Oji, Vinzenz 1974-
VIAF ID: 20744171 ( Personal )
Permalink: http://viaf.org/viaf/20744171
Preferred Forms
- 100 1 _ ‡a Oji, Vinzenz ‡d 1974-
- 100 1 _ ‡a Oji, Vinzenz ‡d 1974-
4xx's: Alternate Name Forms (2)
5xx's: Related Names (2)
- 500 1 _ ‡a Hoppe, Vinzenz ‡d 1974-
- 551 _ _ ‡a Potsdam ‡4 ortg ‡4 http://d-nb.info/standards/elementset/gnd#placeOfBirth
Works
Title | Sources |
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Corneodesmosin und die Genetik der Psoriasis vulgaris unter Betrachtung geschlechtsspezifischer Allel-Transmissionen im MHC | |
Epidemiology of inherited Epidermolysis bullosa in Germany | |
Erythrokeratodermia variabilis-like phenotype in patients carrying ABCA12 mutations | |
Genetic analysis of MPO variants in four psoriasis subtypes in patients from Germany | |
Mutational spectrum of the ABCA12 gene and genotype–phenotype correlation in a cohort of 64 patients with autosomal recessive congenital ichthyosis | |
Proposal for a 6‐step approach for differential diagnosis of neonatal erythroderma | |
Quality of life and clinical characteristics of self‐improving congenital ichthyosis within the disease spectrum of autosomal recessive congenital ichthyosis | |
Ulceration in prolidase deficiency: successful treatment with anticoagulants | |
Untersuchungen der Protease-Aktivität und Expression bei Filaggrin Mangel |