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Anne-Laure Bedat-Millet

University of Rouen

19

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238

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Association of fingerprint bodies with rods is due to mutations in the LMOD3 gene: Fingerprint body myopathy and LMOD3

2019 Neuromuscular Disorders
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Prospective study of the additional benefit of plexus MRI in the diagnosis of CIDP

2019 European Journal of Neurology
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Gender as a Modifying Factor Influencing Myotonic Dystrophy Type 1 Phenotype Severity and Mortality : A Nationwide Multiple Databases Cross-Sectional Observational Study

2016 PLOS ONE
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Anti-MuSK myasthenia gravis with prolonged remission

2016 Neuromuscular Disorders
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A novel DNAJB6 mutation causing variable phenotypic expression: From distal myopathy to limb girdle muscular dystrophy

2016 Neuromuscular Disorders
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The wide POLG-related spectrum: An integrated view

2016 Journal of the Neurological Sciences
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Recurrent diplopia over a 30-year period: natural history of a Lewis and Sumner syndrome

2012 Acta Neurologica Belgica
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Results of Prolonged Follow-Up of Late-Onset Pompe Disease Treated with Alglucosidase Alfa (Myozyme®)

2011 Clinical Therapeutics
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An Autopsy Case of Amyotrophic Lateral Sclerosis with Waldenström Macroglobulinemia and Anti-MAG Gammopathy

2011 Case Reports in Neurology
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P4.50 Results of prolonged follow-up of late-onset Pompe disease treated with alglucosidase alfa (Myozyme)

2010 Neuromuscular Disorders
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