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There are 30428 results for: content related to: Patient with dyschromatosis symmetrica hereditaria treated with miniature punch grafting, followed by excimer light therapy

  1. You have free access to this content
    Dyschromatosis symmetrica hereditaria

    The Journal of Dermatology

    Volume 40, Issue 5, May 2013, Pages: 336–343, Masahiro Hayashi and Tamio Suzuki

    Version of Record online : 14 SEP 2012, DOI: 10.1111/j.1346-8138.2012.01661.x

  2. Dyschromatosis symmetrica hereditaria (reticulate acropigmentation of Dohi): report of a Japanese family with the condition and a literature review of 185 cases

    British Journal of Dermatology

    Volume 140, Issue 3, March 1999, Pages: 491–496, OYAMA, SHIMIZU, OHATA, TAJIMA and NISHIKAWA

    Version of Record online : 24 DEC 2001, DOI: 10.1046/j.1365-2133.1999.02716.x

  3. Dyschromatosis universalis hereditaria: Familial case and ultrastructural skin investigation

    American Journal of Medical Genetics Part A

    Volume 125A, Issue 3, 15 March 2004, Pages: 261–266, Ulrike A. Nuber, Sigrid Tinschert, Stefan Mundlos and Ingrid Hauber

    Version of Record online : 29 SEP 2003, DOI: 10.1002/ajmg.a.20519

  4. Mutation Analysis of the ADAR1 Gene in a Chinese Family with Dyschromatosis Symmetrica Hereditaria

    Australasian Journal of Dermatology

    Volume 55, Issue 1, February 2014, Pages: 92–93, Yijin Huang, Xiaoyan Zhao, Qin Mei, Bo Cheng, Yan Zhao and Zhaoshui Shangguan

    Version of Record online : 17 JAN 2014, DOI: 10.1111/ajd.12132

  5. Dyschromatosis symmetrica hereditaria: report of a sporadic case

    International Journal of Dermatology

    Volume 49, Issue 8, August 2010, Pages: 918–920, Javier Consigli, Maria S. Gómez Zanni, Luciana Ragazzini and Cristian Danielo

    Version of Record online : 19 JUL 2010, DOI: 10.1111/j.1365-4632.2010.04472.x

  6. Six novel mutations of the ADAR1 gene in patients with dyschromatosis symmetrica hereditaria: Histological observation and comparison of genotypes and clinical phenotypes

    The Journal of Dermatology

    Volume 35, Issue 7, July 2008, Pages: 395–406, Taisuke KONDO, Tamio SUZUKI, Yoshihiko MITSUHASHI, Shiro ITO, Michihiro KONO, Mayumi KOMINE, Hirotaka AKITA and Yasushi TOMITA

    Version of Record online : 10 JUL 2008, DOI: 10.1111/j.1346-8138.2008.00493.x

  7. A novel nonsense mutation of ADAR1 gene in a Chinese patient with dyschromatosis symmetrica hereditaria

    Journal of the European Academy of Dermatology and Venereology

    Volume 28, Issue 12, December 2014, Pages: 1832–1833, Q.-Y. Wu, W.-W. Li, N. Li, T.-F. Li, C. Zhang, T. Ni, Y.-X. Cui, X.-J. Li and X.-Y. Xia

    Version of Record online : 14 FEB 2014, DOI: 10.1111/jdv.12381

  8. You have free access to this content
    Infancy- and childhood-onset dyschromatoses

    Clinical and Experimental Dermatology

    Volume 36, Issue 8, December 2011, Pages: 833–839, V. Vachiramon, K. Thadanipon and K. Chanprapaph

    Version of Record online : 10 NOV 2011, DOI: 10.1111/j.1365-2230.2011.04162.x

  9. Two novel mutations of the ADAR1 gene in Chinese patients with dyschromatosis symmetrica hereditaria successfully treated with fractional CO2 laser

    Journal of the European Academy of Dermatology and Venereology

    Volume 30, Issue 6, June 2016, Pages: 1035–1038, X.G. Xu, Y. Lv, J.L. Zhai, Y.H. Li, X.H. Gao and H.D. Chen

    Version of Record online : 12 MAR 2015, DOI: 10.1111/jdv.13090

  10. Genetic Epidermal Syndromes: Disorders Characterized by Reticulated Hyperpigmentation

    The Pigmentary System: Physiology and Pathophysiology, Second Edition

    Eulalia Baselga, Nancy Burton Esterly, Pages: 780–808, 2007

    Published Online : 26 OCT 2007, DOI: 10.1002/9780470987100.ch44

  11. Effective treatment with Dabrafenib and Trametinib for a BRAF-mutated metastatic dedifferentiated malignant spindle cell neoplasm

