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

Year Number of Results
1966 1
1967 4
1968 2
1970 3
1971 1
1972 3
1973 3
1974 3
1975 11
1976 6
1977 14
1978 5
1979 8
1980 10
1981 16
1982 10
1983 16
1984 25
1985 19
1986 25
1987 16
1988 23
1989 26
1990 35
1991 27
1992 41
1993 60
1994 69
1995 57
1996 64
1997 74
1998 58
1999 85
2000 95
2001 86
2002 91
2003 123
2004 129
2005 118
2006 164
2007 177
2008 163
2009 147
2010 192
2011 218
2012 215
2013 225
2014 252
2015 237
2016 276
2017 328
2018 303
2019 268
2020 312
2021 336
2022 293
2023 229
2024 63

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5,257 results

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Page 1
Huntington's disease: a clinical review.
McColgan P, Tabrizi SJ. McColgan P, et al. Eur J Neurol. 2018 Jan;25(1):24-34. doi: 10.1111/ene.13413. Epub 2017 Sep 22. Eur J Neurol. 2018. PMID: 28817209 Review.
Huntington's disease (HD) is a fully penetrant neurodegenerative disease caused by a dominantly inherited CAG trinucleotide repeat expansion in the huntingtin gene on chromosome 4. ...Early macroscopic changes are seen in the striatum with involvement of the
Huntington's disease (HD) is a fully penetrant neurodegenerative disease caused by a dominantly inherited CAG trinucleo
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.
Huntington's disease (HD) is an inherited neurodegenerative disease characterised by neuropsychiatric symptoms, a movement disorder (most commonly choreiform) and progressive cognitive impairment. ...Though diagnosis is usually straightforward, unusual presen
Huntington's disease (HD) is an inherited neurodegenerative disease characterised by neuropsychiatric symptoms, a movem
Huntington's Disease: Mechanisms of Pathogenesis and Therapeutic Strategies.
Jimenez-Sanchez M, Licitra F, Underwood BR, Rubinsztein DC. Jimenez-Sanchez M, et al. Cold Spring Harb Perspect Med. 2017 Jul 5;7(7):a024240. doi: 10.1101/cshperspect.a024240. Cold Spring Harb Perspect Med. 2017. PMID: 27940602 Free PMC article. Review.
Huntington's disease is a late-onset neurodegenerative disease caused by a CAG trinucleotide repeat in the gene encoding the huntingtin protein. ...Finally, we outline some of the therapeutic strategies that are currently being pursued to slow down the dis
Huntington's disease is a late-onset neurodegenerative disease caused by a CAG trinucleotide repeat in the gene encodin
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. ...Evidence suggests that this tail confers a toxic gain
Huntington's disease is an autosomal-dominant, progressive neurodegenerative disorder with a distinct phenotype, including cho
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.
Huntington disease (HD) is a rare neurodegenerative disorder of the central nervous system characterized by unwanted choreatic movements, behavioral and psychiatric disturbances and dementia. ...In some cases symptoms start before the age of 20 years with behavior d
Huntington disease (HD) is a rare neurodegenerative disorder of the central nervous system characterized by unwanted choreatic
Physical Therapy and Exercise Interventions in Huntington's Disease: A Mixed Methods Systematic Review.
Fritz NE, Rao AK, Kegelmeyer D, Kloos A, Busse M, Hartel L, Carrier J, Quinn L. Fritz NE, et al. J Huntingtons Dis. 2017;6(3):217-235. doi: 10.3233/JHD-170260. J Huntingtons Dis. 2017. PMID: 28968244 Free PMC article. Review.
BACKGROUND: A number of studies evaluating physical therapy and exercise interventions in Huntington's disease have been conducted over the past 15 years. However, an assessment of the quality and strength of the evidence in support of these interventions is lacking …
BACKGROUND: A number of studies evaluating physical therapy and exercise interventions in Huntington's disease have been condu …
Huntington disease: natural history, biomarkers and prospects for therapeutics.
Ross CA, Aylward EH, Wild EJ, Langbehn DR, Long JD, Warner JH, Scahill RI, Leavitt BR, Stout JC, Paulsen JS, Reilmann R, Unschuld PG, Wexler A, Margolis RL, Tabrizi SJ. Ross CA, et al. Nat Rev Neurol. 2014 Apr;10(4):204-16. doi: 10.1038/nrneurol.2014.24. Epub 2014 Mar 11. Nat Rev Neurol. 2014. PMID: 24614516 Free article. Review.
Huntington disease (HD) can be seen as a model neurodegenerative disorder, in that it is caused by a single genetic mutation and is amenable to predictive genetic testing, with estimation of years to predicted onset, enabling the entire range of disease natur
Huntington disease (HD) can be seen as a model neurodegenerative disorder, in that it is caused by a single genetic mutation a
Clinical Features of Huntington's Disease.
Ghosh R, Tabrizi SJ. Ghosh R, et al. Adv Exp Med Biol. 2018;1049:1-28. doi: 10.1007/978-3-319-71779-1_1. Adv Exp Med Biol. 2018. PMID: 29427096 Review.
Huntington's disease (HD) is the most common monogenic neurodegenerative disease and the commonest genetic dementia in the developed world. ...Since the discovery of the gene over 20 years ago much progress has been made in HD research, and although there are
Huntington's disease (HD) is the most common monogenic neurodegenerative disease and the commonest genetic dementia in
New Avenues for the Treatment of Huntington's Disease.
Kim A, Lalonde K, Truesdell A, Gomes Welter P, Brocardo PS, Rosenstock TR, Gil-Mohapel J. Kim A, et al. Int J Mol Sci. 2021 Aug 4;22(16):8363. doi: 10.3390/ijms22168363. Int J Mol Sci. 2021. PMID: 34445070 Free PMC article. Review.
Huntington's disease (HD) is a neurodegenerative disorder caused by a CAG expansion in the HD gene. The disease is characterized by neurodegeneration, particularly in the striatum and cortex. ...
Huntington's disease (HD) is a neurodegenerative disorder caused by a CAG expansion in the HD gene. The disease is char
Huntington disease.
Bates GP, Dorsey R, Gusella JF, Hayden MR, Kay C, Leavitt BR, Nance M, Ross CA, Scahill RI, Wetzel R, Wild EJ, Tabrizi SJ. Bates GP, et al. Nat Rev Dis Primers. 2015 Apr 23;1:15005. doi: 10.1038/nrdp.2015.5. Nat Rev Dis Primers. 2015. PMID: 27188817 Review.
Huntington disease is devastating to patients and their families - with autosomal dominant inheritance, onset typically in the prime of adult life, progressive course, and a combination of motor, cognitive and behavioural features. ...We describe the relationship be
Huntington disease is devastating to patients and their families - with autosomal dominant inheritance, onset typically in the
5,257 results