1-20 of 20
Authors: V. Oji
Journal Article
Development of a pathogenesis‐based therapy for peeling skin syndrome type 1
British Journal of Dermatology, Volume 184, Issue 6, 1 June 2021, Pages 1123–1131, https://doi.org/10.1111/bjd.19546
Published: 01 June 2021
Journal Article
Refining the dermatological spectrum in primary immunodeficiency: mucosa‐associated lymphoid tissue lymphoma translocation protein 1 deficiency mimicking Netherton/Omenn syndromes Get access
British Journal of Dermatology, Volume 182, Issue 1, 1 January 2020, Pages 202–207, https://doi.org/10.1111/bjd.18091
Published: 01 January 2020
Journal Article
LEKTI domains D6, D7 and D8+9 serve as substrates for transglutaminase 1: implications for targeted therapy of Netherton syndrome Get access
British Journal of Dermatology, Volume 181, Issue 5, 1 November 2019, Pages 999–1008, https://doi.org/10.1111/bjd.17820
Published: 01 November 2019
Includes: Multimedia
Journal Article
Management of congenital ichthyoses: European guidelines of care, part two
British Journal of Dermatology, Volume 180, Issue 3, 1 March 2019, Pages 484–495, https://doi.org/10.1111/bjd.16882
Published: 01 March 2019
Journal Article
先天性鱼鳞病 : 欧洲护理指南, 第二部分 Get access
British Journal of Dermatology, Volume 180, Issue 3, 1 March 2019, Page e96, https://doi.org/10.1111/bjd.17568
Published: 01 March 2019
Journal Article
Congenital ichthyoses: European guidelines of care, part two Get access
British Journal of Dermatology, Volume 180, Issue 3, 1 March 2019, Page e80, https://doi.org/10.1111/bjd.17552
Published: 01 March 2019
Journal Article
Management of congenital ichthyoses: European guidelines of care, part one
British Journal of Dermatology, Volume 180, Issue 2, 1 February 2019, Pages 272–281, https://doi.org/10.1111/bjd.17203
Published: 01 February 2019
Journal Article
The genetic basis for most patients with pustular skin disease remains elusive
British Journal of Dermatology, Volume 178, Issue 3, 1 March 2018, Pages 740–748, https://doi.org/10.1111/bjd.15867
Published: 01 March 2018
Journal Article
Functional implications of novel ADAM10 mutations in reticulate acropigmentation of Kitamura Get access
British Journal of Dermatology, Volume 177, Issue 6, 1 December 2017, Pages e340–e343, https://doi.org/10.1111/bjd.16024
Published: 01 December 2017
Journal Article
Diminished protein‐bound ω‐hydroxylated ceramides in the skin of patients with ichthyosis with 12R‐lipoxygenase (LOX) or eLOX‐3 deficiency Get access
British Journal of Dermatology, Volume 177, Issue 4, 1 October 2017, Pages e119–e121, https://doi.org/10.1111/bjd.15406
Published: 01 October 2017
Journal Article
Sixteen novel mutations in PNPLA1 in patients with autosomal recessive congenital ichthyosis reveal the importance of an extended patatin domain in PNPLA1 that is essential for proper human skin barrier function Get access
British Journal of Dermatology, Volume 177, Issue 2, 1 August 2017, Pages 445–455, https://doi.org/10.1111/bjd.15308
Published: 01 August 2017
Journal Article
Association analysis of psoriasis vulgaris and psoriatic arthritis with loss‐of‐function mutations in IL36RN in German patients
British Journal of Dermatology, Volume 175, Issue 3, 1 September 2016, Pages 639–641, https://doi.org/10.1111/bjd.14624
Published: 01 September 2016
Journal Article
Association of Cole disease with novel heterozygous mutations in the somatomedin‐B domains of the ENPP1 gene: necessary, but not always sufficient Get access
British Journal of Dermatology, Volume 174, Issue 5, 1 May 2016, Pages 1152–1156, https://doi.org/10.1111/bjd.14328
Published: 01 May 2016
Journal Article
Expanding the keratin mutation database: novel and recurrent mutations and genotype–phenotype correlations in 28 patients with epidermolytic ichthyosis Get access
British Journal of Dermatology, Volume 164, Issue 2, 1 February 2011, Pages 442–447, https://doi.org/10.1111/j.1365-2133.2010.10096.x
Published: 01 February 2011
Journal Article
Acral self‐healing collodion baby: report of a new clinical phenotype caused by a novel TGM1 mutation Get access
British Journal of Dermatology, Volume 161, Issue 2, 1 August 2009, Pages 456–463, https://doi.org/10.1111/j.1365-2133.2009.09277.x
Published: 01 August 2009
Journal Article
Ichthyosis vulgaris: novel FLG mutations in the German population and high presence of CD1a+ cells in the epidermis of the atopic subgroup Get access
British Journal of Dermatology, Volume 160, Issue 4, 1 April 2009, Pages 771–781, https://doi.org/10.1111/j.1365-2133.2008.08999.x
Published: 01 April 2009
Journal Article
Novel and recurrent mutations in the 1B domain of keratin 1 in palmoplantar keratoderma with tonotubules Get access
British Journal of Dermatology, Volume 160, Issue 2, 1 February 2009, Pages 446–449, https://doi.org/10.1111/j.1365-2133.2008.08831.x
Published: 01 February 2009
Journal Article
A newly identified splice site mutation in ZMPSTE24 causes restrictive dermopathy in the Middle East Get access
British Journal of Dermatology, Volume 159, Issue 4, 1 October 2008, Pages 961–967, https://doi.org/10.1111/j.1365-2133.2008.08772.x
Published: 01 October 2008
Journal Article
Plasminogen activator inhibitor‐2 is expressed in different types of congenital ichthyosis: in vivo evidence for its cross‐linking into the cornified cell envelope by transglutaminase‐1 Get access
British Journal of Dermatology, Volume 154, Issue 5, 1 May 2006, Pages 860–867, https://doi.org/10.1111/j.1365-2133.2005.07109.x
Published: 01 May 2006
Journal Article
Topical pimecrolimus: a novel therapeutic option for Netherton syndrome Get access
British Journal of Dermatology, Volume 153, Issue 5, 1 November 2005, Pages 1067–1068, https://doi.org/10.1111/j.1365-2133.2005.06884.x
Published: 01 November 2005
