Search Results

There are 3259 results for: content related to: Congenital hair loss disorders: Rare, but not too rare

  1. 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

  2. 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

  3. Ectodermal Dysplasias

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

    Yuka Asai, Alan D. Irvine, Pages: 127.1–127.104, 2011

    Published Online : 24 MAY 2011, DOI: 10.1002/9781444345384.ch127

  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. 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

  6. 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

  7. You have full text access to this OnlineOpen article
    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

  8. 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

  9. Marie Unna Hypotrichosis in a Chinese Family

    Pediatric Dermatology

    Volume 19, Issue 3, May/June2002, Pages: 250–255, S. N. Wong, Y. C. Giam and Y. S. Lee

    Version of Record online : 13 JUN 2002, DOI: 10.1046/j.1525-1470.2002.00070.x

  10. 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

  11. Multiple familial and pigmented basal cell carcinomas in early childhood – Bazex–Dupré–Christol syndrome

    Journal of the European Academy of Dermatology and Venereology

    Volume 26, Issue 1, January 2012, Pages: 117–121, F. Abuzahra, L.J.M.T. Parren and J. Frank

    Version of Record online : 24 MAR 2011, DOI: 10.1111/j.1468-3083.2011.04048.x

  12. Disorders of Hair

    Rook's Textbook of Dermatology, Seventh Edition

    D. A. R. De Berker, A. G. Messenger, R. D. Sinclair, Pages: 3199–3318, 2008

    Published Online : 4 FEB 2008, DOI: 10.1002/9780470750520.ch63

  13. 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

  14. Marie Unna Hypotrichosis in an Asian Family

    The Journal of Dermatology

    Volume 28, Issue 3, March 2001, Pages: 149–152, Hong Suk Kim, Soo-Chan Kim and Won-Soo Lee

    Version of Record online : 22 JUL 2014, DOI: 10.1111/j.1346-8138.2001.tb00109.x

  15. Expression studies of a novel splice site mutation in the LIPH gene identified in a Japanese patient with autosomal recessive woolly hair

    The Journal of Dermatology

    Volume 41, Issue 10, October 2014, Pages: 890–894, Ryota Hayashi, Shigeki Inui, Muhammad Farooq, Masaaki Ito and Yutaka Shimomura

    Version of Record online : 1 OCT 2014, DOI: 10.1111/1346-8138.12623

  16. Genetics of Alopecia

    Standard Article


    Shigeki Inui

    Published Online : 16 APR 2012, DOI: 10.1002/9780470015902.a0023882

  17. 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

  18. A novel nonsense CDH3 mutation in hypotrichosis with juvenile macular dystrophy

    International Journal of Dermatology

    Volume 51, Issue 3, March 2012, Pages: 325–327, Emily Avitan-Hersh, Margarita Indelman, Ziyad Khamaysi, Rina Leibu and Reuven Bergman

    Version of Record online : 20 FEB 2012, DOI: 10.1111/j.1365-4632.2011.04973.x

  19. 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

  20. Identification of 736T>A mutation of lipase H in Japanese siblings with autosomal recessive woolly hair

    The Journal of Dermatology

    Volume 38, Issue 9, September 2011, Pages: 900–904, Takashi YOSHIMASU, Nobuo KANAZAWA, Naotomo KAMBE, Motonobu NAKAMURA and Fukumi FURUKAWA

    Version of Record online : 1 FEB 2011, DOI: 10.1111/j.1346-8138.2010.01101.x