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

Year Number of Results
1934 1
1946 1
1959 1
1967 1
1971 1
1974 3
1975 13
1976 8
1977 8
1978 15
1979 9
1980 11
1981 16
1982 20
1983 24
1984 19
1985 17
1986 26
1987 32
1988 24
1989 27
1990 32
1991 44
1992 37
1993 47
1994 55
1995 37
1996 31
1997 35
1998 60
1999 69
2000 95
2001 62
2002 81
2003 73
2004 98
2005 83
2006 106
2007 108
2008 114
2009 137
2010 144
2011 142
2012 158
2013 178
2014 192
2015 213
2016 230
2017 297
2018 299
2019 310
2020 358
2021 399
2022 425
2023 428
2024 200

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4,957 results

Results by year

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Page 1
Wilson Disease: An Overview and Approach to Management.
Mulligan C, Bronstein JM. Mulligan C, et al. Neurol Clin. 2020 May;38(2):417-432. doi: 10.1016/j.ncl.2020.01.005. Epub 2020 Feb 28. Neurol Clin. 2020. PMID: 32279718 Review.
Wilson's disease is one of the few preventable movement disorders in which there are therapies that modify disease progression. ...This article reviews the clinical presentation, epidemiology, genetics, pathophysiology, diagnosis, and management of Wilson dis …
Wilson's disease is one of the few preventable movement disorders in which there are therapies that modify disease progression …
Corneal wound healing.
Wilson SE. Wilson SE. Exp Eye Res. 2020 Aug;197:108089. doi: 10.1016/j.exer.2020.108089. Epub 2020 Jun 15. Exp Eye Res. 2020. PMID: 32553485 Free PMC article. Review.
Saul-Wilson Syndrome.
Ferreira C. Ferreira C. 2020 Feb 20. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2020 Feb 20. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 32078278 Free Books & Documents. Review.
CLINICAL CHARACTERISTICS: Saul-Wilson syndrome (SWS) is a skeletal dysplasia characterized by profound short stature, distinctive craniofacial features, short distal phalanges of fingers and toes, and often clubfoot. ...
CLINICAL CHARACTERISTICS: Saul-Wilson syndrome (SWS) is a skeletal dysplasia characterized by profound short stature, distinctive cra …
Mowat-Wilson Syndrome.
Adam MP, Conta J, Bean LJH. Adam MP, et al. 2007 Mar 28 [updated 2019 Jul 25]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2007 Mar 28 [updated 2019 Jul 25]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 20301585 Free Books & Documents. Review.
CLINICAL CHARACTERISTICS: Mowat-Wilson syndrome (MWS) is characterized by distinctive facial features (widely spaced eyes, broad eyebrows with a medial flare, low-hanging columella, prominent or pointed chin, open-mouth expression, and uplifted earlobes with a central depr …
CLINICAL CHARACTERISTICS: Mowat-Wilson syndrome (MWS) is characterized by distinctive facial features (widely spaced eyes, broad eyeb …
[Wilson disease].
Huster D. Huster D. Internist (Berl). 2018 Feb;59(2):159-174. doi: 10.1007/s00108-017-0378-x. Internist (Berl). 2018. PMID: 29340742 Review. German.
Wilson disease is a rare hereditary disorder of copper metabolism. ...
Wilson disease is a rare hereditary disorder of copper metabolism. ...
Wilson disease-treatment perspectives.
Litwin T, Dzieżyc K, Członkowska A. Litwin T, et al. Ann Transl Med. 2019 Apr;7(Suppl 2):S68. doi: 10.21037/atm.2018.12.09. Ann Transl Med. 2019. PMID: 31179305 Free PMC article. Review.
Wilson disease (WD) is a genetic disorder caused by pathological tissue copper accumulation with secondary damage of affected organs (mainly, but not limited to, the liver and brain). ...
Wilson disease (WD) is a genetic disorder caused by pathological tissue copper accumulation with secondary damage of affected organs …
Eye Movement Disorders in Movement Disorders.
Kassavetis P, Kaski D, Anderson T, Hallett M. Kassavetis P, et al. Mov Disord Clin Pract. 2022 Feb 16;9(3):284-295. doi: 10.1002/mdc3.13413. eCollection 2022 Apr. Mov Disord Clin Pract. 2022. PMID: 35402641 Free PMC article. Review.
Gaze impersistence in a patient with chorea suggests Huntington's disease, but in a patient with dystonia or tremor, Wilson's disease is more likely. Finally, functional eye movements can reinforce the clinical impression of a functional movement disorder....
Gaze impersistence in a patient with chorea suggests Huntington's disease, but in a patient with dystonia or tremor, Wilson's …
Wilson disease - liver pathology.
Pronicki M. Pronicki M. Handb Clin Neurol. 2017;142:71-75. doi: 10.1016/B978-0-444-63625-6.00007-0. Handb Clin Neurol. 2017. PMID: 28433112 Review.
The liver in Wilson disease may demonstrate a wide range of damage patterns. Some patients may present almost no detectable microscopic pathology, while others display lesions consistent with fulminant hepatitis or acute liver failure. ...The possibility of Wilson d …
The liver in Wilson disease may demonstrate a wide range of damage patterns. Some patients may present almost no detectable microscop …
Functional anatomy of thalamus and basal ganglia.
Herrero MT, Barcia C, Navarro JM. Herrero MT, et al. Childs Nerv Syst. 2002 Aug;18(8):386-404. doi: 10.1007/s00381-002-0604-1. Epub 2002 Jul 26. Childs Nerv Syst. 2002. PMID: 12192499 Review.
Involvement of the basal ganglia is related to involuntary and stereotyped movements or paucity of movements without involvement of voluntary motor functions, as in Parkinson's disease, Wilson's disease, progressive supranuclear palsy or Huntington's disease. ...
Involvement of the basal ganglia is related to involuntary and stereotyped movements or paucity of movements without involvement of voluntar …
4,957 results