CHUST, Manuel y Claudia Rosas Lauro (Eds.). El Perú en revolución. Independencia y guerra: un proceso, 1780-1826. Lima: Editorial Universitat Jaume I, El Colegio de Michoacán, Fond... von Cusi Tejada, Cristian Félix

Volltext

Reseña de "El Cusco Insurrecto. La Revolución de 1814, doscientos años después", de Roberto Ojeda Escalante von Cristian Félix Cusi Tejada

Volltext

Key with Movable Wards von EUGEN GERBER, FELIX CUSI

Volltext bestellen

Schlüssel mit einem am Schafte angelenkten, beim Einstecken in das Schlüsselloch selbsttätig aus der gestreckten in die Gebrauchslage übergeführten Bart von EUGEN GERBER, FELIX CUSI

Volltext bestellen

Schloß mit Schlüssel von EUGEN GERBER, FELIX CUSI

Volltext bestellen

Nouvelle clef dont le panneton est articulé à la tige et est logé dans une douille qui peut glisser sur ladite tige, tandis qu'il sort automatiquement de ladite douille pour occupe... von GERBER EUGEN, CUSI FELIX

Volltext bestellen

Quality control and conduct of genome-wide association meta-analyses von Winkler, Thomas W, Day, Felix R, Croteau-Chonka, Damien C, Wood, Andrew R, Locke, Adam E, Mägi, Reedik, Ferreira, Teresa, Fall, Tove, Graff, Mariaelisa, Justice, Anne E, Luan, Jian'an, Gustafsson, Stefan, Randall, Joshua C, Vedantam, Sailaja, Workalemahu, Tsegaselassie, Kilpeläinen, Tuomas O, Scherag, André, Esko, Tonu, Kutalik, Zoltán, Heid, Iris M, Loos, Ruth J F

Volltext

Low-Frequency and Rare-Coding Variation Contributes to Multiple Sclerosis Risk von Patsopoulos, Nikolaos A., Beecham, Ashley H., Goris, An, Dubois, Bénédicte, D’hooghe, Marie B., Van Damme, Philip, Søndergaard, Helle Bach, Sellebjerg, Finn, Ullum, Henrik, Thørner, Lise W., Werge, Thomas, Damotte, Vincent, Fontaine, Bertrand, Lathrop, Mark, Gourraud, Pierre-Antoine, Pongratz, Viola, Gasperi, Christiane, Bayas, Antonios, Heesen, Christoph, Linker, Ralf, Paul, Friedemann, Stangel, Martin, Tackenberg, Björn, Bergh, Florian Then, Wildemann, Brigitte, Tumani, Hayrettin, Gold, Ralf, Grummel, Verena, Knier, Benjamin, Lill, Christina M., Dardiotis, Efthimios, Agliardi, Cristina, Barizzone, Nadia, Mascia, Elisabetta, Bernardinelli, Luisa, Cusi, Daniele, Ferrè, Laura, Comi, Cristoforo, Galimberti, Daniela, Leone, Maurizio A., Mescheriakova, Julia, Hintzen, Rogier, van Duijn, Cornelia, Teunissen, Charlotte E., Bos, Steffan D., Myhr, Kjell-Morten, Celius, Elisabeth G., Lie, Benedicte A., Comabella, Manuel, Montalban, Xavier, Alfredsson, Lars, Stridh, Pernilla, Hillert, Jan, Piehl, Fredrik, Jelčić, Ilijas, Martin, Roland, Sospedra, Mireia, Hawkins, Clive, Hysi, Pirro, Karpe, Fredrik, Khadake, Jyoti, Lachance, Genevieve, Neville, Matthew, Santaniello, Adam, Caillier, Stacy J., Calabresi, Peter A., Cross, Anne, Davis, Mary F., de Bakker, Paul I.W., Delgado, Silvia, Dembele, Marieme, Edwards, Keith, Fitzgerald, Kathryn C., Hakonarson, Hakon, Konidari, Ioanna, Lathi, Ellen, Manrique, Clara P., Pericak-Vance, Margaret A., Piccio, Laura, Schaefer, Cathy, McCabe, Cristin, Hadjigeorgiou, Georgios, Taylor, Bruce, Tajouri, Lotti, Charlesworth, Jac, Booth, David R., Harbo, Hanne F., Ivinson, Adrian J., Hauser, Stephen L., Compston, Alastair, Stewart, Graeme, Zipp, Frauke, Barcellos, Lisa F., Baranzini, Sergio E., Martinelli-Boneschi, Filippo, Ziegler, Andreas, McCauley, Jacob L., Sawcer, Stephen J., De Jager, Philip L., Kockum, Ingrid

