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Page 1
Machado-Joseph disease/spinocerebellar ataxia type 3.
Paulson H. Paulson H. Handb Clin Neurol. 2012;103:437-49. doi: 10.1016/B978-0-444-51892-7.00027-9. Handb Clin Neurol. 2012. PMID: 21827905 Free PMC article. Review.
Machado-Joseph disease (MJD), also known as spinocerebellar ataxia type 3 (SCA3), may be the most common dominantly inherited ataxia in the world. ...The specific properties of MJD/SCA3 and its disease protein are discussed …
Machado-Joseph disease (MJD), also known as spinocerebellar ataxia type 3 (SCA3), may be th …
Autophagy in Spinocerebellar Ataxia Type 3: From Pathogenesis to Therapeutics.
Paulino R, Nóbrega C. Paulino R, et al. Int J Mol Sci. 2023 Apr 17;24(8):7405. doi: 10.3390/ijms24087405. Int J Mol Sci. 2023. PMID: 37108570 Free PMC article. Review.
Machado-Joseph disease (MJD) or spinocerebellar ataxia 3 (SCA3) is a rare, inherited, monogenic, neurodegenerative disease, and the most common SCA worldwide. ...Due to these facts, there is a huge research effort to develop therapeutic strategies for …
Machado-Joseph disease (MJD) or spinocerebellar ataxia 3 (SCA3) is a rare, inherited, monogenic, neurodegenerative d …
The Neuropathology of Spinocerebellar Ataxia Type 3/Machado-Joseph Disease.
Koeppen AH. Koeppen AH. Adv Exp Med Biol. 2018;1049:233-241. doi: 10.1007/978-3-319-71779-1_11. Adv Exp Med Biol. 2018. PMID: 29427106 Review.
Spinocerebellar ataxia type 3 (SCA-3)/Machado-Joseph disease (MJD), the most common autosomal dominant ataxia, affects many regions of the brain and spinal cord. ...Almost invariably, the substantia nigra and the dentate nucleus of …
Spinocerebellar ataxia type 3 (SCA-3)/Machado-Joseph disease (MJD), the most common autosom …
Spinocerebellar ataxia type 3 (Machado-Joseph disease).
Dulski J, Al-Shaikh RH, Sulek A, Kasprzak J, Sławek J, Wszolek ZK. Dulski J, et al. Pol Arch Intern Med. 2022 Oct 21;132(10):16322. doi: 10.20452/pamw.16322. Epub 2022 Aug 22. Pol Arch Intern Med. 2022. PMID: 35997122 Free article. No abstract available.
Spinocerebellar Ataxia Type 3: A Case Report and Literature Review.
McCord MR, Bigio EH, Kam KL, Fischer V, Obeidin F, White CL, Brat DJ, Muller WA, Mao Q. McCord MR, et al. J Neuropathol Exp Neurol. 2020 Jun 1;79(6):641-646. doi: 10.1093/jnen/nlaa033. J Neuropathol Exp Neurol. 2020. PMID: 32346735 Review.
Spinocerebellar ataxia type 3 (SCA3), also known by the eponym Machado-Joseph disease, is an autosomal dominant CAG trinucleotide (polyglutamine) repeat disease that presents in young- to middle-aged adults. ...Here, we desc …
Spinocerebellar ataxia type 3 (SCA3), also known by the eponym Machado-Joseph disease, is a …
Mutant Ataxin-3-Containing Aggregates (MATAGGs) in Spinocerebellar Ataxia Type 3: Dynamics of the Disorder.
Raj K, Akundi RS. Raj K, et al. Mol Neurobiol. 2021 Jul;58(7):3095-3118. doi: 10.1007/s12035-021-02314-z. Epub 2021 Feb 24. Mol Neurobiol. 2021. PMID: 33629274 Review.
Spinocerebellar ataxia type 3 (SCA3) is the most common type of SCA worldwide caused by abnormal polyglutamine expansion in the coding region of the ataxin-3 gene. ...This review provides an exhaustive assessment of the various pathogenic mechanisms un …
Spinocerebellar ataxia type 3 (SCA3) is the most common type of SCA worldwide caused by abnormal polyglutamine e …
The Role of MicroRNAs in Spinocerebellar Ataxia Type 3.
Krauss S, Evert BO. Krauss S, et al. J Mol Biol. 2019 Apr 19;431(9):1729-1742. doi: 10.1016/j.jmb.2019.01.019. Epub 2019 Jan 18. J Mol Biol. 2019. PMID: 30664869 Free article. Review.
For example, microRNAs (miRNAs) are important regulatory RNAs that control gene expression in various biological processes and human diseases. In spinocerebellar ataxia type 3 (SCA3), a devastating neurodegenerative disease, miRNAs are involved …
For example, microRNAs (miRNAs) are important regulatory RNAs that control gene expression in various biological processes and human disease …
Machado-Joseph disease/spinocerebellar ataxia type 3: lessons from disease pathogenesis and clues into therapy.
Matos CA, de Almeida LP, Nóbrega C. Matos CA, et al. J Neurochem. 2019 Jan;148(1):8-28. doi: 10.1111/jnc.14541. Epub 2018 Oct 5. J Neurochem. 2019. PMID: 29959858 Free article. Review.
Machado-Joseph disease (MJD), also known as spinocerebellar ataxia type 3 (SCA3), is an incurable disorder, widely regarded as the most common form of spinocerebellar ataxia in the world. ...The current review analyses the availabl …
Machado-Joseph disease (MJD), also known as spinocerebellar ataxia type 3 (SCA3), is an inc …
Experimental and Clinical Strategies for Treating Spinocerebellar Ataxia Type 3.
Wang Z. Wang Z. Neuroscience. 2018 Feb 10;371:138-154. doi: 10.1016/j.neuroscience.2017.11.051. Epub 2017 Dec 8. Neuroscience. 2018. PMID: 29229556 Review.
Spinocerebellar ataxia type 3 (SCA3), or Machado-Joseph disease (MJD), is an autosomal dominant neurodegenerative disorder caused by the expansion of a polyglutamine (polyQ) tract in the ataxin-3 protein. To date, there is no effec …
Spinocerebellar ataxia type 3 (SCA3), or Machado-Joseph disease (MJD), is an autosomal domi …
Stage-Dependent Biomarker Changes in Spinocerebellar Ataxia Type 3.
Faber J, Berger M, Wilke C, Hubener-Schmid J, Schaprian T, Santana MM, Grobe-Einsler M, Onder D, Koyak B, Giunti P, Garcia-Moreno H, Gonzalez-Robles C, Lima M, Raposo M, Melo ARV, de Almeida LP, Silva P, Pinto MM, van de Warrenburg BP, van Gaalen J, de Vries J, Oz G, Joers JM, Synofzik M, Schols L, Riess O, Infante J, Manrique L, Timmann D, Thieme A, Jacobi H, Reetz K, Dogan I, Onyike C, Povazan M, Schmahmann J, Ratai EM, Schmid M, Klockgether T. Faber J, et al. Ann Neurol. 2024 Feb;95(2):400-406. doi: 10.1002/ana.26824. Epub 2023 Dec 5. Ann Neurol. 2024. PMID: 37962377
Spinocerebellar ataxia type 3/Machado-Joseph disease is the most common autosomal dominant ataxia. In view of the development of targeted therapies, knowledge of early biomarker changes is needed. We analyzed cross-sectional data o …
Spinocerebellar ataxia type 3/Machado-Joseph disease is the most common autosomal dominant …
1,606 results