Prediction and digital mapping of soil carbon storage in the Lower Namoi Valley von MINASNY, Budiman, MCBRATNEY, Alex. B, MENDONCA-SANTOS, M. L, ODEH, I. O. A, GUYON, Brice

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Importance of Combining Advanced Particle Size Analysis Techniques To Characterize Cell-Penetrating Peptide–Ferrocifen Self-Assemblies von Guyon, Léna, Lepeltier, Elise, Gimel, Jean-Christophe, Calvignac, Brice, Franconi, Florence, Lautram, Nolwenn, Dupont, Aurélien, Bourgaux, Claudie, Pigeon, Pascal, Saulnier, Patrick, Jaouen, Gérard, Passirani, Catherine

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Spastin mutations are frequent in sporadic spastic paraparesis and their spectrum is different from that observed in familial cases von Depienne, C, Tallaksen, C, Lephay, J Y, Bricka, B, Poea-Guyon, S, Fontaine, B, Labauge, P, Brice, A, Durr, A

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Well-Differentiated Papillary Mesothelioma of the Peritoneum: A Retrospective Study from the RENAPE Observational Registry von Vogin, Guillaume, Hettal, Liza, Vignaud, Jean-Michel, Dartigues, Peggy, Goere, Diane, Ferron, Gwenaël, Heyd, Bruno, Bereder, Jean-Marc, Tuech, Jean-Jacques, Glehen, Olivier, de Chaisemartin, Cécile, Lherm, Yoann, Villeneuve, Laurent, Kepenekian, Vahan, Marchal, Frédéric

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Spastic paraplegia 5: Locus refinement, candidate gene analysis and clinical description von Klebe, Stephan, Durr, Alexandra, Bouslam, Naima, Grid, Djamel, Paternotte, Caroline, Depienne, Christel, Hanein, Sylvain, Bouhouche, Ahmed, Elleuch, Nizar, Azzedine, Hamid, Poea-Guyon, Sandrine, Forlani, Sylvie, Denis, Elodie, Charon, Céline, Hazan, Jamile, Brice, Alexis, Stevanin, Giovanni

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NIPA1 (SPG6) mutations are a rare cause of autosomal dominant spastic paraplegia in Europe von Klebe, Stephan, Lacour, Arnaud, Durr, Alexandra, Stojkovic, Tanya, Depienne, Christel, Forlani, Sylvie, Poea-Guyon, Sandrine, Vuillaume, Isabelle, Sablonniere, Bernard, Vermersch, Patrick, Brice, Alexis, Stevanin, Giovanni

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Gene symbol: SPAST. Disease: spastic paraparesis. Accession #Hs0515 von Depienne, C, Tallaksen, C, Lephay, J Y, Bricka, B, Poea-Guyon, S, Fontaine, B, Labauge, P, Brice, A, Durr, A

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Gene symbol: SPAST. Disease: Spastic paraparesis. Accession #Hd0519 von Depienne, C, Tallaksen, C, Lephay, J Y, Bricka, B, Poea-Guyon, S, Fontaine, B, Labauge, P, Brice, A, Durr, A

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Gene symbol: SPAST (SPG4). Disease: Spastic paraparesis. Accession #Hm0552 von Depienne, C, Tallaksen, C, Lephay, J Y, Bricka, B, Poea-Guyon, S, Fontaine, B, Labauge, P, Brice, A, Durr, A

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Gene symbol: SPAST. Disease: Spastic paraparesis. Accession #Hm0553 von Depienne, C, Tallaksen, C, Lephay, J Y, Bricka, B, Poea-Guyon, S, Fontaine, B, Labauge, P, Brice, A, Durr, A

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Gene symbol: SPAST. Disease: Spastic paraparesis. Accession #Hm0557 von Depienne, C, Tallaksen, C, Lephay, J Y, Bricka, B, Poea-Guyon, S, Fontaine, B, Labauge, P, Brice, A, Durr, A