Volltext

Identification of risk loci for primary aldosteronism in genome-wide association studies von Le Floch, Edith, Cosentino, Teresa, Larsen, Casper K., Beuschlein, Felix, Reincke, Martin, Amar, Laurence, Rossi, Gian-Paolo, De Sousa, Kelly, Baron, Stéphanie, Chantalat, Sophie, Saintpierre, Benjamin, Lenzini, Livia, Frouin, Arthur, Giscos-Douriez, Isabelle, Ferey, Matthis, Abdellatif, Alaa B., Meatchi, Tchao, Empana, Jean-Philippe, Jouven, Xavier, Gieger, Christian, Waldenberger, Melanie, Peters, Annette, Cusi, Daniele, Salvi, Erika, Meneton, Pierre, Touvier, Mathilde, Deschasaux, Mélanie, Druesne-Pecollo, Nathalie, Boulkroun, Sheerazed, Fernandes-Rosa, Fabio L., Deleuze, Jean-François, Jeunemaitre, Xavier, Zennaro, Maria-Christina

Volltext

Targeting pheochromocytoma/paraganglioma with polyamine inhibitors von Rai, Sudhir Kumar, Bril, Fernando, Hatch, Heather M., Xu, Yiling, Shelton, Laura, Kalavalapalli, Srilaxmi, Click, Arielle, Lee, Douglas, Beecher, Chris, Kirby, Austin, Kong, Kimi, Trevino, Jose, Jha, Abhishek, Jatav, Shashank, Kriti, Kriti, Luthra, Soumya, Garrett, Timothy J., Guingab-Cagmat, Joy, Plant, Daniel, Bose, Prodip, Cusi, Kenneth, Hromas, Robert A., Tischler, Arthur S., Powers, James F., Gupta, Priyanka, Bibb, James, Beuschlein, Felix, Robledo, Mercedes, Calsina, Bruna, Timmers, Henri, Taieb, David, Kroiss, Matthias, Richter, Susan, Langton, Katharina, Eisenhofer, Graeme, Bergeron, Raymond, Pacak, Karel, Tevosian, Sergei G., Ghayee, Hans K.

Volltext

THU612 SDHx Pheochromocytoma/Paraganglioma Has Elevation Of Arginine And Lysine Metabolites von Ghayee, Hans Kumar, Richter, Susan, Bechmann, Nicole, Kalavalapalli, Srilaxmi, Joy, Guingab-Cagmat, Xu, Yiling, Cusi, Kenneth, Tischler, Arthur, Powers, James F, Beuschlein, Felix, Robledo, Mercedes, Fliedner, Steffi, Quinkler, Marcus, Fassnacht, Martin, Timmers, Henri, Pacak, Karel, Eisenhofer, Graeme, Garrett, Timothy J

