Search Results

There are 4455 results for: content related to: The gastrointestinal manifestations of telomere-mediated disease

  1. Dyskeratosis congenita: clinical report and review of the literature

    International Journal of Dental Hygiene

    Volume 8, Issue 1, February 2010, Pages: 68–74, I Baran, R Nalcaci and M Kocak

    Version of Record online : 11 JUN 2009, DOI: 10.1111/j.1601-5037.2009.00364.x

  2. You have free access to this content
    Dyskeratosis congenita in all its forms

    British Journal of Haematology

    Volume 110, Issue 4, September 2000, Pages: 768–779, Inderjeet Dokal

    Version of Record online : 24 DEC 2001, DOI: 10.1046/j.1365-2141.2000.02109.x

  3. You have free access to this content
    Unraveling the pathogenesis of Hoyeraal–Hreidarsson syndrome, a complex telomere biology disorder

    British Journal of Haematology

    Volume 170, Issue 4, August 2015, Pages: 457–471, Galina Glousker, Fabien Touzot, Patrick Revy, Yehuda Tzfati and Sharon A. Savage

    Version of Record online : 4 MAY 2015, DOI: 10.1111/bjh.13442

  4. Congenital Epidermal Hypermelanoses

    The Pigmentary System: Physiology and Pathophysiology, Second Edition

    Susan Bayliss Mallory, Peggy L. Chern, Sharon A. Foley, Pages: 898–906, 2007

    Published Online : 26 OCT 2007, DOI: 10.1002/9780470987100.ch49

  5. Warty dyskeratoma/focal acantholytic dyskeratosis – an update on a rare oral lesion

    Journal of Oral Pathology & Medicine

    Volume 41, Issue 3, March 2012, Pages: 261–267, Irit Allon and Amos Buchner

    Version of Record online : 21 SEP 2011, DOI: 10.1111/j.1600-0714.2011.01082.x

  6. Dyskeratosis congenita with linear areas of severe cutaneous involvement

    American Journal of Medical Genetics

    Volume 75, Issue 5, 17 February 1998, Pages: 492–496, Eulalia Baselga, Beth A. Drolet, Peter van Tuinen, Nancy B. Esterly and Rudolf Happle

    Version of Record online : 6 DEC 1998, DOI: 10.1002/(SICI)1096-8628(19980217)75:5<492::AID-AJMG7>3.0.CO;2-P

  7. Rothmund–Thomson Syndrome, Bloom Syndrome, Dyskeratosis Congenita, Fanconi Anaemia

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

    Alan D. Irvine, Peter H. Hoeger, Albert C. Yan, Pages: 136.1–136.13, 2011

    Published Online : 24 MAY 2011, DOI: 10.1002/9781444345384.ch136

  8. You have free access to this content
    Advances in the understanding of dyskeratosis congenita

    British Journal of Haematology

    Volume 145, Issue 2, April 2009, Pages: 164–172, Amanda J. Walne and Inderjeet Dokal

    Version of Record online : 4 FEB 2009, DOI: 10.1111/j.1365-2141.2009.07598.x

  9. The Inherited Bone Marrow Failure Syndromes: Fanconi Anemia, Dyskeratosis Congenita and Diamond-Blackfan Anemia

    Reviews in Clinical and Experimental Hematology

    Volume 4, Issue 3, September 2000, Pages: 183–215, Inderjeet Dokal

    Version of Record online : 25 DEC 2001, DOI: 10.1046/j.1468-0734.2000.00015.x

  10. Cytogenetic studies of skin fibroblast cultures from a karyotypically normal female with dyskeratosis congenita

    Clinical Genetics

    Volume 41, Issue 3, March 1992, Pages: 129–134, Hildegard Kehrer, Winfrid Krone, Oetlav Schindler, Roland Kaufmann and Hubert Schrezenmeler

    Version of Record online : 28 JUN 2008, DOI: 10.1111/j.1399-0004.1992.tb03648.x

  11. Genetics and Genodermatoses

    Rook's Textbook of Dermatology, Eighth Edition

    A. D. Irvine, J. E. Mellerio, Pages: 1–97, 2010

    Published Online : 6 MAY 2010, DOI: 10.1002/9781444317633.ch15

  12. Dyskeratosis congenita: Hematologic evaluation of a sibship and review of the literature

    American Journal of Hematology

    Volume 3, Issue 2, 1977, Pages: 143–152, Dr. Arthur A. Trowbridge, Chintana Sirinavin and James W. Linman

    Version of Record online : 28 MAY 2013, DOI: 10.1002/ajh.2830030205

  13. Dyskeratosis congenita: a genetic disorder of many faces

    Clinical Genetics

    Volume 73, Issue 2, February 2008, Pages: 103–112, M Kirwan and I Dokal

    Version of Record online : 15 NOV 2007, DOI: 10.1111/j.1399-0004.2007.00923.x

  14. Genetic Defects of Nails and Nail Growth

    Standard Article

    Rook's Textbook of Dermatology, Ninth Edition

    Adam Rubin and Amy S. Paller

    Published Online : 9 OCT 2016, DOI: 10.1002/9781118441213.rtd0070

  15. Oral Focal Acantholytic Dyskeratosis

    The Journal of Dermatologic Surgery and Oncology

    Volume 16, Issue 6, June 1990, Pages: 510–515, SUSAN L. ZUNT and CHARLES E. TOMICH

    Version of Record online : 21 JUN 2013, DOI: 10.1111/j.1524-4725.1990.tb00072.x

  16. Chromosome abnormalities in cell cultures derived from the leukoplakia of a female patient with dyskeratosis congenita

    American Journal of Medical Genetics

    Volume 42, Issue 2, 15 January 1992, Pages: 217–218, Hildegard Kehrer, Winfrid Krone and Dr. Bruno Dallapiccola

    Version of Record online : 8 JUN 2005, DOI: 10.1002/ajmg.1320420219

  17. Dyskeratosis Congenita Associated with Elevated Fetal Hemoglobin, X-Linked Ocular Albinism, and Juvenile-Onset Diabetes Mellitus

    Pediatric Dermatology

    Volume 9, Issue 2, June 1992, Pages: 103–106, Martin Reichel, Arthur C. Grix and R. Rivkah Isseroff

    Version of Record online : 20 MAR 2008, DOI: 10.1111/j.1525-1470.1992.tb01223.x

  18. The wide-ranging clinical implications of the short telomere syndromes

    Internal Medicine Journal

    Volume 46, Issue 4, April 2016, Pages: 393–403, P. M. Barbaro, D. S. Ziegler and R. R. Reddel

    Version of Record online : 7 APR 2016, DOI: 10.1111/imj.12868

  19. Poikiloderma Syndromes

    Standard Article

    Rook's Textbook of Dermatology, Ninth Edition

    Alan D. Irvine and Jemima E. Mellerio

    Published Online : 9 OCT 2016, DOI: 10.1002/9781118441213.rtd0078

  20. Somatic ATP2A2 mutation in a case of papular acantholytic dyskeratosis: mosaic Darier disease

    Journal of Cutaneous Pathology

    Volume 42, Issue 11, November 2015, Pages: 853–857, Eleanor A. Knopp, Corey Saraceni, Jeremy Moss, Jennifer M. McNiff and Keith A. Choate

    Version of Record online : 12 AUG 2015, DOI: 10.1111/cup.12551