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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 16
2022 17
2023 10
2024 0

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316 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 …
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 …
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 …
Movement disorders and neuropathies: overlaps and mimics in clinical practice.
Gentile F, Bertini A, Priori A, Bocci T. Gentile F, et al. J Neurol. 2022 Sep;269(9):4646-4662. doi: 10.1007/s00415-022-11200-0. Epub 2022 Jun 3. J Neurol. 2022. PMID: 35657406 Review.
Finally, genetic causes should be pursued in case of positive family history, young onset or multisystemic involvement, and examined for neuroacanthocytosis, spinocerebellar ataxias, mitochondrial disorders and less common causes of adult-onset cerebellar ataxias and spast …
Finally, genetic causes should be pursued in case of positive family history, young onset or multisystemic involvement, and examined for …
Deep brain stimulation for chorea-acanthocytosis: a systematic review.
Wu Y, Xu YY, Gao Y, Li JM, Liu XW, Wang MQ, Deng H, Xiao LL, Ren HB, Xiong BT, Pan W, Zhou XW, Wang W. Wu Y, et al. Neurosurg Rev. 2022 Jun;45(3):1861-1871. doi: 10.1007/s10143-022-01735-1. Epub 2022 Jan 12. Neurosurg Rev. 2022. PMID: 35020105 Review.
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.
316 results