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Quoted phrase not found in phrase index: "Machado-Joseph disease type 2"
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 prevalence range of dominant HCA was 0.0-5.6/10(5), with an average of 2.7/10(5) (1.5-4.0/10(5)). Spinocerebellar ataxia type 3 (SCA3)/Machado-Joseph disease was the most common dominant ataxia, followed by SCA2 and SCA6. ...The prevalence o …
The prevalence range of dominant HCA was 0.0-5.6/10(5), with an average of 2.7/10(5) (1.5-4.0/10(5)). Spinocerebellar ataxia type …
The ASAS-OMERACT core domain set for axial spondyloarthritis.
Navarro-Compán V, Boel A, Boonen A, Mease P, Landewé R, Kiltz U, Dougados M, Baraliakos X, Bautista-Molano W, Carlier H, Chiowchanwisawakit P, Dagfinrud H, de Peyrecave N, El-Zorkany B, Fallon L, Gaffney K, Garrido-Cumbrera M, Gensler LS, Haroon N, Kwan YH, Machado PM, Maksymowych WP, Poddubnyy D, Protopopov M, Ramiro S, Shea B, Song IH, van Weely S, van der Heijde D. Navarro-Compán V, et al. Semin Arthritis Rheum. 2021 Dec;51(6):1342-1349. doi: 10.1016/j.semarthrit.2021.07.021. Epub 2021 Aug 1. Semin Arthritis Rheum. 2021. PMID: 34489113
The development process consisted of: i) Identifying candidate domains using a systematic literature review and qualitative studies; ii) Selection of the most relevant domains for different stakeholders through a 3-round Delphi survey involving axSpA patients and axSpA experts; i …
The development process consisted of: i) Identifying candidate domains using a systematic literature review and qualitative studies; ii) Sel …
Neurocognitive Changes in Spinocerebellar Ataxia Type 3: A Systematic Review with a Narrative Design.
Yap KH, Kessels RPC, Azmin S, van de Warrenburg B, Mohamed Ibrahim N. Yap KH, et al. Cerebellum. 2022 Apr;21(2):314-327. doi: 10.1007/s12311-021-01282-3. Epub 2021 Jul 7. Cerebellum. 2022. PMID: 34231180 Review.
Spinocerebellar ataxia type 3 (SCA3), the commonest dominantly inherited ataxia worldwide, is characterized by disruption in the cerebellar-cerebral and striatal-cortical networks. ...
Spinocerebellar ataxia type 3 (SCA3), the commonest dominantly inherited ataxia worldwide, is characterized by disruption in the cere …
Genetic risk factors for modulation of age at onset in Machado-Joseph disease/spinocerebellar ataxia type 3: a systematic review and meta-analysis.
de Mattos EP, Kolbe Musskopf M, Bielefeldt Leotti V, Saraiva-Pereira ML, Jardim LB. de Mattos EP, et al. J Neurol Neurosurg Psychiatry. 2019 Feb;90(2):203-210. doi: 10.1136/jnnp-2018-319200. Epub 2018 Oct 18. J Neurol Neurosurg Psychiatry. 2019. PMID: 30337442
OBJECTIVES: To perform a systematic review and meta-analysis of genetic risk factors for age at onset (AO) in spinocerebellar ataxia type 3/Machado-Joseph disease (SCA3/MJD). METHODS: Two authors independently reviewed reports on the mathematical relat …
OBJECTIVES: To perform a systematic review and meta-analysis of genetic risk factors for age at onset (AO) in spinocerebellar ataxia type …
Tremor-spectrum in spinocerebellar ataxia type 3.
Bonnet C, Apartis E, Anheim M, Legrand AP, Baizabal-Carvallo JF, Bonnet AM, Durr A, Vidailhet M. Bonnet C, et al. J Neurol. 2012 Nov;259(11):2460-70. doi: 10.1007/s00415-012-6531-5. Epub 2012 May 17. J Neurol. 2012. PMID: 22592286 Review.
Spinocerebellar ataxia type 3 (SCA3) can be present with a combination of cerebellar, neuropathic, pyramidal, or extrapyramidal symptoms. ...Electrophysiological study including polymyographic recording was possible in 4/6 patients and DaTSCAN in 2/6. The authors al …
Spinocerebellar ataxia type 3 (SCA3) can be present with a combination of cerebellar, neuropathic, pyramidal, or extrapyramidal sympt …