Items where Author or Editor is "Melchers, I." - Kölner UniversitätsPublikationsServer

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Number of items: 11.

Dieude, P., Bouaziz, M., Guedj, M., Riemekasten, G., Airo, P., Mueller, M., Cusi, D., Matucci-Cerinic, M., Melchers, I., Koenig, W., Salvi, E., Wichmann, H. E., Cuomo, G., Hachulla, E., Diot, E., Hunzelmann, N., Caramaschi, P., Mouthon, L., Riccieri, V., Distler, J., Tarner, I., Avouac, J., Meyer, O., Kahan, A., Chiocchia, G., Boileau, C. and Allanore, Y. (2011). Evidence of the contribution of the X chromosome to systemic sclerosis susceptibility: Association with the functional IRAK1 196Phe/532Ser haplotype. Arthritis Rheum., 63 (12). S. 3979 - 3988. HOBOKEN: WILEY. ISSN 1529-0131

Dieude, P., Guedj, M., Wipff, J., Ruiz, B., Riemekasten, G., Matucci-Cerinic, M., Melchers, I., Hachulla, E., Airo, P., Diot, E., Hunzelmann, N., Cabane, J., Mouthon, L., Cracowski, J. L., Riccieri, V., Distler, J., Meyer, O., Kahan, A., Boileau, C. and Allanore, Y. (2010). Association of the TNFAIP3 rs5029939 variant with systemic sclerosis in the European Caucasian population. Ann. Rheum. Dis., 69 (11). S. 1958 - 1965. LONDON: BMJ PUBLISHING GROUP. ISSN 1468-2060

Hunzelmann, N., Moinzadeh, P., Riemekasten, G., Becker, M., Kreuter, A., Mueller-Ladner, U., Meier, F., Wozel, G., Melchers, I., Srdy, M., Sunderkoetter, C., Herrgott, I., Graefenstein, K., Zeidler, G., Fierlbeck, G., Pfeiffer, C., Worm, M., Lee, H., Burkhardt, H., Koehm, M., Henes, J., Mensing, H., Kuhr, K. and Krieg, T. (2015). Low risk for digital ulcer development in SSc patients with increasing disease duration and lack of Scl-70 autoantibodies. Exp. Dermatol., 24 (3). S. E11 - 1. HOBOKEN: WILEY-BLACKWELL. ISSN 1600-0625

Hunzelmann, N., Riemekasten, G., Becker, M. O., Moinzadeh, P., Kreuter, A., Melchers, I., Mueller-Ladner, U., Meier, F., Worm, M., Lee, H., Herrgott, I., Pfeiffer, C., Fierlbeck, G., Henes, J., Juche, A., Zeidler, G., Mensing, H., Guenther, C., Sardy, M., Burkhardt, H., Koehm, M., Kuhr, K., Krieg, T. and Sunderkoetter, C. (2016). The Predict Study: low risk for digital ulcer development in patients with systemic sclerosis with increasing disease duration and lack of topoisomerase-1 antibodies. Br. J. Dermatol., 174 (6). S. 1384 - 1388. HOBOKEN: WILEY. ISSN 1365-2133

Hunzelmann, Nicolas, Riemekasten, G., Becker, M.O., Moinzadeh, Pia ORCID: 0000-0002-8784-8615, Kreuter, Alexander ORCID: 0000-0003-2275-499X, Melchers, I., Müller‐Ladner, Ulf, Meier, Friedegund ORCID: 0000-0003-4340-9706, Worm, Margitta ORCID: 0000-0002-3449-1245, Lee, H., Herrgott, I., Pfeiffer, C., Fierlbeck, G., Henes, J., Juche, A., Zeidler, G., Mensing, H., Günther, C., Sardy, Miklos ORCID: 0000-0003-4306-5093, Burkhardt, H., Koehm, M., Kuhr, K., Krieg, Thomas M. ORCID: 0000-0001-5616-8476 and Sunderkötter, C. (2016). The Predict Study: low risk for digital ulcer development in patients with systemic sclerosis with increasing disease duration and lack of topoisomerase‐1 antibodies. British Journal of Dermatology, 174 (6). pp. 1384-1387. Oxford University Press. ISSN 0007-0963

Moinzadeh, P., Aberer, E., Ahmadi-Simab, K., Blank, N., Distler, J. H. W., Fierlbeck, G., Genth, E., Guenther, C., Hein, R., Henes, J., Herich, L., Herrgott, I., Koetter, I., Kreuter, A., Krieg, T., Kuhr, K., Lorenz, H. -M., Meier, F., Melchers, I., Mensing, H., Mueller-Ladner, U., Pfeiffer, C., Riemekasten, G., Sardy, M., Schmalzing, M., Sunderkoetter, C., Susok, L., Tarner, I. H., Vaith, P., Worm, M., Wozel, G., Zeidler, G. and Hunzelmann, N. (2014). SSC-OVERLAP SYNDROMES: A DISTINCT CLINICAL SUBGROUP WITH SIGNIFICANT DIFFERENCES IN DISEASE PROGRESSION COMPARED TO LSSC AND DSSC PATIENTS. Clin. Exp. Rheumatol., 32 (2). S. S119 - 2. PISA: CLINICAL & EXPER RHEUMATOLOGY. ISSN 1593-098X

