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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1970 1
1975 1
1977 1
1979 1
1985 2
1986 1
1990 1
1991 1
1994 1
1995 3
1996 4
1998 5
1999 3
2000 7
2001 1
2002 4
2003 10
2004 9
2005 6
2006 13
2007 14
2008 12
2009 11
2010 14
2011 16
2012 11
2013 14
2014 21
2015 19
2016 18
2017 22
2018 23
2019 32
2020 23
2021 39
2022 31
2023 26
2024 15

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382 results

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Page 1
Cerebral Iron Deposition in Neurodegeneration.
Dusek P, Hofer T, Alexander J, Roos PM, Aaseth JO. Dusek P, et al. Biomolecules. 2022 May 17;12(5):714. doi: 10.3390/biom12050714. Biomolecules. 2022. PMID: 35625641 Free PMC article. Review.
Yet, other disorders such as aceruloplasminemia, neuroferritinopathy, or Wilson disease manifest with diffuse iron accumulation in the deep gray matter in a pattern comparable to or even more extensive than that observed during normal aging. ...
Yet, other disorders such as aceruloplasminemia, neuroferritinopathy, or Wilson disease manifest with diffuse iron accumulatio …
Zinc: an essential micronutrient.
Saper RB, Rash R. Saper RB, et al. Am Fam Physician. 2009 May 1;79(9):768-72. Am Fam Physician. 2009. PMID: 20141096 Free PMC article.
Zinc in combination with antioxidants may be modestly effective in slowing the progression of intermediate and advanced age-related macular degeneration. Zinc is an effective treatment for Wilson disease. Current data do not support zinc supplementation as effective …
Zinc in combination with antioxidants may be modestly effective in slowing the progression of intermediate and advanced age-related macular …
Dietary Trace Minerals.
Tako E. Tako E. Nutrients. 2019 Nov 19;11(11):2823. doi: 10.3390/nu11112823. Nutrients. 2019. PMID: 31752257 Free PMC article.
Trace mineral imbalances can result from hereditary disorders (e.g., hemochromatosis, Wilson disease), kidney dialysis, parenteral nutrition, restrictive diets prescribed for people with inborn errors of metabolism, or various popular diet plans. ...
Trace mineral imbalances can result from hereditary disorders (e.g., hemochromatosis, Wilson disease), kidney dialysis, parent …
Copper metabolism in cell death and autophagy.
Xue Q, Kang R, Klionsky DJ, Tang D, Liu J, Chen X. Xue Q, et al. Autophagy. 2023 Aug;19(8):2175-2195. doi: 10.1080/15548627.2023.2200554. Epub 2023 Apr 16. Autophagy. 2023. PMID: 37055935 Free PMC article. Review.
Pathologically, impaired copper metabolism due to environmental or genetic causes is implicated in a variety of human diseases, such as rare Wilson disease and common cancers. Therapeutically, copper-based compounds are potential chemotherapeutic agents that can be …
Pathologically, impaired copper metabolism due to environmental or genetic causes is implicated in a variety of human diseases, such as rare …
Wilson disease.
Aggarwal A, Bhatt M. Aggarwal A, et al. Curr Opin Neurol. 2020 Aug;33(4):534-542. doi: 10.1097/WCO.0000000000000837. Curr Opin Neurol. 2020. PMID: 32657896 Review.
PURPOSE OF REVIEW: The aim of this article is to review recent developments in the areas of the disease features and treatment of Wilson disease, and survey disorders that share its pathophysiology or clinical symptoms. ...A disease phenotype with dominant psychiatr …
PURPOSE OF REVIEW: The aim of this article is to review recent developments in the areas of the disease features and treatment of Wilson …
Mutation analysis of the ATP7B gene and genotype-phenotype correlation in Chinese patients with Wilson disease.
Li M, Ma J, Wang W, Yang X, Luo K. Li M, et al. BMC Gastroenterol. 2021 Sep 1;21(1):339. doi: 10.1186/s12876-021-01911-5. BMC Gastroenterol. 2021. PMID: 34470610 Free PMC article.
AIM: To discover the novel ATP7B mutations in 103 southern Chinese patients with Wilson disease (WD), and to determine the spectrum and frequency of mutations in the ATP7B gene and genotype-phenotype correlation in a large-scale sample of Chinese WD patients. ...
AIM: To discover the novel ATP7B mutations in 103 southern Chinese patients with Wilson disease (WD), and to determine the spe …
Wilson disease in children and adolescents.
Fernando M, van Mourik I, Wassmer E, Kelly D. Fernando M, et al. Arch Dis Child. 2020 May;105(5):499-505. doi: 10.1136/archdischild-2018-315705. Epub 2020 Jan 23. Arch Dis Child. 2020. PMID: 31974298 Review.
Wilson disease (WD) is a rare, recessively inherited disorder of copper metabolism mainly affecting liver and brain. ...
Wilson disease (WD) is a rare, recessively inherited disorder of copper metabolism mainly affecting liver and brain. ...
Movement disorders.
Harris MK, Shneyder N, Borazanci A, Korniychuk E, Kelley RE, Minagar A. Harris MK, et al. Med Clin North Am. 2009 Mar;93(2):371-88, viii. doi: 10.1016/j.mcna.2008.09.002. Med Clin North Am. 2009. PMID: 19272514 Review.
The disorders discussed are Parkinson disease, essential tremor, restless legs syndrome, Huntington disease, drug-induced movement disorder, Wilson disease, and Tourette syndrome....
The disorders discussed are Parkinson disease, essential tremor, restless legs syndrome, Huntington disease, drug-induced movement disorder, …
The genetics of Wilson disease.
Chang IJ, Hahn SH. Chang IJ, et al. Handb Clin Neurol. 2017;142:19-34. doi: 10.1016/B978-0-444-63625-6.00003-3. Handb Clin Neurol. 2017. PMID: 28433102 Free PMC article. Review.
Wilson disease has poor genotype-phenotype correlation, although a few possible modifiers have been proposed. Improving molecular genetic studies continue to advance our understanding of the pathogenesis, diagnosis, and screening for Wilson disease....
Wilson disease has poor genotype-phenotype correlation, although a few possible modifiers have been proposed. Improving molecu …
Trientine tetrahydrochloride versus penicillamine for maintenance therapy in Wilson disease (CHELATE): a randomised, open-label, non-inferiority, phase 3 trial.
Schilsky ML, Czlonkowska A, Zuin M, Cassiman D, Twardowschy C, Poujois A, Gondim FAA, Denk G, Cury RG, Ott P, Moore J, Ala A, D'Inca R, Couchonnal-Bedoya E, D'Hollander K, Dubois N, Kamlin COF, Weiss KH; CHELATE trial investigators. Schilsky ML, et al. Lancet Gastroenterol Hepatol. 2022 Dec;7(12):1092-1102. doi: 10.1016/S2468-1253(22)00270-9. Epub 2022 Sep 30. Lancet Gastroenterol Hepatol. 2022. PMID: 36183738 Clinical Trial.
We enrolled patients aged 18-75 years with stable Wilson disease who were treated for at least 1 year with penicillamine. ...INTERPRETATION: The efficacy of TETA4 as oral maintenance therapy was non-inferior to penicillamine and well tolerated in adults with Wils …
We enrolled patients aged 18-75 years with stable Wilson disease who were treated for at least 1 year with penicillamine. ...I …
382 results