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Year Number of Results
2009 2
2012 3
2014 2
2016 1
2018 1
2020 1
2021 1
2022 2
2024 0

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Page 1
The global epidemiology of hereditary ataxia and spastic paraplegia: a systematic review of prevalence studies.
Ruano L, Melo C, Silva MC, Coutinho P. Ruano L, et al. Neuroepidemiology. 2014;42(3):174-83. doi: 10.1159/000358801. Epub 2014 Mar 5. Neuroepidemiology. 2014. PMID: 24603320 Free article. Review.
The autosomal recessive (AR) HCA (AR-HCA) prevalence range was 0.0-7.2/10(5), the average being 3.3/10(5) (1.8-4.9/10(5)). Friedreich ataxia was the most frequent AR-HCA, followed by ataxia with oculomotor apraxia or ataxia-telangiectasia. ...
The autosomal recessive (AR) HCA (AR-HCA) prevalence range was 0.0-7.2/10(5), the average being 3.3/10(5) (1.8-4.9/10(5)). Friedreich …
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.
Zesiewicz TA, Wilmot G, Kuo SH, Perlman S, Greenstein PE, Ying SH, Ashizawa T, Subramony SH, Schmahmann JD, Figueroa KP, Mizusawa H, Schöls L, Shaw JD, Dubinsky RM, Armstrong MJ, Gronseth GS, Sullivan KL. Zesiewicz TA, et al. Neurology. 2018 Mar 6;90(10):464-471. doi: 10.1212/WNL.0000000000005055. Epub 2018 Feb 9. Neurology. 2018. PMID: 29440566 Free PMC article.
For patients with ataxia of mixed etiology, riluzole probably improves ataxia signs at 8 weeks (1 Class I study). For patients with Friedreich ataxia or spinocerebellar ataxia (SCA), riluzole probably improves ataxia signs at 12 months (1 Class I study). ...For pati …
For patients with ataxia of mixed etiology, riluzole probably improves ataxia signs at 8 weeks (1 Class I study). For patients with Fried …
The cognitive profile of Friedreich ataxia: a systematic review and meta-analysis.
Naeije G, Schulz JB, Corben LA. Naeije G, et al. BMC Neurol. 2022 Mar 17;22(1):97. doi: 10.1186/s12883-022-02615-3. BMC Neurol. 2022. PMID: 35300598 Free PMC article.
BACKGROUND: Study the cognitive profile of individuals with Friedreich ataxia (FRDA) and seek evidence for correlations between clinical, genetic and imaging characteristics and neuropsychological impairments. ...
BACKGROUND: Study the cognitive profile of individuals with Friedreich ataxia (FRDA) and seek evidence for correlations betwee …
Antioxidants and other pharmacological treatments for Friedreich ataxia.
Kearney M, Orrell RW, Fahey M, Pandolfo M. Kearney M, et al. Cochrane Database Syst Rev. 2012 Apr 18;(4):CD007791. doi: 10.1002/14651858.CD007791.pub3. Cochrane Database Syst Rev. 2012. PMID: 22513953 Updated. Review.
BACKGROUND: Friedreich ataxia is a rare inherited autosomal recessive neurological disorder, characterised initially by unsteadiness in standing and walking, slowly progressing to wheelchair dependency usually in the late teens or early twenties. ...MAIN RESULTS: Mo …
BACKGROUND: Friedreich ataxia is a rare inherited autosomal recessive neurological disorder, characterised initially by unstea …
Treatment for speech disorder in Friedreich ataxia and other hereditary ataxia syndromes.
Vogel AP, Folker J, Poole ML. Vogel AP, et al. Cochrane Database Syst Rev. 2014 Oct 28;(10):CD008953. doi: 10.1002/14651858.CD008953.pub2. Cochrane Database Syst Rev. 2014. PMID: 25348587 Review.