Moinzadeh, P., Aberer, E., Ahmadi-Simab, K., Blank, N., Distler, J. W., Fierlbeck, G., Genth, E., Guenther, C., Hein, R., Henes, J., Herich, L., Herrgott, I., Koetter, I., Kreuter, A., Krieg, T., Kuhr, K., Lorenz, H. M., Meier, F., Melchers, I., Mensing, H., Mueller-Ladner, U., Pfeiffer, C., Riemekasten, G., Sardy, M., Schmalzing, M., Sunderkoetter, C., Susok, L., Tarner, I. H., Vaith, P., Worm, M., Zeidler, G. and Hunzelmann, N. (2014). SSc-overlap syndromes: a distinct clinical subgroup with significant differences in disease progression compared to lSSc and dSSc patients. Data of the German Network for Systemic Scleroderma (DNSS). Exp. Dermatol., 23 (3). S. E13 - 1. HOBOKEN: WILEY-BLACKWELL. ISSN 1600-0625

Moinzadeh, P., Elisabeth, A., Blank, N., Distler, J., Fierlbeck, G., Genth, E., Guenther, C., Hein, R., Henes, J., Hellmich, M., Herrgott, I., Koetter, I., Kreuter, A., Krieg, T., Melchers, I., Mensing, H., Mueller-Ladner, U., Pfeiffer, C., Riemekasten, G., Sardy, M., Susok, L., Worm, M., Wozel, G., Zeidler, G., Sunderkoetter, C. and Hunzelmann, N. (2014). ANALYSIS OF REAL LIFE VASOACTIVE THERAPY IN OVER 3000 PATIENTS WITH SYSTEMIC SCLEROSIS (SSC) REVEALS CONSIDERABLE UNDERTREATMENT AND SIGNIFICANT CHANGES OF TREATMENT PRACTICE SINCE 2004. Ann. Rheum. Dis., 73. S. 564 - 565. LONDON: BMJ PUBLISHING GROUP. ISSN 1468-2060

Terao, C., Kawaguchi, T., Dieude, P., Varga, J., Kuwana, M., Hudson, M., Kawaguchi, Y., Matucci-Cerinic, M., Ohmura, K., Riemekasten, G., Kawasaki, A., Airo, P., Horita, T., Oka, A., Hachulla, E., Yoshifuji, H., Caramaschi, P., Hunzelmann, N., Baron, M., Atsumi, T., Hassouns, P., Tochimoto, A., Ayuzawa, N., Yanagida, H., Furukawa, H., Tohma, S., Hasegawa, M., Fujimoto, M., Ishikawa, O., Yamamoto, T., Goto, D., Asano, Y., Jinnin, M., Endo, H., Takahashi, H., Takehara, K., Sato, S., Ihn, H., Raychaudhuri, S., Liao, K., Gregersen, P., Tsuchiya, N., Riccieri, V., Melchers, I., Valentini, G., Cauvet, A., Martinez, M., Mimori, T., Matsuda, F. and Allanore, Y. (2017). TRANS-ETHNIC META-ANALYSIS OF GENOME-WIDE ASSOCIATION STUDIES IDENTIFIES GSDMA AND PRDM1 AS SUSCEPTIBILITY GENES TO SYSTEMIC SCLEROSIS. Ann. Rheum. Dis., 76. S. 202 - 203. LONDON: BMJ PUBLISHING GROUP. ISSN 1468-2060

Wipff, J., Dieude, P., Guedj, M., Ruiz, B., Riemekasten, G., Cracowski, J. L., Matucci-Cerinic, M., Melchers, I., Humbert, M., Hachulla, E., Airo, P., Diot, E., Hunzelmann, N., Caramaschi, P., Sibilia, J., Valentini, G., Tiev, K., Girerd, B., Mouthon, L., Riccieri, V., Carpentier, P. H., Distler, J., Amoura, Z., Tarner, I., Degano, B., Avouac, J., Meyer, O., Kahan, A., Boileau, C. and Allanore, Y. (2010). Association of a KCNA5 Gene Polymorphism With Systemic Sclerosis-Associated Pulmonary Arterial Hypertension in the European Caucasian Population. Arthritis Rheum., 62 (10). S. 3093 - 3101. HOBOKEN: WILEY. ISSN 1529-0131

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