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

Year Number of Results
1802 1
1806 2
1809 1
1820 1
1837 1
1856 2
1863 1
1866 1
1870 1
1872 1
1879 1
1880 1
1882 1
1886 1
1887 1
1888 1
1896 1
1900 2
1901 1
1902 2
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 29
1955 14
1956 22
1957 32
1958 28
1959 36
1960 39
1961 30
1962 40
1963 57
1964 57
1965 69
1966 39
1967 61
1968 78
1969 70
1970 66
1971 71
1972 64
1973 63
1974 82
1975 141
1976 132
1977 135
1978 128
1979 133
1980 145
1981 165
1982 172
1983 184
1984 181
1985 208
1986 211
1987 287
1988 279
1989 319
1990 361
1991 369
1992 361
1993 408
1994 446
1995 459
1996 441
1997 444
1998 466
1999 552
2000 944
2001 584
2002 611
2003 678
2004 748
2005 819
2006 806
2007 902
2008 935
2009 1010
2010 1007
2011 1180
2012 1278
2013 1426
2014 1707
2015 1911
2016 2016
2017 2136
2018 2387
2019 2458
2020 2778
2021 2388
2022 1
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35,600 results
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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 …
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 …
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: 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
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
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.
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 …
Biomarkers for diagnosis of Wilson's disease.
Ryan A, Nevitt SJ, Tuohy O, Cook P. Ryan A, et al. Cochrane Database Syst Rev. 2019 Nov 19;2019(11):CD012267. doi: 10.1002/14651858.CD012267.pub2. Cochrane Database Syst Rev. 2019. PMID: 31743430 Free PMC article.
BACKGROUND: Wilson's disease, first described by Samuel Wilson in 1912, is an autosomal recessive metabolic disorder resulting from mutations in the ATP7B gene. ...The index tests covered by this Cochrane Review are caeruloplasmin, 24-hour urinary copper and …
BACKGROUND: Wilson's disease, first described by Samuel Wilson in 1912, is an autosomal recessive metabolic disorder re …
[Wilson's disease].
Brůha R, Marecek Z, Martásek P, Nevsímalová S, Petrtýl J, Urbánek P, Kalistová H, Pospísilová L. Brůha R, et al. Cas Lek Cesk. 2009;148(11):544-8. Cas Lek Cesk. 2009. PMID: 20662462 Review. Czech.
Wilson's disease is an inherited disorder leading to accumulation of copper in tissues, mainly in the liver and brain. ...The manifestation of Wilson's disease is usually hepatic or neurologic. Hepatic form is manifested by acute or chronic hepatitis,
Wilson's disease is an inherited disorder leading to accumulation of copper in tissues, mainly in the liver and brain. ...The
Sleep Disorders in Wilson's Disease.
Cochen De Cock V, Woimant F, Poujois A. Cochen De Cock V, et al. Curr Neurol Neurosci Rep. 2019 Nov 13;19(11):84. doi: 10.1007/s11910-019-1001-4. Curr Neurol Neurosci Rep. 2019. PMID: 31720864 Review.
PURPOSE OF REVIEW: We aimed to review the sleep disorders described in Wilson's disease (WD), focusing on their mechanisms and treatments. ...
PURPOSE OF REVIEW: We aimed to review the sleep disorders described in Wilson's disease (WD), focusing on their mechanisms and …
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