Publications by authors named "Vinzenz Oji"

58Publications

Genetic variants in FBLIM1 gene do not contribute to SAPHO syndrome and chronic recurrent multifocal osteomyelitis in typical patient groups.

BMC Med Genet 2020 05 12;21(1):102. Epub 2020 May 12.

Institute of Human Genetics, University Hospital Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg, Schwabachanlage 10, 91054, Erlangen, Germany.

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http://dx.doi.org/10.1186/s12881-020-01037-7DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7216525PMC
May 2020

Ichthyosen im klinischen Alltag: Umgang mit einer seltenen Erkrankungsgruppe.

J Dtsch Dermatol Ges 2020 Mar;18(3):225-245

Klinik für Dermatologie und Venerologie, Universitätsklinikum Münster Reference Center for Ichthyoses and Palmoplantar keratoderma (ReCIP) ERN-Skin.

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http://dx.doi.org/10.1111/ddg.14049_gDOI Listing
March 2020

Ichthyoses in everyday practice: management of a rare group of diseases.

J Dtsch Dermatol Ges 2020 Mar 2;18(3):225-243. Epub 2020 Mar 2.

Department of Dermatology and Venereology, Münster University Medical Center, Münster, Germany.

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http://dx.doi.org/10.1111/ddg.14049DOI Listing
March 2020

Ulceration in Prolidase Deficiency: Successful Treatment with Anticoagulants.

Acta Derm Venereol 2020 Jan 7;100(1):adv00002. Epub 2020 Jan 7.

Department of Dermatology, University Hospital of Münster, 48149 Münster, Germany.

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http://dx.doi.org/10.2340/00015555-3324DOI Listing
January 2020

Epidermolytische Ichthyose mit Nachweis einer De-novo-Missense-Mutation c.1307T>C; p.Leu436Pro in KRT10.

J Dtsch Dermatol Ges 2019 Jan;17(1):82-84

Klinik und Poliklinik für Dermatologie, Universitätsklinikum Carl Gustav Carus, Technische Universität Dresden.

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http://dx.doi.org/10.1111/ddg.13720_gDOI Listing
January 2019

Rezidivierendes akutes hämorrhagisches Ödem des Kindesalters (AHEI) in der Pubertät.

J Dtsch Dermatol Ges 2018 Dec;16(12):1496-1498

Abteilung für Translationale Dermatoinfektiologie, Universitätsklinikum Münster.

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http://dx.doi.org/10.1111/ddg.13699_gDOI Listing
December 2018

Epidermolytic ichthyosis due to a de novo missense mutation c.1307T> C; p.Leu436Pro in KRT10.

J Dtsch Dermatol Ges 2019 Jan 6;17(1):82-84. Epub 2018 Dec 6.

Department of Dermatology, Carl Gustav Carus University Medical Center, Dresden Technical University, Dresden, Germany.

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http://dx.doi.org/10.1111/ddg.13720DOI Listing
January 2019

Recurrent acute hemorrhagic edema of infancy (AHEI) during puberty.

J Dtsch Dermatol Ges 2018 Dec 9;16(12):1496-1498. Epub 2018 Nov 9.

Department of Translational Dermatoinfectiology, Münster University Medical Center, Münster, Germany.

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http://dx.doi.org/10.1111/ddg.13699DOI Listing
December 2018

Mutation update for CYP4F22 variants associated with autosomal recessive congenital ichthyosis.

Hum Mutat 2018 10 7;39(10):1305-1313. Epub 2018 Aug 7.

Faculty of Medicine, Institute of Human Genetics, University Medical Center Freiburg, University of Freiburg, Freiburg, Germany.

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http://dx.doi.org/10.1002/humu.23594DOI Listing
October 2018

Transcriptomic Analysis of Two Cdsn-Deficient Mice Shows Gene Signatures Biologically Relevant for Peeling Skin Disease.

J Invest Dermatol 2018 06 23;138(6):1431-1435. Epub 2017 Dec 23.

Unité Différenciation Epithéliale et Autoimmunité Rhumatoïde, UMR 1056 Inserm-Université de Toulouse, Place du Dr Baylac, Hôpital Purpan, Toulouse, France. Electronic address:

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http://dx.doi.org/10.1016/j.jid.2017.12.020DOI Listing
June 2018

Ocular manifestations, complications and management of congenital ichthyoses: a new look.

Br J Ophthalmol 2018 05 3;102(5):586-592. Epub 2017 Nov 3.

Department of Dermatology, University Hospital Münster, Munster, Germany.

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http://dx.doi.org/10.1136/bjophthalmol-2017-310615DOI Listing
May 2018

Munchausen by proxy syndrome mimicking systemic autoinflammatory disease: case report and review of the literature.

Pediatr Rheumatol Online J 2017 Apr 5;15(1):19. Epub 2017 Apr 5.

Department of Paediatric Rheumatology and Immunology, University Children's Hospital Muenster, Albert-Schweitzer-Campus 1, Bld. W30, D-48149, Muenster, Germany.

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http://dx.doi.org/10.1186/s12969-017-0152-6DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5382472PMC
April 2017

Ein mehrstufiger Algorithmus zur Diagnose seltener Genodermatosen.

J Dtsch Dermatol Ges 2016 Oct;14(10):969-987

Klinik für Dermatologie und Venerologie, Universitätsklinikum Freiburg.

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http://dx.doi.org/10.1111/ddg.13140_gDOI Listing
October 2016

A multistep approach to the diagnosis of rare genodermatoses.

