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There are 7861849 results for: content related to: Cause of death in Wilson disease

  1. 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

  2. Identification of three novel mutations and a high frequency of the Arg778Leu mutation in Korean patients with Wilson disease

    Human Mutation

    Volume 11, Issue 4, 1998, Pages: 275–278, Eun Kyung Kim, Ook Joon Yoo, Kyu Young Song, Han Wook Yoo, Sang Yong Choi, Sung Won Cho and Si Houn Hahn

    Version of Record online : 22 NOV 1999, DOI: 10.1002/(SICI)1098-1004(1998)11:4<275::AID-HUMU4>3.0.CO;2-L

  3. Genotype–phenotype correlations for a wide spectrum of mutations in the Wilson disease gene (ATP7B)

    American Journal of Medical Genetics Part A

    Volume 131A, Issue 2, 1 December 2004, Pages: 168–173, Eleni Panagiotakaki, Maria Tzetis, Nina Manolaki, Giorgos Loudianos, Athanasios Papatheodorou, Emmanuel Manesis, Sanda Nousia-Arvanitakis, Syriopoulou V and Emmanuel Kanavakis

    Version of Record online : 2 NOV 2004, DOI: 10.1002/ajmg.a.30345

  4. Molecular characterization of Wilson disease in the Sardinian population—Evidence of a founder effect

    Human Mutation

    Volume 14, Issue 4, October 1999, Pages: 294–303, Georgios Loudianos, Valeria Dessi, Mario Lovicu, Andrea Angius, Annalena Figus, Franco Lilliu, Stefano De Virgiliis, Anna Maria Nurchi, Angelo Deplano, Paolo Moi, Mario Pirastu and Antonio Cao

    Version of Record online : 28 SEP 1999, DOI: 10.1002/(SICI)1098-1004(199910)14:4<294::AID-HUMU4>3.0.CO;2-9

  5. Haplotype and mutation analysis in Mediterranean patients with Wilson disease

    The Journal of Trace Elements in Experimental Medicine

    Volume 12, Issue 4, 1999, Pages: 315–319, Georgios Loudianos, Valeria Dessi, Mario Lovicu, Andrea Angius, Mario Pirastu and Antonio Cao

    Version of Record online : 19 NOV 1999, DOI: 10.1002/(SICI)1520-670X(1999)12:4<315::AID-JTRA4>3.0.CO;2-#

  6. 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

  7. A study of Wilson disease mutations in Britain

    Human Mutation

    Volume 14, Issue 4, October 1999, Pages: 304–311, Diana Curtis, Miranda Durkie, Pauline Balac (Morris), Donna Sheard, Anne Goodeve, Ian Peake, Oliver Quarrell and Stuart Tanner

    Version of Record online : 28 SEP 1999, DOI: 10.1002/(SICI)1098-1004(199910)14:4<304::AID-HUMU5>3.0.CO;2-W

  8. Mutation analysis of Wilson disease in the Spanish population – identification of a prevalent substitution and eight novel mutations in the ATP7B gene

    Clinical Genetics

    Volume 68, Issue 1, July 2005, Pages: 61–68, E Margarit, V Bach, D Gómez, M Bruguera, P Jara, R Queralt and F Ballesta

    Version of Record online : 31 MAR 2005, DOI: 10.1111/j.1399-0004.2005.00439.x

  9. You have free access to this content
    Use of the molecular adsorbents recirculating system as a treatment for acute decompensated wilson disease

    Liver Transplantation

    Volume 14, Issue 10, October 2008, Pages: 1512–1516, Alexander Chiu, Nai Shun Tsoi and Sheung Tat Fan

    Version of Record online : 29 SEP 2008, DOI: 10.1002/lt.21553

  10. Mutation analysis of Wilson disease in Taiwan and description of six new mutations

    Human Mutation

    Volume 12, Issue 6, 1998, Pages: 370–376, Chang-Hai Tsai, Fuu-Jen Tsai, Jer-Yuarn Wu, Jang-Gowth Chang, Cheng-Chun Lee, Shuan-Pei Lin, Chi-Fan Yang, Yuh-Jyh Jong and Man-Chi Lo

    Version of Record online : 7 JAN 1999, DOI: 10.1002/(SICI)1098-1004(1998)12:6<370::AID-HUMU2>3.0.CO;2-S