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RISTRETTO: reflected-light exoplanet spectroscopy at the diffraction limit of the VLT von Lovis, Christophe, Blind, Nicolas, Chazelas, Bruno, Shinde, Muskan, Bugatti, Maddalena, Restori, Nathanaël, Dinis, Isaac, Genolet, Ludovic, Hughes, Ian, Sordet, Michaël, Schnell, Robin, Rihs, Samuel, Crausaz, Adrien, Turbet, Martin, Billot, Nicolas, Fusco, Thierry, Neichel, Benoit, Sauvage, Jean-François, Pablo Santos Diaz, Houelle, Mathilde, Blackman, Joshua, Lanotte, Audrey, Kühn, Jonas, Hagelberg, Janis, Guyon, Olivier, Martinez, Patrice, Spang, Alain, Mordasini, Christoph, Ehrenreich, David, Brice-Olivier Demory, Bolmont, Emeline

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Gene symbol: SPAST. Disease: Spastic paraparesis. Accession #Hs0516 von Depienne, C, Tallaksen, C, Lephay, J Y, Bricka, B, Poea-Guyon, S, Fontaine, B, Brice, A, Durr, A

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Gene symbol: SPAST. Disease: Spastic paraparesis. Accession #Hm0555 von Depienne, C, Tallaksen, C, Lephay, J Y, Bricka, B, Poea-Guyon, S, Fontaine, B, Brice, A, Durr, A

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Gene symbol: SPAST. Disease: Spastic paraparesis. Accession #Hm0556 von Depienne, C, Tallaksen, C, Lephay, J Y, Bricka, B, Poea-Guyon, S, Fontaine, B, Labauge, P, Brice, A, Durr, A

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Gene symbol: SPAST. Disease: Spastic paraparesis. Accession #Hm0554 von Depienne, C, Tallaksen, C, Lephay, J Y, Bricka, B, Poea-Guyon, S, Fontaine, B, Labauge, P, Brice, A, Durr, A

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M - 10 Mutations du gène NIPA1 (SPG6) : une cause rare de paraparésie spastique héréditaire en Europe von Klebe, S., Lacour, A., Durr, A., Stojkovic, T., Depienne, C., Forlani, S., Poca-Guyon, S., Vuillaume, I., Sablonniere, B., Vermersch, P., Brice, A., Stevanin, G.

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NIPA1 (SPG6) mutations are a rare cause of autosomal dominant spastic paraplegia in Europe von Klebe, Stephan, Lacour, Arnaud, Durr, Alexandra, Stojkovic, Tanya, Depienne, Christel, lani, Sylvie, Poea-Guyon, Sandrine, Vuillaume, Isabelle, Sablonniere, Bernard, Vermersch, Patrick, Brice, Alexis, Stevanin, Giovanni

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ESA Voyage 2050 White Paper: Detecting life outside our solar system with a large high-contrast-imaging mission von Snellen, Ignas, Albrecht, Simon, Anglada-Escude, Guillem, Baraffe, Isabelle, Baudoz, Pierre, Benz, Willy, Beuzit, Jean-Luc, Biller, Beth, Birkby, Jayne, Boccaletti, Anthony, Boekel, Roy van, Boer, Jos de, Brogi, Matteo, Buchhave, Lars, Carone, Ludmila, Claire, Mark, Claudi, Riccardo, Demory, Brice-Olivier, Desert, Jean-Michel, Desidera, Silvano, Gaudi, Scott, Gratton, Raffaele, Gillon, Michael, Grenfell, John Lee, Guyon, Olivier, Henning, Thomas, Hinkley, Sasha, Huby, Elsa, Janson, Markus, Helling, Christiane, Heng, Kevin, Kasper, Markus, Keller, Christoph, Kenworthy, Matthew, Krause, Oliver, Kreidberg, Laura, Nikku, Madhusudhan, Lagrange, Anne-Marie, Launhardt, Ralf, Lenton, Tim, Lopez-Puertas, Manuel, Maire, Anne-Lise, Mayne, Nathan, Meadows, Victoria, Mennesson, Bertrand, Micela, Giuseppina, Miguel, Yamila, Milli, Julien, Min, Michiel, Mooij, Ernst de, Mouillet, David, N'Diaye, Mamadou, D'Orazi, Valentina, Palle, Enric, Pagano, Isabella, Piotto, Giampaolo, Queloz, Didier, Rauer, Heike, Ribas, Ignasi, Ruane, Garreth, Selsis, Franck, Snik, Frans, Sozzetti, Alessandro, Stam, Daphne, Stark, Christopher, Vigan, Arthur, Visser, Pieter de

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