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There are 10722 results for: content related to: Wilson's Disease

  1. Pathogenesis and management of Wilson disease

    Hepatology Research

    Volume 44, Issue 4, April 2014, Pages: 395–402, Masaru Harada

    Version of Record online : 6 MAR 2014, DOI: 10.1111/hepr.12301

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    Diagnosis and treatment of Wilson disease: An update

    Hepatology

    Volume 47, Issue 6, June 2008, Pages: 2089–2111, Eve A. Roberts and Michael L. Schilsky

    Version of Record online : 4 FEB 2008, DOI: 10.1002/hep.22261

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    A practice guideline on Wilson disease

    Hepatology

    Volume 37, Issue 6, June 2003, Pages: 1475–1492, Eve A. Roberts and Michael L. Schilsky

    Version of Record online : 30 DEC 2003, DOI: 10.1053/jhep.2003.50252

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    DKWSLLL, a Versatile DXXXLL-Type Signal with Distinct Roles in the Cu+-Regulated Trafficking of ATP7B

    Traffic

    Volume 15, Issue 8, August 2014, Pages: 839–860, Vasiliki Lalioti, Sonia Hernandez-Tiedra and Ignacio V. Sandoval

    Version of Record online : 24 JUN 2014, DOI: 10.1111/tra.12176

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    Laser ablation inductively coupled plasma mass spectrometry imaging of metals in experimental and clinical Wilson's disease

    Journal of Cellular and Molecular Medicine

    Volume 19, Issue 4, April 2015, Pages: 806–814, Sorina Georgiana Boaru, Uta Merle, Ricarda Uerlings, Astrid Zimmermann, Christa Flechtenmacher, Claudia Willheim, Elisabeth Eder, Peter Ferenci, Wolfgang Stremmel and Ralf Weiskirchen

    Version of Record online : 20 FEB 2015, DOI: 10.1111/jcmm.12497

  6. EGFP Tags Affect Cellular Localization of ATP7B Mutants

    CNS Neuroscience & Therapeutics

    Volume 19, Issue 5, May 2013, Pages: 346–351, Min Zhu, Wang Ni, Yi Dong and Zhi-Ying Wu

    Version of Record online : 22 APR 2013, DOI: 10.1111/cns.12091

  7. Distinct clinical courses according to presenting phenotypes and their correlations to ATP7B mutations in a large Wilson's disease cohort

    Liver International

    Volume 31, Issue 6, July 2011, Pages: 831–839, Beom H. Lee, Joo H. Kim, Sun Y. Lee, Hye Y. Jin, Kwi-Joo Kim, Jin-Joo Lee, Jung-Young Park, Gu-Hwan Kim, Jin-Ho Choi, Kyung M. Kim and Han-Wook Yoo

    Version of Record online : 13 MAR 2011, DOI: 10.1111/j.1478-3231.2011.02503.x

  8. Evidence for a critical role of ceruloplasmin oxidase activity in iron metabolism of Wilson disease gene knockout mice

    Journal of Gastroenterology and Hepatology

    Volume 25, Issue 6, June 2010, Pages: 1144–1150, Uta Merle, Sabine Tuma, Thomas Herrmann, Valer Muntean, Martin Volkmann, Sven G. Gehrke and Wolfgang Stremmel

    Version of Record online : 5 NOV 2009, DOI: 10.1111/j.1440-1746.2009.06173.x

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    Copper Directs ATP7B to the Apical Domain of Hepatic Cells via Basolateral Endosomes

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    Volume 15, Issue 12, December 2014, Pages: 1344–1365, Lydia K. Nyasae, Michael J. Schell and Ann L. Hubbard

    Version of Record online : 27 OCT 2014, DOI: 10.1111/tra.12229

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    Corrigendum: Copper Directs ATP7B to the Apical Domain of Hepatic Cells via Basolateral Endosomes

    Vol. 16, Issue 1, 99, Version of Record online: 22 DEC 2014

  10. Sequence variation in the ATP-binding domain of the Wilson disease transporter, ATP7B, affects copper transport in a yeast model system

    Human Mutation

    Volume 29, Issue 4, April 2008, Pages: 491–501, Gloria Hsi, Lara M. Cullen, Georgina Macintyre, Matthew M. Chen, D. Moira Glerum and Diane W. Cox