Volltext

Low-Frequency and Rare-Coding Variation Contributes to Multiple Sclerosis Risk von Patsopoulos, Nikolaos A., Beecham, Ashley H., Goris, An, Dubois, Bénédicte, D’hooghe, Marie B., Van Damme, Philip, Søndergaard, Helle Bach, Sellebjerg, Finn, Ullum, Henrik, Thørner, Lise W., Werge, Thomas, Damotte, Vincent, Fontaine, Bertrand, Lathrop, Mark, Gourraud, Pierre-Antoine, Pongratz, Viola, Gasperi, Christiane, Bayas, Antonios, Heesen, Christoph, Linker, Ralf, Paul, Friedemann, Stangel, Martin, Tackenberg, Björn, Bergh, Florian Then, Wildemann, Brigitte, Tumani, Hayrettin, Gold, Ralf, Grummel, Verena, Knier, Benjamin, Lill, Christina M., Dardiotis, Efthimios, Agliardi, Cristina, Barizzone, Nadia, Mascia, Elisabetta, Bernardinelli, Luisa, Cusi, Daniele, Ferrè, Laura, Comi, Cristoforo, Galimberti, Daniela, Leone, Maurizio A., Mescheriakova, Julia, Hintzen, Rogier, van Duijn, Cornelia, Teunissen, Charlotte E., Bos, Steffan D., Myhr, Kjell-Morten, Celius, Elisabeth G., Lie, Benedicte A., Comabella, Manuel, Montalban, Xavier, Alfredsson, Lars, Stridh, Pernilla, Hillert, Jan, Piehl, Fredrik, Jelčić, Ilijas, Martin, Roland, Sospedra, Mireia, Hawkins, Clive, Hysi, Pirro, Karpe, Fredrik, Khadake, Jyoti, Lachance, Genevieve, Neville, Matthew, Santaniello, Adam, Caillier, Stacy J., Calabresi, Peter A., Cross, Anne, Davis, Mary F., de Bakker, Paul I.W., Delgado, Silvia, Dembele, Marieme, Edwards, Keith, Fitzgerald, Kathryn C., Hakonarson, Hakon, Konidari, Ioanna, Lathi, Ellen, Manrique, Clara P., Pericak-Vance, Margaret A., Piccio, Laura, Schaefer, Cathy, McCabe, Cristin, Hadjigeorgiou, Georgios, Taylor, Bruce, Tajouri, Lotti, Charlesworth, Jac, Booth, David R., Harbo, Hanne F., Ivinson, Adrian J., Hauser, Stephen L., Compston, Alastair, Stewart, Graeme, Zipp, Frauke, Barcellos, Lisa F., Baranzini, Sergio E., Martinelli-Boneschi, Filippo, Ziegler, Andreas, McCauley, Jacob L., Sawcer, Stephen J., De Jager, Philip L., Kockum, Ingrid

Volltext

Low-Frequency and Rare-Coding Variation Contributes to Multiple Sclerosis Risk von Patsopoulos, Nikolaos A., Beecham, Ashley H., Goris, An, Dubois, Bénédicte, D’hooghe, Marie B., Van Damme, Philip, Søndergaard, Helle Bach, Sellebjerg, Finn, Ullum, Henrik, Thørner, Lise W., Werge, Thomas, Damotte, Vincent, Fontaine, Bertrand, Lathrop, Mark, Gourraud, Pierre-Antoine, Pongratz, Viola, Gasperi, Christiane, Bayas, Antonios, Heesen, Christoph, Linker, Ralf, Paul, Friedemann, Stangel, Martin, Tackenberg, Björn, Bergh, Florian Then, Wildemann, Brigitte, Tumani, Hayrettin, Gold, Ralf, Grummel, Verena, Knier, Benjamin, Lill, Christina M., Dardiotis, Efthimios, Agliardi, Cristina, Barizzone, Nadia, Mascia, Elisabetta, Bernardinelli, Luisa, Cusi, Daniele, Ferrè, Laura, Comi, Cristoforo, Galimberti, Daniela, Leone, Maurizio A., Mescheriakova, Julia, Hintzen, Rogier, van Duijn, Cornelia, Teunissen, Charlotte E., Bos, Steffan D., Myhr, Kjell-Morten, Celius, Elisabeth G., Lie, Benedicte A., Comabella, Manuel, Montalban, Xavier, Alfredsson, Lars, Stridh, Pernilla, Hillert, Jan, Piehl, Fredrik, Jelčić, Ilijas, Martin, Roland, Sospedra, Mireia, Hawkins, Clive, Hysi, Pirro, Karpe, Fredrik, Khadake, Jyoti, Lachance, Genevieve, Neville, Matthew, Santaniello, Adam, Caillier, Stacy J., Calabresi, Peter A., Cross, Anne, Davis, Mary F., de Bakker, Paul I.W., Delgado, Silvia, Dembele, Marieme, Edwards, Keith, Fitzgerald, Kathryn C., Hakonarson, Hakon, Konidari, Ioanna, Lathi, Ellen, Manrique, Clara P., Pericak-Vance, Margaret A., Piccio, Laura, Schaefer, Cathy, McCabe, Cristin, Hadjigeorgiou, Georgios, Taylor, Bruce, Tajouri, Lotti, Charlesworth, Jac, Booth, David R., Harbo, Hanne F., Ivinson, Adrian J., Hauser, Stephen L., Compston, Alastair, Stewart, Graeme, Zipp, Frauke, Barcellos, Lisa F., Baranzini, Sergio E., Martinelli-Boneschi, Filippo, Ziegler, Andreas, McCauley, Jacob L., Sawcer, Stephen J., De Jager, Philip L., Kockum, Ingrid

