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There are 8135416 results for: content related to: Marie Unna hereditary hypotrichosis: a recurrent c.74C>T mutation in the U2HR gene and literature review

  1. Identification of a novel U2HR mutation in a Korean woman with Marie Unna hereditary hypotrichosis

    International Journal of Dermatology

    Volume 53, Issue 11, November 2014, Pages: 1358–1361, Seok-Kweon Yun, Yong-Gon Cho, Ki Hun Song, Su-Ran Hwang, Sung-Joo Kim Yoon, Keon-Woo Choi, Han-Uk Kim and Jin Park

    Version of Record online : 25 JUN 2014, DOI: 10.1111/ijd.12545

  2. You have free access to this content
    Marie Unna hereditary hypotrichosis caused by a novel mutation in the human hairless transcript

    Experimental Dermatology

    Volume 19, Issue 8, August 2010, Pages: e320–e322, Yuval Ramot, Liran Horev, Irena Smolovich, Vered Molho-Pessach and Abraham Zlotogorski

    Version of Record online : 16 FEB 2010, DOI: 10.1111/j.1600-0625.2009.01042.x

  3. Genetics of human isolated hereditary hair loss disorders

    Clinical Genetics

    Volume 88, Issue 3, September 2015, Pages: 203–212, S. Basit, S. Khan and W. Ahmad

    Version of Record online : 22 NOV 2014, DOI: 10.1111/cge.12531

  4. A novel deletion mutation in the DSG4 gene underlies autosomal recessive hypotrichosis with variable phenotype in two unrelated consanguineous families

    Clinical and Experimental Dermatology

    Volume 40, Issue 1, January 2015, Pages: 78–84, A. Ullah, S. I. Raza, R. H. Ali, A. K. Naveed, A. Jan, S. D. A. Rizvi, R. Satti and W. Ahmad

    Version of Record online : 23 SEP 2014, DOI: 10.1111/ced.12457

  5. Digenic inheritance of an autosomal recessive hypotrichosis in two consanguineous pedigrees

    Clinical Genetics

    Volume 79, Issue 3, March 2011, Pages: 273–281, S Basit, A Wali, A Aziz, N Muhammad, M Jelani and W Ahmad

    Version of Record online : 23 APR 2010, DOI: 10.1111/j.1399-0004.2010.01455.x

  6. 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

  7. Prevalent founder mutation c.736T>A of LIPH in autosomal recessive woolly hair of Japanese leads to variable severity of hypotrichosis in adulthood

    Journal of the European Academy of Dermatology and Venereology

    Volume 27, Issue 9, September 2013, Pages: 1182–1184, K. Tanahashi, K. Sugiura, T. Takeichi, H. Takama, S. Shinkuma, H. Shimizu and M. Akiyama

    Version of Record online : 26 MAR 2012, DOI: 10.1111/j.1468-3083.2012.04526.x

  8. Identification of a U2HR gene mutation in Turkish families with Marie Unna hereditary hypotrichosis

    Clinical and Experimental Dermatology

    Volume 34, Issue 8, December 2009, Pages: e953–e956, S. Düzenli, S. Redler, M. Müller, M. Polat, D. Dogruer, S. M. Pasternack and R. C. Betz

    Version of Record online : 13 NOV 2009, DOI: 10.1111/j.1365-2230.2009.03644.x

  9. Marie Unna hereditary hypotrichosis: A Turkish family with loss of eyebrows and a U2HR mutation

    American Journal of Medical Genetics Part A

    Volume 152A, Issue 10, October 2010, Pages: 2628–2633, Ayse Tulin Mansur, Nursel H. Elcioglu, Silke Redler, Zehra A. Serdar, Sule Cetinel, Regina C. Betz and Nurten A. Akarsu

    Version of Record online : 2 SEP 2010, DOI: 10.1002/ajmg.a.33649

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    Long-term safety and efficacy of bimatoprost solution 0·03% application to the eyelid margin for the treatment of idiopathic and chemotherapy-induced eyelash hypotrichosis: a randomized controlled trial

    British Journal of Dermatology

    Volume 172, Issue 5, May 2015, Pages: 1384–1394, D.A. Glaser, P. Hossain, W. Perkins, T. Griffiths, G. Ahluwalia, E. Weng and F.C. Beddingfield