    Journal of the European Academy of Dermatology and Venereology

    Volume 30, Issue 7, July 2016, Pages: 1224–1226, I. Escandell, M. Cabezas, J.M. Martín, L. Terradez and M.I. Pinazo

    Version of Record online : 27 APR 2015, DOI: 10.1111/jdv.13155

  12. The Racket Graft

    Dermatologic Surgery

    Volume 39, Issue 11, November 2013, Pages: 1714–1717, Erich Vargas-Diez

    Version of Record online : 1 NOV 2013, DOI: 10.1111/dsu.12323

  13. Dyschromatosis symmetrica hereditaria complicated by intracranial hemangiomas and Parry–Romberg syndrome

    The Journal of Dermatology

    Saki Yanagishita, Kazuyoshi Fukai, Daisuke Tsuruta, Toshiyuki Seto, Taro Shimono, Ken Okamura, Yutaka Hozumi and Tamio Suzuki

    Version of Record online : 4 APR 2016, DOI: 10.1111/1346-8138.13353

  14. Surgical Treatment of Speckled Skin Caused by Dyschromatosis Symmetrica Hereditaria

    The Journal of Dermatology

    Volume 13, Issue 6, December 1986, Pages: 471–473, Tadashi Taki, Sadao Kozuka, Yohei Izawa, Mitsuyoshi Hiramatsu, Toshikazu Usuda, Kazuhisa Yokoo, Toshiki Matsuda, Tomihiko Kou and Taisuke Kobayashi

    Version of Record online : 9 APR 2015, DOI: 10.1111/j.1346-8138.1986.tb02978.x

  15. Dyschromatosis symmetrica hereditaria with long hair on the forearms, hypo/hyperpigmented hair, and dental anomalies: Report of a novel ADAR1 mutation

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 9, September 2012, Pages: 2258–2265, Piranit Nik Kantaputra, Wannapa Chinadet, Atsushi Ohazama and Michihiro Kono

    Version of Record online : 20 JUL 2012, DOI: 10.1002/ajmg.a.35488

  16. Dyschromatosis Universalis Hereditaria: Report of a case and Review of the Literature

    Pediatric Dermatology

    Volume 19, Issue 6, November 2002, Pages: 523–526, Khalid Al Hawsawi, Khalid Al Aboud, V. Ramesh and Daifullah Al Aboud

    Version of Record online : 23 NOV 2002, DOI: 10.1046/j.1525-1470.2002.00225.x

  17. Evaluation and improving the success rate of protein identification by peptide mass fingerprinting using matrix-assisted laser desorption/ionization time-of-flight mass spectrometry

    Rapid Communications in Mass Spectrometry

    Volume 19, Issue 17, 15 September 2005, Pages: 2465–2468, Freek Bouwman, Dennis Suylen, Johan Renes and Edwin Mariman

    Version of Record online : 29 JUL 2005, DOI: 10.1002/rcm.2073

  18. Dyschromatosis Universalis Hereditaria with Oral Leukokeratosis—A Case of Mistaken Identity and Review of the Literature

    Pediatric Dermatology

    Volume 32, Issue 6, November/December 2015, Pages: e283–e287, Robert H. Sorensen, Kimberly A. Werner and Todd T. Kobayashi

    Version of Record online : 13 AUG 2015, DOI: 10.1111/pde.12652

  19. Novel ADAR1 mutations including a single amino acid deletion in the deaminase domain underlie dyschromatosis symmetrica hereditaria in Japanese families

    International Journal of Dermatology

    Volume 53, Issue 3, March 2014, Pages: e194–e196, Michihiro Kono, Mutsumi Suganuma, Yasutomo Ito, Hideyuki Ujiie, Kenichi Morimoto and Masashi Akiyama

    Version of Record online : 28 APR 2013, DOI: 10.1111/j.1365-4632.2012.05765.x

  20. Two Taiwanese siblings with dyschromatosis universalis hereditaria

    Clinical and Experimental Dermatology

    Volume 34, Issue 8, December 2009, Pages: e666–e669, C. Y. Wu and W. H. Huang

    Version of Record online : 17 JUN 2009, DOI: 10.1111/j.1365-2230.2009.03385.x