J Dtsch Dermatol Ges 2016 Oct;14(10):969-986

Department of Dermatology, University of Freiburg, Germany.

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http://dx.doi.org/10.1111/ddg.13140DOI Listing
October 2016

Role of steroid sulfatase in steroid homeostasis and characterization of the sulfated steroid pathway: Evidence from steroid sulfatase deficiency.

Mol Cell Endocrinol 2016 12 13;437:142-153. Epub 2016 Aug 13.

Steroid Research & Mass Spectrometry Unit, Division of Pediatric Endocrinology & Diabetology, Center of Child and Adolescent Medicine, Justus Liebig University, Feulgenstrasse 12, 35392, Giessen, Germany.

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http://dx.doi.org/10.1016/j.mce.2016.08.019DOI Listing
December 2016

The skin in psoriasis: assessment and challenges.

Clin Exp Rheumatol 2015 Sep-Oct;33(5 Suppl 93):S14-9. Epub 2015 Oct 15.

Department of Dermatology, University Hospital Münster, Germany.

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December 2015

Simultaneous quantification of cholesterol sulfate, androgen sulfates, and progestagen sulfates in human serum by LC-MS/MS.

J Lipid Res 2015 Sep 2;56(9):1843-51. Epub 2015 Aug 2.

Steroid Research and Mass Spectrometry Unit, Division of Pediatric Endocrinology and Diabetology, Center of Child and Adolescent Medicine, Justus-Liebig-University, 35392 Giessen, Germany.

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http://dx.doi.org/10.1194/jlr.D061499DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4548788PMC
September 2015

Increased expression of caspase-1 and interleukin-18 in peeling skin disease, and a novel mutation of corneodesmosin.

Acta Derm Venereol 2015 Nov;95(8):1019-21

Department of Dermatology, University of Münster, Von-Esmarch-Str. 58, DE-48149 Münster, Germany.

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http://dx.doi.org/10.2340/00015555-2142DOI Listing
November 2015

High levels of oxysterol sulfates in serum of patients with steroid sulfatase deficiency.

J Lipid Res 2015 Feb 11;56(2):403-12. Epub 2014 Dec 11.

Steroid Research and Mass Spectrometry Unit, Division of Pediatric Endocrinology and Diabetology, Center of Child and Adolescent Medicine, Justus-Liebig University, 35392 Giessen, Germany.

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http://www.jlr.org/lookup/doi/10.1194/jlr.M055608
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http://dx.doi.org/10.1194/jlr.M055608DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4306693PMC
February 2015

Nonsyndromic types of ichthyoses - an update.

J Dtsch Dermatol Ges 2014 Feb 11;12(2):109-21. Epub 2013 Oct 11.

Department of Dermatology, University of Münster, Germany.

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http://dx.doi.org/10.1111/ddg.12229DOI Listing
February 2014

Mutations in the prostaglandin transporter SLCO2A1 cause primary hypertrophic osteoarthropathy with digital clubbing.

J Invest Dermatol 2012 Oct 14;132(10):2473-2476. Epub 2012 Jun 14.

Center for Human Genetics, Bioscientia, Ingelheim, Germany; Department of Human Genetics, RWTH Aachen University, Aachen, Germany; Center for Clinical Research, University Hospital Freiburg, Freiburg, Germany. Electronic address:

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http://dx.doi.org/10.1038/jid.2012.146DOI Listing
October 2012

rAAV2-mediated restoration of LEKTI in LEKTI-deficient cells from Netherton patients.

J Dermatol Sci 2011 Mar 21;61(3):194-8. Epub 2010 Dec 21.

Division of Environmental Dermatology and Allergy, ZAUM Center for Allergy and Environment, Technische Universität München, Munich, Germany.

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http://dx.doi.org/10.1016/j.jdermsci.2010.12.004DOI Listing
March 2011

Ichthyosis: clinical manifestations and practical treatment options.

Am J Clin Dermatol 2009 ;10(6):351-64

Department of Dermatology, University of Münster, Münster, Germany.

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http://link.springer.com/10.2165/11311070-000000000-00000
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http://dx.doi.org/10.2165/11311070-000000000-00000DOI Listing
December 2009

Ichthyoses - Part 1: Differential diagnosis of vulgar ichthyoses and therapeutic options.

J Dtsch Dermatol Ges 2009 Jun;7(6):511-9

Department of Dermatology, University of Tübingen, Germany.

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http://dx.doi.org/10.1111/j.1610-0387.2008.06969.xDOI Listing
June 2009

Ichthyoses--Part 2: Congenital ichthyoses.

J Dtsch Dermatol Ges 2009 Jul;7(7):577-88

Department of Dermatology, University of Tübingen, Germany.

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http://dx.doi.org/10.1111/j.1610-0387.2008.06970.xDOI Listing
July 2009

Ichthyoses: differential diagnosis and molecular genetics.

Eur J Dermatol 2006 Jul-Aug;16(4):349-59

Department of Dermatology, University Hospital, Von-Esmarch-Str. 58, 48149 Münster, Germany.

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March 2007

SPINK5 and Netherton syndrome: novel mutations, demonstration of missing LEKTI, and differential expression of transglutaminases.

J Invest Dermatol 2004 Sep;123(3):474-83

Department of Dermatology, University Hospital, University of Münster, Von-Esmarch-Strasse 58, D-48149 Münster, Germany.

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http://dx.doi.org/10.1111/j.0022-202X.2004.23220.xDOI Listing
September 2004