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There are 6877 results for: content related to: Mendelian Disorders of Cornification (MEDOC): The Erythrokeratodermas

  1. Disorders of Keratinization

    Rook's Textbook of Dermatology, Seventh Edition

    M. R. Judge, W. H. I. McLean, C. S. Munro, Pages: 1619–1730, 2008

    Published Online : 4 FEB 2008, DOI: 10.1002/9780470750520.ch34

  2. Overview of skin diseases linked to connexin gene mutations

    International Journal of Dermatology

    Volume 53, Issue 2, February 2014, Pages: 192–205, Lyubov Avshalumova, Jordan Fabrikant and Angie Koriakos

    Article first published online : 15 MAY 2013, DOI: 10.1111/ijd.12062

  3. Erythrokeratodermas: A classification in a state of flux?

    Australasian Journal of Dermatology

    Volume 46, Issue 3, August 2005, Pages: 127–143, Maureen Rogers

    Article first published online : 7 JUL 2005, DOI: 10.1111/j.1440-0960.2005.00165.x

  4. Disorders of Keratinization

    Connective Tissue and Its Heritable Disorders: Molecular, Genetic, and Medical Aspects, Second Edition

    Meral J. Arin, Daniel Hohl, Dennis R. Roop, Pages: 1025–1068, 2003

    Published Online : 30 APR 2003, DOI: 10.1002/0471221929.ch24

  5. Disorders of Keratinization

    Rook's Textbook of Dermatology, Eighth Edition

    M. R. Judge, W. H. I. McLean, C. S. Munro, Pages: 1–122, 2010

    Published Online : 6 MAY 2010, DOI: 10.1002/9781444317633.ch19

  6. Gap junction diseases of the skin

    American Journal of Medical Genetics Part C: Seminars in Medical Genetics

    Volume 131C, Issue 1, 15 November 2004, Pages: 12–19, M.A.M. van Steensel

    Article first published online : 5 OCT 2004, DOI: 10.1002/ajmg.c.30030

  7. Connexin gene pathology

    Clinical and Experimental Dermatology

    Volume 28, Issue 4, July 2003, Pages: 397–409, G. Richard

    Article first published online : 19 JUN 2003, DOI: 10.1046/j.1365-2230.2003.01312.x

  8. The missense mutation G12D in connexin30.3 can cause both erythrokeratodermia variabilis of Mendes da Costa and progressive symmetric erythrokeratodermia of Gottron

    American Journal of Medical Genetics Part A

    Volume 149A, Issue 4, April 2009, Pages: 657–661, M.A.M. van Steensel, A.P. Oranje, J.G. van der Schroeff, A. Wagner and M. van Geel

    Article first published online : 16 MAR 2009, DOI: 10.1002/ajmg.a.32744

  9. Mendelian Disorders of Cornification (MEDOC): The Ichthyoses

    Harper's Textbook of Pediatric Dermatology, Volume 1, 2, Third Edition

    Daniel Hohl, Mary Williams, Pages: 121.1–121.70, 2011

    Published Online : 24 MAY 2011, DOI: 10.1002/9781444345384.ch121

  10. Extending the Phenotypic Spectrum of Keratitis-Ichthyosis-Deafness Syndrome: Report of a Patient with GJB2 (G12R) Connexin 26 Mutation and Unusual Clinical Findings

    Pediatric Dermatology

    Volume 29, Issue 3, May/June 2012, Pages: 349–357, Tamara Lazic, Qiaoli Li, Michael Frank, Jouni Uitto and Linda H. Zhou

    Article first published online : 20 OCT 2011, DOI: 10.1111/j.1525-1470.2011.01425.x

  11. You have free access to this content
    Connexins: a connection with the skin

    Experimental Dermatology

    Volume 9, Issue 2, April 2000, Pages: 77–96, Gabriela Richard

    Article first published online : 24 DEC 2001, DOI: 10.1034/j.1600-0625.2000.009002077.x

  12. Erythrokeratodermia Variabilis Present at Birth: Case Report and Review of the Literature

    Pediatric Dermatology

    Volume 12, Issue 4, December 1995, Pages: 351–354, John D. Hendrix Jr. and Kenneth E. Greer

    Article first published online : 28 JUN 2008, DOI: 10.1111/j.1525-1470.1995.tb00200.x

  13. GJB2 mutations in keratitis-ichthyosis-deafness syndrome including its fatal form

    American Journal of Medical Genetics Part A

    Volume 133A, Issue 2, 1 March 2005, Pages: 128–131, Andreas R. Janecke, Hans Christian Hennies, Barbara Günther, Gabriele Gansl, Josef Smolle, Elisabeth M. Messmer, Gerd Utermann and Olaf Rittinger

    Article first published online : 4 JAN 2005, DOI: 10.1002/ajmg.a.30515

  14. Is erythrokeratoderma one disorder? A clinical and ultrastructural study of two siblings

    British Journal of Dermatology

    Volume 124, Issue 5, May 1991, Pages: 487–491, A.W. MACFARLANE, S.J. CHAPMAN and J.L. VERBOV

    Article first published online : 29 JUL 2006, DOI: 10.1111/j.1365-2133.1991.tb00632.x

  15. Autosomal Recessive Inheritance of Erythrokeratoderma Variabilis

    Pediatric Dermatology

    Volume 14, Issue 5, September 1997, Pages: 355–358, D. K. B. Armstrong, T. H. Hutchinson, M. Y. Walsh and J. C. McMillan

    Article first published online : 28 JUN 2008, DOI: 10.1111/j.1525-1470.1997.tb00980.x

  16. A case of erythrokeratoderma variabilis without mutations in connexin 31

    British Journal of Dermatology

    Volume 143, Issue 6, December 2000, Pages: 1283–1287, A. Ishida-Yamamoto, D. Kelsell, J. Common, M.J. Houseman, M. Hashimoto, H. Shibaki, K. Asano, H. Takahashi, Y. Hashimoto, T. Senshu, I.M. Leigh and H. Iizuka

    Article first published online : 24 DEC 2001, DOI: 10.1046/j.1365-2133.2000.03902.x

  17. Drug-induced aphthous ulcers

    British Journal of Dermatology

    Volume 143, Issue 6, December 2000, Pages: 1138–1139, R.I. McLeod

    Article first published online : 24 DEC 2001, DOI: 10.1046/j.1365-2133.2000.04002.x

  18. You have free access to this content
    Index

    Harper's Textbook of Pediatric Dermatology, Volume 1, 2, Third Edition

    Alan D. Irvine, Peter H. Hoeger, Albert C. Yan, Pages: 1–76, 2011

    Published Online : 24 MAY 2011, DOI: 10.1002/9781444345384.index

  19. Mendelian Disorders of Cornification (MEDOC): The Keratodermas

    Harper's Textbook of Pediatric Dermatology, Volume 1, 2, Third Edition

    Maurice A. M. van Steensel, Peter M. Steijlen, Pages: 120.1–120.26, 2011

    Published Online : 24 MAY 2011, DOI: 10.1002/9781444345384.ch120

  20. No exonic mutations at GJB2, GJB3, GJB4, GJB6, ARS (Component B), and LOR genes responsible for a Chinese patient affected by progressive symmetric erythrokeratodermia with pseudoainhum

    International Journal of Dermatology

    Volume 53, Issue 9, September 2014, Pages: 1111–1113, Fusheng Zhou, Hongyang Fu, Linghua Liu, Yong Cui, Zhengzhong Zhang, Ruixue Chang, Zhen Yue, Sen Yang and Xuejun Zhang

    Article first published online : 25 JUN 2014, DOI: 10.1111/ijd.12494