Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

My NCBI Filters
Results by year

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

Year Number of Results
1806 1
1812 1
1842 1
1844 1
1871 2
1875 1
1888 1
1897 1
1906 1
1908 1
1910 1
1913 1
1916 1
1920 1
1922 1
1923 3
1926 1
1927 1
1928 2
1930 1
1931 1
1934 1
1935 1
1936 2
1937 2
1938 1
1939 1
1941 1
1942 1
1944 1
1945 5
1946 14
1947 17
1948 18
1949 12
1950 29
1951 32
1952 49
1953 46
1954 60
1955 48
1956 47
1957 64
1958 53
1959 61
1960 56
1961 52
1962 65
1963 108
1964 100
1965 90
1966 73
1967 101
1968 124
1969 126
1970 109
1971 140
1972 120
1973 138
1974 125
1975 157
1976 152
1977 142
1978 139
1979 140
1980 153
1981 200
1982 166
1983 192
1984 189
1985 226
1986 250
1987 267
1988 281
1989 270
1990 281
1991 289
1992 282
1993 325
1994 360
1995 362
1996 400
1997 380
1998 411
1999 446
2000 811
2001 490
2002 528
2003 576
2004 637
2005 689
2006 714
2007 735
2008 819
2009 883
2010 896
2011 1077
2012 1114
2013 1233
2014 1372
2015 1347
2016 1381
2017 1431
2018 1508
2019 1607
2020 1640
2021 3
Text availability
Article attribute
Article type
Publication date

