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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 16
1976 11
1977 15
1978 28
1979 16
1980 22
1981 21
1982 14
1983 21
1984 31
1985 28
1986 21
1987 29
1988 36
1989 42
1990 49
1991 56
1992 64
1993 78
1994 90
1995 104
1996 88
1997 115
1998 93
1999 152
2000 135
2001 192
2002 158
2003 163
2004 160
2005 172
2006 204
2007 196
2008 178
2009 180
2010 179
2011 190
2012 267
2013 273
2014 261
2015 199
2016 263
2017 236
2018 324
2019 276
2020 307
2021 277
2022 237
2023 170

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6,023 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. ...
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 …
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.
Cerebellar ataxia results from damage to the cerebellum and presents as movement incoordination and variability, gait impairment, and slurred speech. ...There are many genetic causes for cerebellar ataxia, and the common autosomal dominant and recessive at …
Cerebellar ataxia results from damage to the cerebellum and presents as movement incoordination and variability, gait impairme …
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 …
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.
Gait variability is characteristic and may arise from a combination of balance impairments, interlimb incoordination, and incoordination between postural activity and leg movement. ...Walking aids, orthoses, specialized footwear and seating may be required for more …
Gait variability is characteristic and may arise from a combination of balance impairments, interlimb incoordination, and incoordi …
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 …
Opsoclonus-myoclonus-ataxia syndrome in children.
Bhatia P, Heim J, Cornejo P, Kane L, Santiago J, Kruer MC. Bhatia P, et al. J Neurol. 2022 Feb;269(2):750-757. doi: 10.1007/s00415-021-10536-3. Epub 2021 Mar 29. J Neurol. 2022. PMID: 33779841 Review.
Opsoclonus-myoclonus-ataxia syndrome is a rare neuroimmunologic disorder typically presenting in previously healthy infants and toddlers. It is characterized by a clinical triad of (1) erratic saccadic intrusions; (2) myoclonus and/or ataxia; (3) behavioral features …
Opsoclonus-myoclonus-ataxia syndrome is a rare neuroimmunologic disorder typically presenting in previously healthy infants and toddl …
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.
PURPOSE OF REVIEW: Neurodegenerative cerebellar ataxia is a diverse collection of diseases that are unified by gait and balance abnormalities, appendicular incoordination, and abnormalities of eye movement and speech. ...SUMMARY: Neurodegenerative cerebellar atax …
PURPOSE OF REVIEW: Neurodegenerative cerebellar ataxia is a diverse collection of diseases that are unified by gait and balance abnor …
6,023 results