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There are 6390 results for: content related to: Mendelian Disorders of Cornification (MEDOC): The Erythrokeratodermas

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

    Australasian Journal of Dermatology

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

    Version of Record online : 7 JUL 2005, DOI: 10.1111/j.1440-0960.2005.00165.x

  2. 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

  3. Inherited Disorders of Cornification

    Standard Article

    Rook's Textbook of Dermatology

    Vinzenz Oji, Dieter Metze and Heiko Traupe

    Published Online : 9 OCT 2016, DOI: 10.1002/9781118441213.rtd0066

  4. 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

    Version of Record online : 15 MAY 2013, DOI: 10.1111/ijd.12062

  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. 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

    Version of Record online : 28 JUN 2008, DOI: 10.1111/j.1525-1470.1995.tb00200.x

  7. 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

    Version of Record online : 5 OCT 2004, DOI: 10.1002/ajmg.c.30030

  8. 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

    Version of Record online : 28 JUN 2008, DOI: 10.1111/j.1525-1470.1997.tb00980.x

  9. 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

    Version of Record online : 24 DEC 2001, DOI: 10.1046/j.1365-2133.2000.03902.x

  10. Erythrokeratoderma variabilis: case report and review of the literature

    Journal of the European Academy of Dermatology and Venereology

    Volume 11, Issue 2, September 1998, Pages: 180–183, E. Papadavid, E. Koumantaki and R.P.R. Dawber

    Version of Record online : 29 SEP 2006, DOI: 10.1111/j.1468-3083.1998.tb00777.x

  11. Acitretin for Erythrokeratodermia Variabilis in a 9-Year-Old Girl

    Pediatric Dermatology

    Volume 19, Issue 6, November 2002, Pages: 510–512, Robin A. C. Graham-Brown and Toby A. Chave

    Version of Record online : 23 NOV 2002, DOI: 10.1046/j.1525-1470.2002.00221.x

  12. A new, recurrent mutation of GJB3 (Cx31) in erythrokeratodermia variabilis

    British Journal of Dermatology

    Volume 152, Issue 6, June 2005, Pages: 1143–1148, S.M. Morley, M.I. White, M. Rogers, D. Wasserman, P. Ratajczak, W.H.I. Mclean and G. Richard

    Version of Record online : 8 JUN 2005, DOI: 10.1111/j.1365-2133.2005.06610.x

  13. You have free access to this content
    Erythrokeratodermia variabilis et progressiva

    The Journal of Dermatology

    Volume 43, Issue 3, March 2016, Pages: 280–285, Akemi Ishida-Yamamoto

    Version of Record online : 5 MAR 2016, DOI: 10.1111/1346-8138.13220

  14. Connexin gene pathology

    Clinical and Experimental Dermatology

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

    Version of Record online : 19 JUN 2003, DOI: 10.1046/j.1365-2230.2003.01312.x

  15. 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

    Version of Record online : 29 JUL 2006, DOI: 10.1111/j.1365-2133.1991.tb00632.x

  16. Evidence for the absence of mutations at GJB3, GJB4 and LOR in progressive symmetrical erythrokeratodermia

    Clinical and Experimental Dermatology

    Volume 36, Issue 4, June 2011, Pages: 399–405, S. Wei, Y. Zhou, T. D. Zhang, Z. M. Huang, X. B. Zhang, H. L. Zhu, B. H. Liang, L. Lin and L. Deng

    Version of Record online : 24 DEC 2010, DOI: 10.1111/j.1365-2230.2010.03974.x

  17. Erythrokeratodermia Variabilis with Erythema Gyratum Repens-Like Lesions

    Pediatric Dermatology

    Volume 19, Issue 4, July 2002, Pages: 285–292, Marina Landau, Meirav Cohen-Bar-Dayan, Daniel Hohl, Joseph Ophir, Charles R. Wolf, Andrea Gat and Barukh Mevorah

    Version of Record online : 13 SEP 2002, DOI: 10.1046/j.1525-1470.2002.00085.x

  18. Erythrokeratoderma Variabilis: Case Report and Review of the Literature

    Pediatric Dermatology

    Volume 12, Issue 1, March 1995, Pages: 21–23, Ronald C. Knipe, Franklin P. Flowers, Franklin R. Johnson Jr., Franklin L. DeBusk and Francisco A. Ramos-Caro

    Version of Record online : 28 JUN 2008, DOI: 10.1111/j.1525-1470.1995.tb00118.x

  19. Erythrokeratodermia variabilis in a Jewish Kurdish family

    Clinical Genetics

    Volume 13, Issue 5, May 1978, Pages: 404–408, Shoshana Hacham-Zadeh and Zvi Even-Paz

    Version of Record online : 28 JUN 2008, DOI: 10.1111/j.1399-0004.1978.tb04138.x

  20. Erythrokeratodermia variabilis (EKV) – eine Störung der epidermalen Expression von Gap-Junction-Proteinen

    JDDG: Journal der Deutschen Dermatologischen Gesellschaft

    Volume 3, Issue 5, May 2005, Pages: 354–358, Sonja Ständer, Antje Stadelmann, Otto Traub, Heiko Traupe and Dieter Metze

    Version of Record online : 14 APR 2005, DOI: 10.1111/j.1610-0387.2005.05711.x