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

Year Number of Results
1963 5
1964 5
1965 1
1966 1
1967 6
1968 8
1969 12
1970 10
1971 23
1972 15
1973 14
1974 11
1975 14
1976 11
1977 12
1978 28
1979 16
1980 21
1981 19
1982 13
1983 20
1984 32
1985 29
1986 21
1987 27
1988 34
1989 40
1990 47
1991 52
1992 59
1993 79
1994 90
1995 104
1996 91
1997 115
1998 95
1999 152
2000 140
2001 194
2002 159
2003 166
2004 161
2005 170
2006 200
2007 199
2008 183
2009 184
2010 185
2011 195
2012 273
2013 277
2014 265
2015 201
2016 270
2017 238
2018 335
2019 280
2020 310
2021 283
2022 214
2023 18
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5,928 results
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Ataxia.
Kuo SH. Kuo SH. Continuum (Minneap Minn). 2019 Aug;25(4):1036-1054. doi: 10.1212/CON.0000000000000753. Continuum (Minneap Minn). 2019. PMID: 31356292 Free PMC article. Review.
When these molecular pathways become dysfunctional, patients develop cerebellar ataxia. In addition, several ongoing clinical trials for Friedreich ataxia and spinocerebellar ataxia will likely result in novel symptomatic and disease-modifying therapies for …
When these molecular pathways become dysfunctional, patients develop cerebellar ataxia. In addition, several ongoing clinical trials …
Acute cerebellar ataxia: differential diagnosis and clinical approach.
Pedroso JL, Vale TC, Braga-Neto P, Dutra LA, França MC Jr, Teive HAG, Barsottini OGP. Pedroso JL, et al. Arq Neuropsiquiatr. 2019 Mar;77(3):184-193. doi: 10.1590/0004-282X20190020. Arq Neuropsiquiatr. 2019. PMID: 30970132 Free article. Review.
Acute ataxia usually results in hospitalization and extensive laboratory investigation. ...This review focuses on the etiologic and diagnostic considerations for acute ataxia....
Acute ataxia usually results in hospitalization and extensive laboratory investigation. ...This review focuses on the etiologic and d …
Spinocerebellar ataxia: an update.
Sullivan R, Yau WY, O'Connor E, Houlden H. Sullivan R, et al. J Neurol. 2019 Feb;266(2):533-544. doi: 10.1007/s00415-018-9076-4. Epub 2018 Oct 3. J Neurol. 2019. PMID: 30284037 Free PMC article. Review.
Spinocerebellar ataxia (SCA) is a heterogeneous group of neurodegenerative ataxic disorders with autosomal dominant inheritance. ...
Spinocerebellar ataxia (SCA) is a heterogeneous group of neurodegenerative ataxic disorders with autosomal dominant inheritance. ...
Ataxia.
Ashizawa T, Xia G. Ashizawa T, et al. Continuum (Minneap Minn). 2016 Aug;22(4 Movement Disorders):1208-26. doi: 10.1212/CON.0000000000000362. Continuum (Minneap Minn). 2016. PMID: 27495205 Free PMC article. Review.
PURPOSE OF REVIEW: This article introduces the background and common etiologies of ataxia and provides a general approach to assessing and managing the patient with ataxia. ...Pure ataxia is rare in acquired ataxia disorders, and associated symptoms an …
PURPOSE OF REVIEW: This article introduces the background and common etiologies of ataxia and provides a general approach to assessin …
Epilepsy and episodic ataxia type 2: family study and review of the literature.
Verriello L, Pauletto G, Nilo A, Lonigro I, Betto E, Valente M, Curcio F, Gigli GL. Verriello L, et al. J Neurol. 2021 Nov;268(11):4296-4302. doi: 10.1007/s00415-021-10555-0. Epub 2021 May 13. J Neurol. 2021. PMID: 33983550 Review.
