Free article.

6

Molecular deletion patterns in families from southern France with Duchenne/Becker muscular dystrophies.

Claustres M, Tuffery S, Chevron MP, Jozelon MP, Martinez P, Echenne B, Demaille J. Claustres M, et al. Hum Genet. 1991 Dec;88(2):179-84. doi: 10.1007/BF00206068. Hum Genet. 1991. PMID: 1684565

7

[Monogenetic dystonia: revisiting the dopaminergic hypothesis].

Blanchard A, Roubertie A, Frédéric MY, Claustres M, Collod-Béroud G. Blanchard A, et al. Among authors: claustres m. Rev Neurol (Paris). 2010 Apr;166(4):389-99. doi: 10.1016/j.neurol.2009.09.007. Rev Neurol (Paris). 2010. PMID: 19836812 Free article. Review. French.

8

[Movement disorders in childhood: classification and genetic update].

Roubertie A, Rivier F, Tuffery-Giraud S, Humbertclaude V, Claustres M, Cheminal R, Echenne B. Roubertie A, et al. Among authors: claustres m. Arch Pediatr. 2003 Nov;10(11):994-1002. doi: 10.1016/j.arcped.2003.07.003. Arch Pediatr. 2003. PMID: 14613695 Review. French.

9

Mutation analysis of the dystrophin gene in Southern French DMD or BMD families: from Southern blot to protein truncation test.

Tuffery S, Chambert S, Bareil C, Sarda P, Coubes C, Echenne B, Demaille J, Claustres M. Tuffery S, et al. Among authors: claustres m. Hum Genet. 1998 Mar;102(3):334-42. doi: 10.1007/s004390050702. Hum Genet. 1998. PMID: 9544849

10

Becker muscular dystrophy: demonstration of the carrier status of a female by immunoblotting and immunostaining.

Chevron MP, Tuffery S, Echenne B, Demaille J, Claustres M. Chevron MP, et al. Among authors: claustres m. Neuromuscul Disord. 1992;2(1):47-50. doi: 10.1016/0960-8966(92)90026-3. Neuromuscul Disord. 1992. PMID: 1525558

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