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Validation of genetic modifiers for Duchenne muscular dystrophy: a multicentre study assessing SPP1 and LTBP4 variants.
van den Bergen JC, Hiller M, Böhringer S, Vijfhuizen L, Ginjaar HB, Chaouch A, Bushby K, Straub V, Scoto M, Cirak S, Humbertclaude V, Claustres M, Scotton C, Passarelli C, Lochmüller H, Muntoni F, Tuffery-Giraud S, Ferlini A, Aartsma-Rus AM, Verschuuren JJ, 't Hoen PA, Spitali P. van den Bergen JC, et al. Among authors: claustres m. J Neurol Neurosurg Psychiatry. 2015 Oct;86(10):1060-5. doi: 10.1136/jnnp-2014-308409. Epub 2014 Dec 4. J Neurol Neurosurg Psychiatry. 2015. PMID: 25476005 Free PMC article.
[Genotypic diagnosis of Duchenne and Becker muscular dystrophies].
Tuffery-Giraud S, Chambert S, Demaille J, Claustres M. Tuffery-Giraud S, et al. Among authors: claustres m. Ann Biol Clin (Paris). 1999 Jul-Aug;57(4):417-26. Ann Biol Clin (Paris). 1999. PMID: 10432364 Free article. Review. French.
[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.
The role of muscle biopsy in analysis of the dystrophin gene in Duchenne muscular dystrophy: experience of a national referral centre.
Tuffery-Giraud S, Saquet C, Chambert S, Echenne B, Marie Cuisset J, Rivier F, Cossée M, Philippe C, Monnier N, Bieth E, Recan D, Antoinette Voelckel M, Perelman S, Lambert JC, Malcolm S, Claustres M. Tuffery-Giraud S, et al. Among authors: claustres m. Neuromuscul Disord. 2004 Oct;14(10):650-8. doi: 10.1016/j.nmd.2004.05.002. Neuromuscul Disord. 2004. PMID: 15351422
299 results