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

Year Number of Results
1963 2
1966 1
1967 4
1968 3
1969 3
1970 9
1971 7
1972 5
1973 7
1974 5
1975 14
1976 7
1977 15
1978 7
1979 10
1980 12
1981 17
1982 13
1983 20
1984 29
1985 23
1986 25
1987 17
1988 32
1989 27
1990 29
1991 27
1992 42
1993 53
1994 54
1995 56
1996 63
1997 60
1998 47
1999 83
2000 77
2001 77
2002 67
2003 88
2004 83
2005 76
2006 102
2007 99
2008 86
2009 77
2010 113
2011 147
2012 118
2013 105
2014 150
2015 133
2016 124
2017 164
2018 147
2019 126
2020 140
2021 130
2022 108
2023 86
2024 1

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3,191 results

Results by year

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Page 1
Huntington's disease: diagnosis and management.
Stoker TB, Mason SL, Greenland JC, Holden ST, Santini H, Barker RA. Stoker TB, et al. Pract Neurol. 2022 Feb;22(1):32-41. doi: 10.1136/practneurol-2021-003074. Epub 2021 Aug 19. Pract Neurol. 2022. PMID: 34413240 Review.
Current treatments are symptomatic, and largely directed at the chorea and neurobehavioural problems, although supporting trial evidence for these is often limited....
Current treatments are symptomatic, and largely directed at the chorea and neurobehavioural problems, although supporting trial evide …
Huntington's disease.
Walker FO. Walker FO. Lancet. 2007 Jan 20;369(9557):218-28. doi: 10.1016/S0140-6736(07)60111-1. Lancet. 2007. PMID: 17240289 Review.
Huntington's disease is an autosomal-dominant, progressive neurodegenerative disorder with a distinct phenotype, including chorea and dystonia, incoordination, cognitive decline, and behavioural difficulties. ...
Huntington's disease is an autosomal-dominant, progressive neurodegenerative disorder with a distinct phenotype, including chorea and …
Chorea.
Termsarasab P. Termsarasab P. Continuum (Minneap Minn). 2019 Aug;25(4):1001-1035. doi: 10.1212/CON.0000000000000763. Continuum (Minneap Minn). 2019. PMID: 31356291 Review.
PURPOSE OF REVIEW: This article provides an overview of the approach to chorea in clinical practice, beginning with a discussion of the phenomenologic features of chorea and how to differentiate it from other movement disorders. ...SUMMARY: Clinical features remain …
PURPOSE OF REVIEW: This article provides an overview of the approach to chorea in clinical practice, beginning with a discussion of t …
Huntington's disease: a clinical review.
Roos RA. Roos RA. Orphanet J Rare Dis. 2010 Dec 20;5:40. doi: 10.1186/1750-1172-5-40. Orphanet J Rare Dis. 2010. PMID: 21171977 Free PMC article. Review.
In some cases symptoms start before the age of 20 years with behavior disturbances and learning difficulties at school (Juvenile Huntington's disease; JHD). The classic sign is chorea that gradually spreads to all muscles. All psychomotor processes become severely retarded …
In some cases symptoms start before the age of 20 years with behavior disturbances and learning difficulties at school (Juvenile Huntington' …
Movement disorders and stroke.
Defebvre L, Krystkowiak P. Defebvre L, et al. Rev Neurol (Paris). 2016 Aug-Sep;172(8-9):483-487. doi: 10.1016/j.neurol.2016.07.006. Epub 2016 Jul 28. Rev Neurol (Paris). 2016. PMID: 27476417 Review.
Movement Disorders in Multiple Sclerosis: An Update.
Ghosh R, Roy D, Dubey S, Das S, Benito-León J. Ghosh R, et al. Tremor Other Hyperkinet Mov (N Y). 2022 May 4;12:14. doi: 10.5334/tohm.671. eCollection 2022. Tremor Other Hyperkinet Mov (N Y). 2022. PMID: 35601204 Free PMC article. Review.
RESULTS: The most prevalent movement disorders described in MS include restless leg syndrome, tremor, ataxia, parkinsonism, paroxysmal dyskinesias, chorea and ballism, facial myokymia, including hemifacial spasm and spastic paretic hemifacial contracture, tics, and tourett …
RESULTS: The most prevalent movement disorders described in MS include restless leg syndrome, tremor, ataxia, parkinsonism, paroxysmal dyski …
Chorea in children: etiology, diagnostic approach and management.
Baizabal-Carvallo JF, Cardoso F. Baizabal-Carvallo JF, et al. J Neural Transm (Vienna). 2020 Oct;127(10):1323-1342. doi: 10.1007/s00702-020-02238-3. Epub 2020 Aug 9. J Neural Transm (Vienna). 2020. PMID: 32776155 Review.
Chorea may present at all stages of life, from newborns to elderly individuals. ...Sydenham chorea is considered the most common cause of acute childhood-onset chorea, but its prevalence has decreased in Western countries. ...
Chorea may present at all stages of life, from newborns to elderly individuals. ...Sydenham chorea is considered the most comm …
Huntington's Disease-Update on Treatments.
Wyant KJ, Ridder AJ, Dayalu P. Wyant KJ, et al. Curr Neurol Neurosci Rep. 2017 Apr;17(4):33. doi: 10.1007/s11910-017-0739-9. Curr Neurol Neurosci Rep. 2017. PMID: 28324302 Review.
Despite the discovery of the underlying genetic mutation more than 20 years ago, treatment remains focused on symptomatic management. Chorea, the most recognizable symptom, responds to medication that reduces dopaminergic neurotransmission. ...
Despite the discovery of the underlying genetic mutation more than 20 years ago, treatment remains focused on symptomatic management. Cho …
Chorea.
Stimming EF, Bega D. Stimming EF, et al. Continuum (Minneap Minn). 2022 Oct 1;28(5):1379-1408. doi: 10.1212/CON.0000000000001169. Continuum (Minneap Minn). 2022. PMID: 36222771 Review.
PURPOSE OF REVIEW: This article provides an overview of the diagnostic and therapeutic approach to a patient with chorea. The phenomenology of chorea is described in addition to other common hyperkinetic movements that may be mistaken for or coexist with chorea …
PURPOSE OF REVIEW: This article provides an overview of the diagnostic and therapeutic approach to a patient with chorea. The phenome …
Recommendations for the diagnosis and treatment of paroxysmal kinesigenic dyskinesia: an expert consensus in China.
Cao L, Huang X, Wang N, Wu Z, Zhang C, Gu W, Cong S, Ma J, Wei L, Deng Y, Fang Q, Niu Q, Wang J, Wang Z, Yin Y, Tian J, Tian S, Bi H, Jiang H, Liu X, Lü Y, Sun M, Wu J, Xu E, Chen T, Chen T, Chen X, Li W, Li S, Li Q, Song X, Tang Y, Yang P, Yang Y, Zhang M, Zhang X, Zhang Y, Zhang R, Ouyang Y, Yu J, Hu Q, Ke Q, Yao Y, Zhao Z, Zhao X, Zhao G, Liang F, Cheng N, Han J, Peng R, Chen S, Tang B. Cao L, et al. Transl Neurodegener. 2021 Feb 16;10(1):7. doi: 10.1186/s40035-021-00231-8. Transl Neurodegener. 2021. PMID: 33588936 Free PMC article. Review.
3,191 results