OBJECTIVES: To assess the effects of interventions for speech disorder in adults and children with Friedreich ataxia and other hereditary ataxias. SEARCH METHODS: On 14 October 2013, we searched the Cochrane Neuromuscular Disease Group Specialized Register, CENTRAL, …
OBJECTIVES: To assess the effects of interventions for speech disorder in adults and children with Friedreich ataxia and other …
Antioxidants and other pharmacological treatments for Friedreich ataxia.
Kearney M, Orrell RW, Fahey M, Pandolfo M. Kearney M, et al. Cochrane Database Syst Rev. 2009 Oct 7;(4):CD007791. doi: 10.1002/14651858.CD007791.pub2. Cochrane Database Syst Rev. 2009. PMID: 19821439 Updated. Review.
BACKGROUND: Friedreich ataxia is a rare inherited, autosomal recessive, neurological disorder characterised initially by unsteadiness in standing and walking, slowly progressing to wheelchair dependency usually in the late teens or early twenties. ...MAIN RESULTS: O …
BACKGROUND: Friedreich ataxia is a rare inherited, autosomal recessive, neurological disorder characterised initially by unste …
Characterising the neuropathology and neurobehavioural phenotype in Friedreich ataxia: a systematic review.
Corben LA, Georgiou-Karistianis N, Bradshaw JL, Evans-Galea MV, Churchyard AJ, Delatycki MB. Corben LA, et al. Adv Exp Med Biol. 2012;769:169-84. doi: 10.1007/978-1-4614-5434-2_11. Adv Exp Med Biol. 2012. PMID: 23560311 Review.
Friedreich ataxia (FRDA), the most common of the hereditary ataxias, is an autosomal recessive, multisystem disorder characterised by progressive ataxia, sensory symptoms, weakness, scoliosis and cardiomyopathy. ...
Friedreich ataxia (FRDA), the most common of the hereditary ataxias, is an autosomal recessive, multisystem disorder character …
Pharmacological treatments for Friedreich ataxia.
Kearney M, Orrell RW, Fahey M, Brassington R, Pandolfo M. Kearney M, et al. Cochrane Database Syst Rev. 2016 Aug 30;2016(8):CD007791. doi: 10.1002/14651858.CD007791.pub4. Cochrane Database Syst Rev. 2016. PMID: 27572719 Free PMC article. Review.
BACKGROUND: Friedreich ataxia is a rare inherited autosomal recessive neurological disorder, characterised initially by unsteadiness in standing and walking, slowly progressing to wheelchair dependency usually in the late teens or early twenties. ...SELECTION CRITER …
BACKGROUND: Friedreich ataxia is a rare inherited autosomal recessive neurological disorder, characterised initially by unstea …
Ataxia rating scales--psychometric profiles, natural history and their application in clinical trials.
Saute JA, Donis KC, Serrano-Munuera C, Genis D, Ramirez LT, Mazzetti P, Pérez LV, Latorre P, Sequeiros J, Matilla-Dueñas A, Jardim LB; Iberoamerican Multidisciplinary Network for the Study of Movement Disorders (RIBERMOV) Study Group. Saute JA, et al. Cerebellum. 2012 Jun;11(2):488-504. doi: 10.1007/s12311-011-0316-8. Cerebellum. 2012. PMID: 21964941 Review.
A systematic review of disease prevalence, health-related quality of life, and economic outcomes associated with Friedreich's Ataxia.
Buesch K, Zhang R. Buesch K, et al. Curr Med Res Opin. 2022 Oct;38(10):1739-1749. doi: 10.1080/03007995.2022.2112870. Epub 2022 Aug 23. Curr Med Res Opin. 2022. PMID: 35983717
INTRODUCTION: Friedreich ataxia (FA) is a rare, inherited neuromuscular disease characterized by an early onset and progressive limb and gait ataxia. ...
INTRODUCTION: Friedreich ataxia (FA) is a rare, inherited neuromuscular disease characterized by an early onset and progressiv …
13 results