For: | Kim JW, Kim JH, Seo JK, Ko JS, Chang JY, Yang HR, Kang KH. Genetically confirmed Wilson disease in a 9-month old boy with elevations of aminotransferases. World J Hepatol 2013; 5(3): 156-159 [PMID: 23556051 DOI: 10.4254/wjh.v5.i3.156] |
---|---|
URL: | https://www.wjgnet.com/1948-5182/full/v5/i3/156.htm |
Number | Citing Articles |
1 |
Oliver Bandmann, Karl Heinz Weiss, Stephen G Kaler. Wilson's disease and other neurological copper disorders. The Lancet Neurology 2015; 14(1): 103 doi: 10.1016/S1474-4422(14)70190-5
|
2 |
Corinne Collet, Jean-Louis Laplanche, Justine Page, Hélène Morel, France Woimant, Aurélia Poujois. High genetic carrier frequency of Wilson’s disease in France: discrepancies with clinical prevalence. BMC Medical Genetics 2018; 19(1) doi: 10.1186/s12881-018-0660-3
|
3 |
Duaa Al‐Sadeq, Taghreed Abunada, Rajaa Dalloul, Sara Fahad, Sara Taleb, Kholoud Aljassim, Fatima Alzahra Al Hamed, Hatem Zayed. Spectrum of mutations of cystic fibrosis in the 22 Arab countries: A systematic review. Respirology 2019; 24(2): 127 doi: 10.1111/resp.13437
|
4 |
Ulrike Reuner, Jürgen Dinger. Morbus Wilson – das Wichtigste ist: „daran zu denken“. Neuroradiologie Scan 2021; 11(03): 195 doi: 10.1055/a-1494-0499
|
5 |
|
6 |
Cynthia Abou Zeid, Ling Yi, Stephen G. Kaler. The Liver. 2020; : 207 doi: 10.1002/9781119436812.ch18
|
7 |
Michelle Camarata, Regino P. Gonzalez-Peralta. Management of Wilson Disease. Clinical Gastroenterology 2018; : 161 doi: 10.1007/978-3-319-91527-2_9
|
8 |
Amelie Stalke, Eva-Doreen Pfister, Ulrich Baumann, Marlies Eilers, Vera Schäffer, Thomas Illig, Bernd Auber, Brigitte Schlegelberger, Renate Brackmann, Holger Prokisch, Simon Krooss, Jens Bohne, Britta Skawran. Homozygous frame shift variant in ATP7B exon 1 leads to bypass of nonsense-mediated mRNA decay and to a protein capable of copper export. European Journal of Human Genetics 2019; 27(6): 879 doi: 10.1038/s41431-019-0345-1
|
9 |
Michael L. Schilsky, Eve A. Roberts, Jeff M. Bronstein, Anil Dhawan, James P. Hamilton, Anne Marie Rivard, Mary Kay Washington, Karl Heinz Weiss, Paula C. Zimbrean. A multidisciplinary approach to the diagnosis and management of Wilson disease: 2022 Practice Guidance on Wilson disease from the American Association for the Study of Liver Diseases. Hepatology 2022; doi: 10.1002/hep.32801
|
10 |
|
11 |
Peter Ferenci. Phenotype–genotype correlations in patients with Wilson's disease. Annals of the New York Academy of Sciences 2014; 1315(1): 1 doi: 10.1111/nyas.12340
|
12 |
Eve A. Roberts, Piotr Socha. Wilson Disease. Handbook of Clinical Neurology 2017; 142: 141 doi: 10.1016/B978-0-444-63625-6.00012-4
|
13 |
Simin Li, Yunting Lin, Shehong Chen, Wen Zhang, Yu‐ming Chen, Xinshuo Lu, Yongxian Shao, Zhikun Lu, Huiying Sheng, Zhihong Guan, Ruidan Zheng, Cuili Liang, Yaoyong Chen, Li Liu, Chunhua Zeng. Clinical characteristics and prognosis of early diagnosed Wilson's disease: A large cohort study. Liver International 2024; 44(9): 2424 doi: 10.1111/liv.16009