Volltext

Multiple sclerosis genomic map implicates peripheral immune cells and microglia in susceptibility von Patsopoulos, Nikolas A, Baranzini, Sergio E, Santaniello, Adams, Shoostari, Parisa, Cotsapas, Chris, Wong, Garrett, Beecham, Ashley H, James, Tojo, Replogle, Joseph, Vlachos, Ioannis S, McCabe, Cristin, Pers, Tune H, Brandes, Aaron, White, Charles, Keenan, Brendan, Cimpean, Maria, Winn, Phoebe, Panteliadis, Ioannis-Pavlos, Robbins, Allison, Andlauer, Till F.M, Zarzycki, Onigiusz, Dubois, Bénédicte, Goris, An, Sondergaard, Helle Bach, Sellebjerg, Finn, Sorensen, Per Soelberg, Ullum, Henrik, Thorner, Lise Wegner, Saarela, Janna, Cournu-Rebeix, Isabelle, Damotte, Vincent, Fontaine, Bertrand, Guillot-Noel, Lena, Lathrop, Mark, Vukusic, Sandra, Berthele, Achim, Pongratz, Viola, Gasperi, Christiane, Graetz, Christiane, Grummel, Verena, Hemmer, Bernhard, Hoshi, Muni, Knier, Benjamin, Korn, Thomas, Lill, Christina M, Luessi, Felix, Muehlau, Mark, Zipp, Frauke, Dardiotis, Efthimios, Agliardi, Cristina, Amoroso, Antonio, Barizzone, Nadia, Benedetti, Maria D, Bernardinelli, Luisa, Cavalla, Paola, Clarelli, Ferdinando, Comi, Giancarlo, Cusi, Daniele, Esposito, Federica, Ferre, Laura, Galimberti, Daniela, Guaschino, Clara, Leone, Maurizio A, Martinelli, Vittorio, Moiola, Lucia, Salvetti, Marco, Sorosina, Melissa, Vecchio, Domizia, Zauli, Andrea, Santoro, Silvia, Mancini, Nicasio, Zuccala, Miriam, Mescheriakova, Julia, van Duijn, Cornelia, Bos, Steffan D, Celius, Elisabeth G, Spurkland, Anne, Comabella, Manuel, Montalban, Xavier, Alfredsson, Lars, Bomfim, Izaura L, Gomez-Cabrero, David, Hillert, Jan, Jagodic, Maja, Linden, Magdalena, Piehl, Fredrik, Jelcic, Ilijas, Martin, Roland, Sospedra, Mirela, Baker, Amie, Ban, Maria, Hawkins, Clive, Hysi, Pirro, Kalra, Seema, Karpe, Fredrik, Khadake, Jyoti, Lachance, Genevieve, Molyneux, Paul, Neville, Matthew, Thorpe, John

Volltext

Low-Frequency and Rare-Coding Variation Contributes to Multiple Sclerosis Risk von Int Multiple Sclerosis Genetics, Mitrovic, Mitja, Patsopoulos, Nikoloas, Beecham, Ashley, Dankowski, Theresa, Goris, An, Dubois, Bénédicte, D'hooghe, Marie B, Lemmens, Robin, Van Damme, Philip, Bach Sondergaard, Helle, Sellebjerg, Finn, Soelberg Sorensen, Per, Ullum, Henrik, Thorner, Lise W, Werge, Thomas, Saarela, Janna, Cournu-Rebeix, Isabelle, Damotte, Vincent, Fontaine, Bertrand, Guillot-Noel, Lena, Lathrop, Mark, Vukusik, Sandra, Gourraud, Pierre-Antoine, Andlauer, Till F.M, Pongratz, Viola, Buck, Dorothea, Gasperi, Christiane, Bayas, Antonios, Heesen, Christoph, Kümpfel, Tania, Linker, Ralf, Friedemann, Paul, Stangel, Martin, Tackenberg, Björn, Then Bergh, Florian, Warnke, Clemens, Wiendl, Heinz, Wildemann, Brigitte, Zettl, Uwe, Ziemann, Ulf, Tumani, Hayrettin, Gold, Ralf, Grummel, Verena, Hemmer, Bernhard, Knier, Benjamin, Lill, Christina, Luessi, Felix, Dardiotis, Efthimios, Agliardi, Cristina, Barizzone, Nadia, Mascia, Elisabetta, Bernardinelli, Luisa, Comi, Giancarlo, Cusi, Daniele, Esposito, Federica, Ferrè, Laura, Comi, Cristoforo, Galimberti, Daniela, Leone, Maurizio A, Sorosina, Melissa, Mescheriakova, Julia, Hintzen, Rogier, van Duijn, Cornelia, Theunissen, Charlotte E, Bos, Steffan D, Myhr, Kjell-Morten, Celius, Elisabeth G, Lie, Benedicte A, Spurkland, Anne, Comabella, Manuel, Montalban, Xavier, Alfredsson, Lars, Stridh, Pernilla, Hillert, Jan, Jagodic, Maja, Piehl, Fredrik, Jelcic, Ilijas, Martin, Roland, Sospedra, Mireia, Ban, Maria, Hawkins, Clive, Hysi, Pirro, Kalra, Seema, Karpe, Fredrik, Khadake, Jyoti, Lachance, Genevieve, Neville, Matthew, Santaniello, Adam, Caillier, Stacy J, Calavresi, Peter A, Cree, Bruce A.C, Cross, Anne, Davis, Mary F, Haines, Jonathan L, de Bakker, Paul I.W, Delgado, Silvia, Dembele, Marieme, Edwards, Keith, Fitzgerald, Kathryn C

