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Neurology|June 1, 1992
31P NMR spectroscopy and ergometer exercise test as evidence for muscle oxidative performance improvement with coenzyme Q in mitochondrial myopathiesD Bendahan, C Desnuelle, D Vanuxem, et al.
Lancet (London, England)|August 26, 1998
Macrophagic myofasciitis: an emerging entity. Groupe d'Etudes et Recherche sur les Maladies Musculaires Acquises et Dysimmunitaires (GERMMAD) de l'Association Française contre les Myopathies (AFM)R K Gherardi, M Coquet, P Chérin, et al.
Arthritis and Rheumatism|March 29, 2002
Investigation of fluoroquinolone-induced myalgia using (31)P magnetic resonance spectroscopy and in vitro contracture testsS Guis, D Bendahan, G Kozak-Ribbens, et al.
Annals of the Rheumatic Diseases|October 14, 2015
Patients with ankylosing spondylitis have been breast fed less often than healthy controls: a case-control retrospective studyJ Montoya, N B Matta, P Suchon, et al.
European Journal of Human Genetics : EJHG|April 11, 2000
Linkage of X-linked myopathy with excessive autophagy (XMEA) to Xq28L Villard, V des Portes, N Levy, et al.
Revue Neurologique|April 3, 2001
[Proximal myotonial myopathy (PROMM): clinical and histology study]G Bassez, S Attarian, P Laforêt, et al.
Human Molecular Genetics|April 18, 1998
Correlation between varying levels of PMP22 expression and the degree of demyelination and reduction in nerve conduction velocity in transgenic miceC Huxley, E Passage, A M Robertson, et al.
Diagnostic and Interventional Imaging|July 24, 2019
Assessment of proximal femur microarchitecture using ultra-high field MRI at 7 TeslaD Guenoun, M Pithioux, J-C Souplet, et al.
Neurology|June 11, 2003
Histopathological differences of myotonic dystrophy type 1 (DM1) and PROMM/DM2A Vihola, G Bassez, G Meola, et al.
Brain : a Journal of Neurology|September 24, 2002
PMP22 overexpression causes dysmyelination in miceA Robaglia-Schlupp, J Pizant, J-C Norreel, et al.
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