Phenotype of Arylsulfatase A-Deficient Mice: Relationship to Human Metachromatic Leukodystrophy von Hess, Barbara, Saftig, Paul, Hartmann, Dieter, Coenen, Ruth, Lullmann-Rauch, Renate, Goebel, Hans H., Evers, Meike, Von Figura, Kurt, D'Hooge, Rudi, Nagels, Guy, De Deyn, Peter, Peters, Christoph, Gieselmann, Volkmar

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Targeted Disruption of the Lysosomal α-Mannosidase Gene Results in Mice Resembling a Mild form of Human α-Mannosidosis von Stinchi, Sofia, Lüllmann-Rauch, Renate, Hartmann, Dieter, Coenen, Ruth, Beccari, Tommaso, Orlacchio, Aldo, von Figura, Kurt, Saftig, Paul

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Decline in brainstem auditory-evoked potentials coincides with loss of spiral ganglion cells in arylsulfatase A-deficient mice von D'Hooge, Rudi, Coenen, Ruth, Gieselmann, Volkmar, Lüllmann-Rauch, Renate, De Deyn, Peter P.

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Phenotype of arylsufatase A-deficient mice: Relationship to human metachromatic leukodystrophy von Hess, Barbara, Saftig, Paul, Hartmann, Dieter, Coenen, Ruth

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Targeted Disruption of the Lysosomal  -Mannosidase Gene Results in Mice Resembling a Mild form of Human  -Mannosidosis von Stinchi, S., Lullmann-Rauch, R., Hartmann, D., Coenen, R., Beccari, T., Orlacchio, A., von Figura, K., Saftig, P.

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Methine dyestuffs von MULLER WERNER, WEISSEL OSKAR, COENEN HELLA, COENEN RUTH, COENEN GERDA, RAUE RODERICH, COENEN BARBARA

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3-dimethyl-substituted indoline dyestuffs von MULLER WERNER, WEISSEL OSKAR, COENEN HELLA, COENEN RUTH, COENEN GERDA, RAUE RODERICH, COENEN BARBARA

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Mesolimbic Functional Magnetic Resonance Imaging Activations during Reward Anticipation Correlate with Reward-Related Ventral Striatal Dopamine Release von Schott, Bjorn H, Minuzzi, Luciano, Krebs, Ruth M, Elmenhorst, David, Lang, Markus, Winz, Oliver H, Seidenbecher, Constanze I, Coenen, Heinz H, Heinze, Hans-Jochen, Zilles, Karl, Duzel, Emrah, Bauer, Andreas

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Deep brain stimulation of the supero-lateral branch of the medial forebrain bundle does not lead to changes in personality in patients suffering from severe depression von Bewernick, Bettina H., Kilian, Hannah M., Schmidt, Klaudius, Reinfeldt, Ruth E., Kayser, Sarah, Coenen, Volker A., Markett, Sebastian, Schlaepfer, Thomas E.

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The PTPN22 R263Q polymorphism is a risk factor for rheumatoid arthritis in Caucasian case–control samples von Rodríguez‐Rodríguez, Luis, Taib, Wan Rohani Wan, Topless, Ruth, Steer, Sophia, González‐Escribano, María F., Balsa, Alejandro, Pascual‐Salcedo, Dora, González‐Gay, Miguel A., Raya, Enrique, Fernandez‐Gutierrez, Benjamín, González‐Álvaro, Isidoro, Bottini, Nunzio, Witte, Torsten, Viken, Marte K., Coenen, Marieke J. H., van Riel, Piet L. C. M., Franke, Barbara, den Heijer, Martin, Radstake, Timothy R. D. J., Wordsworth, Paul, Lie, Benedicte A., Merriman, Tony R., Martín, Javier

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Depletion of LAG‐3+ T Cells Translated to Pharmacology and Improvement in Psoriasis Disease Activity: A Phase I Randomized Study of mAb GSK2831781 von Ellis, Joanne, J.B. Marks, Daniel, Srinivasan, Naren, Barrett, Christine, Hopkins, Thomas G., Richards, Anna, Fuhr, Rainard, Albayaty, Muna, Coenen, Martin, Liefaard, Lia, Leavens, Karen, Nevin, Katherine L., Tang, Shuo, Hughes, Stephen A., Fortunato, Léa, Edwards, Ken, Cui, Yi, Anselm, Rabia, Delves, Christopher J., Charles, Emilie, Feeney, Maria, Webb, Thomas M., Brett, Sara J., Schmidt, Tim S., Stone, John, Savage, Caroline O.S., Wisniacki, Nicolas, Tarzi, Ruth M.