Volltext

Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals von Winkler, Thomas W, Rasheed, Humaira, Teumer, Alexander, Gorski, Mathias, Rowan, Bryce X, Stanzick, Kira J, Thomas, Laurent F, Tin, Adrienne, Hoppmann, Anselm, Chu, Audrey Y, Tayo, Bamidele, Thio, Chris H L, Cusi, Daniele, Chai, Jin-Fang, Sieber, Karsten B, Horn, Katrin, Li, Man, Scholz, Markus, Cocca, Massimiliano, Wuttke, Matthias, van der Most, Peter J, Yang, Qiong, Ghasemi, Sahar, Nutile, Teresa, Li, Yong, Pontali, Giulia, Günther, Felix, Dehghan, Abbas, Correa, Adolfo, Parsa, Afshin

Volltext

Genetic loci associated with heart rate variability and their effects on cardiac disease risk von Nolte, Ilja M, Tragante, Vinicius, Amare, Azmeraw T, Jansen, Rick, Vaez, Ahmad, Von Der Heyde, Benedikt, Avery, Christy L, Bis, Joshua C, Dierckx, Bram, van Dongen, Jenny, Gogarten, Stephanie M, Hernesniemi, Jussi, Hwang, Shih-Jen, Jaju, Deepali, Kerr, Kathleen F, Kluttig, Alexander, Krijthe, Bouwe P, Kumar, Jitender, Van Der Laan, Sander W, Maihofer, Adam X, van der Most, Peter J, Müller-Nurasyid, Martina, Nivard, Michel G, Salvi, Erika, Thayer, Julian F, Zabaneh, Delilah, Zafarmand, Mohammad Hadi, Abdellaoui, Abdel, Ashar, Foram N, Axelsson, Tomas, Baker, Dewleen G, Bayoumi, Riad, Boomsma, Dorret I, Ehret, George B, Franco, Oscar H, Gademan, Maaike G.J, Geyer, Mark A, Hemerich, Daiane, Hottenga, Jouke-Jan, Huikuri, Heikki V, Hutri-Kähönen, Nina, Junttila, Juhani, Juonala, Markus, Kiviniemi, Antti M, Kumari, Meena, Kuznetsova, Tatiana, Laurie, Cathy C, Li, Yun R, Limacher, Marian C, Lin, Henry J, Mahajan, Anubha, McKnight, Barbara, Meyer Zu Schwabedissen, Henriette, Nalls, Mike A, Nikus, Kjell, North, Kari E, Ormel, Johan, Perz, Siegfried, Peters, Annette, Psaty, Bruce M, Raitakari, Olli T, Risbrough, Victoria B, Sinner, Moritz F, Siscovick, David S, Smith, Nicholas L, Soliman, Elsayed Z, Staessen, Jan A, Stein, Phyllis K, Strauch, Konstantin, Sundström, Johan, Swenne, Cees A, Syvänen, Ann-Christine, Tardif, Jean-Claude, Thornton, Timothy A, Tinker, Lesley E, Uitterlinden, André G, Van Setten, Jessica, Voss, Andreas, Waldenberger, Melanie, Wilhelmsen, Kirk C, Wong, Quenna, Zonderman, Alan B, Cusi, Daniele, van der Harst, Pim, Hassan, Mohammad, Kääb, Stefan, Kähönen, Mika, Lehtimäki, Terho, Lind, Lars, Oldehinkel, Albertine J, Reiner, Alexander P, Riese, Harriëtte, Rioux, John D, Rotter, Jerome I, Stricker, Bruno H, Vrijkotte, Tanja G M, Asselbergs, Folkert W, Brundel, Bianca J.J.M, Heckbert, Susan R, den Hoed, Marcel

