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Year Number of Results
1802 1
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1809 1
1820 1
1837 1
1842 2
1843 1
1844 1
1856 2
1862 1
1863 1
1866 1
1867 1
1870 1
1872 1
1874 2
1879 1
1880 1
1882 2
1884 1
1886 1
1887 1
1888 1
1892 1
1896 2
1899 2
1900 2
1901 2
1902 3
1905 2
1906 2
1912 1
1913 2
1914 2
1915 19
1916 26
1917 16
1918 10
1919 10
1920 10
1921 6
1922 8
1923 4
1924 12
1925 15
1926 7
1927 8
1928 3
1929 5
1930 3
1931 5
1932 1
1933 6
1934 8
1935 5
1936 7
1937 3
1938 3
1939 3
1940 2
1941 3
1942 9
1943 7
1944 3
1945 13
1946 10
1947 11
1948 13
1949 12
1950 23
1951 27
1952 30
1953 28
1954 30
1955 14
1956 22
1957 32
1958 28
1959 36
1960 39
1961 30
1962 41
1963 57
1964 57
1965 70
1966 40
1967 61
1968 80
1969 72
1970 69
1971 72
1972 66
1973 66
1974 93
1975 336
1976 338
1977 353
1978 345
1979 341
1980 466
1981 540
1982 534
1983 622
1984 599
1985 664
1986 709
1987 797
1988 806
1989 837
1990 879
1991 936
1992 963
1993 1005
1994 1144
1995 1073
1996 1159
1997 1107
1998 1150
1999 1306
2000 1723
2001 1392
2002 1550
2003 1618
2004 1786
2005 1975
2006 1850
2007 2086
2008 2152
2009 2347
2010 2466
2011 2704
2012 2846
2013 3121
2014 3264
2015 3415
2016 3058
2017 2835
2018 3523
2019 3600
2020 4001
2021 4133
2022 3955
2023 3645
2024 861

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Page 1
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'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
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 diagnosis, and tr …
Despite a long history, Wilson's disease, an autosomal recessive disease caused by mutations in the ATP7B gene, remains a comm …
EASL Clinical Practice Guidelines: Wilson's disease.
European Association for Study of Liver. European Association for Study of Liver. J Hepatol. 2012 Mar;56(3):671-85. doi: 10.1016/j.jhep.2011.11.007. J Hepatol. 2012. PMID: 22340672 Free article.
This Clinical Practice Guideline (CPG) has been developed to assist physicians and other healthcare providers in the diagnosis and management of patients with Wilson's disease. The goal is to describe a number of generally accepted approaches for diagnosis, preventi …
This Clinical Practice Guideline (CPG) has been developed to assist physicians and other healthcare providers in the diagnosis and managemen …
A genetic study of Wilson's disease in the United Kingdom.
Coffey AJ, Durkie M, Hague S, McLay K, Emmerson J, Lo C, Klaffke S, Joyce CJ, Dhawan A, Hadzic N, Mieli-Vergani G, Kirk R, Elizabeth Allen K, Nicholl D, Wong S, Griffiths W, Smithson S, Giffin N, Taha A, Connolly S, Gillett GT, Tanner S, Bonham J, Sharrack B, Palotie A, Rattray M, Dalton A, Bandmann O. Coffey AJ, et al. Brain. 2013 May;136(Pt 5):1476-87. doi: 10.1093/brain/awt035. Epub 2013 Mar 21. Brain. 2013. PMID: 23518715 Free PMC article.
Previous studies have failed to identify mutations in the Wilson's disease gene ATP7B in a significant number of clinically diagnosed cases. ...The likelihood of mutations in genes other than ATP7B causing a Wilson's disease phenotype is therefore very …
Previous studies have failed to identify mutations in the Wilson's disease gene ATP7B in a significant number of clinically di …
Wilson's disease: Revisiting an old friend.
Lucena-Valera A, Perez-Palacios D, Muñoz-Hernandez R, Romero-Gómez M, Ampuero J. Lucena-Valera A, et al. World J Hepatol. 2021 Jun 27;13(6):634-649. doi: 10.4254/wjh.v13.i6.634. World J Hepatol. 2021. PMID: 34239699 Free PMC article. Review.
Wilson's disease (WD) is a rare condition caused by copper accumulation primarily in the liver and secondly in other organs, such as the central nervous system. ...
Wilson's disease (WD) is a rare condition caused by copper accumulation primarily in the liver and secondly in other organs, s
Wilson's disease: Food therapy out of trace elements.
Li WJ, Chen HL, Wang B, Yao L, Wang XP. Li WJ, et al. Front Cell Dev Biol. 2022 Dec 21;10:1091580. doi: 10.3389/fcell.2022.1091580. eCollection 2022. Front Cell Dev Biol. 2022. PMID: 36619859 Free PMC article. Review.
Hepatolenticular degeneration, also known as Wilson's disease (WD), is an autosomal recessive inheritance nervous disorder of copper metabolism. ...
Hepatolenticular degeneration, also known as Wilson's disease (WD), is an autosomal recessive inheritance nervous disorder of …
Wilson's disease.
Pfeiffer RF. Pfeiffer RF. Handb Clin Neurol. 2011;100:681-709. doi: 10.1016/B978-0-444-52014-2.00049-5. Handb Clin Neurol. 2011. PMID: 21496616 Review.
The genetic basis for Wilson's disease - mutation within the ATP7B gene - has been identified. ...In this chapter, the clinical manifestations, diagnostic evaluation, and treatment approaches for Wilson's disease are discussed....
The genetic basis for Wilson's disease - mutation within the ATP7B gene - has been identified. ...In this chapter, the clinica …
Elastography of the Liver in Wilson's Disease.
Nehring P, Szeligowska J, Przybyłkowski A. Nehring P, et al. Diagnostics (Basel). 2023 May 29;13(11):1898. doi: 10.3390/diagnostics13111898. Diagnostics (Basel). 2023. PMID: 37296749 Free PMC article. Review.
Staging of liver fibrosis is of special significance in Wilson's disease as it determines the patient's prognosis and treatment. Histopathological examination is a standard method for fibrosis assessment; however, non-invasive methods like transient elastogra …
Staging of liver fibrosis is of special significance in Wilson's disease as it determines the patient's prognosis and t …
Wilson's Disease: A Review for the General Pediatrician.
Capone K, Azzam RK. Capone K, et al. Pediatr Ann. 2018 Nov 1;47(11):e440-e444. doi: 10.3928/19382359-20181026-01. Pediatr Ann. 2018. PMID: 30423186 Review.
Wilson's disease, also known as hepatolenticular degeneration, is an autosomal recessive genetic disorder due to a mutation of the ATP7B gene resulting in impaired hepatic copper excretion and copper accumulation in various tissues. ...The general pediatrician may b
Wilson's disease, also known as hepatolenticular degeneration, is an autosomal recessive genetic disorder due to a mutation of
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