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[Proximal myotonial myopathy (PROMM): clinical and histology study].
Bassez G, Attarian S, Laforêt P, Azulay JP, Rouche A, Ferrer X, Urtizberea JA, Pellissier JF, Duboc D, Fardeau M, Pouget J, Eymard B. Bassez G, et al. Among authors: rouche a. Rev Neurol (Paris). 2001 Feb;157(2):209-18. Rev Neurol (Paris). 2001. PMID: 11283467 French.
Clinical and histologic findings in autosomal centronuclear myopathy.
Jeannet PY, Bassez G, Eymard B, Laforêt P, Urtizberea JA, Rouche A, Guicheney P, Fardeau M, Romero NB. Jeannet PY, et al. Among authors: rouche a. Neurology. 2004 May 11;62(9):1484-90. doi: 10.1212/01.wnl.0000124388.67003.56. Neurology. 2004. PMID: 15136669 Review.
Phenotype genotype analysis in 15 patients presenting a congenital myasthenic syndrome due to mutations in DOK7.
Ben Ammar A, Petit F, Alexandri N, Gaudon K, Bauché S, Rouche A, Gras D, Fournier E, Koenig J, Stojkovic T, Lacour A, Petiot P, Zagnoli F, Viollet L, Pellegrini N, Orlikowski D, Lazaro L, Ferrer X, Stoltenburg G, Paturneau-Jouas M, Hentati F, Fardeau M, Sternberg D, Hantaï D, Richard P, Eymard B. Ben Ammar A, et al. Among authors: rouche a. J Neurol. 2010 May;257(5):754-66. doi: 10.1007/s00415-009-5405-y. Epub 2009 Dec 11. J Neurol. 2010. PMID: 20012313
[About the technique of muscle biopsy (III). The contribution of elctron microscopy, yesterday, and at the time of the molecular genetics era. A historical overview].
Fardeau M, Rouche A, Vassilopoulos S, Romero NB; l’équipe de microscopie électronique de l’Unité Morphologie Neuromusculaire de la Division Risler (G. Brochier, M.T. Bui, C. Labasse, A. Madelaine). Fardeau M, et al. Among authors: rouche a. Med Sci (Paris). 2016 Nov;32 Hors série n°2:6-9. doi: 10.1051/medsci/201632s202. Epub 2016 Nov 21. Med Sci (Paris). 2016. PMID: 27869068 Free article. French. No abstract available.
23 results