    Version of Record online : 7 MAR 2015, DOI: 10.1111/bjd.13443

  11. Novel D323G mutation of DSG4 gene in a girl with localized autosomal recessive hypotrichosis clinically overlapped with monilethrix

    International Journal of Dermatology

    Volume 54, Issue 10, October 2015, Pages: 1163–1168, Jia-Man Wang, Yu-Juan Xiao and Yan-Hua Liang

    Version of Record online : 14 JUL 2015, DOI: 10.1111/ijd.12889

  12. Localization of a novel autosomal recessive hypotrichosis locus (LAH3) to chromosome 13q14.11–q21.32

    Clinical Genetics

    Volume 72, Issue 1, July 2007, Pages: 23–29, A Wali, MS Chishti, M Ayub, M Yasinzai, , G Ali, P John and W Ahmad

    Version of Record online : 27 MAY 2007, DOI: 10.1111/j.1399-0004.2007.00818.x

  13. Mutations in the P2RY5 gene underlie autosomal recessive hypotrichosis in 13 Pakistani families

    British Journal of Dermatology

    Volume 160, Issue 5, May 2009, Pages: 1006–1010, M. Tariq, M. Ayub, M. Jelani, S. Basit, G. Naz, N. Wasif, S.I. Raza, A.K. Naveed, S. Ullah Khan, Z. Azeem, M. Yasinzai, A. Wali, G. Ali, M.S. Chishti and W. Ahmad

    Version of Record online : 9 MAR 2009, DOI: 10.1111/j.1365-2133.2009.09046.x

  14. Hereditary hypotrichosis of the scalp

    American Journal of Medical Genetics

    Volume 39, Issue 2, 1 May 1991, Pages: 125–129, Dr. Russell O. Hess and Hideo Uno

    Version of Record online : 6 JUN 2005, DOI: 10.1002/ajmg.1320390202

  15. Congenital hair loss disorders: Rare, but not too rare

    The Journal of Dermatology

    Volume 39, Issue 1, January 2012, Pages: 3–10, Yutaka SHIMOMURA

    Version of Record online : 2 NOV 2011, DOI: 10.1111/j.1346-8138.2011.01395.x

  16. Marie-Unna Hereditary Hypotrichosis or Autosomal Recessive Hereditary Hypotrichosis with Woolly Hair: The Diagnostic Dilemma of Labeling Cases with Hypotrichosis

    Pediatric Dermatology

    Volume 28, Issue 6, November/December 2011, Pages: 750–751, KHALID AL ABOUD and DAIFULLAH AL ABOUD

    Version of Record online : 15 NOV 2011, DOI: 10.1111/j.1525-1470.2011.01601.x

  17. Identification of a novel heterozygous mutation in the first Japanese case of Marie Unna hereditary hypotrichosis

    The Journal of Dermatology

    Volume 40, Issue 4, April 2013, Pages: 278–280, Taisuke Ito, Yutaka Shimomura, Masaaki Ogai, Jun-Ichi Sakabe and Yoshiki Tokura

    Version of Record online : 7 JAN 2013, DOI: 10.1111/1346-8138.12068

  18. A Sporadic Case of Congenital Hypotrichosis Simplex of the Scalp: Difficulties in Diagnosis and Classification

    Pediatric Dermatology

    Volume 16, Issue 4, July/August 1999, Pages: 301–304, Stefano Cambiaghi and Mauro Barbareschi

    Version of Record online : 4 JAN 2002, DOI: 10.1046/j.1525-1470.1999.00079.x

  19. Hallermann–Streiff syndrome with cutaneous manifestations

    International Journal of Dermatology

    Volume 54, Issue 9, September 2015, Pages: 1068–1070, Adarsh Lata Singh, Meenakshi Chandak, Divya Jain and Rupali Mogre

    Version of Record online : 29 OCT 2013, DOI: 10.1111/ijd.12172

  20. Mutation in ribosomal protein L21 underlies hereditary hypotrichosis simplex

    Human Mutation

    Volume 32, Issue 7, July 2011, Pages: 710–714, Cheng Zhou, Dongjie Zang, Yan Jin, Huafeng Wu, Zhengyi Liu, Juan Du and Jianzhong Zhang

    Version of Record online : 26 APR 2011, DOI: 10.1002/humu.21503