Wilson Disease: Diagnostic Challenges and Differential Diagnoses
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Publisher
Springer Science and Business Media LLC
Link
https://link.springer.com/content/pdf/10.1007/s12018-024-09294-3.pdf
Reference121 articles.
1. Wilson SAK. Dégéneration lenticulaire progressive maladie nerveuse familiale associée á la cirrhose du foie. Masson for the Société français de neurologie; 1912.
2. Członkowska A, Dzieżyc-Jaworska K, Kłysz B, Barbara R-O, Litwin T. Difficulties in diagnosis and treatment of Wilson disease—a case series of five patients. Ann Transl Med. 2019;7(Suppl 2):S73.
3. Zimbrean PC, Schilsky ML. Psychiatric aspects of Wilson disease: a review. Gen Hosp Psychiatry. 2014;36(1):53–62.
4. Sapuppo A, Pavone P, Praticò AD, Ruggieri M, Bertino G, Fiumara A. Genotype-phenotype variable correlation in Wilson disease: clinical history of two sisters with the similar genotype. BMC Med Genet. 2020;21:1–6.
5. Gupta A, et al. Molecular pathogenesis of Wilson disease among Indians: a perspective on mutation spectrum in ATP7B gene, prevalent defects, clinical heterogeneity and implication towards diagnosis. Cell Mol Neurobiol. 2007;27(8):1023–33.
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