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Early Moves: a protocol for a population-based prospective cohort study to establish general movements as an early biomarker of cognitive impairment in infants von Elliott, Catherine, Alexander, Caroline, Salt, Alison, Spittle, Alicia J, Boyd, Roslyn N, Badawi, Nadia, Morgan, Catherine, Silva, Desiree, Geelhoed, Elizabeth, Ware, Robert S, Ali, Alishum, McKenzie, Anne, Bloom, David, Sharp, Mary, Ward, Roslyn, Bora, Samudragupta, Prescott, Susan, Woolfenden, Susan, Le, Vuong, Davidson, Sue-Anne, Thornton, Ashleigh, Finlay-Jones, Amy, Jensen, Lynn, Amery, Natasha, Valentine, Jane, Valentine, Jane, Salt, Alison, Silva, Desiree, Alexander, Caroline, Amery, Natasha, Coenen, Arlette, Morie, Rose, Moore, Jennifer, OConnor, Madeleine, Srinivasjois, Ravisha, Tan, Jason, Jongeling, Brad, Downie, Elayne, Last, Ruth, Sharp, Mary, Wray, John, Davidson, Sue-Anne, Thornton, Ashleigh

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Material deposition and migration processes with resonant magnetic perturbation fields at TEXTOR von Laengner, Ruth, Schmitz, O., Brezinsek, S., Coenen, J.W., Eich, T., Freisinger, M., Kirschner, A., Kreter, A., Möller, S., Laengner, M., Philipps, V., Pospieszczyk, A., Reimer, H., Samm, U., Wienhold, P.

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Erratum: The PTPN22 R263Q polymorphism is a risk factor for rheumatoid arthritis in Caucasian case–control samples von Rodríguez‐Rodríguez, Luis, Taib, Wan Rohani Wan, Topless, Ruth, Steer, Sophia, González‐Escribano, María F., Balsa, Alejandro, Pascual‐Salcedo, Dora, González‐Gay, Miguel A., Raya, Enrique, Fernandez‐Gutierrez, Benjamín, González‐Álvaro, Isidoro, Bottini, Nunzio, Witte, Torsten, Viken, Marte K., Coenen, Marieke J. H., van Riel, Piet L. C. M., Franke, Barbara, den Heijer, Martin, Radstake, Timothy R. D. J., Wordsworth, Paul, Lie, Benedicte A., Merriman, Tony R., Martín, Javier

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Report on the Annual Meeting of the Study Groups 'Host-Parasite Interactions' and 'Mycology' 2010 von Albarouki, Emad, Deising, Holger B., Djulic, Alma, Vögele, Ralf T., Campe, Ruth, Schaffrath, Ulrich, Conrath, Uwe, Göllner, Katharina, Delventhal, Rhoda, Zellerhoff, Nina, Mogga, Valerie, Weidenbach, Denise, Andresen, Karsten, Thines, Eckhard, Langenbach, Caspar, Löhrer, Marco, Botterweck, Marco, Behr, Michael, Humbeck, Klaus, Hause, Gerd, Motyka, Vaclav, Wirsel, Stefan G.R., Leroch, Michaela, Kleber, Astrid, Coenen, Bettina, Peter, Christine, Hahn, Matthias, Beninweck, Ndambi, Heller, Annerose, Elzein, Abuelgasim, Cadisch, Georg, Neumann, Martin, Beckers, Gerold, Jaskiewicz, Michal, Liu, Yidong, Zhang, Shuqun, Pretsch, Klara, Geiger, Matthias, Kernen, Ariane, Kernen, Eric, Mendgen, Kurt, Voegele, Ralf Thomas, Treitschke, Steffi, Döhlemann, Gunther, Schuster, Martin, Martín-Urdíroz, Magdalena, Steinberg, Gero, Lang, Patrick, Link, Tobias, Voegele, Ralf T., Andrade, Diana, Rexer, Karl-Heinz, Kost, Gerhard, Restrepo, Silvia, Grosch, Rita, de Garcia, Maria Caridad Cepero, Maximova, Eugenia, Krumbein, Angelika, Franken, Philipp, Bogs, Carolin, Wielgoss, Anna, Nechwatal, Jan, Farahani-Kofoet, Roxana Djalali, Römer, Peter, Kofoet, Andreas, Hegebarth, Daniela, Stammler, Gerd, Trück, Thomas, Spring, Otmar

