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Cited by in CrossRef
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 disordersThe 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 prevalenceBMC 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 reviewRespirology 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
D. Huster. Morbus WilsonDer Gastroenterologe 2018; 13(3): 199 doi: 10.1007/s11377-018-0260-y
6
Cynthia Abou Zeid, Ling Yi, Stephen G. Kaler. The Liver2020; : 207 doi: 10.1002/9781119436812.ch18
7
Michelle Camarata, Regino P. Gonzalez-Peralta. Management of Wilson DiseaseClinical 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 exportEuropean 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 DiseasesHepatology 2022;  doi: 10.1002/hep.32801
10
D. Huster. Morbus WilsonDer Internist 2018; 59(2): 159 doi: 10.1007/s00108-017-0378-x
11
Peter Ferenci. Phenotype–genotype correlations in patients with Wilson's diseaseAnnals of the New York Academy of Sciences 2014; 1315(1): 1 doi: 10.1111/nyas.12340
12
Eve A. Roberts, Piotr Socha. Wilson DiseaseHandbook of Clinical Neurology 2017; 142: 141 doi: 10.1016/B978-0-444-63625-6.00012-4
13
Harvey S. Singer, Jonathan W. Mink, Donald L. Gilbert, Joseph Jankovic. Movement Disorders in Childhood2022; : 443 doi: 10.1016/B978-0-12-820552-5.00018-8
14
Nanda Kerkar, Eve A. Roberts. Clinical and Translational Perspectives on WILSON DISEASE2019; : 179 doi: 10.1016/B978-0-12-810532-0.00017-3
15
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 childrenBMC Gastroenterology 2022; 22(1) doi: 10.1186/s12876-022-02186-0
16
Dorothy A. Kieffer, Valentina Medici. Wilson disease: At the crossroads between genetics and epigenetics—A review of the evidenceLiver Research 2017; 1(2): 121 doi: 10.1016/j.livres.2017.08.003
17
Eduardo Martínez-Morillo, Josep Miquel Bauça. Actualización en el diagnóstico bioquímico de la enfermedad de WilsonAdvances in Laboratory Medicine / Avances en Medicina de Laboratorio 2022; 3(2): 114 doi: 10.1515/almed-2021-0089
18
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 RatPLoS ONE 2013; 8(12): e82323 doi: 10.1371/journal.pone.0082323
19
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 patientsMolecular Genetics and Metabolism Reports 2023; 36: 100984 doi: 10.1016/j.ymgmr.2023.100984
20
Eve A. Roberts. Update on the Diagnosis and Management of Wilson DiseaseCurrent Gastroenterology Reports 2018; 20(12) doi: 10.1007/s11894-018-0660-7
21
Harvey S. Singer, Jonathan W. Mink, Donald L. Gilbert, Joseph Jankovic. Movement Disorders in Childhood2016; : 337 doi: 10.1016/B978-0-12-411573-6.00017-6
22
Nora V. Bergasa. Clinical Cases in Hepatology2022; : 371 doi: 10.1007/978-1-4471-4715-2_12
23
Christine Lo, Oliver Bandmann. Wilson DiseaseHandbook of Clinical Neurology 2017; 142: 7 doi: 10.1016/B978-0-444-63625-6.00002-1
24
Peter Ferenci. Whom and how to screen for Wilson diseaseExpert Review of Gastroenterology & Hepatology 2014; 8(5): 513 doi: 10.1586/17474124.2014.899898
25
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 DiseaseJournal of Clinical and Translational Hepatology 2019; 7(X): 1 doi: 10.14218/JCTH.2019.00042
26
Caitlin Mulligan, Jeff M. Bronstein. Wilson DiseaseNeurologic Clinics 2020; 38(2): 417 doi: 10.1016/j.ncl.2020.01.005
27
Pamela L. Valentino, Eve A. Roberts, Stacey Beer, Tamir Miloh, Ronen Arnon, Jennifer M. Vittorio, Michael L. Schilsky. Management of Wilson Disease Diagnosed in InfancyJournal of Pediatric Gastroenterology and Nutrition 2020; 70(5): 547 doi: 10.1097/MPG.0000000000002608
28
Kuerbanjiang Abuduxikuer, Li-Ting Li, Yi-Ling Qiu, Neng-Li Wang, Jian-She Wang. Wilson disease with hepatic presentation in an eight-month-old boyWorld Journal of Gastroenterology 2015; 21(29): 8981-8984 doi: 10.3748/wjg.v21.i29.8981
29
W. Hermann, D. Huster. Diagnostik des Morbus WilsonDer Nervenarzt 2018; 89(2): 115 doi: 10.1007/s00115-017-0452-6
30
Ulrike Reuner, Jürgen Dinger. Morbus Wilson – das Wichtigste ist: „daran zu denken“Neurologie up2date 2021; 4(01): 71 doi: 10.1055/a-0956-2573
31
K Gaur, P Sakhuja, RN Mandal, S Kapoor. Indian childhood cirrhosis – down but not outJournal of Postgraduate Medicine 2018; 64(2): 104 doi: 10.4103/jpgm.JPGM_359_17
32
Wei Song, Ling Xin, Jiemei Wang. A grading method for Kayser Fleischer ring images based on ResNetHeliyon 2023; 9(5): e16149 doi: 10.1016/j.heliyon.2023.e16149
33
Jorge Júlvez, Duygu Dikicioglu, Stephen G. Oliver. Handling variability and incompleteness of biological data by flexible nets: a case study for Wilson diseasenpj Systems Biology and Applications 2018; 4(1) doi: 10.1038/s41540-017-0044-x
34
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 mappingActa Radiologica 2018; 59(11): 1380 doi: 10.1177/0284185118759821
35
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 diseaseClinical Genetics 2023; 104(2): 174 doi: 10.1111/cge.14352
36
Eduardo Martínez-Morillo, Josep Miquel Bauça. Biochemical diagnosis of Wilson’s disease: an updateAdvances in Laboratory Medicine / Avances en Medicina de Laboratorio 2022; 3(2): 103 doi: 10.1515/almed-2022-0020