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2025

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

Year Number of Results
1963 1
1964 1
1966 1
1967 5
1968 6
1969 7
1970 7
1971 12
1972 10
1973 9
1974 7
1975 6
1976 5
1977 11
1978 15
1979 10
1980 15
1981 14
1982 6
1983 15
1984 25
1985 17
1986 14
1987 15
1988 9
1989 22
1990 25
1991 27
1992 30
1993 36
1994 43
1995 53
1996 42
1997 58
1998 44
1999 57
2000 63
2001 73
2002 63
2003 57
2004 60
2005 75
2006 58
2007 78
2008 63
2009 57
2010 66
2011 66
2012 99
2013 81
2014 90
2015 69
2016 106
2017 84
2018 153
2019 120
2020 132
2021 120
2022 115
2023 126
2024 120
2025 6

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2,632 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.
PURPOSE OF REVIEW: This article reviews the symptoms, laboratory and neuroimaging diagnostic tests, genetics, and management of cerebellar ataxia. RECENT FINDINGS: Recent advances in genetics have led to the identification of novel genetic causes for ataxia a …
PURPOSE OF REVIEW: This article reviews the symptoms, laboratory and neuroimaging diagnostic tests, genetics, and management of cerebella
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.
Patients with cerebellar ataxia can also have cognitive and mood changes. Although the identification of causes for cerebellar ataxia can be complex, age of presentation, chronicity, family history, and associated movement disorders may provide diagnos …
Patients with cerebellar ataxia can also have cognitive and mood changes. Although the identification of causes for cerebel
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.
Cerebellar ataxia is a common finding in neurological practice and has a wide variety of causes, ranging from the chronic and slowly-progressive cerebellar degenerations to the acute cerebellar lesions due to infarction, edema and hemorrhage, configuri
Cerebellar ataxia is a common finding in neurological practice and has a wide variety of causes, ranging from the chronic and
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.
These improvements increase clinicians' ability to identify the etiology of neurodegenerative cerebellar ataxia and suggest future treatments. Although no medication has been approved by the US Food and Drug Administration (FDA) for treatment of cerebellar
These improvements increase clinicians' ability to identify the etiology of neurodegenerative cerebellar ataxia and suggest fu …
CACNA1A-Related Channelopathies: Clinical Manifestations and Treatment Options.
Indelicato E, Boesch S. Indelicato E, et al. Handb Exp Pharmacol. 2023;279:227-248. doi: 10.1007/164_2022_625. Handb Exp Pharmacol. 2023. PMID: 36592223 Review.
In the last decade, variants in the Ca(2+) channel gene CACNA1A emerged as a frequent aetiology of rare neurological phenotypes sharing a common denominator of variable paroxysmal manifestations and chronic cerebellar dysfunction. The spectrum of paroxysmal manifestations …
In the last decade, variants in the Ca(2+) channel gene CACNA1A emerged as a frequent aetiology of rare neurological phenotypes sharing a co …
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 ca
Ataxia-telangiectasia is a rare, neurodegenerative, and multisystem disease, characterized by cerebellar ataxia, oculoc
The inherited cerebellar ataxias: an update.
Coarelli G, Wirth T, Tranchant C, Koenig M, Durr A, Anheim M. Coarelli G, et al. J Neurol. 2023 Jan;270(1):208-222. doi: 10.1007/s00415-022-11383-6. Epub 2022 Sep 24. J Neurol. 2023. PMID: 36152050 Free PMC article. Review.
Initial approach facing a patient with cerebellar ataxia requires family medical history, physical examination, exclusions of acquired causes and genetic analysis, including Next-Generation Sequencing (NGS). ...Diagnostic difficulties arise from allelic and phenotyp …
Initial approach facing a patient with cerebellar ataxia requires family medical history, physical examination, exclusions of …
Neurological Syndromes Associated with Anti-GAD Antibodies.
Dade M, Berzero G, Izquierdo C, Giry M, Benazra M, Delattre JY, Psimaras D, Alentorn A. Dade M, et al. Int J Mol Sci. 2020 May 24;21(10):3701. doi: 10.3390/ijms21103701. Int J Mol Sci. 2020. PMID: 32456344 Free PMC article. Review.
GAD antibodies (Ab) have been associated with multiple neurological syndromes, including stiff-person syndrome, cerebellar ataxia, and limbic encephalitis, which are all considered to result from reduced GABAergic transmission. ...
GAD antibodies (Ab) have been associated with multiple neurological syndromes, including stiff-person syndrome, cerebellar ataxia
Cerebellar ataxia.
Marsden JF. Marsden JF. Handb Clin Neurol. 2018;159:261-281. doi: 10.1016/B978-0-444-63916-5.00017-3. Handb Clin Neurol. 2018. PMID: 30482319 Review.
The cerebellum plays an integral role in the control of limb and ocular movements, balance, and walking. Cerebellar disorders may be classified as sporadic or hereditary with clinical presentation varying with the extent and site of cerebellar damage and extracerebe …
The cerebellum plays an integral role in the control of limb and ocular movements, balance, and walking. Cerebellar disorders may be …
Cerebellar ataxia, neuropathy and vestibular areflexia syndrome (CANVAS): genetic and clinical aspects.
Cortese A, Curro' R, Vegezzi E, Yau WY, Houlden H, Reilly MM. Cortese A, et al. Pract Neurol. 2022 Feb;22(1):14-18. doi: 10.1136/practneurol-2020-002822. Epub 2021 Aug 13. Pract Neurol. 2022. PMID: 34389644 Review.
Cerebellar ataxia, neuropathy and vestibular areflexia syndrome (CANVAS) typically presents in middle life with a combination of neuropathy, ataxia and vestibular disease, with patients reporting progressive imbalance, oscillopsia, sensory disturbance and a d
Cerebellar ataxia, neuropathy and vestibular areflexia syndrome (CANVAS) typically presents in middle life with a combination
2,632 results