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Exercise efficiency impairment in metabolic myopathies.
Noury JB, Zagnoli F, Petit F, Marcorelles P, Rannou F. Noury JB, et al. Among authors: petit f. Sci Rep. 2020 May 29;10(1):8765. doi: 10.1038/s41598-020-65770-y. Sci Rep. 2020. PMID: 32472082 Free PMC article.
Exercise testing-based algorithms to diagnose McArdle disease and MAD defects.
Noury JB, Zagnoli F, Carré JL, Drouillard I, Petit F, Le Maréchal C, Marcorelles P, Rannou F. Noury JB, et al. Among authors: petit f. Acta Neurol Scand. 2018 Oct;138(4):301-307. doi: 10.1111/ane.12957. Epub 2018 May 10. Acta Neurol Scand. 2018. PMID: 29749052 Clinical Trial.
[Exercise-induced muscle pain due to phosphofrutokinase deficiency: Diagnostic contribution of metabolic explorations (exercise tests, 31P-nuclear magnetic resonance spectroscopy)].
Drouet A, Zagnoli F, Fassier T, Rannou F, Baverel F, Piraud M, Bahuau M, Petit F, Streichenberger N, Marcorelles P, Vital Durand D. Drouet A, et al. Among authors: petit f. Rev Neurol (Paris). 2013 Aug-Sep;169(8-9):613-24. doi: 10.1016/j.neurol.2013.02.006. Epub 2013 Sep 4. Rev Neurol (Paris). 2013. PMID: 24011984 French.
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: petit f. J Neurol. 2010 May;257(5):754-66. doi: 10.1007/s00415-009-5405-y. Epub 2009 Dec 11. J Neurol. 2010. PMID: 20012313
503 results