Congential scoliosis in Wilson’s disease: case report and review of the literature
Author:
Publisher
Springer Science and Business Media LLC
Subject
General Medicine,Surgery
Link
http://link.springer.com/content/pdf/10.1186/1471-2482-14-71.pdf
Reference14 articles.
1. Rosencrantz R, Schilsky M: Wilson disease: pathogenesis and clinical considerations in diagnosis and treatment. Semin Liver Dis. 2011, 31: 245-259. 10.1055/s-0031-1286056.
2. Compston A: Progressive lenticular degeneration: a familial nervous disease associated with cirrhosis of the liver, by S. A. Kinnier Wilson, (From the National Hospital, and the Laboratory of the National Hospital, Queen Square, London) Brain 1912: 34; 295-509. Brain. 2009, 132: 1997-2001. 10.1093/brain/awp193.
3. Bull PC, Thomas GR, Rommens JM, Forbes JR, Cox DW: The Wilson disease gene is a putative copper transporting P-type ATPase similar to the Menkes gene. Nat Genet. 1993, 5: 327-337. 10.1038/ng1293-327.
4. Burkhead JL, Gray LW, Lutsenko S: Systems biology approach to Wilson's disease. Biometals. 2011, 24: 455-466. 10.1007/s10534-011-9430-9.
5. Warnock CG: Hepatolenticular degeneration; Wilson's disease; a report of five cases, with commentary. Ulster Med J. 1952, 21: 155-171.
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