Labarre-Vila A - Search Results

1

Using EMG data to constrain optimization procedure improves finger tendon tension estimations during static fingertip force production.

Vigouroux L, Quaine F, Labarre-Vila A, Amarantini D, Moutet F. Vigouroux L, et al. J Biomech. 2007;40(13):2846-56. doi: 10.1016/j.jbiomech.2007.03.010. Epub 2007 May 7. J Biomech. 2007. PMID: 17482624

2

Estimation of finger muscle tendon tensions and pulley forces during specific sport-climbing grip techniques.

Vigouroux L, Quaine F, Labarre-Vila A, Moutet F. Vigouroux L, et al. J Biomech. 2006;39(14):2583-92. doi: 10.1016/j.jbiomech.2005.08.027. Epub 2005 Oct 12. J Biomech. 2006. PMID: 16225880

3

A knowledge-driven agent-centred framework for data mining in EMG.

Balter J, Labarre-Vila A, Ziébelin D, Garbay C. Balter J, et al. C R Biol. 2002 Apr;325(4):375-82. doi: 10.1016/s1631-0691(02)01434-8. C R Biol. 2002. PMID: 12161917 Free article.

4

[Assessment of muscle function in pathology with surface electrode EMG].

Labarre-Vila A. Labarre-Vila A. Rev Neurol (Paris). 2006 Apr;162(4):459-65. doi: 10.1016/s0035-3787(06)75037-8. Rev Neurol (Paris). 2006. PMID: 16585907 Review. French.

5

A homozygous splicing mutation causing a depletion of skeletal muscle RYR1 is associated with multi-minicore disease congenital myopathy with ophthalmoplegia.

Monnier N, Ferreiro A, Marty I, Labarre-Vila A, Mezin P, Lunardi J. Monnier N, et al. Hum Mol Genet. 2003 May 15;12(10):1171-8. doi: 10.1093/hmg/ddg121. Hum Mol Genet. 2003. PMID: 12719381

6

[Surface electromyography procedure].

Labarre-Vila A. Labarre-Vila A. Rev Med Liege. 2004;59 Suppl 1:176-83. Rev Med Liege. 2004. PMID: 15244174 Free article. Review. French.

7

Exercise test in muscle channelopathies and other muscle disorders.

Kuntzer T, Flocard F, Vial C, Kohler A, Magistris M, Labarre-Vila A, Gonnaud PM, Ochsner F, Soichot P, Chan V, Monnier G. Kuntzer T, et al. Muscle Nerve. 2000 Jul;23(7):1089-94. doi: 10.1002/1097-4598(200007)23:7<1089::aid-mus12>3.0.co;2-q. Muscle Nerve. 2000. PMID: 10883004 Clinical Trial.

8

Absence of beta-tropomyosin is a new cause of Escobar syndrome associated with nemaline myopathy.

Monnier N, Lunardi J, Marty I, Mezin P, Labarre-Vila A, Dieterich K, Jouk PS. Monnier N, et al. Among authors: labarre vila a. Neuromuscul Disord. 2009 Feb;19(2):118-23. doi: 10.1016/j.nmd.2008.11.009. Epub 2009 Jan 19. Neuromuscul Disord. 2009. PMID: 19155175

9

Evidence for a dominant negative disease mechanism in cap myopathy due to TPM3.

Waddell LB, Kreissl M, Kornberg A, Kennedy P, McLean C, Labarre-Vila A, Monnier N, North KN, Clarke NF. Waddell LB, et al. Among authors: labarre vila a. Neuromuscul Disord. 2010 Jul;20(7):464-6. doi: 10.1016/j.nmd.2010.05.012. Epub 2010 Jun 15. Neuromuscul Disord. 2010. PMID: 20554445

10

Mutations in TPM3 are a common cause of congenital fiber type disproportion.

Clarke NF, Kolski H, Dye DE, Lim E, Smith RL, Patel R, Fahey MC, Bellance R, Romero NB, Johnson ES, Labarre-Vila A, Monnier N, Laing NG, North KN. Clarke NF, et al. Among authors: labarre vila a. Ann Neurol. 2008 Mar;63(3):329-37. doi: 10.1002/ana.21308. Ann Neurol. 2008. PMID: 18300303

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