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There are 9548 results for: content related to: Marie-Unna Hereditary Hypotrichosis or Autosomal Recessive Hereditary Hypotrichosis with Woolly Hair: The Diagnostic Dilemma of Labeling Cases with Hypotrichosis

  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. 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

  3. Inherited Hair Disorders

    Standard Article

    Rook's Textbook of Dermatology, Ninth Edition

    Eli Sprecher

    Published Online : 9 OCT 2016, DOI: 10.1002/9781118441213.rtd0069

  4. 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

  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. Congenital hypotrichosis

    International Journal of Dermatology

    Volume 38, Issue S1, May 1999, Pages: 25–33, David De Berker

    Version of Record online : 25 DEC 2001, DOI: 10.1046/j.1365-4362.1999.00005.x

  8. Genetics of Alopecia

    Standard Article


    Shigeki Inui

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

  9. 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

  10. 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

  11. 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

  12. 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

  13. 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

  14. 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

  15. Hair Restoration Surgery in Patients with Pubic Atrichosis or Hypotrichosis: Review of Technique and Clinical Consideration of 507 Cases

    Dermatologic Surgery

    Volume 32, Issue 11, November 2006, Pages: 1327–1335, YOUNG-RAN LEE, SANG-JUN LEE, JUNG-CHUL KIM and HIDEOKI OGAWA

    Version of Record online : 3 NOV 2006, DOI: 10.1111/j.1524-4725.2006.32302.x

  16. 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

  17. 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

  18. 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

  19. Mutations in the LPAR6 and LIPH genes underlie autosomal recessive hypotrichosis/woolly hair in 17 consanguineous families from Pakistan

    Clinical and Experimental Dermatology

    Volume 36, Issue 6, August 2011, Pages: 652–654, S. Khan, R. Habib, H. Mir,   Umm-e-Kalsoom, G. Naz, M. Ayub, S. Shafique, T. Yamin, N. Ali, S. Basit, N. Wasif, S. Kamran-ul-Hassan Naqvi, G. Ali, A. Wali, M. Ansar and W. Ahmad

    Version of Record online : 21 MAR 2011, DOI: 10.1111/j.1365-2230.2011.04014.x

  20. Autosomal recessive woolly hair with hypotrichosis caused by a novel homozygous mutation in the P2RY5 gene

    Experimental Dermatology

    Volume 18, Issue 3, March 2009, Pages: 218–221, Yutaka Shimomura, Maria C. Garzon, Leonard Kristal, Lawrence Shapiro and Angela M. Christiano

    Version of Record online : 18 SEP 2008, DOI: 10.1111/j.1600-0625.2008.00788.x