Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

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

Year Number of Results
1796 1
1797 2
1799 1
1800 2
1802 2
1803 2
1804 1
1806 2
1808 3
1809 3
1811 2
1812 3
1814 2
1815 1
1820 3
1821 2
1823 1
1828 2
1829 5
1830 1
1837 1
1838 2
1841 5
1842 11
1843 5
1844 5
1845 2
1846 2
1849 3
1851 2
1852 2
1853 6
1854 4
1855 11
1856 10
1858 1
1859 1
1860 1
1861 2
1862 3
1863 1
1864 3
1865 5
1866 5
1867 3
1869 3
1870 3
1871 18
1872 10
1874 4
1875 2
1876 2
1877 4
1878 10
1879 11
1880 11
1881 6
1882 10
1883 2
1884 3
1885 3
1886 5
1887 10
1888 8
1889 12
1890 7
1891 5
1892 7
1893 4
1894 9
1895 4
1896 3
1897 10
1898 12
1899 19
1900 10
1901 17
1902 12
1903 6
1904 5
1905 12
1906 12
1907 15
1908 9
1909 14
1910 13
1911 13
1912 11
1913 24
1914 13
1915 42
1916 45
1917 33
1918 26
1919 24
1920 30
1921 23
1922 15
1923 22
1924 36
1925 36
1926 27
1927 35
1928 26
1929 17
1930 26
1931 29
1932 21
1933 30
1934 24
1935 33
1936 36
1937 25
1938 18
1939 30
1940 17
1941 26
1942 28
1943 27
1944 12
1945 64
1946 200
1947 202
1948 192
1949 196
1950 224
1951 253
1952 245
1953 256
1954 256
1955 219
1956 209
1957 229
1958 279
1959 298
1960 272
1961 239
1962 308
1963 367
1964 420
1965 433
1966 397
1967 501
1968 543
1969 565
1970 628
1971 676
1972 691
1973 754
1974 746
1975 804
1976 875
1977 822
1978 893
1979 917
1980 988
1981 1016
1982 1004
1983 1113
1984 1088
1985 1250
1986 1328
1987 1393
1988 1449
1989 1483
1990 1545
1991 1574
1992 1609
1993 1741
1994 1907
1995 1828
1996 1936
1997 1755
1998 1821
1999 1973
2000 2472
2001 2186
2002 2368
2003 2466
2004 2763
2005 3058
2006 2993
2007 3308
2008 3448
2009 3612
2010 3843
2011 4137
2012 4473
2013 4826
2014 4983
2015 5210
2016 5444
2017 5392
2018 5594
2019 5860
2020 6595
2021 6914
2022 6439
2023 6194
2024 2381

Text availability

Article attribute

Article type

Publication date

Search Results

141,161 results

Results by year

Filters applied: . Clear all
The following term was not found in PubMed: Zuniga-Sarango
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 …
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 …
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 …
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 …
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 elastography and …
Staging of liver fibrosis is of special significance in Wilson's disease as it determines the patient's prognosis and treatmen …
Late-Onset Wilson's Disease.
Žigrai M, Vyskočil M, Tóthová A, Vereš P, Bluska P, Valkovič P. Žigrai M, et al. Front Med (Lausanne). 2020 Feb 6;7:26. doi: 10.3389/fmed.2020.00026. eCollection 2020. Front Med (Lausanne). 2020. PMID: 32118011 Free PMC article.
Wilson's disease is a rare autosomal recessive disease, caused by impaired secretion of copper into bile due to a defective function of the ATPase 7B enzyme. Clinical manifestation is predominantly hepatic and neurological. Wilson's disease is traditio …
Wilson's disease is a rare autosomal recessive disease, caused by impaired secretion of copper into bile due to a defective fu …
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 …
Cataplexy.
Wilson SA. Wilson SA. J Neurol Psychopathol. 1933 Jul;14(53):45-51. doi: 10.1136/jnnp.s1-14.53.45. J Neurol Psychopathol. 1933. PMID: 21610759 Free PMC article. No abstract available.
Classification and differential diagnosis of Wilson's disease.
Hermann W. Hermann W. Ann Transl Med. 2019 Apr;7(Suppl 2):S63. doi: 10.21037/atm.2019.02.07. Ann Transl Med. 2019. PMID: 31179300 Free PMC article. Review.
Wilson's disease is characterized by hepatic and extrapyramidal movement disorders (EPS) with variable manifestation primarily between age 5 and 45. ...The recently described manganese storage disease presents another rare metabolic disorder with symptoms similar to …
Wilson's disease is characterized by hepatic and extrapyramidal movement disorders (EPS) with variable manifestation primarily …
141,161 results
You have reached the last available page of results. Please see the User Guide for more information.