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

Year Number of Results
1966 1
1969 1
1970 1
1971 2
1972 5
1975 7
1976 8
1977 6
1978 10
1979 8
1980 7
1981 9
1982 7
1983 8
1984 16
1985 18
1986 16
1987 9
1988 18
1989 17
1990 17
1991 14
1992 20
1993 24
1994 35
1995 27
1996 31
1997 40
1998 32
1999 44
2000 33
2001 52
2002 37
2003 45
2004 55
2005 59
2006 57
2007 61
2008 87
2009 60
2010 71
2011 83
2012 90
2013 111
2014 101
2015 79
2016 109
2017 110
2018 113
2019 113
2020 137
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2022 122
2023 96
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2,259 results

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Quoted phrase not found in phrase index: "Brachydactyly-nystagmus-cerebellar ataxia syndrome"
Page 1
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 cerebellar ataxia is a syndrome that occurs in less than 72 hours, in previously healthy subjects. ...This review focuses on the etiologic and diagnostic considerations for acute ataxia....
Acute cerebellar ataxia is a syndrome that occurs in less than 72 hours, in previously healthy subjects. ...This review focuse …
GAA-FGF14 ataxia (SCA27B): phenotypic profile, natural history progression and 4-aminopyridine treatment response.
Wilke C, Pellerin D, Mengel D, Traschütz A, Danzi MC, Dicaire MJ, Neumann M, Lerche H, Bender B, Houlden H; RFC1 study group; Züchner S, Schöls L, Brais B, Synofzik M. Wilke C, et al. Brain. 2023 Oct 3;146(10):4144-4157. doi: 10.1093/brain/awad157. Brain. 2023. PMID: 37165652
Ataxia due to an autosomal dominant intronic GAA repeat expansion in FGF14 [GAA-FGF14 ataxia, spinocerebellar ataxia 27B (SCA27B)] has recently been identified as one of the most common genetic late-onset ataxias. ...Cross-sectional and longitudinal as …
Ataxia due to an autosomal dominant intronic GAA repeat expansion in FGF14 [GAA-FGF14 ataxia, spinocerebellar ataxia 27 …
Immune-mediated ataxias.
Joubert B, Rostásy K, Honnorat J. Joubert B, et al. Handb Clin Neurol. 2018;155:313-332. doi: 10.1016/B978-0-444-64189-2.00021-4. Handb Clin Neurol. 2018. PMID: 29891069 Review.
Both acute and progressive progressions are possible. Different syndromes have been identified, including CA associated with anti-GAD antibodies, the cerebellar type of Hashimoto encephalopathy, primary autoimmune CA, gluten ataxia, opsoclonus-myoclonus syndrome …
Both acute and progressive progressions are possible. Different syndromes have been identified, including CA associated with anti-GAD …
Nonprogressive congenital ataxias.
Bertini E, Zanni G, Boltshauser E. Bertini E, et al. Handb Clin Neurol. 2018;155:91-103. doi: 10.1016/B978-0-444-64189-2.00006-8. Handb Clin Neurol. 2018. PMID: 29891079 Review.
The terminology of nonprogressive congenital ataxia (NPCA) refers to a clinically and genetically heterogeneous group of disorders characterized by congenital or early-onset ataxia, but no progression or even improvement on follow-up. Ataxia is preceded by mu …
The terminology of nonprogressive congenital ataxia (NPCA) refers to a clinically and genetically heterogeneous group of disorders ch …
Diagnostic approach to paediatric movement disorders: a clinical practice guide.
Brandsma R, van Egmond ME, Tijssen MAJ; Groningen Movement Disorder Expertise Centre. Brandsma R, et al. Dev Med Child Neurol. 2021 Mar;63(3):252-258. doi: 10.1111/dmcn.14721. Epub 2020 Nov 5. Dev Med Child Neurol. 2021. PMID: 33150968 Free PMC article.
