The MFN2 gene is responsible for mitochondrial DNA instability and optic atrophy 'plus' phenotype von Rouzier, Cécile, Bannwarth, Sylvie, Chaussenot, Annabelle, Chevrollier, Arnaud, Verschueren, Annie, Bonello-Palot, Nathalie, Fragaki, Konstantina, Cano, Aline, Pouget, Jean, Pellissier, Jean-François, Procaccio, Vincent, Chabrol, Brigitte, Paquis-Flucklinger, Véronique

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Macrophagic myofasciitis lesions assess long-term persistence of vaccine-derived aluminium hydroxide in muscle von Gherardi, R. K., Coquet, M., Cherin, P., Belec, L., Moretto, P., Dreyfus, P. A., Pellissier, J.-F., Chariot, P., Authier, F.-J.

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Ascorbic acid treatment corrects the phenotype of a mouse model of Charcot-Marie-Tooth disease von Fontés, Michel, Passage, Edith, Norreel, Jean Chrétien, Noack-Fraissignes, Pauline, Sanguedolce, Véronique, Pizant, Josette, Thirion, Xavier, Robaglia-Schlupp, Andrée, Pellissier, Jean François

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The severity of phenotype linked to SUCLG1 mutations could be correlated with residual amount of SUCLG1 protein von Rouzier, C, Le Guédard-Méreuze, S, Fragaki, K, Serre, V, Miro, J, Tuffery-Giraud, S, Chaussenot, A, Bannwarth, S, Caruba, C, Ostergaard, E, Pellissier, J-F, Richelme, C, Espil, C, Chabrol, B, Paquis-Flucklinger, V

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Diagnostic evaluation of clinically normal subjects with chronic hyperCKemia von FERNANDEZ, C, DE PAULA, A. Maues, FIGARELLA-BRANGER, D, KRAHN, M, GIORGI, R, CHABROL, B, MONFORT, M.-F, POUGET, J, PELLISSIER, J.-F

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Pituicytomas, a mis-diagnosed benign tumor of the neurohypophysis: report of three cases von FIGARELLA-BRANGER, D, DUFOUR, H, FERNANDEZ, C, BOUVIER-LABIT, C, GRISOLI, F, PELLISSIER, J. F

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Q-TWiST analysis to assess benefit-risk of pembrolizumab in patients with PD-L1-positive advanced or metastatic NSCLC von Huang, M., Pietanza, M.C., Samkari, A., Pellissier, J., Burke, T., Chandwani, S., Kong, F., Pickard, A.S.

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The Lipid Phosphatase Myotubularin Is Essential for Skeletal Muscle Maintenance but Not for Myogenesis in Mice von Buj-Bello, Anna, Laugel, Vincent, Messaddeq, Nadia, Zahreddine, Hala, Laporte, Jocelyn, Pellissier, Jean-François, Mandel, Jean-Louis

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Histopathological differences of myotonic dystrophy type 1 (DM1) and PROMM/DM2 von Vihola, A, Bassez, G, Meola, G, Zhang, S, Haapasalo, H, Paetau, A, Mancinelli, E, Rouche, A, Hogrel, J Y, Laforêt, P, Maisonobe, T, Pellissier, J F, Krahe, R, Eymard, B, Udd, B

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A Long‐Term Watershed‐Scale Partnership to Restore Bull Trout Across Federal, State, Private, and Historic Tribal Land Near Crater Lake National Park, Oregon von Buktenica, M. W., Hering, D. K., Scott, N., Lambert, C., McKee, J., Maletis, E., Pellissier, J., Tinniswood, W., Banish, N.

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PMP22 overexpression causes dysmyelination in mice von Robaglia‐Schlupp, A., Pizant, J., Norreel, J.‐C., Passage, E., Sabéran‐Djoneidi, D., Ansaldi, J.‐L., Vinay, L., Figarella‐Branger, D., Lévy, N., Clarac, F., Cau, P., Pellissier, J.‐F., Fontés, M.

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CCR2A and CCR2B, the two isoforms of the monocyte chemoattractant protein-1 receptor are up-regulated and expressed by different cell subsets in idiopathic inflammatory myopathies von BARTOLI, C, CIVATTE, M, PELLISSIER, J. F, FIGARELLA-BRANGER, D

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Macrophagic myofasciitis: an emerging entity von Gherardi, RK, Coquet, M, Chérin, P, Authier, F-J, Laforêt, P, Bélec, L, Figarella-Branger, D, Mussini, J-M, Pellissier, J-F, Fardeau, M

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The Incidence of Herpes Zoster in a United States Administrative Database von Insinga, Ralph P., Itzler, Robbin F., Pellissier, James M., Saddier, Patricia, Nikas, Alexander A.

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Foreword - macrophage mediated myofasciites von Guis, S, Pellissier, J F

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Class I MHC detection as a diagnostic tool in noninformative muscle biopsies of patients suffering from dermatomyositis (DM) von Civatte, M., Schleinitz, N., Krammer, P., Fernandez, C., Guis, S., Veit, V., Pouget, J., Harlé, J.-R., Pellissier, J.-F., Figarella-Branger, D.

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Cost effectiveness of anterior cruciate ligament reconstruction in young adults von GOTTLOB, C. A, BAKER, C. L, PELLISSIER, J. M, COLVIN, L

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Expression of the β chemokines CCL3, CCL4, CCL5 and their receptors in idiopathic inflammatory myopathies von Civatte, M., Bartoli, C., Schleinitz, N., Chetaille, B., Pellissier, J. F., Figarella-Branger, D.

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Construction of a Mouse Model of Charcot-Marie-Tooth Disease Type 1A by Pronuclear Injection of Human YAC DNA von Huxley, C., Passage, E., Manson, A., Putzu, G., Figarella-Branger, D., Pellissier, J. F., Fontés, M.

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Correlation Between Varying Levels of PMP22 Expression and the Degree of Demyelination and Reduction in Nerve Conduction Velocity in Transgenic Mice von Huxley, C., Passage, E., Robertson, A. M., Youl, B., Huston, S., Manson, A., Sabéran-Djoniedi, D., Figarella-Branger, D., Pellissier, J. F., Thomas, P. K., Fontés, M.

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