Volltext

Genetic loci associated with heart rate variability and their effects on cardiac disease risk von Nolte, IM, Tragante, V, Amare, AT, Jansen, R, Vaez, A, Von der Heyde, B, Avery, CL, Dierckx, B, Van Dongen, J, Gogarten, SM, Goyette, P, Huikari, V, Hwang, S-J, Jaju, D, Kerr, KF, Krijthe, BP, Kumar, J, Maihofer, AX, Minassian, A, Van der Most, PJ, Nivard, M, Verweij, N, Zabaneh, D, Albarwani, S, Albert, C, Axelsson, T, Baker, DG, De Bakker, PIW, Bayoumi, R, Bieringa, RJ, Boucher, G, Dietrich, A, Ehret, GB, Ellinor, PT, Felix, JF, Floras, JS, Friberg, P, Geyer, MA, Giedraitis, V, Hartman, CA, Hofman, A, Juonala, M, Kumari, M, Kuznetsova, T, Laurie, CC, Lefrandt, JD, Liao, D, Limacher, MC, Lin, HJ, Mahajan, A, Zu Schwabedissen, HM, Milaneschi, Y, Mononen, N, Morris, AP, Nalls, MA, Neijts, M, Nikus, K, O'Connor, DT, Peters, A, Raitakari, OT, Risbrough, VB, Siscovick, D, Smit, JH, Smith, NL, Soliman, EZ, Staessen, JA, Stein, PK, Sundstrom, J, Swenne, CA, Tardif, J-C, Taylor, KD, Teumer, A, Thornton, TA, Van Setten, J, Waldenberger, M, Wilhelmsen, KC, Willemsen, G, Wong, Q, Zhang, Z-M, Zonderman, AB, Cusi, D, Evans, MK, Ingelsson, E, Jarvelin, M-R, Lehtimaki, T, Lind, L, Nievergelt, CM, O'Donnell, CJ, Oldehinkel, AJ, Penninx, B, Reiner, AP, Riese, H, Van Roon, AM, Rioux, JD, Rotter, JI, Vrijkotte, TGM, Asselbergs, FW, Den Hoed, M, Snieder, H, De Geus, EJC

Volltext

MON-199 Targeting Pheochromocytoma/Paraganglioma with Polyamine Inhibitors von Ghayee, Hans Kumar, Rai, Sudhir, Bril, Fernando, Hatch, Heather, Xu, Yiling, Kalavalapalli, Srilaxami, Garrett, Timothy, Plant, Dan, Bose, Prodip, Hromas, Robert, Cusi, Kenneth, Tischler, Arthur, Gupta, Priyanaka, Bibb, James, Beuschlein, Felix, Robledo, Mercedes, Calsina, Bruna, Timmers, Henri, Taieb, David, Kroiss, Matthias, Richter, Susan, Eisenhofer, Graeme, Bergeron, Raymond, Pacak, Karel, Tevosian, Sergei G

Volltext

Identification of risk loci for primary aldosteronism in genome-wide association studies von Le Floch, Edith, Cosentino, Teresa, Larsen, Casper K, Beuschlein, Felix, Reincke, Martin, Amar, Laurence, Rossi, Gian-Paolo, De Sousa, Kelly, Baron, Stéphanie, Chantalat, Sophie, Saintpierre, Benjamin, Lenzini, Livia, Frouin, Arthur, Giscos-Douriez, Isabelle, Ferey, Matthis, Abdellatif, Alaa B, Meatchi, Tchao, Empana, Jean-Philippe, Jouven, Xavier, Gieger, Christian, Waldenberger, Melanie, Peters, Annette, Cusi, Daniele, Salvi, Erika, Meneton, Pierre, Touvier, Mathilde, Deschasaux, Mélanie, Druesne-Pecollo, Nathalie, Boulkroun, Sheerazed, Fernandes-Rosa, Fabio L, Deleuze, Jean-François, Jeunemaitre, Xavier, Zennaro, Maria-Christina

Volltext bestellen