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Show 1 to 10 of 68 results

Oji, Vinzenz

Response to dupilumab in two children with Netherton syndrome: Improvement of pruritus and scaling Sussmuth K, Traupe H, Loser K, Ständer S, Kessel C, Wittkowski H, Oji V (2021) In: Journal of the European Academy of Dermatology and Venereology, 35(2). Research article (journal)
Increased Prevalence of Filaggrin Deficiency in 51 Patients with Recessive X-Linked Ichthyosis Presenting for Dermatological Examination Süßmuth K, Gruber R, Rodriguez E, Traupe H, Amler S, Sánchez-Guijo A, Valentin F, Tarinski T, Straub N, Metze D, Schneider SW, Hausser I, Baurecht H, Weidinger S, Oji V (2017) In: ((Bitte Journal prüfen)), 2017. Research article (journal)
The genetic basis in most patients with pustular skin disease remains elusive Mössner R, Wilsmann-Theis D, Oji V, Gkogkolou P, Löhr S*, Schulz P, Körber A, Christoph -Prinz J, Renner R, Schäkel K, Vogelsang L, Peters K-P, Philipp S, Reich K, Ständer H, Jacobi J, Weyergraf A, Kingo K, Kõks S, Gerdes S, Steinz K, Schill T, Griewank K G, Müller M, Frey S, Ebertsch L, Uebe S, Sticherling M, Sticht H, Hüffmeier U (2017) In: British Journal of Dermatology, Epub. Research article (journal)
Munchausen by proxy syndrome mimicking systemic autoinflammatory disease: case report and review of the literature Wittkowski H, Hinze C, Häfner-Harms S, Oji V, Masjosthusmann K, Monninger M, Grenzebach U, Foell D (2017) In: ((Bitte Journal prüfen)), 2017(15(1):19). Research article (journal)
Guideline (S1) for diagnostics and management of the ichthyoses (update) Oji V, Preil ML, Kleinow B, Wehr G, Fischer J, Hennies HC, Hausser I, Aufenvenne K, Stieler K, Tantcheva-Poór I, Weidinger S, Emmert S, Hamm H, Perusquia-Ortiz AM, Diem A, Giehl K, Fölster-Holst R, Höger P, Ott H, Traupe H (2017) In: ((Bitte Journal prüfen)), 2017. Research article (journal)
16 novel mutations in {PNPLA}1 in patients with autosomal recessive congenital ichthyosis reveal the importance of an extended patatin domain in {PNPLA}1 that is essential for proper human skin barrier function Zimmer A, Kim G, Hotz A, Bourrat E, Hausser I, Has C, Oji V, Stieler K, Vahlquist A, Kunde V, Weber B, Radner F, Leclerc-Mercier S, Schlipf N, Demmer P, Küsel J, Fischer J (2017) In: British Journal of Dermatology, 2017. Research article (journal)
Diminished Protein-Bound $\upomega$-Hydroxylated Ceramides In The Skin Of Ichthyosis Patients With 12r-Lox Or Elox-3 Deficiency In: .
Expanding the Clinical and Genetic Spectrum of {KRT}1, {KRT}2 and {KRT}10 Mutations in Keratinopathic Ichthyosis In: .
Association of Cole disease with novel heterozygous mutations in the somatomedin-B domains of {theENPP}1gene: necessary, but not always sufficient In: .
Association analysis of psoriasis vulgaris and psoriatic arthritis with loss-of-function mutations in {IL}36RN in German patients In: .

Dick A, Tantcheva-Po{ó}}r I, Oji V, Giehl K, Fischer J, Krieg P, Schneider H, Rauh M

(2017)

British Journal of Dermatology

, 2017

Research article (journal)

Hotz A, Oji V, Bourrat E, Jonca N, Mazereeuw-Hautier J, Betz R, Blume-Peytavi U, Stieler K, Morice-Picard F, Schönbuchner I, Markus S, Schlipf N, Fischer J

(2016)

((Bitte Journal prüfen))

, 96

(4)

Research article (journal)

Schlipf N, Traupe H, Gilaberte Y, Peitsch W, Hausser I, Oji V, Schmieder A, Schneider S, Demmer P, Rösler B, Fischer J

(2016)

British Journal of Dermatology

, 174

(5)

Research article (journal)

Löhr S, Uebe S, Behrens F, Böhm B, Köhm M, Traupe H, Oji V, Burkhardt H, Reis A, Hüffmeier U

(2016)

British Journal of Dermatology

, 175

(3)

Research article (journal)