Ngā hua rapu - Melchers, Inga

5HT(2A )polymorphism His452Tyr in a German Caucasian systemic sclerosis population mā Kirsten, Holger, Burkhardt, Jana, Hantmann, Helene, Hunzelmann, Nico, Vaith, Peter, Ahnert, Peter, Melchers, Inga

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High frequency of corticosteroid and immunosuppressive therapy in patients with systemic sclerosis despite limited evidence for efficacy mā Hunzelmann, Nicolas, Moinzadeh, Pia, Genth, Ekkehard, Krieg, Thomas, Lehmacher, Walter, Melchers, Inga, Meurer, Michael, Müller-Ladner, Ulf, Olski, Thorsten M, Pfeiffer, Christiane, Riemekasten, Gabriela, Schulze-Lohoff, Eckhard, Sunderkoetter, Cord, Weber, Manfred

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Myelin Basic Protein as a Novel Genetic Risk Factor in Rheumatoid Arthritis—A Genome-Wide Study Combined with Immunological Analyses mā Terao, Chikashi, Ohmura, Koichiro, Katayama, Masaki, Takahashi, Meiko, Kokubo, Miki, Diop, Gora, Toda, Yoshinobu, Yamamoto, Natsuki, Shinkura, Reiko, Shimizu, Masakazu, Gut, Ivo, Heath, Simon, Melchers, Inga, Manabe, Toshiaki, Lathrop, Mark, Mimori, Tsuneyo, Yamada, Ryo, Matsuda, Fumihiko

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Frequency of disease-associated and other nuclear autoantibodies in patients of the German network for systemic scleroderma: correlation with characteristic clinical features mā Mierau, Rudolf, Moinzadeh, Pia, Riemekasten, Gabriela, Melchers, Inga, Meurer, Michael, Reichenberger, Frank, Buslau, Michael, Worm, Margitta, Blank, Norbert, Hein, Rüdiger, Müller-Ladner, Ulf, Kuhn, Annegret, Sunderkötter, Cord, Juche, Aaron, Pfeiffer, Christiane, Fiehn, Christoph, Sticherling, Michael, Lehmann, Percy, Stadler, Rudolf, Schulze-Lohoff, Eckhard, Seitz, Cornelia, Foeldvari, Ivan, Krieg, Thomas, Genth, Ekkehard, Hunzelmann, Nicolas

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Disease progression in systemic sclerosis-overlap syndrome is significantly different from limited and diffuse cutaneous systemic sclerosis mā Moinzadeh, Pia, Aberer, Elisabeth, Ahmadi-Simab, Keihan, Blank, Norbert, Distler, Joerg H W, Fierlbeck, Gerhard, Genth, Ekkehard, Guenther, Claudia, Hein, Ruediger, Henes, Joerg, Herich, Lena, Herrgott, Ilka, Koetter, Ina, Kreuter, Alexander, Krieg, Thomas, Kuhr, Kathrin, Lorenz, Hanns-Martin, Meier, Florian, Melchers, Inga, Mensing, Hartwig, Mueller-Ladner, Ulf, Pfeiffer, Christiane, Riemekasten, Gabriela, Sárdy, Miklós, Schmalzing, Marc, Sunderkoetter, Cord, Susok, Laura, Tarner, Ingo H, Vaith, Peter, Worm, Margitta, Wozel, Gottfried, Zeidler, Gabriele, Hunzelmann, Nicolas

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Genome-Wide Scan Identifies TNIP1, PSORS1C1, and RHOB as Novel Risk Loci for Systemic Sclerosis mā Allanore, Yannick, Saad, Mohamad, Dieudé, Philippe, Avouac, Jérôme, Distler, Jorg H. W., Amouyel, Philippe, Matucci-Cerinic, Marco, Riemekasten, Gabriella, Airo, Paolo, Melchers, Inga, Hachulla, Eric, Cusi, Daniele, Wichmann, H.-Erich, Wipff, Julien, Lambert, Jean-Charles, Hunzelmann, Nicolas, Tiev, Kiet, Caramaschi, Paola, Diot, Elisabeth, Kowal-Bielecka, Otylia, Valentini, Gabriele, Mouthon, Luc, Czirják, László, Damjanov, Nemanja, Salvi, Erika, Conti, Costanza, Müller, Martina, Müller-Ladner, Ulf, Riccieri, Valeria, Ruiz, Barbara, Cracowski, Jean-Luc, Letenneur, Luc, Dupuy, Anne Marie, Meyer, Oliver, Kahan, André, Munnich, Arnold, Boileau, Catherine, Martinez, Maria

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Defective removal of ribonucleotides from DNA promotes systemic autoimmunity mā Günther, Claudia, Kind, Barbara, Reijns, Martin A.M., Berndt, Nicole, Martinez-Bueno, Manuel, Wolf, Christine, Tüngler, Victoria, Chara, Osvaldo, Lee, Young Ae, Hübner, Norbert, Bicknell, Louise, Blum, Sophia, Krug, Claudia, Schmidt, Franziska, Kretschmer, Stefanie, Koss, Sarah, Astell, Katy R., Ramantani, Georgia, Bauerfeind, Anja, Morris, David L., Cunninghame Graham, Deborah S., Bubeck, Doryen, Leitch, Andrea, Ralston, Stuart H., Blackburn, Elizabeth A., Gahr, Manfred, Witte, Torsten, Vyse, Timothy J., Melchers, Inga, Mangold, Elisabeth, Nöthen, Markus M., Aringer, Martin, Kuhn, Annegret, Lüthke, Kirsten, Unger, Leonore, Bley, Annette, Lorenzi, Alice, Isaacs, John D., Alexopoulou, Dimitra, Conrad, Karsten, Dahl, Andreas, Roers, Axel, Alarcon-Riquelme, Marta E., Jackson, Andrew P., Lee-Kirsch, Min Ae

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Transethnic meta-analysis identifies GSDMA and PRDM1 as susceptibility genes to systemic sclerosis mā Terao, Chikashi, Kawaguchi, Takahisa, Dieude, Philippe, Varga, John, Kuwana, Masataka, Hudson, Marie, Kawaguchi, Yasushi, Matucci-Cerinic, Marco, Ohmura, Koichiro, Riemekasten, Gabriela, Kawasaki, Aya, Airo, Paolo, Horita, Tetsuya, Oka, Akira, Hachulla, Eric, Yoshifuji, Hajime, Caramaschi, Paola, Hunzelmann, Nicolas, Baron, Murray, Atsumi, Tatsuya, Hassoun, Paul, Torii, Takeshi, Takahashi, Meiko, Tabara, Yasuharu, Shimizu, Masakazu, Tochimoto, Akiko, Ayuzawa, Naho, Yanagida, Hidetoshi, Furukawa, Hiroshi, Tohma, Shigeto, Hasegawa, Minoru, Fujimoto, Manabu, Ishikawa, Osamu, Yamamoto, Toshiyuki, Goto, Daisuke, Asano, Yoshihide, Jinnin, Masatoshi, Endo, Hirahito, Takahashi, Hiroki, Takehara, Kazuhiko, Sato, Shinichi, Ihn, Hironobu, Raychaudhuri, Soumya, Liao, Katherine, Gregersen, Peter, Tsuchiya, Naoyuki, Riccieri, Valeria, Melchers, Inga, Valentini, Gabriele, Cauvet, Anne, Martinez, Maria, Mimori, Tsuneyo, Matsuda, Fumihiko, Allanore, Yannick

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