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

Year Number of Results
1966 1
1976 1
1987 1
1989 1
1993 1
1994 1
1995 2
1996 1
1997 2
1998 1
1999 1
2000 3
2002 2
2003 3
2007 1
2009 1
2010 1
2011 3
2014 2
2016 2
2018 2
2019 4
2020 2
2021 2
2022 2
2023 2
2024 0

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Page 1
Ataxia with Vitamin E Deficiency May Present with Cervical Dystonia.
Becker AE, Vargas W, Pearson TS. Becker AE, et al. Tremor Other Hyperkinet Mov (N Y). 2016 May 17;6:374. doi: 10.7916/D8B85820. eCollection 2016. Tremor Other Hyperkinet Mov (N Y). 2016. PMID: 27274910 Free PMC article.
Dystonia has been reported rarely. CASE REPORT: An 11-year-old female presented with dystonic head tremor and cervical and bilateral arm dystonia. Her 14-year-old older brother had dystonic head tremor and generalized dystonia. One year later, t
Dystonia has been reported rarely. CASE REPORT: An 11-year-old female presented with dystonic head tremor and cervical and bil
Aceruloplasminemia.
Miyajima H, Hosoi Y. Miyajima H, et al. 2003 Aug 12 [updated 2018 Sep 27]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2003 Aug 12 [updated 2018 Sep 27]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 20301666 Free Books & Documents. Review.
The neurologic findings of movement disorder (blepharospasm, grimacing, facial and neck dystonia, tremors, chorea) and ataxia (gait ataxia, dysarthria) correspond to regions of iron deposition in the brain. ...MANAGEMENT: Treatment of manifestations: Iron chelating agents …
The neurologic findings of movement disorder (blepharospasm, grimacing, facial and neck dystonia, tremors, chorea) and ataxia (gait a …
Myoclonus-dystonia syndrome.
Nardocci N. Nardocci N. Handb Clin Neurol. 2011;100:563-75. doi: 10.1016/B978-0-444-52014-2.00041-0. Handb Clin Neurol. 2011. PMID: 21496608 Review.
Myoclonus dystonia syndrome (MDS) refers to a group of heterogeneous nondegenerative clinical conditions characterized by the association of myoclonus and dystonia as the only or prominent symptom. ...Dopa-responsive dystonia due to mutation in the GTP-CH gen …
Myoclonus dystonia syndrome (MDS) refers to a group of heterogeneous nondegenerative clinical conditions characterized by the associa …
Ataxia with vitamin E deficiency and severe dystonia: report of a case.
Roubertie A, Biolsi B, Rivier F, Humbertclaude V, Cheminal R, Echenne B. Roubertie A, et al. Brain Dev. 2003 Sep;25(6):442-5. doi: 10.1016/s0387-7604(03)00054-8. Brain Dev. 2003. PMID: 12907280
Mutation of the gene for alpha-tocopherol transfer protein causes ataxia with isolated vitamin E deficiency, a disorder usually stabilized or improved after vitamin E supplementation. Dystonia has rarely been described in ataxia with isolated …
Mutation of the gene for alpha-tocopherol transfer protein causes ataxia with isolated vitamin E deficiency, a disorder usuall …
Tardive Dyskinesia.
Tarsy D. Tarsy D. Curr Treat Options Neurol. 2000 May;2(3):205-214. doi: 10.1007/s11940-000-0003-4. Curr Treat Options Neurol. 2000. PMID: 11096748
Anticholinergic drugs are unhelpful and may aggravate TD but, similar to their effect in idiopathic dystonia, may be effective in tardive dystonia. Botulinum toxin injections are of considerable value in managing localized forms of tardive dystonia, such as r …
Anticholinergic drugs are unhelpful and may aggravate TD but, similar to their effect in idiopathic dystonia, may be effective in tar …
Myoclonic dystonia as unique presentation of isolated vitamin E deficiency in a young patient.
Angelini L, Erba A, Mariotti C, Gellera C, Ciano C, Nardocci N. Angelini L, et al. Mov Disord. 2002 May;17(3):612-4. doi: 10.1002/mds.10026. Mov Disord. 2002. PMID: 12112220
We describe a young patient affected by vitamin E deficiency with mutation in the tocopherol transfer protein alleles and the unique presentation as myoclonic dystonia, which was practically the only symptom for 6 years before ataxia became evident. Vitami
We describe a young patient affected by vitamin E deficiency with mutation in the tocopherol transfer protein alleles and the …
[Treatment of tardive syndromes].
Horváth K, Aschermann Z, Komoly S, Kovács A, Kovács N. Horváth K, et al. Psychiatr Hung. 2014;29(2):214-24. Psychiatr Hung. 2014. PMID: 25041749 Review. Hungarian.
Tardive syndromes associated with dopamine-receptor blocking agents have heterogeneous appearance. The treatment of tardive dyskinesia, dystonia, myoclonus, tourettism, tremor and akathisia is challenging for both psychiatrists and neurologists. ...Although lowering or sto …
Tardive syndromes associated with dopamine-receptor blocking agents have heterogeneous appearance. The treatment of tardive dyskinesia, d
40 results