  11. Wilson disease

    Textbook of Clinical Gastroenterology and Hepatology, Second Edition

    C. J. Hawkey, Jaime Bosch, Joel E. Richter, Guadalupe Garcia-Tsao, Francis K. L. Chan, Pages: 689–694, 2012

    Published Online : 16 APR 2012, DOI: 10.1002/9781118321386.ch92

  12. You have free access to this content
    Mutation analysis in patients with Wilson disease: Identification of 4 novel mutations

    Human Mutation

    Volume 14, Issue 1, 1999, Page: 88, Regina Haas, Bertha Gutierrez-Rivero, Judith Knoche, Klaus Böker, Michael P. Manns and Hartmut H.-J. Schmidt

    Version of Record online : 1 JUL 1999, DOI: 10.1002/(SICI)1098-1004(1999)14:1<88::AID-HUMU15>3.0.CO;2-H

  13. Late diagnosed Wilson disease with hepatic and neurological manifestations

    Hepatology Research

    Volume 41, Issue 3, March 2011, Pages: 270–276, Yuichi Honma, Masaru Harada, Miyuki Sato, Yuka Katsuki, Masaaki Hiura, Michihiko Shibata, Ryoichi Narita, Riko Harada, Shintaro Abe, Akinari Tabaru, Nobuyoshi Tajiri and Shohei Shimajiri

    Version of Record online : 21 FEB 2011, DOI: 10.1111/j.1872-034X.2010.00754.x

  14. Proteomic analyzes of copper metabolism in an in vitro model of Wilson disease using surface enhanced laser desorption/ionization-time of flight-mass spectrometry

    Journal of Cellular Biochemistry

    Volume 93, Issue 4, 1 November 2004, Pages: 732–740, Dr. Han Roelofsen, Reshma Balgobind and Roel J. Vonk

    Version of Record online : 11 AUG 2004, DOI: 10.1002/jcb.20226

  15. Diagnostic significance of reduced serum caeruloplasmin concentration in neurological disease

    Movement Disorders

    Volume 20, Issue 12, December 2005, Pages: 1658–1661, John M. Walshe

    Version of Record online : 9 AUG 2005, DOI: 10.1002/mds.20628

  16. Three novel mutations (P760L, L1305P, Q1351Stop) causing Wilson disease

    Human Mutation

    Volume 17, Issue 2, February 2001, Page: 156, Janine Genschel, Anna Czlonkowska, Grit Sommer, Carsten Buettner, Bettina Bochow, Herbert Lochs and Hartmut H-J. Schmidt

    Version of Record online : 23 JAN 2001, DOI: 10.1002/1098-1004(200102)17:2<156::AID-HUMU18>3.0.CO;2-0

  17. Novel ATP7B mutations causing Wilson disease in several Israeli ethnic groups

    Human Mutation

    Volume 11, Issue 2, 1998, Pages: 145–151, Hagar Kalinsky, Adina Funes, Alina Zeldin, Yehuda Pel-Or, Misha Korostishevsky, Ruth Gershoni-Baruch, Lindsay A. Farrer and Batsheva Bonne-Tamir

    Version of Record online : 7 JAN 1999, DOI: 10.1002/(SICI)1098-1004(1998)11:2<145::AID-HUMU7>3.0.CO;2-I

  18. Diagnosis and phenotypic classification of Wilson disease

    Liver International

    Volume 23, Issue 3, June 2003, Pages: 139–142, Peter Ferenci, Karel Caca, Georgios Loudianos, Georgina Mieli-Vergani, Stuart Tanner, Irmin Sternlieb, Michael Schilsky, Diane Cox and Frieder Berr

    Version of Record online : 7 MAY 2003, DOI: 10.1034/j.1600-0676.2003.00824.x

  19. Hemolytic anemia in wilson disease: Clinical findings and biochemical mechanisms

    American Journal of Hematology

    Volume 9, Issue 3, November 1980, Pages: 269–275, Stephen J. Forman, K. Sree Kumar, Allan G. Redeker and Paul Hochstein

    Version of Record online : 11 JUL 2006, DOI: 10.1002/ajh.2830090305

  20. Metabolic Diseases of the Liver

    Textbook of Gastroenterology

    Tadataka Yamada, Pages: 2223–2246, 2009

    Published Online : 17 FEB 2009, DOI: 10.1002/9781444303254.ch87