|
14 |
Harvey S. Singer, Jonathan W. Mink, Donald L. Gilbert, Joseph Jankovic. Movement Disorders in Childhood. 2022; : 443 doi: 10.1016/B978-0-12-820552-5.00018-8
|
15 |
Nanda Kerkar, Eve A. Roberts. Clinical and Translational Perspectives on WILSON DISEASE. 2019; : 179 doi: 10.1016/B978-0-12-810532-0.00017-3
|
16 |
Xinshuo Lu, Simin Li, Wen Zhang, Yunting Lin, Zhikun Lu, Yanna Cai, Xueying Su, Yongxian Shao, Zongcai Liu, Huiying Sheng, Yonglan Huang, Li Liu, Chunhua Zeng. Assessment of the diagnostic value of serum ceruloplasmin for Wilson’s disease in children. BMC Gastroenterology 2022; 22(1) doi: 10.1186/s12876-022-02186-0
|
17 |
Dorothy A. Kieffer, Valentina Medici. Wilson disease: At the crossroads between genetics and epigenetics—A review of the evidence. Liver Research 2017; 1(2): 121 doi: 10.1016/j.livres.2017.08.003
|
18 |
Eduardo Martínez-Morillo, Josep Miquel Bauça. Actualización en el diagnóstico bioquímico de la enfermedad de Wilson. Advances in Laboratory Medicine / Avances en Medicina de Laboratorio 2022; 3(2): 114 doi: 10.1515/almed-2021-0089
|
19 |
Françoise Schmitt, Guillaume Podevin, Joël Poupon, Jérôme Roux, Pierre Legras, Jean-Marc Trocello, France Woimant, Olivier Laprévote, Tuan Huy NGuyen, Souleiman El Balkhi, Fanis Missirlis. Evolution of Exchangeable Copper and Relative Exchangeable Copper through the Course of Wilson's Disease in the Long Evans Cinnamon Rat. PLoS ONE 2013; 8(12): e82323 doi: 10.1371/journal.pone.0082323
|
20 |
Hasan M Isa, Fawzeya A Alahmed, Maryam Y Busehail, Zahra H Isa, Kawthar M Abdulla. Genetically Confirmed Wilson Disease: A Retrospective Cohort Study From Bahrain. Cureus 2024; doi: 10.7759/cureus.71805
|
21 |
Karima Lafhal, Es-said Sabir, Abdelmalek Hakmaoui, Miloud Hammoud, Abdelmohcine Aimrane, Samira Najeh, Imane Assiri, Abdelaati Berrachid, Najwa Imad, Chaima Ait Boujemaa, Faissal Aziz, Fatima Zahra El Hanafi, Abdessamad Lalaoui, Hasna Aamri, Iryna Boyko, Ana Sánchez-Monteagudo, Carmen Espinós, Imane Ait Sab, Nisrine Aboussair, Aicha Bourrahouat, Naima Fdil. Clinical, biochemical and molecular characterization of Wilson's disease in Moroccan patients. Molecular Genetics and Metabolism Reports 2023; 36: 100984 doi: 10.1016/j.ymgmr.2023.100984
|
22 |
Eve A. Roberts. Update on the Diagnosis and Management of Wilson Disease. Current Gastroenterology Reports 2018; 20(12) doi: 10.1007/s11894-018-0660-7
|
23 |
Harvey S. Singer, Jonathan W. Mink, Donald L. Gilbert, Joseph Jankovic. Movement Disorders in Childhood. 2016; : 337 doi: 10.1016/B978-0-12-411573-6.00017-6
|
24 |
|
25 |
Christine Lo, Oliver Bandmann. Wilson Disease. Handbook of Clinical Neurology 2017; 142: 7 doi: 10.1016/B978-0-444-63625-6.00002-1
|
26 |
Peter Ferenci. Whom and how to screen for Wilson disease. Expert Review of Gastroenterology & Hepatology 2014; 8(5): 513 doi: 10.1586/17474124.2014.899898
|
27 |
