OC-0634 Lymphocyte Sparing Radiation Therapy for stage III NSCLC: a dosimetric study von Fernandes, P., Jourani, Y., Birkfellner, W., Charlier, F., Ferreira, A., Van de Ven, G., Moretti, L., Fardeau, E., Van Gestel, D., Reynaert, N.

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Uveitic macular edema von Fardeau, C, Champion, E, Massamba, N, LeHoang, P

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Macellibacteroides fermentans gen. nov., sp. nov., a member of the family Porphyromonadaceae isolated from an upflow anaerobic filter treating abattoir wastewaters von Jabari, Linda, Gannoun, Hana, Cayol, Jean-Luc, Hedi, Abdeljabbar, Sakamoto, Mitsuo, Falsen, Enevold, Ohkuma, Moriya, Hamdi, Moktar, Fauque, Guy, Ollivier, Bernard, Fardeau, Marie-Laure

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Processes Governing Phosphorus Availability in Temperate Soils von Frossard, E., Condron, L. M., Oberson, A., Sinaj, S., Fardeau, J. C.

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Serratia glossinae sp. nov., isolated from the midgut of the tsetse fly Glossina palpalis gambiensis von GEIGER, A, FARDEAU, M.-L, FALSEN, E, OLLIVIER, B, CUNY, G

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Biocorrosion of carbon steel alloys by an hydrogenotrophic sulfate-reducing bacterium Desulfovibrio capillatus isolated from a Mexican oil field separator von Miranda, E., Bethencourt, M., Botana, F.J., Cano, M.J., Sánchez-Amaya, J.M., Corzo, A., de Lomas, J. García, Fardeau, M.L., Ollivier, B.

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Hydrogen Sulfide: A Toxic Gas Produced by Dissimilatory Sulfate and Sulfur Reduction and Consumed by Microbial Oxidation von Barton, Larry L., Fardeau, Marie-Laure, Fauque, Guy D.

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Characterization of extracellular polymers synthesized by tropical intertidal biofilm bacteria von Ortega-Morales, B.O, Santiago-García, J.L, Chan-Bacab, M.J, Moppert, X, Miranda-Tello, E, Fardeau, M.L, Carrero, J.C, Bartolo-Pérez, P, Valadéz-González, A, Guezennec, J

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Mutations in dynamin 2 cause dominant centronuclear myopathy von Bitoun, Marc, Maugenre, Svetlana, Jeannet, Pierre-Yves, Lacène, Emmanuelle, Ferrer, Xavier, Laforêt, Pascal, Martin, Jean-Jacques, Laporte, Jocelyn, Lochmüller, Hanns, Beggs, Alan H, Fardeau, Michel, Eymard, Bruno, Romero, Norma B, Guicheney, Pascale

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NEW GENES AND DISEASES von Moulay, G., Nelson, I., Lainé, J., Cohen, E., Lemaître, M., Mamchaoui, K., Julien, L., Brochier, G., Beuvin, M., Yaou, R. Ben, Malfatti, E., Fardeau, C., Fardeau, M., Romero, N., Bitoun, M., Stojkovic, T., Bonne, G., Vassilopoulos, S.

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NEW GENES AND DISEASES: EP.301 The alpha2-subunit of the AP2 clathrin adaptor as the causal gene in an atypical myopathy with granulofilamentous inclusions von Moulay, G., Nelson, I., Lainé, J., Cohen, E., Lemaître, M., Mamchaoui, K., Julien, L., Brochier, G., Beuvin, M., Yaou, R. Ben, Malfatti, E., Fardeau, C., Fardeau, M., Romero, N., Bitoun, M., Stojkovic, T., Bonne, G., Vassilopoulos, S.

