References analysis of the Wikipedia article "Wilson's disease" in the English version

books.google.com

Lynn DJ, Newton HB, Rae-Grant A (2004). The 5-minute Neurology Consult. Lippincott Williams & Wilkins. p. 442. ISBN 9780683307238. Archived from the original on 2016-11-07.

Sahani DV, Samir AE (2016). Abdominal Imaging: Expert Radiology Series (2 ed.). Elsevier Health Sciences. p. 400. ISBN 9780323431613. Archived from the original on 2016-11-07.

doi.org

Ala A, Walker AP, Ashkan K, Dooley JS, Schilsky ML (2007). "Wilson's disease". Lancet. 369 (9559): 397–408. doi:10.1016/S0140-6736(07)60196-2. PMID 17276780. S2CID 24663871.

Merle U, Schaefer M, Ferenci P, Stremmel W (2007). "Clinical presentation, diagnosis and long-term outcome of Wilson's disease: a cohort study". Gut. 56 (1): 115–20. doi:10.1136/gut.2005.087262. PMC 1856673. PMID 16709660.

Lorincz MT (2010). "Neurologic Wilson's disease" (PDF). Annals of the New York Academy of Sciences. 1184 (1): 173–87. Bibcode:2010NYASA1184..173L. doi:10.1111/j.1749-6632.2009.05109.x. hdl:2027.42/78731. PMID 20146697. S2CID 2989668.

Roberts EA, Schilsky ML (2008). "Diagnosis and treatment of Wilson disease: An update". Hepatology. 47 (6): 2089–2111. doi:10.1002/hep.22261. PMID 18506894.

Roberts EA, Schilsky ML (7 September 2023). "Current and Emerging Issues in Wilson's Disease". New England Journal of Medicine. 389 (10): 922–938. doi:10.1056/NEJMra1903585. PMID 37672695. S2CID 261581755.

Roberts EA, Schilsky ML (2003). "A practice guideline on Wilson disease". Hepatology. 37 (6): 1475–92. doi:10.1053/jhep.2003.50252. PMID 12774027. S2CID 263620.

de Bie P, Muller P, Wijmenga C, Klomp LW (November 2007). "Molecular pathogenesis of Wilson and Menkes disease: correlation of mutations with molecular defects and disease phenotypes". J. Med. Genet. 44 (11): 673–88. doi:10.1136/jmg.2007.052746. PMC 2752173. PMID 17717039.

Kumar M, Gaharwar U, Paul S, Poojary M, Pandhare K, Scaria V, Bk B (2020-06-03). "WilsonGen a comprehensive clinically annotated genomic variant resource for Wilson's Disease". Scientific Reports. 10 (1): 9037. Bibcode:2020NatSR..10.9037K. doi:10.1038/s41598-020-66099-2. ISSN 2045-2322. PMC 7270127. PMID 32493955.

Grubenbecher S, Stüve O, Hefter H, Korth C (2006). "Prion protein gene codon 129 modulates clinical course of neurological Wilson disease". NeuroReport. 17 (5): 549–52. doi:10.1097/01.wnr.0000209006.48105.90. PMID 16543824. S2CID 37186426.

Shaver WA, Bhatt H, Combes B (1986). "Low serum alkaline phosphatase activity in Wilson's disease". Hepatology. 6 (5): 859–63. doi:10.1002/hep.1840060509. PMID 3758940. S2CID 24055787.

Das SK, Ray K (September 2006). "Wilson's disease: an update". Nat Clin Pract Neurol. 2 (9): 482–93. doi:10.1038/ncpneuro0291. PMID 16932613. S2CID 205340375.

Ferenci P (2006-06-22). "Regional distribution of mutations of the ATP7B gene in patients with Wilson disease: impact on genetic testing". Human Genetics. 120 (2): 151–159. doi:10.1007/s00439-006-0202-5. ISSN 0340-6717. PMID 16791614. S2CID 10124665.

Walshe JM (July 1996). "Treatment of Wilson's disease: the historical background". QJM. 89 (7): 553–55. doi:10.1093/qjmed/89.7.553. PMID 8759497.

Brewer GJ, Askari FK (2005). "Wilson's disease: clinical management and therapy". Journal of Hepatology. 42 (Suppl 1): 13–21. doi:10.1016/j.jhep.2004.11.013. PMID 15777568.

Kinnier Wilson SA (1912). "Progressive lenticular degeneration: a familial nervous disease associated with cirrhosis of the liver". Brain. 34 (1): 295–507. doi:10.1093/brain/34.4.295.

