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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