Paediatric movement disorders (PMDs) comprise a large group of disorders (tics, myoclonus, tremor, dystonia, chorea, Parkinsonism, ataxia), often with mixed phenotypes. Determination of the underlying aetiology can be difficult given the broad differential diagnosis and th …
Paediatric movement disorders (PMDs) comprise a large group of disorders (tics, myoclonus, tremor, dystonia, chorea, Parkinsonism, ataxia …
Episodic Ataxias: Primary and Secondary Etiologies, Treatment, and Classification Approaches.
Hassan A. Hassan A. Tremor Other Hyperkinet Mov (N Y). 2023 Mar 28;13:9. doi: 10.5334/tohm.747. eCollection 2023. Tremor Other Hyperkinet Mov (N Y). 2023. PMID: 37008993 Free PMC article. Review.
METHODS: A systematic literature review was performed in October 2022 for 'episodic ataxia' and 'paroxysmal ataxia', restricted to publications in the last 10 years to focus on recent clinical advances. ...EA may also be caused by gene mutations associated with chro …
METHODS: A systematic literature review was performed in October 2022 for 'episodic ataxia' and 'paroxysmal ataxia', restricte …
Immune-mediated ataxias: Guide to clinicians.
Meira AT, de Moraes MPM, Ferreira MG, Franklin GL, Rezende Filho FM, Teive HAG, Barsottini OGP, Pedroso JL. Meira AT, et al. Parkinsonism Relat Disord. 2023 Dec;117:105861. doi: 10.1016/j.parkreldis.2023.105861. Epub 2023 Sep 20. Parkinsonism Relat Disord. 2023. PMID: 37748994 Review.
Immune-mediated cerebellar ataxias were initially described as a clinical entity in the 1980s, and since then, an expanding body of evidence has contributed to our understanding of this topic. These ataxias encompass various etiologies, including postinfectious cere …
Immune-mediated cerebellar ataxias were initially described as a clinical entity in the 1980s, and since then, an expanding body of e …
Spinocerebellar degenerations.
Perlman SL. Perlman SL. Handb Clin Neurol. 2011;100:113-40. doi: 10.1016/B978-0-444-52014-2.00006-9. Handb Clin Neurol. 2011. PMID: 21496573 Review.
The common recessive ataxias with associated hyperkinetic movements are ataxia telangiectasia and Friedreich's ataxia. Fragile X tremor-ataxia syndrome (FXTAS) and multiple-system atrophy (a sporadic ataxia which is felt to have a genetic …
The common recessive ataxias with associated hyperkinetic movements are ataxia telangiectasia and Friedreich's ataxia. …
Cerebellar ataxias: an update.
Manto M, Gandini J, Feil K, Strupp M. Manto M, et al. Curr Opin Neurol. 2020 Feb;33(1):150-160. doi: 10.1097/WCO.0000000000000774. Curr Opin Neurol. 2020. PMID: 31789706 Review.
Relevant animal models have paved the way for rationale therapies of numerous disorders affecting the cerebellum. RECENT FINDINGS: Clinically, the cerebellar syndrome is now divided into a cerebellar motor syndrome, vestibulocerebellar syndrome and cerebellar …
Relevant animal models have paved the way for rationale therapies of numerous disorders affecting the cerebellum. RECENT FINDINGS: Clinicall …
Episodic ataxias.
Jen JC, Wan J. Jen JC, et al. Handb Clin Neurol. 2018;155:205-215. doi: 10.1016/B978-0-444-64189-2.00013-5. Handb Clin Neurol. 2018. PMID: 29891059 Review.
Primary episodic ataxias (EAs) are a group of dominantly inherited disorders characterized by transient recurrent incoordination and truncal instability, often triggered by physical exertion and emotional stress, variably associated with progressive baseline ataxia. …
Primary episodic ataxias (EAs) are a group of dominantly inherited disorders characterized by transient recurrent incoordination and …
2,259 results