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HLA-DRB1*01 and macrophagic myofasciitis.
Guis S, Pellissier JF, Nicoli F, Reviron D, Mattei JP, Gherardi RK, Pelletier J, Kaplanski G, Figarella-Branger D, Roudier J. Guis S, et al. Arthritis Rheum. 2002 Sep;46(9):2535-7. doi: 10.1002/art.10465. Arthritis Rheum. 2002. PMID: 12355502 Free article. No abstract available.
Electron microscopy in neuromuscular disorders.
Fernandez C, Figarella-Branger D, Meyronet D, Cassote E, Tong S, Pellissier JF. Fernandez C, et al. Ultrastruct Pathol. 2005 Nov-Dec;29(6):437-50. doi: 10.1080/01913120500323175. Ultrastruct Pathol. 2005. PMID: 16316944 Review.
Molecular characterization of myophosphorylase deficiency (McArdle disease) in 34 patients from Southern France: identification of 10 new mutations. Absence of genotype-phenotype correlation.
Aquaron R, Bergé-Lefranc JL, Pellissier JF, Montfort MF, Mayan M, Figarella-Branger D, Coquet M, Serratrice G, Pouget J. Aquaron R, et al. Neuromuscul Disord. 2007 Mar;17(3):235-41. doi: 10.1016/j.nmd.2006.12.014. Epub 2007 Feb 26. Neuromuscul Disord. 2007. PMID: 17324573
589 results