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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 2
1966 1
1967 6
1968 8
1969 12
1970 10
1971 23
1972 15
1973 14
1974 11
1975 14
1976 11
1977 13
1978 28
1979 16
1980 21
1981 19
1982 14
1983 20
1984 31
1985 29
1986 21
1987 28
1988 35
1989 41
1990 49
1991 54
1992 64
1993 78
1994 88
1995 103
1996 90
1997 115
1998 91
1999 153
2000 134
2001 196
2002 158
2003 167
2004 174
2005 172
2006 211
2007 202
2008 177
2009 182
2010 182
2011 198
2012 268
2013 275
2014 265
2015 207
2016 269
2017 240
2018 324
2019 279
2020 308
2021 280
2022 239
2023 226
2024 78

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6,186 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 …
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 …
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. ...
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.
We also report on key clinical points for the diagnosis of the main ICAs, including Friedreich ataxia, CANVAS, polyglutamine spinocerebellar ataxias, Fragile X-associated tremor/ataxia syndrome. ...To complicate the phenotype, cerebellar cognitive affective syndrome …
We also report on key clinical points for the diagnosis of the main ICAs, including Friedreich ataxia, CANVAS, polyglutamine spinocer …
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 …
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.
The spectrum of paroxysmal manifestations encompasses migraine with hemiplegic aura, episodic ataxia, epilepsy and paroxysmal non-epileptic movement disorders. Additional chronic neurological symptoms range from severe developmental phenotypes in early-onset cases to neuro …
The spectrum of paroxysmal manifestations encompasses migraine with hemiplegic aura, episodic ataxia, epilepsy and paroxysmal non-epi …
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. .. …
6,186 results