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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 31
1985 28
1986 20
1987 27
1988 34
1989 40
1990 46
1991 52
1992 58
1993 75
1994 88
1995 101
1996 87
1997 112
1998 90
1999 150
2000 133
2001 189
2002 156
2003 161
2004 159
2005 166
2006 196
2007 194
2008 174
2009 178
2010 179
2011 189
2012 264
2013 269
2014 259
2015 196
2016 261
2017 233
2018 321
2019 273
2020 305
2021 274
2022 234
2023 201
2024 26

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5,956 results

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Page 1
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 …
Neurodegenerative Cerebellar Ataxia.
Rosenthal LS. Rosenthal LS. Continuum (Minneap Minn). 2022 Oct 1;28(5):1409-1434. doi: 10.1212/CON.0000000000001180. Continuum (Minneap Minn). 2022. PMID: 36222772 Review.
SUMMARY: Neurodegenerative cerebellar ataxia is characterized by dysarthria, dysmetria, oculomotor abnormalities, and ataxic gait. ...Although no medications have been approved specifically for cerebellar ataxia, treatment options are available to improve patients' …
SUMMARY: Neurodegenerative cerebellar ataxia is characterized by dysarthria, dysmetria, oculomotor abnormalities, and ataxic gait. .. …
Evaluation of Cerebellar Ataxic Patients.
Radmard S, Zesiewicz TA, Kuo SH. Radmard S, et al. Neurol Clin. 2023 Feb;41(1):21-44. doi: 10.1016/j.ncl.2022.05.002. Epub 2022 Aug 31. Neurol Clin. 2023. PMID: 36400556 Free PMC article. Review.
There are many genetic causes for cerebellar ataxia, and the common autosomal dominant and recessive ataxia are due to genetic repeat expansions. ...Symptomatic and potential disease-modifying therapies may benefit patients with cerebellar ataxia....
There are many genetic causes for cerebellar ataxia, and the common autosomal dominant and recessive ataxia are due to genetic …
Ataxia-telangiectasia: recommendations for multidisciplinary treatment.
van Os NJH, Haaxma CA, van der Flier M, Merkus PJFM, van Deuren M, de Groot IJM, Loeffen J, van de Warrenburg BPC, Willemsen MAAP; A-T Study Group. van Os NJH, et al. Dev Med Child Neurol. 2017 Jul;59(7):680-689. doi: 10.1111/dmcn.13424. Epub 2017 Mar 20. Dev Med Child Neurol. 2017. PMID: 28318010 Free article. Review.
Ataxia-telangiectasia is a rare, neurodegenerative, and multisystem disease, characterized by cerebellar ataxia, oculocutaneous telangiectasia, immunodeficiency, progressive respiratory failure, and an increased risk of malignancies. It demands specialized care tail
Ataxia-telangiectasia is a rare, neurodegenerative, and multisystem disease, characterized by cerebellar ataxia, oculocutaneou
Chiari Malformation Type 1: A Systematic Review of Natural History and Conservative Management.
Langridge B, Phillips E, Choi D. Langridge B, et al. World Neurosurg. 2017 Aug;104:213-219. doi: 10.1016/j.wneu.2017.04.082. Epub 2017 Apr 21. World Neurosurg. 2017. PMID: 28435116 Free article. Review.
RESULTS: In symptomatic patients who did not undergo surgery, headaches and nausea often improved, whereas ataxia and sensory disturbance tended not to improve spontaneously. ...
RESULTS: In symptomatic patients who did not undergo surgery, headaches and nausea often improved, whereas ataxia and sensory disturb …
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, post-infec …
Immune-mediated cerebellar ataxias (IMCAs), a clinical entity reported for the first time in the 1980s, include gluten ataxia (GA), p …
Machado-Joseph disease/spinocerebellar ataxia type 3: lessons from disease pathogenesis and clues into therapy.
Matos CA, de Almeida LP, Nóbrega C. Matos CA, et al. J Neurochem. 2019 Jan;148(1):8-28. doi: 10.1111/jnc.14541. Epub 2018 Oct 5. J Neurochem. 2019. PMID: 29959858 Free article. Review.
Machado-Joseph disease (MJD), also known as spinocerebellar ataxia type 3 (SCA3), is an incurable disorder, widely regarded as the most common form of spinocerebellar ataxia in the world. ...
Machado-Joseph disease (MJD), also known as spinocerebellar ataxia type 3 (SCA3), is an incurable disorder, widely regarded as the mo …
5,956 results