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Page 1
Ulceration in Prolidase Deficiency: Successful Treatment with Anticoagulants.
Süßmuth K, Metze D, Muresan AM, Lehmberg K, Zur Stadt U, Speckmann C, Park JH, Marquardt T, Oji V, Goerge T. Süßmuth K, et al. Among authors: oji v. Acta Derm Venereol. 2020 Jan 7;100(1):adv00002. doi: 10.2340/00015555-3324. Acta Derm Venereol. 2020. PMID: 31573664 Free PMC article. No abstract available.
Short anagen hair syndrome: association with mono- and biallelic variants in WNT10A and a genetic overlap with male pattern hair loss.
Cesarato N, Schwieger-Briel A, Gossmann Y, Henne SK, Hillmann K, Frommherz LH, Wehner M, Xiong X, Thiele H, Oji V, Milani D, Tantcheva-Poor I, Giehl K, Fölster-Holst R, Teichler A, Braeckmans D, Hoeger PH, Jones G, Frank J, Weibel L, Blume-Peytavi U, Hamm H, Nöthen MM, Geyer M, Heilmann-Heimbach S, Basmanav FB, Betz RC. Cesarato N, et al. Among authors: oji v. Br J Dermatol. 2023 Nov 16;189(6):741-749. doi: 10.1093/bjd/ljad314. Br J Dermatol. 2023. PMID: 37671665
Founder Variants in KRT5 and POGLUT1 Are Implicated in Dowling-Degos Disease.
Kumar S, Borisov O, Maj C, Ralser DJ, Humbatova A, Hanneken S, Schmieder A, Groß J, Maintz L, Heineke A, Knuever J, Fagerberg C, Parmentier L, Anemüller W, Oji V, Tantcheva-Poór I, Fölster-Holst R, Wenzel J, Krawitz PM, Frank J, Betz RC. Kumar S, et al. Among authors: oji v. J Invest Dermatol. 2024 Jan;144(1):181-184. doi: 10.1016/j.jid.2023.04.036. Epub 2023 Jul 17. J Invest Dermatol. 2024. PMID: 37468035 No abstract available.
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. Süßmuth K, et al. Among authors: oji v. J Invest Dermatol. 2018 Mar;138(3):709-711. doi: 10.1016/j.jid.2017.08.047. Epub 2017 Oct 17. J Invest Dermatol. 2018. PMID: 29054605 Free article. No abstract available.
Meta-Analysis of Mutations in ALOX12B or ALOXE3 Identified in a Large Cohort of 224 Patients.
Hotz A, Kopp J, Bourrat E, Oji V, Komlosi K, Giehl K, Bouadjar B, Bygum A, Tantcheva-Poor I, Hellström Pigg M, Has C, Yang Z, Irvine AD, Betz RC, Zambruno G, Tadini G, Süßmuth K, Gruber R, Schmuth M, Mazereeuw-Hautier J, Jonca N, Guez S, Brena M, Hernandez-Martin A, van den Akker P, Bolling MC, Hannula-Jouppi K, Zimmer AD, Alter S, Vahlquist A, Fischer J. Hotz A, et al. Among authors: oji v. Genes (Basel). 2021 Jan 9;12(1):80. doi: 10.3390/genes12010080. Genes (Basel). 2021. PMID: 33435499 Free PMC article.
106 results