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Affected female carriers of MTM1 mutations display a wide spectrum of clinical and pathological involvement: delineating diagnostic clues von Biancalana, Valérie, Scheidecker, Sophie, Miguet, Marguerite, Laquerrière, Annie, Romero, Norma B., Stojkovic, Tanya, Abath Neto, Osorio, Mercier, Sandra, Voermans, Nicol, Tanner, Laura, Rogers, Curtis, Ollagnon-Roman, Elisabeth, Roper, Helen, Boutte, Célia, Ben-Shachar, Shay, Lornage, Xavière, Vasli, Nasim, Schaefer, Elise, Laforet, Pascal, Pouget, Jean, Moerman, Alexandre, Pasquier, Laurent, Marcorelle, Pascale, Magot, Armelle, Küsters, Benno, Streichenberger, Nathalie, Tranchant, Christine, Dondaine, Nicolas, Schneider, Raphael, Gasnier, Claire, Calmels, Nadège, Kremer, Valérie, Nguyen, Karine, Perrier, Julie, Kamsteeg, Erik Jan, Carlier, Pierre, Carlier, Robert-Yves, Thompson, Julie, Boland, Anne, Deleuze, Jean-François, Fardeau, Michel, Zanoteli, Edmar, Eymard, Bruno, Laporte, Jocelyn

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Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy von Bonne, Gisèle, Barletta, Marina Raffaele Di, Varnous, Shaida, Bécane, Henri-Marc, Hammouda, El-Hadi, Merlini, Luciano, Muntoni, Francesco, Greenberg, Cheryl R., Gary, Françoise, Urtizberea, Jon-Andoni, Duboc, Denis, Fardeau, Michel, Toniolo, Daniela, Schwartz, Ketty

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Assessment of phytoavailability of nickel in soils von Echevarria, G. (Lab. of Soil and Environmental Sciences, France.), Morel, J.L, Fardeau, J.C, Leclerc-Cessac, E

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Sarcomeric disorganization and nemaline bodies in muscle biopsies of patients with EXOSC3‐related type 1 pontocerebellar hypoplasia von Pinto, Miguel M., Monges, Soledad, Malfatti, Edoardo, Lubieniecki, Fabiana, Lornage, Xavière, Alias, Laura, Labasse, Clémence, Madelaine, Angéline, Fardeau, Michel, Laporte, Jocelyn, Tizzano, Eduardo F., Romero, Norma B.

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Observational study of QuantiFERON® management for ocular tuberculosis diagnosis: Analysis of 244 consecutive tests von Amara, A, Ben Salah, E, Guihot, A, Fardeau, C, Touitoue, V, Saadoun, D, Bodaghi, B, Sève, P, Trad, S

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DISPOSITIF PORTE-ELECTRODES DESTINE A ETRE IMPLANTE DANS UN ETRE VIVANT von MICHEL FARDEAU ET JEAN-LUC WEBER

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DISPOSITIF PORTE-ELECTRODES DESTINE A ETRE IMPLANTE DANS UN ETRE VIVANT von MICHEL FARDEAU ET JEAN-LUC WEBER

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Clinical and molecular genetic spectrum of autosomal dominant Emery-Dreifuss muscular dystrophy due to mutations of the lamin A/C gene von Bonne, G., Mercuri, E., Muchir, A., Urtizberea, A., Bécane, H. M., Recan, D., Merlini, L., Wehnert, M., Boor, R., Reuner, U., Vorgerd, M., Wicklein, E. M., Eymard, B., Duboc, D., Penisson-Besnier, I., Cuisset, J. M., Ferrer, X., Desguerre, I., Lacombe, D., Bushby, K., Pollitt, C., Toniolo, D., Fardeau, M., Schwartz, K., Muntoni, F.

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MUSK, a new target for mutations causing congenital myasthenic syndrome von Chevessier, Frédéric, Faraut, Brice, Ravel-Chapuis, Aymeric, Richard, Pascale, Gaudon, Karen, Bauché, Stéphanie, Prioleau, Cassandra, Herbst, Ruth, Goillot, Evelyne, Ioos, Christine, Azulay, Jean-Philippe, Attarian, Shahram, Leroy, Jean-Paul, Fournier, Emmanuel, Legay, Claire, Schaeffer, Laurent, Koenig, Jeanine, Fardeau, Michel, Eymard, Bruno, Pouget, Jean, Hantaï, Daniel

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