Robertson WM (February 2000). "Wilson's disease". Arch. Neurol. 57 (2): 276–77. doi:10.1001/archneur.57.2.276. PMID 10681092.

Cumings JN (1948). "The copper and iron content of brain and liver in the normal and in hepato-lenticular degeneration". Brain. 71 (Dec): 410–15. doi:10.1093/brain/71.4.410. PMID 18124738.

McIntyre N, Clink HM, Levi AJ, Cumings JN, Sherlock S (February 1967). "Hemolytic anemia in Wilson's disease". N. Engl. J. Med. 276 (8): 439–44. doi:10.1056/NEJM196702232760804. PMID 6018274.

Cumings JN (March 1951). "The effects of B.A.L. in hepatolenticular degeneration". Brain. 74 (1): 10–22. doi:10.1093/brain/74.1.10. PMID 14830662.

Denny-Brown D, Porter H (December 1951). "The effect of BAL (2,3-dimercaptopropanol) on hepatolenticular degeneration (Wilson's disease)". N. Engl. J. Med. 245 (24): 917–25. doi:10.1056/NEJM195112132452401. PMID 14882450.

Vilensky JA, Robertson WM, Gilman S (September 2002). "Denny-Brown, Wilson's disease, and BAL (British antilewisite [2,3-dimercaptopropanol])". Neurology. 59 (6): 914–16. doi:10.1212/wnl.59.6.914. PMID 12297577.

Walshe JM (January 1956). "Wilson's disease; new oral therapy". Lancet. 270 (6906): 25–26. doi:10.1016/S0140-6736(56)91859-1. PMID 13279157.

Walshe JM (March 1982). "Treatment of Wilson's disease with trientine (triethylene tetramine) dihydrochloride". Lancet. 1 (8273): 643–47. doi:10.1016/S0140-6736(82)92201-2. PMID 6121964. S2CID 205999334.

Harper PL, Walshe JM (December 1986). "Reversible pancytopenia secondary to treatment with tetrathiomolybdate". Br. J. Haematol. 64 (4): 851–53. doi:10.1111/j.1365-2141.1986.tb02250.x. PMID 3801328. S2CID 11546705.

Brewer GJ (January 2000). "Recognition, diagnosis, and management of Wilson's disease". Proc. Soc. Exp. Biol. Med. 223 (1): 39–46. doi:10.1046/j.1525-1373.2000.22305.x (inactive 2024-11-22). PMID 10632959. Archived from the original on 2008-04-09. Retrieved 2008-05-20.{{cite journal}}: CS1 maint: DOI inactive as of November 2024 (link)

Bull PC, Thomas GR, Rommens JM, Forbes JR, Cox DW (1993). "The Wilson disease gene is a putative copper transporting P-type ATPase similar to the Menkes gene". Nat. Genet. 5 (4): 327–37. doi:10.1038/ng1293-327. PMID 8298639. S2CID 1236890.

Tanzi RE, Petrukhin K, Chernov I, et al. (1993). "The Wilson disease gene is a copper transporting ATPase with homology to the Menkes disease gene". Nat. Genet. 5 (4): 344–50. doi:10.1038/ng1293-344. PMID 8298641. S2CID 610188.

van De Sluis B, Rothuizen J, Pearson PL, van Oost BA, Wijmenga C (2002). "Identification of a new copper metabolism gene by positional cloning in a purebred dog population". Hum. Mol. Genet. 11 (2): 165–73. doi:10.1093/hmg/11.2.165. PMID 11809725.

Müller T, van de Sluis B, Zhernakova A, et al. (2003). "The canine copper toxicosis gene MURR1 does not cause non-Wilsonian hepatic copper toxicosis". J. Hepatol. 38 (2): 164–68. doi:10.1016/S0168-8278(02)00356-2. PMID 12547404.

ebmonline.org

nih.gov

pubmed.ncbi.nlm.nih.gov

Ala A, Walker AP, Ashkan K, Dooley JS, Schilsky ML (2007). "Wilson's disease". Lancet. 369 (9559): 397–408. doi:10.1016/S0140-6736(07)60196-2. PMID 17276780. S2CID 24663871.

Pandey N, John S (21 June 2022). "Kayser-Fleischer Ring". StatPearls. Treasure Island, Florida: StatPearls Publishing. PMID 29083643. Retrieved 30 November 2022.

Roberts EA, Schilsky ML (2008). "Diagnosis and treatment of Wilson disease: An update". Hepatology. 47 (6): 2089–2111. doi:10.1002/hep.22261. PMID 18506894.

