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Number of items: 5.

Journal Article

Ahrazoglu, M., Moinzadeh, P. and Hunzelmann, N. (2014). Differential diagnoses of Raynaud's phenomenon. Dtsch. Med. Wochenschr., 139 (20). S. 1064 - 1070. STUTTGART: GEORG THIEME VERLAG KG. ISSN 1439-4413

Belz, D., Ahrazoglu, M., Moinzadeh, P., Rosenkranz, S. and Hunzelmann, N. (2017). Anaemia and Iron Deficiency in patients with systemic sclerosis. J. Dtsch. Dermatol. Ges., 15. S. 89 - 90. HOBOKEN: WILEY. ISSN 1610-0387

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

Moinzadeh, P. ORCID: 0000-0002-8784-8615, Frommolt, Peter ORCID: 0000-0002-1966-8014, Franitza, M., Toliat, Mohammad Reza ORCID: 0000-0002-9248-3200, Becker, K., Nürnberg, Peter ORCID: 0000-0002-7228-428X, Nihtyanova, Svetlana I. ORCID: 0000-0001-5178-9038, Ahrazoglu, M., Belz, Doreen ORCID: 0000-0002-7824-3315, Hunzelmann, N., Abraham, D., Ong, V. H., Mouthon, L., Hesselstrand, R., Denton, C. P. and Krieg, Thomas M. ORCID: 0000-0001-5616-8476 (2020). Whole blood gene expression profiling distinguishes systemic sclerosis‐overlap syndromes from other subsets. Journal of the European Academy of Dermatology and Venereology, 34 (5). Wiley. ISSN 0926-9959

This list was generated on Fri Mar 29 08:18:27 2024 CET.