    Version of Record online : 17 JAN 2008, DOI: 10.1002/humu.20674

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    Reduced expression of ATP7B affected by Wilson disease–causing mutations is rescued by pharmacological folding chaperones 4-phenylbutyrate and curcumin

    Hepatology

    Volume 50, Issue 6, December 2009, Pages: 1783–1795, Peter V. E. van den Berghe, Janneke M. Stapelbroek, Elmar Krieger, Prim de Bie, Stan F. J. van de Graaf, Reinoud E. A. de Groot, Ellen van Beurden, Ellen Spijker, Roderick H. J. Houwen, Ruud Berger and Leo W. J. Klomp

    Version of Record online : 5 AUG 2009, DOI: 10.1002/hep.23209

  12. Molecular Genetics of Wilson Disease

    Standard Article

    eLS

    Eve A Roberts

    Published Online : 15 APR 2013, DOI: 10.1002/9780470015902.a0024373

  13. Wilson's Disease

    Textbook of Hepatology: From Basic Science to Clinical Practice, Third Edition

    Juan Rodés, Jean-Pierre Benhamou, Andres T. Blei, Jürg Reichen, Mario Rizzetto, Pages: 1313–1322, 2008

    Published Online : 15 APR 2008, DOI: 10.1002/9780470691861.ch16a

  14. Identification of novel ATP7B gene mutations and their functional roles in Korean patients with Wilson disease

    Human Mutation

    Volume 28, Issue 11, November 2007, Pages: 1108–1113, Sangwook Park, Jung-Young Park, Gu-Hwan Kim, Jin-Ho Choi, Kyung-Mo Kim, Jong-Bae Kim and Han-Wook Yoo

    Version of Record online : 22 JUN 2007, DOI: 10.1002/humu.20574

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    Localization of the Wilson disease protein in murine intestine

    Journal of Anatomy

    Volume 213, Issue 3, September 2008, Pages: 232–240, Karl Heinz Weiss, Judith Wurz, Daniel Gotthardt, Uta Merle, Wolfgang Stremmel and Joachim Füllekrug

    Version of Record online : 29 JUL 2008, DOI: 10.1111/j.1469-7580.2008.00954.x

  16. Copper Metabolism and the Liver

    The Liver: Biology and Pathobiology, Fifth Edition

    Michael L. Schilsky, Dennis J. Thiele, Pages: 221–233, 2009

    Published Online : 6 OCT 2009, DOI: 10.1002/9780470747919.ch15

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    Cell-Specific Trafficking Suggests a new role for Renal ATP7B in the Intracellular Copper Storage

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    Volume 10, Issue 6, June 2009, Pages: 767–779, Natalie Barnes, Mee Y. Bartee, Lita Braiterman, Arnab Gupta, Vladimir Ustiyan, Vesna Zuzel, Jack H. Kaplan, Ann L. Hubbard and Svetlana Lutsenko

    Version of Record online : 18 FEB 2009, DOI: 10.1111/j.1600-0854.2009.00901.x

  18. Molecular genetics of intracellular copper transport

    The Journal of Trace Elements in Experimental Medicine

    Volume 12, Issue 4, 1999, Pages: 297–313, Nina Horn and Zeynep Tümer

    Version of Record online : 19 NOV 1999, DOI: 10.1002/(SICI)1520-670X(1999)12:4<297::AID-JTRA3>3.0.CO;2-E

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    Wilson Disease Mutation Pattern with Genotype-Phenotype Correlations from Western India: Confirmation of p.C271* as a Common Indian Mutation and Identification of 14 Novel Mutations

    Annals of Human Genetics

    Volume 77, Issue 4, July 2013, Pages: 299–307, Annu Aggarwal, Gursimran Chandhok, Theodor Todorov, Saloni Parekh, Sharada Tilve, Andree Zibert, Mohit Bhatt and Hartmut H.-J. Schmidt

    Version of Record online : 2 APR 2013, DOI: 10.1111/ahg.12024

  20. Modifying factors and phenotypic diversity in Wilson's disease

    Annals of the New York Academy of Sciences

    Volume 1315, Issue 1, May 2014, Pages: 56–63, Svetlana Lutsenko

    Version of Record online : 4 APR 2014, DOI: 10.1111/nyas.12420