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Cited by in CrossRef
For: Kucinskas L, Jeroch J, Vitkauskiene A, Sakalauskas R, Petrenkiene V, Kucinskas V, Naginiene R, Schmidt H, Kupcinskas L. High frequency of the c.3207C>A (p.H1069Q) mutation in ATP7B gene of Lithuanian patients with hepatic presentation of Wilson’s disease. World J Gastroenterol 2008; 14(38): 5876-5879 [PMID: 18855987 DOI: 10.3748/wjg.14.5876]
URL: https://www.wjgnet.com/2307-8960/full/v14/i38/5876.htm
Number Citing Articles
1
Michael L. Schilsky, Aftab Ala. Genetic Testing for Wilson Disease: Availability and UtilityCurrent Gastroenterology Reports 2010; 12(1): 57 doi: 10.1007/s11894-009-0084-5
2
Le Anh Tuan Pham, Trong Tue Nguyen, Hoang Bich Nga Le, Dat Quoc Tran, Cam Tu Ho, Thinh Huy Tran, Van Thanh Ta, The Hung Bui, Van Khanh Tran. Genetic analysis of 55 northern Vietnamese patients with Wilson disease: seven novel mutations in ATP7BJournal of Genetics 2017; 96(6): 933 doi: 10.1007/s12041-017-0857-9
3
Jussi O.T. Sipilä, Laura Kytövuori, Valtteri Kaasinen. Clinical spectrum and genotype-phenotype associations in Finnish patients with Wilson's diseaseJournal of the Neurological Sciences 2023; 448: 120620 doi: 10.1016/j.jns.2023.120620
4
Agnese Zarina, Ieva Tolmane, Madara Kreile, Aleksandrs Chernushenko, Gunta Cernevska, Ieva Pukite, Ieva Micule, Zita Krumina, Astrida Krumina, Baiba Rozentale, Linda Piekuse. Genetic variation spectrum in ATP7B gene identified in Latvian patients with Wilson diseaseMolecular Genetics & Genomic Medicine 2017; 5(4): 405 doi: 10.1002/mgg3.297
5
Julnar Usta, Hussein Abu Daya, Houssam Halawi, Ibraheem Al-Shareef, Omar El-Rifai, Ahmad H. Malli, Ala I. Sharara, Robert H. Habib, Kassem Barada. JIMD Reports - Case and Research Reports, 2012/1JIMD Reports 2011; 4: 129 doi: 10.1007/8904_2011_91
6
Katarzyna Gaweda-Walerych, Emilia J. Sitek, Małgorzata Borczyk, Ewa Narożańska, Bogna Brockhuis, Michał Korostyński, Michał Schinwelski, Mariusz Siemiński, Jarosław Sławek, Cezary Zekanowski. A Patient with Corticobasal Syndrome and Progressive Non-Fluent Aphasia (CBS-PNFA), with Variants in ATP7B, SETX, SORL1, and FOXP1 GenesGenes 2022; 13(12): 2361 doi: 10.3390/genes13122361
7
Kassem Barada, Mazen El-Atrache, Ihab I. El-Hajj, Khaled Rida, Jida El-Hajjar, Ziyad Mahfoud, Julnar Usta. Homozygous Mutations in the Conserved ATP Hinge Region of the Wilson Disease GeneJournal of Clinical Gastroenterology 2010; 44(6): 432 doi: 10.1097/MCG.0b013e3181ce5138
8
Violeta Mihaylova, Teodor Todorov, Hristo Jelev, Iskren Kotsev, Ludmila Angelova, Olga Kosseva, Georgi Georgiev, Ralica Ganeva, Silvia Cherninkova, Ludmila Tankova, Aleksei Savov, Ivailo Tournev. Neurological Symptoms, Genotype-Phenotype Correlations and Ethnic-specific Differences in Bulgarian Patients With Wilson DiseaseThe Neurologist 2012; 18(4): 184 doi: 10.1097/NRL.0b013e31825cf3b7
9
Hartmut H.-J. Schmidt. Role of genotyping in Wilson’s diseaseJournal of Hepatology 2009; 50(3): 449 doi: 10.1016/j.jhep.2008.11.008
10
Jason L. Burkhead, Lawrence W. Gray, Svetlana Lutsenko. Systems biology approach to Wilson’s diseaseBioMetals 2011; 24(3): 455 doi: 10.1007/s10534-011-9430-9
11
Peter Ferenci. Clinical and Translational Perspectives on WILSON DISEASE2019; : 305 doi: 10.1016/B978-0-12-810532-0.00028-8
12
Diagnostic Imaging: Musculoskeletal Non-Traumatic Disease2016; : 134 doi: 10.1016/B978-0-323-39252-5.50036-6
13
New mutations and polymorphisms of the ATP7B gene in sporadic Wilson diseaseEuropean Journal of Medical Genetics 2014; 57(9): 498 doi: 10.1016/j.ejmg.2014.04.016
14
Fei Wu, Jing Wang, Chunwen Pu, Liang Qiao, Chunmeng Jiang. Wilson’s Disease: A Comprehensive Review of the Molecular MechanismsInternational Journal of Molecular Sciences 2015; 16(12): 6419 doi: 10.3390/ijms16036419