Roberts EA, Schilsky ML (2003). "A practice guideline on Wilson disease". Hepatology. 37 (6): 1475–92. doi:10.1053/jhep.2003.50252. PMID 12774027. S2CID 263620.

Shaver WA, Bhatt H, Combes B (1986). "Low serum alkaline phosphatase activity in Wilson's disease". Hepatology. 6 (5): 859–63. doi:10.1002/hep.1840060509. PMID 3758940. S2CID 24055787.

Das SK, Ray K (September 2006). "Wilson's disease: an update". Nat Clin Pract Neurol. 2 (9): 482–93. doi:10.1038/ncpneuro0291. PMID 16932613. S2CID 205340375.

Walshe JM (July 1996). "Treatment of Wilson's disease: the historical background". QJM. 89 (7): 553–55. doi:10.1093/qjmed/89.7.553. PMID 8759497.

Brewer GJ, Askari FK (2005). "Wilson's disease: clinical management and therapy". Journal of Hepatology. 42 (Suppl 1): 13–21. doi:10.1016/j.jhep.2004.11.013. PMID 15777568.

Robertson WM (February 2000). "Wilson's disease". Arch. Neurol. 57 (2): 276–77. doi:10.1001/archneur.57.2.276. PMID 10681092.

Cumings JN (1948). "The copper and iron content of brain and liver in the normal and in hepato-lenticular degeneration". Brain. 71 (Dec): 410–15. doi:10.1093/brain/71.4.410. PMID 18124738.

McIntyre N, Clink HM, Levi AJ, Cumings JN, Sherlock S (February 1967). "Hemolytic anemia in Wilson's disease". N. Engl. J. Med. 276 (8): 439–44. doi:10.1056/NEJM196702232760804. PMID 6018274.

Cumings JN (March 1951). "The effects of B.A.L. in hepatolenticular degeneration". Brain. 74 (1): 10–22. doi:10.1093/brain/74.1.10. PMID 14830662.

Walshe JM (January 1956). "Wilson's disease; new oral therapy". Lancet. 270 (6906): 25–26. doi:10.1016/S0140-6736(56)91859-1. PMID 13279157.

Sternlieb I, Twedt DC, Johnson GF, et al. (1977). "Inherited copper toxicity of the liver in Bedlington terriers". Proc. R. Soc. Med. 70 (Suppl 3): 8–9. PMC 1543595. PMID 122681.

ncbi.nlm.nih.gov

niddk.nih.gov

"Wilson Disease". NIDDK. July 2014. Archived from the original on 2016-10-04. Retrieved 2016-11-06.

"Definition and Facts | NIDDK". National Institute of Diabetes and Digestive and Kidney Diseases. Retrieved 2019-02-01.

semanticscholar.org

api.semanticscholar.org

Ala A, Walker AP, Ashkan K, Dooley JS, Schilsky ML (2007). "Wilson's disease". Lancet. 369 (9559): 397–408. doi:10.1016/S0140-6736(07)60196-2. PMID 17276780. S2CID 24663871.

Roberts EA, Schilsky ML (2003). "A practice guideline on Wilson disease". Hepatology. 37 (6): 1475–92. doi:10.1053/jhep.2003.50252. PMID 12774027. S2CID 263620.

Shaver WA, Bhatt H, Combes B (1986). "Low serum alkaline phosphatase activity in Wilson's disease". Hepatology. 6 (5): 859–63. doi:10.1002/hep.1840060509. PMID 3758940. S2CID 24055787.

Das SK, Ray K (September 2006). "Wilson's disease: an update". Nat Clin Pract Neurol. 2 (9): 482–93. doi:10.1038/ncpneuro0291. PMID 16932613. S2CID 205340375.

web.archive.org

"Wilson Disease". NIDDK. July 2014. Archived from the original on 2016-10-04. Retrieved 2016-11-06.

Lynn DJ, Newton HB, Rae-Grant A (2004). The 5-minute Neurology Consult. Lippincott Williams & Wilkins. p. 442. ISBN 9780683307238. Archived from the original on 2016-11-07.

Sahani DV, Samir AE (2016). Abdominal Imaging: Expert Radiology Series (2 ed.). Elsevier Health Sciences. p. 400. ISBN 9780323431613. Archived from the original on 2016-11-07.

"Whonamedit – dictionary of medical eponyms". www.whonamedit.com. Archived from the original on 2016-11-07. Retrieved 2016-11-06.

Wilson's disease (English Wikipedia)

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