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The genetic architecture of membranous nephropathy and its potential to improve non-invasive diagnosis von Liu, Lili, Mladkova, Nikol, Li, Yifu, Ren, Hong, Wang, Weiming, Cui, Zhao, Lin, Li, Yu, Xialian, Xu, Jing, Sidore, Carlo, Balderes, Olivia, Rosen, Raphael J, Zanoni, Francesca, Zhang, Jun Y, Marasa, Maddalena, Khan, Atlas, Ozay, Fatih, Canetta, Pietro A, Bomback, Andrew S, Appel, Gerald B, Sanna-Cherchi, Simone, Mariani, Laura H, Perkowska-Ptasinska, Agnieszka, Durlik, Magdalena, Mucha, Krzysztof, Moszczuk, Barbara, Foroncewicz, Bartosz, Pączek, Leszek, Habura, Ireneusz, Ars, Elisabet, Ballarín Castan, José Aurelio, Mani, Laila-Yasmin, Vogt, Bruno, Yildiz, Abdülmecit, Arikan, Hakki, Basturk, Taner, Karahan, Gonca, Akgul, Sebahat Usta, Sever, Mehmet Sukru, Zhang, Dan, Santoro, Domenico, Bonomini, Mario, Londrino, Francesco, Gesualdo, Loreto, Reiterova, Jana, Tesar, Vladimir, Izzi, Claudia, Savoldi, Silvana, Spotti, Donatella, Messa, Piergiorgio, Galliani, Marco, Roccatello, Dario, Zaza, Gianluigi, Lugani, Francesca, Ghiggeri, GianMarco, Pisani, Isabella, Allegri, Landino, Sprangers, Ben, Park, Jin-Ho, Cho, BeLong, Kim, Yon Su, Kim, Dong Ki, Suzuki, Hitoshi, Amoroso, Antonio, Cattran, Daniel C, Fervenza, Fernando C, Pani, Antonello, Hamilton, Patrick, Harris, Shelly, Gupta, Sanjana, Cheshire, Chris, Dufek, Stephanie, Issler, Naomi, Connolly, John, Stanescu, Horia C, Kenny, Eimear E, Wuttke, Matthias, Eckardt, Kai-Uwe, Köttgen, Anna, Hofstra, Julia M, Coenen, Marieke J. H, Kiemeney, Lambertus A, Kretzler, Matthias, Beck, Lawrence H, Debiec, Hanna, Ronco, Pierre, Wetzels, Jack F. M, Zoledziewska, Magdalena, Cucca, Francesco, Ionita-Laza, Iuliana, Lee, Hajeong, Hoxha, Elion, Stahl, Rolf A. K, Scolari, Francesco, Zhao, Ming-hui, Gharavi, Ali, Kleta, Robert, Chen, Nan, Kiryluk, Krzysztof, Universitat Autònoma de Barcelona

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The genetic architecture of membranous nephropathy and its potential to improve non-invasive diagnosis von Liu, Lili, Mladkova, Nikol, Li, Yifu, Ren, Hong, Wang, Weiming, Cui, Zhao, Lin, Li, Yu, Xialian, Xu, Jing, Sidore, Carlo, Balderes, Olivia, Rosen, Raphael J, Zanoni, Francesca, Zhang, Jun Y, Marasa, Maddalena, Khan, Atlas, Ozay, Fatih, Canetta, Pietro A, Bomback, Andrew S, Appel, Gerald B, Sanna-Cherchi, Simone, Mariani, Laura H, Perkowska-Ptasinska, Agnieszka, Durlik, Magdalena, Mucha, Krzysztof, Moszczuk, Barbara, Foroncewicz, Bartosz, Pączek, Leszek, Habura, Ireneusz, Ars, Elisabet, Ballarín Castan, José Aurelio, Mani, Laila-Yasmin, Vogt, Bruno, Yildiz, Abdülmecit, Arikan, Hakki, Basturk, Taner, Karahan, Gonca, Akgul, Sebahat Usta, Sever, Mehmet Sukru, Zhang, Dan, Santoro, Domenico, Bonomini, Mario, Londrino, Francesco, Gesualdo, Loreto, Reiterova, Jana, Tesar, Vladimir, Izzi, Claudia, Savoldi, Silvana, Spotti, Donatella, Messa, Piergiorgio, Galliani, Marco, Roccatello, Dario, Zaza, Gianluigi, Lugani, Francesca, Ghiggeri, GianMarco, Pisani, Isabella, Allegri, Landino, Sprangers, Ben, Park, Jin-Ho, Cho, BeLong, Kim, Yon Su, Kim, Dong Ki, Suzuki, Hitoshi, Amoroso, Antonio, Cattran, Daniel C, Fervenza, Fernando C, Pani, Antonello, Hamilton, Patrick, Harris, Shelly, Gupta, Sanjana, Cheshire, Chris, Dufek, Stephanie, Issler, Naomi, Connolly, John, Stanescu, Horia C, Kenny, Eimear E, Wuttke, Matthias, Eckardt, Kai-Uwe, Köttgen, Anna, Hofstra, Julia M, Coenen, Marieke J. H, Kiemeney, Lambertus A, Kretzler, Matthias, Beck, Lawrence H, Debiec, Hanna, Ronco, Pierre, Wetzels, Jack F. M, Zoledziewska, Magdalena, Cucca, Francesco, Ionita-Laza, Iuliana, Lee, Hajeong, Hoxha, Elion, Stahl, Rolf A. K, Scolari, Francesco, Zhao, Ming-hui, Gharavi, Ali G, Kleta, Robert, Chen, Nan, Kiryluk, Krzysztof, Universitat Autònoma de Barcelona

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