Thymoma associated with autoimmune diseases: 85 cases and literature review von Bernard, C, Frih, H, Pasquet, F, Kerever, S, Jamilloux, Y, Tronc, F, Guibert, B, Isaac, S, Devouassoux, M, Chalabreysse, L, Broussolle, C, Petiot, P, Girard, N, Sève, P

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Focal myositis: A review von Devic, P, Gallay, L, Streichenberger, N, Petiot, P

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The pattern and diagnostic criteria of sensory neuronopathy: a case–control study von Camdessanché, Jean-Philippe, Jousserand, Guillemette, Ferraud, Karine, Vial, Christophe, Petiot, Philippe, Honnorat, Jérôme, Antoine, Jean-Christophe

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Sporadic inclusion-body myositis: Recent advances and the state of the art in 2016 von Gallay, L., Petiot, P.

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Antibodies to clustered acetylcholine receptor: expanding the phenotype von Devic, P., Petiot, P., Simonet, T., Stojkovic, T., Delmont, E., Franques, J., Magot, A., Vial, C., Lagrange, E., Nicot, A. S., Risson, V., Eymard, B., Schaeffer, L.

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Dilative arteriopathy and basilar artery dolichoectasia complicating late-onset Pompe disease von LAFORET, P, PETIOT, P, HADRANE, L, ANNANE, D, EYMARD, B, NICOLINO, M, ORLIKOWSKI, D, CAILLAUD, C, PELLEGRINI, N, FROISSART, R, PETITJEAN, T, MAIRE, I, CHABRIAT, H

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Transthyretin amyloid polyneuropathy in France: A cross-sectional study with 413 patients and real-world tafamidis meglumine use (2009–2019) von Adams, D., Cintas, P., Solé, G., Tard, C., Labeyrie, C., Echaniz-Laguna, A., Cauquil, C., Pereon, Y., Magy, L., Morales, R. Juntas, Antoine, J.C., Lagrange, E., Petiot, P., Mallaret, M., Francou, B., Guiochon-Mantel, A., Coste, A., Demarcq, O., Geffroy, C., Famelart, V., Rudant, J, Bartoli, M, Donal, E., Lairez, O., Eicher, J.C., Kharoubi, M., Oghina, S., Trochu, J.N., Inamo, J., Habib, G., Roubille, F., Hagège, A., Morio, F., Cariou, E., Adda, J., Slama, M.S., Charron, P., Algalarrondo, V., Damy, T., Attarian, S.

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Charcot-Marie-Tooth (CMT)-like polyneuropathy revealing neurofibromatosis type 2: A case report and review of the literature von Pegat, A., Ducray, F., Jeannin-Mayer, S., Jouanneau, E., Pinson, S., Petiot, P.

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Effects of a potential D3/5-HT1A antipsychotic compound, F17464, in rat behavioural models of cognitive and negative symptoms of schizophrenia von Auclair, A, Barret-Grevoz, C, Petiot, P, Gatti-McArthur, S

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Thymoma and autoimmune diseases von Jamilloux, Y, Frih, H, Bernard, C, Broussolle, C, Petiot, P, Girard, N, Sève, P

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Phenotype genotype analysis in 15 patients presenting a congenital myasthenic syndrome due to mutations in DOK7 von Ben Ammar, A., Petit, F., Alexandri, N., Gaudon, K., Bauché, S., Rouche, A., Gras, D., Fournier, E., Koenig, J., Stojkovic, T., Lacour, A., Petiot, P., Zagnoli, F., Viollet, L., Pellegrini, N., Orlikowski, D., Lazaro, L., Ferrer, X., Stoltenburg, G., Paturneau-Jouas, M., Hentati, F., Fardeau, M., Sternberg, D., Hantaï, D., Richard, P., Eymard, B.

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Progressive multifocal leukoencephalopathy after liver transplantation can have favorable or unfavorable outcome von Dumortier, J., Guillaud, O., Bosch, A., Coppéré, B., Petiot, P., Roggerone, S., Vukusic, S., Boillot, O.

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Significant response to immune therapies in a case of subacute necrotizing myopathy and FKRP mutations von Svahn, J, Streichenberger, N, Benveniste, O, Menassa, R, Michel, L, Fayolle, H, Petiot, P

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Dramatic improvement after rituximab in a patient with paraneoplastic treatment-refractory Morvan syndrome associated with anti-CASPR2 antibodies von Ong, E., Viaccoz, A., Ducray, F., Pérol, M., Cavillon, G., Rogemond, V., Honnorat, J., Petiot, P.

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The wide POLG -related spectrum: An integrated view von Béreau, M, Anheim, M, Echaniz-Laguna, A, Magot, A, Verny, C, Goideau-Sevrain, M, Barth, M, Amati-Bonneau, P, Allouche, S, Ayrignac, X, Bédat-Millet, A.-L, Guyant-Maréchal, L, Kuntzer, T, Ochsner, F, Petiot, P, Vial, C, Omer, S, Sole, G, Taieb, G, Carvalho, N, Tio, G, Kremer, S, Acquaviva-Bourdain, C, de Camaret, B. Mousson, Tranchant, C

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Distal hereditary motor neuropathy von Devic, P, Petiot, P

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Electrophysiological diagnosis of inflammatory neuropathies von Petiot, P

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L’asymétrie du split-hand index : un marqueur ENMG précoce de SLA ? von Ruel, B., Bouhour, F., Hemmendinger, A., Petiot, P., Bernard, E.

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Necrotizing autoimmune myopathies von Petiot, P, Choumert, A, Hamelin, L, Devic, P, Streichenberger, N

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Respiratory onset in an ALS family with L144F SOD1 mutation von Corcia, P, Petiot, P, Stevic, Z, Vourc'h, P, Morales, R, Gordon, P H, Pageot, N, Andres, C, Camu, W

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