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Page 1
Increased Prevalence of Filaggrin Deficiency in 51 Patients with Recessive X-Linked Ichthyosis Presenting for Dermatological Examination.
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.
Vitamin D Status in Distinct Types of Ichthyosis: Importance of Genetic Type and Severity of Scaling.
Kim MR, Oji V, Valentin F, Traupe H, Nofer JR, Hausser I, Hennies HC, Eckl K, Wudy SA, Sánchez-Guijo A, Kerschke L, Fischer J, Süßmuth K.
Kim MR, et al. Among authors: valentin f.
Acta Derm Venereol. 2021 Sep 15;101(9):adv00546. doi: 10.2340/00015555-3887.
Acta Derm Venereol. 2021.
PMID: 34396419
Free PMC article.
Item in Clipboard
Bathing Suit Variant of Autosomal Recessive Congenital Ichthyosis (ARCI) in Two Indian Patients.
Sathishkumar D, Peter D, Pulimood S, Wiegmann H, Valentin F, Thomas M, Hennies HC, Oji V.
Sathishkumar D, et al. Among authors: valentin f.
Case Rep Dermatol Med. 2018 Dec 30;2018:3140473. doi: 10.1155/2018/3140473. eCollection 2018.
Case Rep Dermatol Med. 2018.
PMID: 30693114
Free PMC article.
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Transcriptomic Analysis of Two Cdsn-Deficient Mice Shows Gene Signatures Biologically Relevant for Peeling Skin Disease.
Zaafouri S, Pichery M, Huchenq A, Valentin F, Oji V, Mazereeuw-Hautier J, Serre G, Jonca N.
Zaafouri S, et al. Among authors: valentin f.
J Invest Dermatol. 2018 Jun;138(6):1431-1435. doi: 10.1016/j.jid.2017.12.020. Epub 2017 Dec 23.
J Invest Dermatol. 2018.
PMID: 29277537
Free article.
No abstract available.
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Increased expression of caspase-1 and interleukin-18 in peeling skin disease, and a novel mutation of corneodesmosin.
Valentin F, Oji V, Hausser I, Liebau E, Tarinski T, Metze D, Breitkreutz D, Traupe H, Jonca N, Terheyden P.
Valentin F, et al.
Acta Derm Venereol. 2015 Nov;95(8):1019-21. doi: 10.2340/00015555-2142.
Acta Derm Venereol. 2015.
PMID: 26014679
Free article.
No abstract available.
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Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome.
Ü Basmanav FB, Cau L, Tafazzoli A, Méchin MC, Wolf S, Romano MT, Valentin F, Wiegmann H, Huchenq A, Kandil R, Garcia Bartels N, Kilic A, George S, Ralser DJ, Bergner S, Ferguson DJP, Oprisoreanu AM, Wehner M, Thiele H, Altmüller J, Nürnberg P, Swan D, Houniet D, Büchner A, Weibel L, Wagner N, Grimalt R, Bygum A, Serre G, Blume-Peytavi U, Sprecher E, Schoch S, Oji V, Hamm H, Farrant P, Simon M, Betz RC.
Ü Basmanav FB, et al. Among authors: valentin f.
Am J Hum Genet. 2016 Dec 1;99(6):1292-1304. doi: 10.1016/j.ajhg.2016.10.004. Epub 2016 Nov 17.
Am J Hum Genet. 2016.
PMID: 27866708
Free PMC article.
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