Is deltoid muscle biopsy useful in isolated camptocormia? A prospective study von Chanson, J.-B., Lannes, B., Echaniz-Laguna, A.

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Population‐based prevalence of eosinophilic fasciitis (Shulman syndrome): a capture–recapture study von Spielmann, L., Arnaud, L., Severac, F., Messer, L., Mahé, A., Meyer, A., Lannes, B., Lipsker, D., Sibilia, J.

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Deciphering the causes of sporadic late-onset cerebellar ataxias: a prospective study with implications for diagnostic work von Gebus, O., Montaut, S., Monga, B., Wirth, T., Cheraud, C., Alves Do Rego, C., Zinchenko, I., Carré, G., Hamdaoui, M., Hautecloque, G., Nguyen-Them, L., Lannes, B., Chanson, J. B., Lagha-Boukbiza, O., Fleury, M. C., Devys, D., Nicolas, G., Rudolf, G., Bereau, M., Mallaret, M., Renaud, M., Acquaviva, C., Koenig, M., Koob, M., Kremer, S., Namer, I. J., Cazeneuve, C., Echaniz-Laguna, A., Tranchant, C., Anheim, Mathieu

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OP0135 Interferon-Beta Induced Reactive Oxygen Species Participate in Muscle Inflammation and Mitochondrial Oxydative Phosphorilation Defects Contributing to Dermatomyositis Muscle... von Meyer, A., Laverny, G., Prevel, N., Echaniz-Laguna, A., Lannes, B., Singh, F., Charles, A.-L., Benveniste, O., Metzger, D., Geny, B., Sibilia, J.

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AB0780 Frequency and characteristics of cancer associated myositis in a cohort of 20 patients with anti-jo-1 positive myositis von Meyer, A., Theulin, A., Chatelus, E., Sordet, C., Javier, R.-M., Lannes, B., Geny, B., Gottenberg, J.-E., Sibilia, J.

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AB0779 Eosinophilic myositis and rheumatoid arthritis as first manifestation in a patient carrying myotonic dystrophy type 2 (CCTG)n expenssion of ZNF9 gene von Meyer, A., Theulin, A., Chatelus, E., Sordet, C., Javier, R.-M., Lannes, B., Echaniz, A., Geny, B., Gottenberg, J.-E., Sibilia, J.

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Immune-mediated necrotizing myopathy associated with antibodies to hydroxy-methyl-glutaryl-coenzyme A reductase von Hinschberger, O, Lohmann, C, Lannes, B, Martzolff, L, Vo, B D, Jaeger-Bizet, F, Ciobanu, E, Kieffer, P

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κ-Opioid Receptor in Humans: cDNA and Genomic Cloning, Chromosomal Assignment, Functional Expression, Pharmacology, and Expression Pattern in the Central Nervous System von Simonin, Frederic, Gaveriaux-Ruff, Claire, Befort, Katia, Matthes, Hans, Lannes, Beatrice, Micheletti, Gabriel, Mattei, Marie-Genevieve, Charron, Gisele, Bloch, Bertrand, Kieffer, Brigitte

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Troubles de la mémoire progressifs, crises d’épilepsie, syndrome cérébelleux chez un homme de 67 ans von Pariente, J., Cretin, B., Lannes, B.

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The human delta-opioid receptor: genomic organization, cDNA cloning, functional expression, and distribution in human brain von Simonin, F, Befort, K, Gavériaux-Ruff, C, Matthes, H, Nappey, V, Lannes, B, Micheletti, G, Kieffer, B

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Increased prevalence of granulovacuolar degeneration in C9orf72 mutation von Riku, Yuichi, Duyckaerts, Charles, Boluda, Susana, Plu, Isabelle, Le Ber, Isabelle, Millecamps, Stéphanie, Salachas, François, Yoshida, Mari, Ando, Takashi, Katsuno, Masahisa, Sobue, Gen, Seilhean, Danielle

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70P Defining the landscape of TIA1 and SQSTM1 digenic myopathy von Fernández-Eulate, G., Panos-Basterra, P., Theuriet, J., Nadaj-Pakleza, A., Magot, A., Lannes, B., Marcorelles, P., Behin, A., Masingue, M., Caillon, F., Malek, Y., Fenouil, T., Bas, J., Menassa, R., Michel-Calemard, L., Streichenberger, N., Simon, J., Bouhour, F., Evangelista, T., Métay, C., Pegat, A., Stojkovic, T.

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Central nervous system abnormalities in patients with PMP22 gene mutations: a prospective study von Chanson, Jean-Baptiste, Echaniz-Laguna, Andoni, Blanc, Frédéric, Lacour, Arnaud, Ballonzoli, Laurent, Kremer, Stéphane, Namer, Izzie-Jacques, Lannes, Béatrice, Tranchant, Christine, Vermersch, Patrick, de Seze, Jérôme

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CONGENITAL MYOPATHIES (CNM) von Lornage, X., Sabouraud, P., Lannes, B., Gaillard, D., Biancalana, V., Böhm, J., Laporte, J.

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CONGENITAL MYOPATHIES (CNM): P.147Novel SPEG mutations in congenital myopathy without centralized nuclei von Lornage, X., Sabouraud, P., Lannes, B., Gaillard, D., Biancalana, V., Böhm, J., Laporte, J.

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Myopathie nécrosante auto-immune associée aux anticorps anti-hydroxy-méthyl-glutaryl-coenzyme A réductase von Hinschberger, O., Lohmann, C., Lannes, B., Martzolff, L., Vo, B.D., Jaeger-Bizet, F., Ciobanu, E., Kieffer, P.

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Au cours des myopathies nécrosantes autoimmunes, les autoanticorps anti-HMGCR exercent un rôle pathogène en bloquant l’HMG-CoA réductase dans le cytoplasme des fibres musculaires... von Giannini, M., Quiring, G., Lannes, B., Oulad-Abdelghani, M., Benveniste, O., Geny, B., Meyer, A.

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A novel mutation in HSPB8 causes dominant adult-onset axial and distal myopathy von Echaniz-Laguna, A., Lornage, X., Lannes, B., Schneider, R., Bierry, G., Dondaine, N., Deleuze, J., Böhm, J., Thompson, J., Laporte, J., Biancalana, V.

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P.74 - A novel mutation in HSPB8 causes dominant adult-onset axial and distal myopathy von Echaniz-Laguna, A., Lornage, X., Lannes, B., Schneider, R., Bierry, G., Dondaine, N., Deleuze, J., Böhm, J., Thompson, J., Laporte, J., Biancalana, V.

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Troubles de la mémoire progressifs, crises d’épilepsie, syndrome cérébelleux chez un homme de 67 ans von Pariente, J., Cretin, B., Lannes, B.

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