Search Results - Oji, V.

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  1. 1
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    Quality of life and clinical characteristics of self-improving congenital ichthyosis within the disease spectrum of autosomal-recessive congenital ichthyosis by Drerup, Lisanne (Author) , Süßmuth, Kira (Author) , Komlosi, K. (Author) , Kopp, J. (Author) , Drerup, C. (Author) , Metze, D. (Author) , Traupe, Heiko (Author) , Haußer-Siller, Ingrid (Author) , Eckl, K. M. (Author) , Hennies, H. C. (Author) , Fischer, Judith (Author) , Oji, V. (Author) ,


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  2. 2
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    Complete filaggrin deficiency in ichthyosis vulgaris is associated with only moderate changes in epidermal permeability barrier function profile by Perusquía Ortiz, Ana María (Author) , Oji, V. (Author) , Sauerland, M.c. (Author) , Tarinski, T. (Author) , Zaraeva, I. (Author) , Seller, N. (Author) , Metze, D. (Author) , Aufenvenne, K. (Author) , Haußer-Siller, Ingrid (Author) , Traupe, H. (Author) ,


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    Expanding the keratin mutation database: novel and recurrent mutations and genotype-phenotype correlations in 28 patients with epidermolytic ichthyosis by Arin, Meral Julia (Author) , Oji, V. (Author) , Emmert, S. (Author) , Haußer-Siller, Ingrid (Author) , Traupe, H. (Author) , Krieg, T. (Author) , Grimberg, G. (Author) ,


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