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Number of items: 8.

Journal Article

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

Johnson, S. R., Soowamber, M. L., Fransen, J., Khanna, D., Van den Hoogen, F., Baron, M., Matucci-Cerinic, M., Denton, C. P., Medsger, T. A., Jr., Carreira, P. E., Riemekasten, G., Distler, J., Gabrielli, A., Steen, V., Chung, L., Silver, R., Varga, J., Mueller-Ladner, U., Vonk, M. C., Walker, U. A., Wollheim, F. A., Herrick, A., Furst, D. E., Czirjak, L., Kowal-Bielecka, O., Del Galdo, F., Cutolo, M., Hunzelmann, N., Murray, C. D., Foeldvari, I., Mouthon, L., Damjanov, N., Kahaleh, B., Frech, T., Assassi, S., Saketkoo, L. A. and Pope, J. E. (2018). There is a need for new systemic sclerosis subset criteria. A content analytic approach. Scand. J. Rheumatol., 47 (1). S. 62 - 71. ABINGDON: TAYLOR & FRANCIS LTD. ISSN 1502-7732

Knobler, R., Moinzadeh, P., Hunzelmann, N., Kreuter, A., Cozzio, A., Mouthon, L., Cutolo, M., Rongioletti, F., Denton, C. P., Rudnicka, L., Frasin, L. A., Smith, V., Gabrielli, A., Aberer, E., Bagot, M., Bali, G., Bouaziz, J., Olesen, A. Braae, Foeldvari, I., Frances, C., Jalili, A., Just, U., Kahari, V., Karpati, S., Kofoed, K., Krasowska, D., Olszewska, M., Orteu, C., Panelius, J., Parodi, A., Petit, A., Quaglino, P., Ranki, A., Sanchez Schmidt, J. M., Seneschal, J., Skrok, A., Sticherling, M., Sunderkoetter, C., Taieb, A., Tanew, A., Wolf, P., Worm, M., Wutte, N. J. and Krieg, T. (2017). European Dermatology Forum S1-guideline on the diagnosis and treatment of sclerosing diseases of the skin, Part 1: localized scleroderma, systemic sclerosis and overlap syndromes. J. Eur. Acad. Dermatol. Venereol., 31 (9). S. 1401 - 1425. HOBOKEN: WILEY. ISSN 1468-3083

Knobler, R., Moinzadeh, P., Hunzelmann, N., Kreuter, A., Cozzio, A., Mouthon, L., Cutolo, M., Rongioletti, F., Denton, C. P., Rudnicka, L., Frasin, L. A., Smith, V., Gabrielli, A., Aberer, E., Bagot, M., Bali, G., Bouaziz, J., Olesen, A. Braae, Foeldvari, I., Frances, C., Jalili, A., Just, U., Kahari, V., Karpati, S., Kofoed, K., Krasowska, D., Olszewska, M., Orteu, C., Panelius, J., Parodi, A., Petit, A., Quaglino, P., Ranki, A., Sanchez Schmidt, J. M., Seneschal, J., Skrok, A., Sticherling, M., Sunderkoetter, C., Taieb, A., Tanew, A., Wolf, P., Worm, M., Wutte, N. J. and Krieg, T. (2017). European dermatology forum S1-guideline on the diagnosis and treatment of sclerosing diseases of the skin, Part 2: Scleromyxedema, scleredema and nephrogenic systemic fibrosis. J. Eur. Acad. Dermatol. Venereol., 31 (10). S. 1581 - 1595. HOBOKEN: WILEY. ISSN 1468-3083

Moinzadeh, P., Frommolt, P., Franitza, M., Toliat, M. R., Becker, K., Nuernberg, P., Nihtyanova, S. I., Ahrazoglu, M., Belz, D., Hunzelmann, N., Abraham, D., Ong, V. H., Mouthon, L., Hesselstrand, R., Denton, C. P. and Krieg, T. (2016). Identification of an expression-based set of genes to predict the subset of patients with systemic scleroderma (SSc). Exp. Dermatol., 25. S. 10 - 11. HOBOKEN: WILEY-BLACKWELL. ISSN 1600-0625

Moinzadeh, P., Frommolt, P., Franitza, M., Toliat, M. R., Becker, K., Nuernberg, P., Nihtyanova, S. I., Ahrazoglu, M., Belz, D., Hunzelmann, N., Abraham, D., Ong, V. H., Mouthon, L., Hesselstrand, R., Denton, C. P. and Krieg, T. (2020). Whole blood gene expression profiling distinguishes systemic sclerosis-overlap syndromes from other subsets. J. Eur. Acad. Dermatol. Venereol., 34 (5). S. E236 - 3. HOBOKEN: WILEY. ISSN 1468-3083

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

This list was generated on Thu Oct 28 18:27:23 2021 CEST.