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Apr 21, 2008 (publication date) through Apr 25, 2024
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World Journal of Gastroenterology
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1007-9327
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Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA
| For: | Simon I, Schaefer M, Reichert J, Stremmel W. Analysis of the human Atox 1 homologue in Wilson patients. World J Gastroenterol 2008; 14(15): 2383-2387 [PMID: 18416466 DOI: 10.3748/wjg.14.2383] |
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| URL: | https://www.wjgnet.com/1007-9327/full/v14/i15/2383.htm |
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Rosanna Squitti, Mariacarla Ventriglia, Massimo Gennarelli, Nicola A. Colabufo, Imane Ghafir El Idrissi, Serena Bucossi, Stefania Mariani, Mauro Rongioletti, Orazio Zanetti, Chiara Congiu, Paolo M. Rossini, Cristian Bonvicini. Non-Ceruloplasmin Copper Distincts Subtypes in Alzheimer’s Disease: a Genetic Study of ATP7B Frequency. Molecular Neurobiology 2017; 54(1): 671 doi: 10.1007/s12035-015-9664-6
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Magdalena Araya, Monica Andrews, Fernando Pizarro, Miguel Arredondo. Chaperones CCS, ATOX and COXIV responses to copper supplementation in healthy adults. BioMetals 2012; 25(2): 383 doi: 10.1007/s10534-011-9511-9
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I. Zh. Zhalsanova, E. A. Fonova, D. I. Zhigalina, N. A. Skryabin. The ATOX1 Gene Role in Copper Metabolism and the Pathogenesis of Copper-Induced Diseases. Russian Journal of Genetics 2023; 59(3): 242 doi: 10.1134/S1022795423030122
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Radan Bruha, Libor Vitek, Zdenek Marecek, Lenka Pospisilova, Sona Nevsimalova, Pavel Martasek, Jaromir Petrtyl, Petr Urbanek, Alena Jiraskova, Ivana Malikova, Martin Haluzik, Peter Ferenci. Decreased serum antioxidant capacity in patients with Wilson disease is associated with neurological symptoms. Journal of Inherited Metabolic Disease 2012; 35(3): 541 doi: 10.1007/s10545-011-9422-5
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Louis C. Penning, Marina Berenguer, Anna Czlonkowska, Kay L. Double, Petr Dusek, Carmen Espinós, Svetlana Lutsenko, Valentina Medici, Wiebke Papenthin, Wolfgang Stremmel, Jose Willemse, Ralf Weiskirchen. A Century of Progress on Wilson Disease and the Enduring Challenges of Genetics, Diagnosis, and Treatment. Biomedicines 2023; 11(2): 420 doi: 10.3390/biomedicines11020420
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Radan Bruha, Zdenek Marecek, Lenka Pospisilova, Sona Nevsimalova, Libor Vitek, Pavel Martasek, Jiri Nevoral, Jaromir Petrtyl, Petr Urbanek, Alena Jiraskova, Peter Ferenci. Long‐term follow‐up of Wilson Disease: natural history, treatment, mutations analysis and phenotypic correlation. Liver International 2011; 31(1): 83 doi: 10.1111/j.1478-3231.2010.02354.x
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I. Zh. Zhalsanova, E. A. Fonova, D. I. Zhigalina, N. A. Skryabin. The <i>ATOX1</i> Gene Role in Copper Metabolism and in the Copper-Induced Diseases Pathogenesis. Генетика 2023; 59(3): 283 doi: 10.31857/S0016675823030128
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Tomasz Litwin, Anna Członkowska. Choroba Wilsona – czynniki wpływające na obraz kliniczny. Neurologia i Neurochirurgia Polska 2013; 47(2): 161 doi: 10.5114/ninp.2013.34397
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Irene J. Chang, Si Houn Hahn. Wilson Disease. Handbook of Clinical Neurology 2017; 142: 19 doi: 10.1016/B978-0-444-63625-6.00003-3
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Niti Kumari, Aman Kumar, Amit Pal, Babu Ram Thapa, Manish Modi, Rajendra Prasad. In-silico analysis of novel p.(Gly14Ser) variant of ATOX1 gene: plausible role in modulating ATOX1–ATP7B interaction. Molecular Biology Reports 2019; 46(3): 3307 doi: 10.1007/s11033-019-04791-x
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| 17 |
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, Han-Wook Yoo. Distinct clinical courses according to presenting phenotypes and their correlations to ATP7B mutations in a large Wilson's disease cohort. Liver International 2011; 31(6): 831 doi: 10.1111/j.1478-3231.2011.02503.x
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Nivedita Singh, Pradeep Kallollimath, Mohd Hussain Shah, Saketh Kapoor, Vishwanath Kumble Bhat, Lakshminarayanapuram Gopal Viswanathan, Madhu Nagappa, Parayil S. Bindu, Arun B. Taly, Sanjib Sinha, Arun Kumar, Andreas R. Janecke. Genetic analysis of ATP7B in 102 south Indian families with Wilson disease. PLOS ONE 2019; 14(5): e0215779 doi: 10.1371/journal.pone.0215779
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T. Litwin, G. Gromadzka, J. Samochowiec, A. Grzywacz, A. Członkowski, A. Członkowska. JIMD Reports - Case and Research Reports, 2012/5. JIMD Reports 2012; 8: 73 doi: 10.1007/8904_2012_163
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Anna Członkowska, Tomasz Litwin, Petr Dusek, Peter Ferenci, Svetlana Lutsenko, Valentina Medici, Janusz K. Rybakowski, Karl Heinz Weiss, Michael L. Schilsky. Wilson disease. Nature Reviews Disease Primers 2018; 4(1) doi: 10.1038/s41572-018-0018-3
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May T. Maung, Alyssa Carlson, Monserrat Olea‐Flores, Lobna Elkhadragy, Kyle M. Schachtschneider, Napoleon Navarro‐Tito, Teresita Padilla‐Benavides. The molecular and cellular basis of copper dysregulation and its relationship with human pathologies. The FASEB Journal 2021; 35(9) doi: 10.1096/fj.202100273RR
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Karolina Dzieżyc, Tomasz Litwin, Grzegorz Chabik, Karolina Gramza, Anna Członkowska. Families with Wilson's disease in subsequent generations: Clinical and genetic analysis. Movement Disorders 2014; 29(14): 1828 doi: 10.1002/mds.26057
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Grażyna Gromadzka, Magdalena Rudnicka, Grzegorz Chabik, Adam Przybyłkowski, Anna Członkowska. Genetic variability in the methylenetetrahydrofolate reductase gene (MTHFR) affects clinical expression of Wilson’s disease. Journal of Hepatology 2011; 55(4): 913 doi: 10.1016/j.jhep.2011.01.030
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Karl Heinz Weiss, Wolfgang Stremmel. Evolving Perspectives in Wilson Disease: Diagnosis, Treatment and Monitoring. Current Gastroenterology Reports 2012; 14(1): 1 doi: 10.1007/s11894-011-0227-3
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