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109 results

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Page 1
Focal myositis: A review.
Devic P, Gallay L, Streichenberger N, Petiot P. Devic P, et al. Among authors: petiot p. Neuromuscul Disord. 2016 Nov;26(11):725-733. doi: 10.1016/j.nmd.2016.08.014. Epub 2016 Aug 26. Neuromuscul Disord. 2016. PMID: 27726926 Review.
Long-term exposure to Myozyme results in a decrease of anti-drug antibodies in late-onset Pompe disease patients.
Masat E, Laforêt P, De Antonio M, Corre G, Perniconi B, Taouagh N, Mariampillai K, Amelin D, Mauhin W, Hogrel JY, Caillaud C, Ronzitti G, Puzzo F, Kuranda K, Colella P, Mallone R, Benveniste O, Mingozzi F; French Pompe Registry Study Group. Masat E, et al. Sci Rep. 2016 Nov 4;6:36182. doi: 10.1038/srep36182. Sci Rep. 2016. PMID: 27812025 Free PMC article.
Genotype-phenotype correlation and course of transthyretin familial amyloid polyneuropathies in France.
Mariani LL, Lozeron P, Théaudin M, Mincheva Z, Signate A, Ducot B, Algalarrondo V, Denier C, Adam C, Nicolas G, Samuel D, Slama MS, Lacroix C, Misrahi M, Adams D; French Familial Amyloid Polyneuropathies Network (CORNAMYL) Study Group. Mariani LL, et al. Ann Neurol. 2015 Dec;78(6):901-16. doi: 10.1002/ana.24519. Epub 2015 Oct 7. Ann Neurol. 2015. PMID: 26369527 Free PMC article.
[Analysis of 12 cases of McArdle's disease diagnosed after 30 years].
Pavic M, Petiot P, Streichenberger N, Dupond JL, Drouet A, Flocard F, Bouhour F, Colin JY, Bielefeld P, Gouttard M, Maire I, Pellat J, Vital Durand D, Rousset H. Pavic M, et al. Among authors: petiot p. Rev Med Interne. 2003 Nov;24(11):716-20. doi: 10.1016/s0248-8663(03)00219-4. Rev Med Interne. 2003. PMID: 14604748 French.
[Autosomal dominant limb-girdle muscular dystrophy associated with conduction defects (LGMD1B): a description of 8 new families with the LMNA gene mutations].
Ben Yaou R, Bécane HM, Demay L, Laforet P, Hannequin D, Bohu PA, Drouin-Garraud V, Ferrer X, Mussini JM, Ollagnon E, Petiot P, Penisson-Besnier I, Streichenberger N, Toutain A, Richard P, Eymard B, Bonne G. Ben Yaou R, et al. Among authors: petiot p. Rev Neurol (Paris). 2005 Jan;161(1):42-54. doi: 10.1016/s0035-3787(05)84972-0. Rev Neurol (Paris). 2005. PMID: 15678000 French.
Granulomatous myositis: a clinical study of thirteen cases.
Le Roux K, Streichenberger N, Vial C, Petiot P, Feasson L, Bouhour F, Ninet J, Lachenal F, Broussolle C, Sève P. Le Roux K, et al. Among authors: petiot p. Muscle Nerve. 2007 Feb;35(2):171-7. doi: 10.1002/mus.20683. Muscle Nerve. 2007. PMID: 17068767 Clinical Trial.
[Distal hereditary motor neuropathy].
Devic P, Petiot P. Devic P, et al. Among authors: petiot p. Rev Neurol (Paris). 2011 Nov;167(11):781-90. doi: 10.1016/j.neurol.2011.03.003. Epub 2011 May 6. Rev Neurol (Paris). 2011. PMID: 21529868 Review. French.
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