Episodic ataxia type 2 (EA2) is a hereditary disorder characterized by paroxysmal attacks of ataxia, vertigo and nausea, due to mutations in the CACNA1A gene, which encodes for alpha1 subunit of the P/Q-type voltage-gated Ca(2+) channel (CaV2.1). ...Our description …
Episodic ataxia type 2 (EA2) is a hereditary disorder characterized by paroxysmal attacks of ataxia, vertigo and nausea, due t …
Machado-Joseph disease/spinocerebellar ataxia type 3.
Paulson H. Paulson H. Handb Clin Neurol. 2012;103:437-49. doi: 10.1016/B978-0-444-51892-7.00027-9. Handb Clin Neurol. 2012. PMID: 21827905 Free PMC article. Review.
Machado-Joseph disease (MJD), also known as spinocerebellar ataxia type 3 (SCA3), may be the most common dominantly inherited ataxia in the world. Here I will review historical, clinical, neuropathological, genetic, and pathogenic features of MJD, and finish with a …
Machado-Joseph disease (MJD), also known as spinocerebellar ataxia type 3 (SCA3), may be the most common dominantly inherited atax
Spinocerebellar ataxia.
Klockgether T, Mariotti C, Paulson HL. Klockgether T, et al. Nat Rev Dis Primers. 2019 Apr 11;5(1):24. doi: 10.1038/s41572-019-0074-3. Nat Rev Dis Primers. 2019. PMID: 30975995 Review.
The spinocerebellar ataxias (SCAs) are a genetically heterogeneous group of autosomal dominantly inherited progressive disorders, the clinical hallmark of which is loss of balance and coordination accompanied by slurred speech; onset is most often in adult life. ...
The spinocerebellar ataxias (SCAs) are a genetically heterogeneous group of autosomal dominantly inherited progressive disorders, the …
Fragile X-Associated Tremor/Ataxia Syndrome (FXTAS): Pathophysiology and Clinical Implications.
Cabal-Herrera AM, Tassanakijpanich N, Salcedo-Arellano MJ, Hagerman RJ. Cabal-Herrera AM, et al. Int J Mol Sci. 2020 Jun 20;21(12):4391. doi: 10.3390/ijms21124391. Int J Mol Sci. 2020. PMID: 32575683 Free PMC article. Review.
The fragile X-associated tremor/ataxia syndrome (FXTAS) is a neurodegenerative disorder seen in older premutation (55-200 CGG repeats) carriers of FMR1. ...The clinical features usually begin in the 60 s with an action or intention tremor followed by cerebellar ataxia
The fragile X-associated tremor/ataxia syndrome (FXTAS) is a neurodegenerative disorder seen in older premutation (55-200 CGG repeats …
Ataxia.
Akbar U, Ashizawa T. Akbar U, et al. Neurol Clin. 2015 Feb;33(1):225-48. doi: 10.1016/j.ncl.2014.09.004. Neurol Clin. 2015. PMID: 25432731 Free PMC article. Review.
While a variety of disorders can cause secondary ataxias, the list of genetic causes of ataxias is growing longer. ...A discussion of the ataxias is presented here with brief mention of acquired ataxias, and a greater focus on inherited ataxias. …
While a variety of disorders can cause secondary ataxias, the list of genetic causes of ataxias is growing longer. ...A discus …
Immune-mediated Cerebellar Ataxias: Practical Guidelines and Therapeutic Challenges.
Mitoma H, Manto M, Hampe CS. Mitoma H, et al. Curr Neuropharmacol. 2019;17(1):33-58. doi: 10.2174/1570159X16666180917105033. Curr Neuropharmacol. 2019. PMID: 30221603 Free PMC article. Review.
Immune-mediated cerebellar ataxias (IMCAs), a clinical entity reported for the first time in the 1980s, include gluten ataxia (GA), paraneoplastic cerebellar degenerations (PCDs), antiglutamate decarboxylase 65 (GAD) antibody-associated cerebellar ataxia, pos …
Immune-mediated cerebellar ataxias (IMCAs), a clinical entity reported for the first time in the 1980s, include gluten ataxia
5,928 results