Hisao Hayashi, Kazumasa Watanabe, Ayano Inui, Ayako Kato, Yasuaki Tatsumi, Akihiko Okumura, Tomoo Fujisawa, Koichi Kato. Alanine Aminotransferase as the First Test Parameter for Wilson’s Disease. Journal of Clinical and Translational Hepatology 2019; 7(X): 1 doi: 10.14218/JCTH.2019.00042
|
28 |
Caitlin Mulligan, Jeff M. Bronstein. Wilson Disease. Neurologic Clinics 2020; 38(2): 417 doi: 10.1016/j.ncl.2020.01.005
|
29 |
Pamela L. Valentino, Eve A. Roberts, Stacey Beer, Tamir Miloh, Ronen Arnon, Jennifer M. Vittorio, Michael L. Schilsky. Management of Wilson Disease Diagnosed in Infancy. Journal of Pediatric Gastroenterology and Nutrition 2020; 70(5): 547 doi: 10.1097/MPG.0000000000002608
|
30 |
Kuerbanjiang Abuduxikuer, Li-Ting Li, Yi-Ling Qiu, Neng-Li Wang, Jian-She Wang. Wilson disease with hepatic presentation in an eight-month-old boy. World Journal of Gastroenterology 2015; 21(29): 8981-8984 doi: 10.3748/wjg.v21.i29.8981
|
31 |
W. Hermann, D. Huster. Diagnostik des Morbus Wilson. Der Nervenarzt 2018; 89(2): 115 doi: 10.1007/s00115-017-0452-6
|
32 |
Ulrike Reuner, Jürgen Dinger. Morbus Wilson – das Wichtigste ist: „daran zu denken“. Neurologie up2date 2021; 4(01): 71 doi: 10.1055/a-0956-2573
|
33 |
Sanjay Kumar, Mohd Irtaza, Biswa Ranjan Patra, Praveen Kumar Rao, Amrit Gopan, Aditya P. Kale, Akash Shukla. Clinical profile of adult and pediatric patients with hepatic Wilson’s disease. Indian Journal of Gastroenterology 2024; 43(2): 425 doi: 10.1007/s12664-024-01586-2
|
34 |
K Gaur, P Sakhuja, RN Mandal, S Kapoor. Indian childhood cirrhosis – down but not out. Journal of Postgraduate Medicine 2018; 64(2): 104 doi: 10.4103/jpgm.JPGM_359_17
|
35 |
Wei Song, Ling Xin, Jiemei Wang. A grading method for Kayser Fleischer ring images based on ResNet. Heliyon 2023; 9(5): e16149 doi: 10.1016/j.heliyon.2023.e16149
|
36 |
Jorge Júlvez, Duygu Dikicioglu, Stephen G. Oliver. Handling variability and incompleteness of biological data by flexible nets: a case study for Wilson disease. npj Systems Biology and Applications 2018; 4(1) doi: 10.1038/s41540-017-0044-x
|
37 |
Sibel Saracoglu, Kazim Gumus, Selim Doganay, Gonca Koc, Ayse Kacar Bayram, Duran Arslan, Hakan Gumus. Brain susceptibility changes in neurologically asymptomatic pediatric patients with Wilson’s disease: evaluation with quantitative susceptibility mapping. Acta Radiologica 2018; 59(11): 1380 doi: 10.1177/0284185118759821
|
38 |
Amelie Stalke, Annika Behrendt, Finja Hennig, Holger Gohlke, Nicole Buhl, Thea Reinkens, Ulrich Baumann, Brigitte Schlegelberger, Thomas Illig, Eva‐Doreen Pfister, Britta Skawran. Functional characterization of novel or yet uncharacterized ATP7B missense variants detected in patients with clinical Wilson's disease. Clinical Genetics 2023; 104(2): 174 doi: 10.1111/cge.14352
|
39 |
Eduardo Martínez-Morillo, Josep Miquel Bauça. Biochemical diagnosis of Wilson’s disease: an update. Advances in Laboratory Medicine / Avances en Medicina de Laboratorio 2022; 3(2): 103 doi: 10.1515/almed-2022-0020
|