Report of the 13th Annual International Pachyonychia Congenita Consortium Symposium-Reference-Cited by-同舟云学术

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Report of the 13th Annual International Pachyonychia Congenita Consortium Symposium

Published:2017-03-27 Issue:5 Volume:176 Page:1144-1147
ISSN:0007-0963
Container-title:British Journal of Dermatology
language:en
Short-container-title:Br J Dermatol

Author:

Rittié L.¹,Kaspar R.L.²,Sprecher E.³,Smith F.J.D.⁴

Affiliation:

1. Department of Dermatology; University of Michigan Medical School; Ann Arbor MI U.S.A

2. TransDerm Inc.; 2161 Delaware Ave Santa Cruz CA 95060 U.S.A

3. Department of Dermatology; Tel Aviv Sourasky Medical Center; Tel Aviv Israel

4. Pachyonychia Congenita Project; Salt Lake City UT U.S.A

Funder

Pachyonychia Congenita Project

Publisher

Wiley

Subject

Dermatology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/bjd.15417/fullpdf

Reference15 articles.

1. A review of the clinical phenotype of 254 patients with genetically confirmed pachyonychia congenita;Eliason;J Am Acad Dermatol,2012

2. The phenotypic and molecular genetic features of pachyonychia congenita;McLean;J Invest Dermatol,2011

3. The molecular genetic analysis of the expanding pachyonychia congenita case collection;Wilson;Br J Dermatol,2014

4. Oxidative stress and dysfunctional NRF2 underlie pachyonychia congenita phenotypes;Kerns;J Clin Invest,2016

5. Identification of stem cell populations in sweat glands and ducts reveals roles in homeostasis and wound repair;Lu;Cell,2012

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1. Genetic Defects of Nails and Nail Growth;Rook's Textbook of Dermatology;2024-02-20

2. Distinctions in the Management, Patient Impact, and Clinical Profiles of Pachyonychia Congenita Subtypes;Skin Appendage Disorders;2021

3. Pain mechanisms in hereditary palmoplantar keratodermas;British Journal of Dermatology;2019-07-24

4. Genetic and developmental disorders of the oral mucosa: Epidemiology; molecular mechanisms; diagnostic criteria; management;Periodontology 2000;2019-05-15

5. Pachyonychia congenita und Steatocystoma multiplex durch Mutation im Keratin-17-Gen;Aktuelle Dermatologie;2019-02

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