[1] Poujois A, Woimant F. Challenges in the diagnosis of Wilson disease. Ann Transl Med, 2019, 7(Suppl 2):S67. [2] Xie JJ, Wu ZY. Wilson's Disease in China. Neurosci Bull, 2017, 33(3):323-330. [3] European Association for Study of Liver. EASL Clinical Practice Guidelines:Wilson's disease. J Hepatol, 2012, 56(3):671-685. [4] Masełbas W, Członkowska A, Litwin T, et al. Persistence with treatment for Wilson disease: a retrospective study. BMC Neurol, 2019, 19(1):278. [5] Zarina A, Tolmane I, Krumina Z, et al. Association of variants in the CP, ATOX1 and COMMD1 genes with Wilson disease symptoms in Latvia. Balkan J Med Genet, 2019, 22(2):37-42. [6] Członkowska A, Litwin T, Dusek P, et al. Wilson disease. Nat Rev Dis Primers, 2018, 4(1):21. [7] Mikol J, Vital C, Wassef M, et al. Extensive cortico-subcortical lesions in Wilson's disease: clinico-pathological study of two cases. Acta Neuropathol, 2005, 110(5):451-458. [8] Li LY, Zhu XQ, Tao WW, et al. Acute onset neurological symptoms in Wilson disease after traumatic, surgical or emotional events: A cross-sectional study. Medicine (Baltimore), 2019, 98(26):e15917. [9] Saroli Palumbo C, Schilsky ML. Clinical practice guidelines in Wilson disease. Ann Transl Med, 2019, 7(Suppl 2):S65. [10] Bobbio E, Forsgard N, Oldfors A, et al. Cardiac arrest in Wilson's disease after curative liver transplantation: a life-threatening complication of myocardial copper excess? ESC Heart Fail, 2019, 6(1):228-231. [11] Hedera P. Wilson's disease: A master of disguise. Parkinsonism Relat Disord, 2019, 59:140-145. [12] Medici V, Weiss KH. Genetic and environmental modifiers of Wilson disease. Handb Clin Neurol, 2017, 142:35-41. [13] Socha P, Janczyk W, Dhawan A, et al. Wilson's disease in children: A position paper by the Hepatology Committee of the European Society for Paediatric Gastroenterology, Hepatology and Nutrition. J Pediatr Gastroenterol Nutr, 2018, 66(2):334-344. [14] Członkowska A, Litwin T, Dziez·yc K, et al. Characteristics of a newly diagnosed Polish cohort of patients with neurological manifestations of Wilson disease evaluated with the unified Wilson's disease rating scale. BMC Neurol, 2018, 18(1):34. [15] Yu XE, Pan M, Han YZ,et al. The study of Wilson disease in pregnancy management. BMC Pregnancy Childbirth, 2019, 19(1):522. [16] Poujois A, Woimant F. Wilson's disease: A 2017 update. Clin Res Hepatol Gastroenterol, 2018, 42(6):512-520. [17] Low QJ, Siaw C, Lee RA, et al. Kayser-Fleischer fings & Wilson's disease.QJM, 2020, 9. pii: hcaa005. [18] Valentino PL, Roberts EA, Beer S, et al. Management of Wilson disease diagnosed in infancy: An appraisal of available experience to generate discussion. J Pediatr Gastroenterol Nutr, 2020[ahead of print] . [19] Poon KS, Teo ZH, Yap JH, et al. Challenges in molecular diagnosis of Wilson disease: viewpoint from the clinical laboratory. J Clin Pathol, 2019, 3. pii: jclinpath-2019-206054. [20] Roberts EA, Schilsky ML, American Association for Study of Liver Diseases (AASLD). Diagnosis and treatment of Wilson disease: an update. Hepatology, 2008, 47(6):2089-2111. [21] Ferenci P, Caca K, Loudianos G, et al. Diagnosis and phenotypic classification of Wilson disease. Liver Int, 2003, 23(3):139-142. [22] Hermann W. Classification and differential diagnosis of Wilson's disease. Ann Transl Med, 2019, 7(Suppl 2):S63. [23] Xu MB, Rong PQ, Jin TY, et al. Chinese herbal medicine for Wilson's disease: A systematic review and Meta-analysis. Front harmacol, 2019, 10:277. [24] Pfeiffenberger J, Beinhardt S, Gotthardt DN, et al. Pregnancy in Wilson's disease: Management and outcome. Hepatology, 2018, 67(4):1261-1269. |