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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
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2023 12
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323 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.
Pandey S. Pandey S. J Assoc Physicians India. 2013 Jul;61(7):471-4, 483. J Assoc Physicians India. 2013. PMID: 24772751 Review.
Genetic test for Huntington's disease is available which may be done for diagnosis and detection of family members at risk of developing disease. Other genetic causes of chorea are neuroacanthocytosis and Wilson's disease. Treatment of genetic causes of chore is usually sy …
Genetic test for Huntington's disease is available which may be done for diagnosis and detection of family members at risk of developing dis …
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 …
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
Inherited movement disorders.
Sharma N, Standaert DG. Sharma N, et al. Neurol Clin. 2002 Aug;20(3):759-78, vii. doi: 10.1016/s0733-8619(01)00014-7. Neurol Clin. 2002. PMID: 12432829 Review.
In addition, gene mutations have been identified in less common movement disorders including Wilson's disease, Hallervorden-Spatz syndrome, paroxysmal kinesogenic choreoathetosis, neuroacanthocytosis, and some forms of dystonia. This article summarizes what is known about …
In addition, gene mutations have been identified in less common movement disorders including Wilson's disease, Hallervorden-Spatz syndrome, …
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.
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.
Sphingolipid and Phospholipid Levels Are Altered in Human Brain in Chorea-Acanthocytosis.
Miltenberger-Miltenyi G, Jones A, Tetlow AM, Conceição VA, Crary JF, Ditzel RM Jr, Farrell K, Nandakumar R, Barton B, Karp BI, Kirby A, Lett DJ, Mente K, Morgello S, Simon DK, Walker RH. Miltenberger-Miltenyi G, et al. Mov Disord. 2023 Aug;38(8):1535-1541. doi: 10.1002/mds.29445. Epub 2023 Jun 12. Mov Disord. 2023. PMID: 37307400
323 results