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Exploring necrotizing autoimmune myopathies with a novel immunoassay for anti-3-hydroxy-3-methyl-glutaryl-CoA reductase autoantibodies.
Drouot L, Allenbach Y, Jouen F, Charuel JL, Martinet J, Meyer A, Hinschberger O, Bader-Meunier B, Kone-Paut I, Campana-Salort E, Eymard B, Tournadre A, Musset L, Sibilia J, Marie I, Benveniste O, Boyer O; French Myositis Network [CN]. Drouot L, et al. Arthritis Res Ther. 2014 Feb 3;16(1):R39. doi: 10.1186/ar4468. Arthritis Res Ther. 2014. PMID: 24484965 Free PMC article.
Correlation between low FAT1 expression and early affected muscle in facioscapulohumeral muscular dystrophy.
Mariot V, Roche S, Hourdé C, Portilho D, Sacconi S, Puppo F, Duguez S, Rameau P, Caruso N, Delezoide AL, Desnuelle C, Bessières B, Collardeau S, Feasson L, Maisonobe T, Magdinier F, Helmbacher F, Butler-Browne G, Mouly V, Dumonceaux J. Mariot V, et al. Among authors: feasson l. Ann Neurol. 2015 Sep;78(3):387-400. doi: 10.1002/ana.24446. Epub 2015 Jul 3. Ann Neurol. 2015. PMID: 26018399
Rational and design of an overfeeding protocol in constitutional thinness: Understanding the physiology, metabolism and genetic background of resistance to weight gain.
Ling Y, Galusca B, Hager J, Feasson L, Valsesia A, Epelbaum J, Alexandre V, Wynn E, Dinet C, Palaghiu R, Peoc'h M, Boirie Y, Montaurier C, Estour B, Germain N. Ling Y, et al. Among authors: feasson l. Ann Endocrinol (Paris). 2016 Oct;77(5):563-569. doi: 10.1016/j.ando.2016.06.001. Epub 2016 Jul 15. Ann Endocrinol (Paris). 2016. PMID: 27424229 Clinical Trial.
PNPLA2 mutation: a paediatric case with early onset but indolent course.
Perrin L, Féasson L, Furby A, Laforêt P, Petit FM, Gautheron V, Chabrier S. Perrin L, et al. Among authors: feasson l. Neuromuscul Disord. 2013 Dec;23(12):986-91. doi: 10.1016/j.nmd.2013.08.008. Epub 2013 Aug 30. Neuromuscul Disord. 2013. PMID: 24074500
145 results