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Year Number of Results
1963 3
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1973 17
1974 11
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1986 13
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2004 97
2005 95
2006 96
2007 89
2008 100
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Page 1
Wilson disease.
Członkowska A, Litwin T, Dusek P, Ferenci P, Lutsenko S, Medici V, Rybakowski JK, Weiss KH, Schilsky ML. Członkowska A, et al. Nat Rev Dis Primers. 2018 Sep 6;4(1):21. doi: 10.1038/s41572-018-0018-3. Nat Rev Dis Primers. 2018. PMID: 30190489 Free PMC article. Review.
Wilson disease (WD) is a potentially treatable, inherited disorder of copper metabolism that is characterized by the pathological accumulation of copper. ...The clinical course of WD can vary in the type and severity of symptoms, but progressive liver disease
Wilson disease (WD) is a potentially treatable, inherited disorder of copper metabolism that is characterized by the pathologi
Wilson's disease and other neurological copper disorders.
Bandmann O, Weiss KH, Kaler SG. Bandmann O, et al. Lancet Neurol. 2015 Jan;14(1):103-13. doi: 10.1016/S1474-4422(14)70190-5. Lancet Neurol. 2015. PMID: 25496901 Free PMC article. Review.
The copper metabolism disorder Wilson's disease was first defined in 1912. Wilson's disease can present with hepatic and neurological deficits, including dystonia and parkinsonism. ...Furthermore, Wilson's disease needs to be differentiat …
The copper metabolism disorder Wilson's disease was first defined in 1912. Wilson's disease can present with hep …
Wilson Disease: An Overview and Approach to Management.
Mulligan C, Bronstein JM. Mulligan C, et al. Neurol Clin. 2020 May;38(2):417-432. doi: 10.1016/j.ncl.2020.01.005. Epub 2020 Feb 28. Neurol Clin. 2020. PMID: 32279718 Review.
Wilson's disease is one of the few preventable movement disorders in which there are therapies that modify disease progression. ...This article reviews the clinical presentation, epidemiology, genetics, pathophysiology, diagnosis, and management of Wilson
Wilson's disease is one of the few preventable movement disorders in which there are therapies that modify disease prog
Wilson's disease: update on pathogenesis, biomarkers and treatments.
Shribman S, Poujois A, Bandmann O, Czlonkowska A, Warner TT. Shribman S, et al. J Neurol Neurosurg Psychiatry. 2021 Oct;92(10):1053-1061. doi: 10.1136/jnnp-2021-326123. Epub 2021 Aug 2. J Neurol Neurosurg Psychiatry. 2021. PMID: 34341141 Review.
Wilson's disease is an autosomal-recessive disorder of copper metabolism caused by mutations in ATP7B and associated with neurological, psychiatric, ophthalmological and hepatic manifestations. ...In this article, we review the current understanding of pathogenesis,
Wilson's disease is an autosomal-recessive disorder of copper metabolism caused by mutations in ATP7B and associated with neur
Wilson's disease: overview.
Lucena-Valera A, Ruz-Zafra P, Ampuero J. Lucena-Valera A, et al. Med Clin (Barc). 2023 Mar 24;160(6):261-267. doi: 10.1016/j.medcli.2022.12.016. Epub 2023 Jan 23. Med Clin (Barc). 2023. PMID: 36697289 Review. English, Spanish.
Wilson's disease (WD) is an uncommon hereditary disorder caused by a deficiency in the ATP7B transporter. ...Lastly, the liver transplant should be an option for patients with end-stage liver disease....
Wilson's disease (WD) is an uncommon hereditary disorder caused by a deficiency in the ATP7B transporter. ...Lastly, the liver
Wilson Disease: Diagnosis, Treatment, and Follow-up.
Schilsky ML. Schilsky ML. Clin Liver Dis. 2017 Nov;21(4):755-767. doi: 10.1016/j.cld.2017.06.011. Epub 2017 Aug 10. Clin Liver Dis. 2017. PMID: 28987261 Review.
Consideration of a diagnosis of Wilson disease is still the critical factor in testing for and establishing disease diagnosis. In association with other clinical and biochemical tests, liver biopsy results and molecular genetic testing can also be used to gen …
Consideration of a diagnosis of Wilson disease is still the critical factor in testing for and establishing disease dia …
Neurologic Wilson's disease.
Lorincz MT. Lorincz MT. Ann N Y Acad Sci. 2010 Jan;1184:173-87. doi: 10.1111/j.1749-6632.2009.05109.x. Ann N Y Acad Sci. 2010. PMID: 20146697 Free article. Review.
Despite a long history, Wilson's disease, an autosomal recessive disease caused by mutations in the ATP7B gene, remains a commonly misdiagnosed import disease. ...This review focuses on the neurologic features of Wilson's disease, its dia …
Despite a long history, Wilson's disease, an autosomal recessive disease caused by mutations in the ATP7B gene, remains …
Wilson disease in children and young adults - State of the art.
Chanpong A, Dhawan A. Chanpong A, et al. Saudi J Gastroenterol. 2022 Jan-Feb;28(1):21-31. doi: 10.4103/sjg.sjg_501_21. Saudi J Gastroenterol. 2022. PMID: 35042319 Free PMC article. Review.
Wilson disease (WD) is an autosomal recessive disorder caused by mutations of the ATP7B gene, with a reported prevalence of 1:30,000-50,000. ...A lack or dysfunction of this enzyme results in a progressive accumulation of copper in several organs, especially in the
Wilson disease (WD) is an autosomal recessive disorder caused by mutations of the ATP7B gene, with a reported prevalence of 1:
Copper Dyshomeostasis in Neurodegenerative Diseases-Therapeutic Implications.
Gromadzka G, Tarnacka B, Flaga A, Adamczyk A. Gromadzka G, et al. Int J Mol Sci. 2020 Dec 4;21(23):9259. doi: 10.3390/ijms21239259. Int J Mol Sci. 2020. PMID: 33291628 Free PMC article. Review.
This knowledge opens up an important new area for potential therapeutic interventions based on copper supplementation or removal in neurodegenerative diseases including Wilson's disease (WD), Menkes disease (MD), Alzheimer's disease (AD), Parkinson's …
This knowledge opens up an important new area for potential therapeutic interventions based on copper supplementation or removal in neurodeg …
Investigation and management of Wilson's disease: a practical guide from the British Association for the Study of the Liver.
Shribman S, Marjot T, Sharif A, Vimalesvaran S, Ala A, Alexander G, Dhawan A, Dooley J, Gillett GT, Kelly D, McNeill A, Warner TT, Wheater V, Griffiths W, Bandmann O; British Association for the Study of the Liver Rare Diseases Special Interest Group. Shribman S, et al. Lancet Gastroenterol Hepatol. 2022 Jun;7(6):560-575. doi: 10.1016/S2468-1253(22)00004-8. Epub 2022 Apr 13. Lancet Gastroenterol Hepatol. 2022. PMID: 35429442 Review.
We also cover treatment initiation, ideally under the guidance of a specialist centre for Wilson's disease, and the principles behind long-term management. This guidance was developed by a multidisciplinary group of Wilson's disease experts formed thro …
We also cover treatment initiation, ideally under the guidance of a specialist centre for Wilson's disease, and the principles …
3,494 results