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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
2011 19
2012 21
2013 14
2014 13
2015 13
2016 14
2017 22
2018 19
2019 18
2020 17
2021 15
2022 15
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305 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.
The differential diagnosis of chorea.
Wild EJ, Tabrizi SJ. Wild EJ, et al. Pract Neurol. 2007 Nov;7(6):360-73. doi: 10.1136/pn.2007.134585. Pract Neurol. 2007. PMID: 18024776 Review.
In this article, the authors discuss the causes of chorea, particularly Huntington's disease and the genetic syndromes that may resemble it, including HDL1-3, inherited prion disease, spinocerebellar ataxias 1, 3 and 17, neuroacanthocytosis, dentatorubro-pallidoluysian atr …
In this article, the authors discuss the causes of chorea, particularly Huntington's disease and the genetic syndromes that may resemble it, …
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 …
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 …
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 …
Progress in the Diagnosis and Management of Chorea-acanthocytosis.
Liu Y, Liu ZY, Wan XH, Guo Y. Liu Y, et al. Chin Med Sci J. 2018 Mar 30;33(1):53-59. doi: 10.24920/21802. Chin Med Sci J. 2018. PMID: 29620515 Review.
Chorea-acanthocytosis (ChAc) is the most common subtype of neuroacanthocytosis syndrome, characterized by the presence of acanthocytes and neurological disorders. ...
Chorea-acanthocytosis (ChAc) is the most common subtype of neuroacanthocytosis syndrome, characterized by the presence of acanthocyte …
Childhood dystonia.
Uc EY, Rodnitzky RL. Uc EY, et al. Semin Pediatr Neurol. 2003 Mar;10(1):52-61. doi: 10.1016/s1071-9091(02)00010-4. Semin Pediatr Neurol. 2003. PMID: 12785748 Review.
Conditions discussed in detail include idiopathic torsion dystonia, dopa-responsive dystonia, Wilson's disease, myoclonus dystonia, rapid-onset dystonia parkinsonism, neurodegeneration with brain iron accumulation (Hallervorden-Spatz syndrome), mitochondrial dystonias, Niemann-Pi …
Conditions discussed in detail include idiopathic torsion dystonia, dopa-responsive dystonia, Wilson's disease, myoclonus dystonia, rapid-on …
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 …
305 results