Romero-Molina A, Ramirez-Garcia G, Chirino-Perez A, Padron-Rivera G, Hernandez-Castillo C, Garcia-Gomar M
PLoS One. 2025; 20(3):e0319505.
PMID: 40029932
PMC: 11875346.
DOI: 10.1371/journal.pone.0319505.
Barcellos I, Hansen C, Strobel G, Geritz J, Munhoz R, Moscovich M
Cerebellum. 2024; 23(5):2109-2121.
PMID: 38869768
DOI: 10.1007/s12311-024-01709-7.
Kurosaki T, Ashizawa T
Front Genet. 2022; 13:936869.
PMID: 36199580
PMC: 9528567.
DOI: 10.3389/fgene.2022.936869.
Ramirez-Garcia S, Sanchez-Corona J, Volpini-Bertran V, Moran-Moguel M, Gutierrez-Rubio S, Castaneda-Cisneros G
Actas Esp Psiquiatr. 2022; 50(1):58-62.
PMID: 35103298
PMC: 10803836.
Veliz-Otani D, Inca-Martinez M, Bampi G, Ortega O, Jardim L, Saraiva-Pereira M
Cerebellum. 2019; 18(5):841-848.
PMID: 31342269
DOI: 10.1007/s12311-019-01057-x.
Frequency of SCA8, SCA10, SCA12, SCA36, FXTAS and C9orf72 repeat expansions in SCA patients negative for the most common SCA subtypes.
Aydin G, Dekomien G, Hoffjan S, Gerding W, Epplen J, Arning L
BMC Neurol. 2018; 18(1):3.
PMID: 29316893
PMC: 5761156.
DOI: 10.1186/s12883-017-1009-9.
Cognitive dysfunction in spinocerebellar ataxias.
Teive H, Arruda W
Dement Neuropsychol. 2017; 3(3):180-187.
PMID: 29213626
PMC: 5618971.
DOI: 10.1590/S1980-57642009DN30300002.
Haplotype Study in SCA10 Families Provides Further Evidence for a Common Ancestral Origin of the Mutation.
Bampi G, Bisso-Machado R, Hunemeier T, Gheno T, Furtado G, Veliz-Otani D
Neuromolecular Med. 2017; 19(4):501-509.
PMID: 28905220
DOI: 10.1007/s12017-017-8464-8.
A Comparative Optical Coherence Tomography Study of Spinocerebellar Ataxia Types 3 and 10.
Tensini F, Sato M, Shiokawa N, Ashizawa T, Teive H
Cerebellum. 2017; 16(4):797-801.
PMID: 28401494
PMC: 6996148.
DOI: 10.1007/s12311-017-0856-7.
Pain in Neurodegenerative Disease: Current Knowledge and Future Perspectives.
de Tommaso M, Arendt-Nielsen L, Defrin R, Kunz M, Pickering G, Valeriani M
Behav Neurol. 2016; 2016:7576292.
PMID: 27313396
PMC: 4904074.
DOI: 10.1155/2016/7576292.
High relative frequency of SCA1 in Poland reflecting a potential founder effect.
Krysa W, Sulek A, Rakowicz M, Szirkowiec W, Zaremba J
Neurol Sci. 2016; 37(8):1319-25.
PMID: 27193757
PMC: 4956719.
DOI: 10.1007/s10072-016-2594-x.
Spinocerebellar ataxias: genotype-phenotype correlations in 104 Brazilian families.
Teive H, Munhoz R, Arruda W, Lopes-Cendes I, Raskin S, Werneck L
Clinics (Sao Paulo). 2012; 67(5):443-9.
PMID: 22666787
PMC: 3351252.
DOI: 10.6061/clinics/2012(05)07.
Spinocerebellar ataxia type 10.
Ashizawa T
Handb Clin Neurol. 2011; 103:507-19.
PMID: 21827910
PMC: 10083001.
DOI: 10.1016/B978-0-444-51892-7.00032-2.
Spinocerebellar ataxia type 10: Frequency of epilepsy in a large sample of Brazilian patients.
Teive H, Munhoz R, Raskin S, Arruda W, de Paola L, Werneck L
Mov Disord. 2010; 25(16):2875-8.
PMID: 20818609
PMC: 3000879.
DOI: 10.1002/mds.23324.
Ancestral origin of the ATTCT repeat expansion in spinocerebellar ataxia type 10 (SCA10).
Almeida T, Alonso I, Martins S, Ramos E, Azevedo L, Ohno K
PLoS One. 2009; 4(2):e4553.
PMID: 19234597
PMC: 2639644.
DOI: 10.1371/journal.pone.0004553.
Lack of variation of ATTCT pentanucleotide repeats at ATXN10 gene between clinically diagnosed ataxia patients and normal individuals originated from Chinese Han.
Wang J, Jiang H, Zhang S, Xu Q, Zhou Y, Liao S
J Genet. 2009; 87(3):283-6.
PMID: 19147916
DOI: 10.1007/s12041-008-0045-z.
Heterozygosity for a protein truncation mutation of sodium channel SCN8A in a patient with cerebellar atrophy, ataxia, and mental retardation.
Trudeau M, Dalton J, Day J, Ranum L, Meisler M
J Med Genet. 2005; 43(6):527-30.
PMID: 16236810
PMC: 2564538.
DOI: 10.1136/jmg.2005.035667.
Clinical, psychological, and genetic characteristics of spinocerebellar ataxia type 19 (SCA19).
Jurgen Schelhaas H, van de Warrenburg B
Cerebellum. 2005; 4(1):51-4.
PMID: 15895560
DOI: 10.1080/14734220510007888.
Recent progress in spinocerebellar ataxia type-10 (SCA10).
Lin X, Ashizawa T
Cerebellum. 2005; 4(1):37-42.
PMID: 15895557
DOI: 10.1080/14734220510007897.