Search Results

27,617 results
Results by year
Filters applied: . Clear all
Page 1
Diagnosis of Wilson disease.
Ferenci P. Ferenci P. Handb Clin Neurol. 2017;142:171-180. doi: 10.1016/B978-0-444-63625-6.00014-8. Handb Clin Neurol. 2017. PMID: 28433100 Review.
Clinical presentation of Wilson disease can vary widely; therefore diagnosis is not always straightforward. Wilson disease is not just a disease of children and young adults, but may present at any age. ...
Clinical presentation of Wilson disease can vary widely; therefore diagnosis is not always straightforward. Wilson d
Wilson Disease.
Pfeiffer RF. Pfeiffer RF. Continuum (Minneap Minn). 2016 Aug;22(4 Movement Disorders):1246-61. doi: 10.1212/CON.0000000000000350. Continuum (Minneap Minn). 2016. PMID: 27495207 Review.
PURPOSE OF REVIEW: This article reviews the clinical features of Wilson disease, focusing on the neurologic and psychiatric abnormalities, and addresses the diagnostic workup and treatment approaches to managing the disease. RECENT FINDINGS: The list of known …
PURPOSE OF REVIEW: This article reviews the clinical features of Wilson disease, focusing on the neurologic and psychiatric ab …
Wilson disease in children.
Roberts EA, Socha P. Roberts EA, et al. Handb Clin Neurol. 2017;142:141-156. doi: 10.1016/B978-0-444-63625-6.00012-4. Handb Clin Neurol. 2017. PMID: 28433098 Review.
Wilson disease (WD) is an inherited disorder mainly of hepatocellular copper disposition, due to dysfunction of the Wilson ATPase, a P(1B)-ATPase encoded by the gene ATP7B. In children, as in older age brackets, clinical disease is highly diverse. Alth
Wilson disease (WD) is an inherited disorder mainly of hepatocellular copper disposition, due to dysfunction of the Wilson
Wilson's Disease in China.
Xie JJ, Wu ZY. Xie JJ, et al. Neurosci Bull. 2017 Jun;33(3):323-330. doi: 10.1007/s12264-017-0107-4. Epub 2017 Mar 6. Neurosci Bull. 2017. PMID: 28265897 Free PMC article. Review.
Wilson's disease (WD) is an autosomal recessive disorder of copper metabolism. ...Genetic diagnosis plays an important role and has gradually become a routine test in China. The first Chinese spectrum of disease-causing mutations of ATP7B has been established
Wilson's disease (WD) is an autosomal recessive disorder of copper metabolism. ...Genetic diagnosis plays an important role an
Wilson disease and related copper disorders.
Lorincz MT. Lorincz MT. Handb Clin Neurol. 2018;147:279-292. doi: 10.1016/B978-0-444-63233-3.00018-X. Handb Clin Neurol. 2018. PMID: 29325617 Review.
Mutations in copper metabolism genes or abnormalities in copper metabolism result in disease from copper excess or deficiency. Wilson disease (WD) is an autosomal-recessive disease caused by mutations in the ATP7B gene which encodes a copper-transporti …
Mutations in copper metabolism genes or abnormalities in copper metabolism result in disease from copper excess or deficiency. Wil
Pathogenesis of Wilson disease.
Scheiber IF, Brůha R, Dušek P. Scheiber IF, et al. Handb Clin Neurol. 2017;142:43-55. doi: 10.1016/B978-0-444-63625-6.00005-7. Handb Clin Neurol. 2017. PMID: 28433109 Review.
Impaired ATP7B function in Wilson disease results in excessive accumulation of copper in liver, brain, and other tissues. ...We will specify the physiologic functions of ATP7B and the consequences of its dysfunction and summarize the current knowledge on the pathoge …
Impaired ATP7B function in Wilson disease results in excessive accumulation of copper in liver, brain, and other tissues. ...W …
Advances in Treatment of Wilson Disease.
Aggarwal A, Bhatt M. Aggarwal A, et al. Tremor Other Hyperkinet Mov (N Y). 2018 Feb 28;8:525. doi: 10.7916/D841881D. eCollection 2018. Tremor Other Hyperkinet Mov (N Y). 2018. PMID: 29520330 Free PMC article. Review.
BACKGROUND: Wilson disease (WD) is an inherited neurometabolic disorder that results in excessive copper deposition in the liver and the brain, affecting children and young adults. Without treatment the disease is invariably fatal. Though treatments for WD ha …
BACKGROUND: Wilson disease (WD) is an inherited neurometabolic disorder that results in excessive copper deposition in the liv …
Wilson disease.
Guindi M. Guindi M. Semin Diagn Pathol. 2019 Nov;36(6):415-422. doi: 10.1053/j.semdp.2019.07.008. Epub 2019 Jul 25. Semin Diagn Pathol. 2019. PMID: 31421978 Review.
Wilson disease (WD) is an inherited disorder of copper metabolism. ...They can overlap with non-WD causes. Patients may present with hepatic or neurological disease or combinations thereof. Approx. 50% of WD patients present with liver disease. ...
Wilson disease (WD) is an inherited disorder of copper metabolism. ...They can overlap with non-WD causes. Patients may presen
Update on the Diagnosis and Management of Wilson Disease.
Roberts EA. Roberts EA. Curr Gastroenterol Rep. 2018 Nov 5;20(12):56. doi: 10.1007/s11894-018-0660-7. Curr Gastroenterol Rep. 2018. PMID: 30397835 Review.
PURPOSE OF REVIEW: Exciting developments relating to Wilson disease (WD) have taken place with respect to both basic biological and clinical research. ...RECENT FINDINGS: The structure of the gene product of ATP7B, abnormal in WD, is being worked out in detail, alon …
PURPOSE OF REVIEW: Exciting developments relating to Wilson disease (WD) have taken place with respect to both basic biologica …
Wilson's disease: A master of disguise.
Hedera P. Hedera P. Parkinsonism Relat Disord. 2019 Feb;59:140-145. doi: 10.1016/j.parkreldis.2019.02.016. Epub 2019 Feb 14. Parkinsonism Relat Disord. 2019. PMID: 30797706 Review.
Wilson's disease (WD), in contrast to many neurogenetic metabolic diseases, can be very effectively treated in acute and chronic stages of the disease. ...Neurologic and neuropsychiatric problems in WD are quite nonspecific and we discuss the most common clin
Wilson's disease (WD), in contrast to many neurogenetic metabolic diseases, can be very effectively treated in acute and chron
27,617 results
You have reached the last page of results. A maximum of 10,000 results are available.
Jump to page
Feedback