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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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2009 | 1 |
2010 | 1 |
2013 | 1 |
2014 | 1 |
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2018 | 1 |
2019 | 1 |
2020 | 1 |
2021 | 1 |
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Comprehensive systematic review summary: Treatment of cerebellar motor dysfunction and ataxia: Report of the Guideline Development, Dissemination, and Implementation Subcommittee of the American Academy of Neurology.
Neurology. 2018 Mar 6;90(10):464-471. doi: 10.1212/WNL.0000000000005055. Epub 2018 Feb 9.
Neurology. 2018.
PMID: 29440566
Free PMC article.
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.
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ACR Appropriateness Criteria® Ataxia.
Expert Panel on Neurologic Imaging:; Juliano AF, Policeni B, Agarwal V, Burns J, Bykowski J, Harvey HB, Hoang JK, Hunt CH, Kennedy TA, Moonis G, Pannell JS, Parsons MS, Powers WJ, Rosenow JM, Schroeder JW, Slavin K, Whitehead MT, Corey AS.
Expert Panel on Neurologic Imaging:, et al.
J Am Coll Radiol. 2019 May;16(5S):S44-S56. doi: 10.1016/j.jacr.2019.02.021.
J Am Coll Radiol. 2019.
PMID: 31054758
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EFNS guidelines on the molecular diagnosis of ataxias and spastic paraplegias.
Gasser T, Finsterer J, Baets J, Van Broeckhoven C, Di Donato S, Fontaine B, De Jonghe P, Lossos A, Lynch T, Mariotti C, Schöls L, Spinazzola A, Szolnoki Z, Tabrizi SJ, Tallaksen CM, Zeviani M, Burgunder JM, Harbo HF; EFNS.
Gasser T, et al.
Eur J Neurol. 2010 Feb;17(2):179-88. doi: 10.1111/j.1468-1331.2009.02873.x. Epub 2009 Dec 28.
Eur J Neurol. 2010.
PMID: 20050888
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[Clinical guideline of gene FMR1-associated diseases: fragile X syndrome, primary ovarian insufficiency and tremor-ataxia syndrome].
Milá M, Ramos F, Tejada MI; Grupo AEGH/CIBERER.
Milá M, et al.
Med Clin (Barc). 2014 Mar 4;142(5):219-25. doi: 10.1016/j.medcli.2013.05.025. Epub 2013 Jul 25.
Med Clin (Barc). 2014.
PMID: 23891128
Spanish.
No abstract available.
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[Investigation of Genetic Aetiology in Neurodegenerative Ataxias: Recommendations from the Group of Neurogenetics of Centro Hospitalar São João, Portugal].
Gomes T, Guimaraes J, Leão M; Grupo de Neurogenetica do Centro Hospitalar Sao Joao.
Gomes T, et al.
Acta Med Port. 2017 Jun 30;30(6):502-512. doi: 10.20344/amp.8797. Epub 2017 Jun 30.
Acta Med Port. 2017.
PMID: 28898621
Free article.
Portuguese.
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