Diagnostic potential of sarcoplasmic myxovirus resistance protein A expression in subsets of dermatomyositis von Uruha, A., Allenbach, Y., Charuel, J.‐L., Musset, L., Aussy, A., Boyer, O., Mariampillai, K., Landon‐Cardinal, O., Rasmussen, C., Bolko, L., Maisonobe, T., Leonard‐Louis, S., Suzuki, S., Nishino, I., Stenzel, W., Benveniste, O.

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Long-term observational study of sporadic inclusion body myositis von Benveniste, Olivier, Guiguet, Marguerite, Freebody, Jane, Dubourg, Odile, Squier, Waney, Maisonobe, Thierry, Stojkovic, Tanya, Leite, Maria Isabel, Allenbach, Yves, Herson, Serge, Brady, Stefen, Eymard, Bruno, Hilton-Jones, David

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Pembrolizumab-induced necrotic myositis in a patient with metastatic melanoma von Vallet, H., Gaillet, A., Weiss, N., Vanhaecke, C., Saheb, S., Touitou, V., Franck, N., Kramkimel, N., Borden, A., Touat, M., Ricard, D., Verny, M., Maisonobe, T., Psimaras, D.

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Neurodystrophic hand dermatitis – Sannino-Barduagni syndrome von Demas, A., Apard, T., Bedat-Millet, A.-L., Maisonobe, T.

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Non-anti-MAG DADS neuropathy as a variant of CIDP: clinical, electrophysiological, laboratory features and response to treatment in 10 cases von Larue, S., Bombelli, F., Viala, K., Neil, J., Maisonobe, T., Bouche, P., Musset, L., Fournier, E., Léger, J. M.

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On/off dropped head syndrome: A severe adverse event after prolonged treatment with MEK inhibitor von Longvert, C., Maisonobe, T., Saiag, P., Auré, K.

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Eosinophilic fasciitis (Shulman disease): new insights into the therapeutic management from a series of 34 patients von Lebeaux, David, Francès, Camille, Barete, Stéphane, Wechsler, Bertrand, Dubourg, Odile, Renoux, Jérôme, Maisonobe, Thierry, Benveniste, Olivier, Gatfossé, Marc, Bourgeois, Pierre, Amoura, Zahir, Cacoub, Patrice, Piette, Jean-Charles, Sène, Damien

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Comparison of Lewis–Sumner syndrome with chronic inflammatory demyelinating polyradiculoneuropathy patients in a tertiary care centre von Fargeot, G., Maisonobe, T., Psimaras, D., Debs, R., Lenglet, T., Adams, D., Vandendries, C., Labeyrie, C., Viala, K.

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Neurolymphomatosis related to direct epineural invasion of the superficial peroneal nerve from subcutaneous B-cell lymphoma von Fargeot, G., Maisonobe, T., Vandendries, C., Le Garff-Tavernier, M., Leblond, V., Viala, K.

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A rare cause of impaired general condition: Muscular and cardiac toxicity of antimalarials von Lenfant, T., Dion, J., Maisonobe, T., Costedoat-Chalumeau, N.

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Neuropathy in lymphoma: a relationship between the pattern of neuropathy, type of lymphoma and prognosis? von Viala, K, Béhin, A, Maisonobe, T, Léger, J-M, Stojkovic, T, Davi, F, Leblond, V, Bouche, P

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Hepatitis C virus–associated polyarteritis nodosa von Saadoun, D., Terrier, B., Semoun, O., Sene, D., Maisonobe, T., Musset, L., Amoura, Z., Rigon, M. Resche, Cacoub, P.

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Intravenous immunoglobulin as short- and long-term therapy of multifocal motor neuropathy: a retrospective study of response to IVIg and of its predictive criteria in 40 patients von Léger, J-M, Viala, K, Cancalon, F, Maisonobe, T, Gruwez, B, Waegemans, T, Bouche, P

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Sarcoidosis occurring during BRAF/MEK inhibitors is associated with paradoxical ERK activation in Erdheim‐Chester patients von Amoura, A., Haroche, J., Emile, J.‐F., Barete, S., Helias‐Rodzewicz, Z., Charlotte, F., Maisonobe, T., Amoura, Z., Cohen Aubart, F.

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Sensory neuronopathy as a major clinical feature of mitochondrial trifunctional protein deficiency in adults von Nadjar, Y., Souvannanorath, S., Maisonobe, T., Brisset, M., De Lonlay, P., Schiff, M., Viala, K., Boutron, A., Nicolas, G., Laforêt, P.

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Comparing ataxias with oculomotor apraxia: a multimodal study of AOA1, AOA2 and AT focusing on video-oculography and alpha-fetoprotein von Mariani, L. L., Rivaud-Péchoux, S., Charles, P., Ewenczyk, C., Meneret, A., Monga, B. B., Fleury, M.-C., Hainque, E., Maisonobe, T., Degos, B., Echaniz-Laguna, A., Renaud, M., Wirth, T., Grabli, D., Brice, A., Vidailhet, M., Stoppa-Lyonnet, D., Dubois-d’Enghien, C., Le Ber, I., Koenig, M., Roze, E., Tranchant, C., Durr, A., Gaymard, B., Anheim, M.

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Antineoplastic agents exacerbating Charcot Marie Tooth disease: red flags to avoid permanent disability von Ibañez-Juliá, M J, Berzero, G, Reyes-Botero, G, Maisonobe, T, Lenglet, T, Slim, M, Louis, S, Balaguer, A, Sanson, M, Le Guern, E, Latour, P, Ricard, D, Stojkovic, T, Psimaras, D

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Encephalopathy associated with a reversible splenial lesion in riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency von Touat, M., Michaud, M., Alamowitch, S., Maisonobe, T., Acquaviva-Bourdain, C., Laforêt, P.

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Follow-up study and response to treatment in 23 patients with Lewis–Sumner syndrome von Viala, K., Renié, L., Maisonobe, T., Béhin, A., Neil, J., Léger, J. M., Bouche, P.

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PHENOTYPE OF A PATIENT WITH RECESSIVE CENTRONUCLEAR MYOPATHY AND A NOVEL BIN1 MUTATION von CLAEYS, K. G, MAISONOBE, T, BÖHM, J, LAPORTE, J, HEZODE, M, ROMERO, N. B, BROCHIER, G, BITOUN, M, CARLIER, R. Y, STOJKOVIC, T

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