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1982
2025

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

Year Number of Results
1982 1
1985 3
1986 1
1988 1
1989 1
1990 1
1991 3
1992 5
1993 1
1994 3
1995 3
1996 6
1997 5
1998 3
1999 4
2000 4
2001 5
2002 4
2003 6
2004 6
2005 6
2006 9
2007 20
2008 13
2009 13
2010 13
2011 19
2012 21
2013 14
2014 13
2015 13
2016 14
2017 22
2018 19
2019 18
2020 17
2021 16
2022 17
2023 12
2024 10
2025 0

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326 results

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Page 1
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.
Chorea-acanthocytosis.
Rashid S, Malek N, Krommyda M. Rashid S, et al. Pract Neurol. 2024 May 29;24(3):223-225. doi: 10.1136/pn-2023-003981. Pract Neurol. 2024. PMID: 38290845
Neuroacanthocytosis.
Walker RH, Jung HH, Danek A. Walker RH, et al. Handb Clin Neurol. 2011;100:141-51. doi: 10.1016/B978-0-444-52014-2.00007-0. Handb Clin Neurol. 2011. PMID: 21496574 Review.
The term "neuroacanthocytosis" describes a heterogeneous group of molecularly-defined disorders which result in progressive neurodegeneration, predominantly of the basal ganglia, and erythrocyte acanthocytosis. The clinical presentation of neuroacanthocytosis syndro …
The term "neuroacanthocytosis" describes a heterogeneous group of molecularly-defined disorders which result in progressive neurodege …
Chorea.
Pandey S. Pandey S. J Assoc Physicians India. 2013 Jul;61(7):471-4, 483. J Assoc Physicians India. 2013. PMID: 24772751 Review.
Other genetic causes of chorea are neuroacanthocytosis and Wilson's disease. Treatment of genetic causes of chore is usually symptomatic with exception of Wilson's disease. ...
Other genetic causes of chorea are neuroacanthocytosis and Wilson's disease. Treatment of genetic causes of chore is usually symptoma …
Neuroacanthocytosis.
Danek A, Walker RH. Danek A, et al. Curr Opin Neurol. 2005 Aug;18(4):386-92. doi: 10.1097/01.wco.0000173464.01888.e9. Curr Opin Neurol. 2005. PMID: 16003113 Review.
PURPOSE OF REVIEW: The term neuroacanthocytosis describes a group of phenotypically and genetically heterogeneous disorders, and thus has long been a source of confusion and diagnostic imprecision. ...SUMMARY: Genetic testing has led to increased diagnostic accuracy of the …
PURPOSE OF REVIEW: The term neuroacanthocytosis describes a group of phenotypically and genetically heterogeneous disorders, and thus …
Neuroacanthocytosis syndromes.
Jung HH, Danek A, Walker RH. Jung HH, et al. Orphanet J Rare Dis. 2011 Oct 25;6:68. doi: 10.1186/1750-1172-6-68. Orphanet J Rare Dis. 2011. PMID: 22027213 Free PMC article. Review.
Neuroacanthocytosis (NA) syndromes are a group of genetically defined diseases characterized by the association of red blood cell acanthocytosis and progressive degeneration of the basal ganglia. ...
Neuroacanthocytosis (NA) syndromes are a group of genetically defined diseases characterized by the association of red blood cell aca
Chorea-acanthocytosis.
Sokolov E, Schneider SA, Bain PG. Sokolov E, et al. Pract Neurol. 2012 Feb;12(1):40-3. doi: 10.1136/practneurol-2011-000045. Pract Neurol. 2012. PMID: 22258171 No abstract available.
Choreo-acanthocytosis.
Bain BJ, Bain PG. Bain BJ, et al. Am J Hematol. 2013 Aug;88(8):712. doi: 10.1002/ajh.23481. Epub 2013 Jun 20. Am J Hematol. 2013. PMID: 23674404 Free article. No abstract available.
The neuropsychiatry of neuroacanthocytosis syndromes.
Walterfang M, Evans A, Looi JC, Jung HH, Danek A, Walker RH, Velakoulis D. Walterfang M, et al. Neurosci Biobehav Rev. 2011 Apr;35(5):1275-83. doi: 10.1016/j.neubiorev.2011.01.001. Epub 2011 Jan 13. Neurosci Biobehav Rev. 2011. PMID: 21237198 Review.
Disruptions to key frontostriatal loops secondary to pathology in the striatum and pallidum appear to predispose individuals to major neuropsychiatric syndromes; however, treatment can be instituted for a number of these manifestations, which lessens the overall burden of disease …
Disruptions to key frontostriatal loops secondary to pathology in the striatum and pallidum appear to predispose individuals to major neurop …
Acanthocytosis and neurological disorders.
Stevenson VL, Hardie RJ. Stevenson VL, et al. J Neurol. 2001 Feb;248(2):87-94. doi: 10.1007/s004150170241. J Neurol. 2001. PMID: 11284140 Review.
In abetalipoproteinaemia, an autosomal recessive condition, vitamin E deficiency results in a progressive spinocerebellar syndrome associated with peripheral neuropathy and retinitis pigmentosa. Neuroacanthocytosis is also probably an autosomal recessive condition and is c …
In abetalipoproteinaemia, an autosomal recessive condition, vitamin E deficiency results in a progressive spinocerebellar syndrome associate …
326 results