195 related articles for article (PubMed ID: 36323979)
21. Variation in DNA Repair System Gene as an Additional Modifier of Age at Onset in Spinocerebellar Ataxia Type 3/Machado-Joseph Disease.
Mergener R; Furtado GV; de Mattos EP; Leotti VB; Jardim LB; Saraiva-Pereira ML
Neuromolecular Med; 2020 Mar; 22(1):133-138. PubMed ID: 31587151
[TBL] [Abstract][Full Text] [Related]
22. Spinocerebellar ataxia type 1 and Machado-Joseph disease: incidence of CAG expansions among adult-onset ataxia patients from 311 families with dominant, recessive, or sporadic ataxia.
Ranum LP; Lundgren JK; Schut LJ; Ahrens MJ; Perlman S; Aita J; Bird TD; Gomez C; Orr HT
Am J Hum Genet; 1995 Sep; 57(3):603-8. PubMed ID: 7668288
[TBL] [Abstract][Full Text] [Related]
23. High frequency of Machado-Joseph disease identified in southeastern Chinese kindreds with spinocerebellar ataxia.
Gan SR; Shi SS; Wu JJ; Wang N; Zhao GX; Weng ST; Murong SX; Lu CZ; Wu ZY
BMC Med Genet; 2010 Mar; 11():47. PubMed ID: 20334689
[TBL] [Abstract][Full Text] [Related]
24. Planning Future Clinical Trials for Machado-Joseph Disease.
Saute JAM; Jardim LB
Adv Exp Med Biol; 2018; 1049():321-348. PubMed ID: 29427112
[TBL] [Abstract][Full Text] [Related]
25. Cerebellar lncRNA Expression Profile Analysis of SCA3/MJD Mice.
Long Z; Li T; Chen Z; Peng Y; Wang C; Hou X; Yuan H; Wang P; Xie Y; He L; Zhou X; Peng H; Qiu R; Xia K; Tang B; Jiang H
Int J Genomics; 2018; 2018():5383517. PubMed ID: 30046585
[TBL] [Abstract][Full Text] [Related]
26. Frequency of the different mutations causing spinocerebellar ataxia (SCA1, SCA2, MJD/SCA3 and DRPLA) in a large group of Brazilian patients.
Lopes-Cendes I; Teive HG; Calcagnotto ME; Da Costa JC; Cardoso F; Viana E; Maciel JA; Radvany J; Arruda WO; Trevisol-Bittencourt PC; Rosa Neto P; Silveira I; Steiner CE; Pinto Júnior W; Santos AS; Correa Neto Y; Werneck LC; Araújo AQ; Carakushansky G; Mello LR; Jardim LB; Rouleau GA
Arq Neuropsiquiatr; 1997 Sep; 55(3B):519-29. PubMed ID: 9629399
[TBL] [Abstract][Full Text] [Related]
27. DNA methylation age acceleration is associated with age of onset in Chinese spinocerebellar ataxia type 3 patients.
Li J; Shu A; Sun Y; Yang W; Tang X; Pu H; Peng Y; Hu X; Qing Y; Wang J; Wan C; Zhou M; Zhang M
Neurobiol Aging; 2022 May; 113():1-6. PubMed ID: 35247757
[TBL] [Abstract][Full Text] [Related]
28. Spinocerebellar ataxia type 3/Machado-Joseph disease: segregation patterns and factors influencing instability of expanded CAG transmissions.
Souza GN; Kersting N; Krum-Santos AC; Santos AS; Furtado GV; Pacheco D; Gonçalves TA; Saute JA; Schuler-Faccini L; Mattos EP; Saraiva-Pereira ML; Jardim LB
Clin Genet; 2016 Aug; 90(2):134-40. PubMed ID: 26693702
[TBL] [Abstract][Full Text] [Related]
29. Machado-Joseph disease/spinocerebellar ataxia type 3.
Paulson H
Handb Clin Neurol; 2012; 103():437-49. PubMed ID: 21827905
[TBL] [Abstract][Full Text] [Related]
30. Analysis of SCA1, DRPLA, MJD, SCA2, and SCA6 CAG repeats in 48 Portuguese ataxia families.
Silveira I; Coutinho P; Maciel P; Gaspar C; Hayes S; Dias A; Guimarães J; Loureiro L; Sequeiros J; Rouleau GA
Am J Med Genet; 1998 Mar; 81(2):134-8. PubMed ID: 9613852
[TBL] [Abstract][Full Text] [Related]
31. The prevalence and wide clinical spectrum of the spinocerebellar ataxia type 2 trinucleotide repeat in patients with autosomal dominant cerebellar ataxia.
Geschwind DH; Perlman S; Figueroa CP; Treiman LJ; Pulst SM
Am J Hum Genet; 1997 Apr; 60(4):842-50. PubMed ID: 9106530
[TBL] [Abstract][Full Text] [Related]
32. Machado-Joseph Disease: from first descriptions to new perspectives.
Bettencourt C; Lima M
Orphanet J Rare Dis; 2011 Jun; 6():35. PubMed ID: 21635785
[TBL] [Abstract][Full Text] [Related]
33. Prenatal diagnosis of Machado-Joseph disease/Spinocerebellar Ataxia Type 3 in Taiwan: early detection of expanded ataxin-3.
Tsai HF; Liu CS; Chen GD; Lin ML; Li C; Chen YY; Wang BT; Hsieh M
J Clin Lab Anal; 2003; 17(5):195-200. PubMed ID: 12938149
[TBL] [Abstract][Full Text] [Related]
34. Machado Joseph disease maps to the same region of chromosome 14 as the spinocerebellar ataxia type 3 locus.
Twist EC; Casaubon LK; Ruttledge MH; Rao VS; Macleod PM; Radvany J; Zhao Z; Rosenberg RN; Farrer LA; Rouleau GA
J Med Genet; 1995 Jan; 32(1):25-31. PubMed ID: 7897622
[TBL] [Abstract][Full Text] [Related]
35. Recent therapeutic prospects for Machado-Joseph disease.
Costa MDC
Curr Opin Neurol; 2020 Aug; 33(4):519-526. PubMed ID: 32657894
[TBL] [Abstract][Full Text] [Related]
36. Mutations in American families with spinocerebellar ataxia (SCA) type 3: SCA3 is allelic to Machado-Joseph disease.
Higgins JJ; Nee LE; Vasconcelos O; Ide SE; Lavedan C; Goldfarb LG; Polymeropoulos MH
Neurology; 1996 Jan; 46(1):208-13. PubMed ID: 8559377
[TBL] [Abstract][Full Text] [Related]
37. Marked phenotypic heterogeneity associated with expansion of a CAG repeat sequence at the spinocerebellar ataxia 3/Machado-Joseph disease locus.
Cancel G; Abbas N; Stevanin G; Dürr A; Chneiweiss H; Néri C; Duyckaerts C; Penet C; Cann HM; Agid Y
Am J Hum Genet; 1995 Oct; 57(4):809-16. PubMed ID: 7573040
[TBL] [Abstract][Full Text] [Related]
38. Spastic paraparesis as the first manifestation of Machado-Joseph disease: A case report and review of the literature.
Lin HC; Chang YY; Chang KH; Chen YF; Lan MY
Clin Neurol Neurosurg; 2018 Sep; 172():137-140. PubMed ID: 30007589
[TBL] [Abstract][Full Text] [Related]
39. Mutational origin of Machado-Joseph disease in the Australian Aboriginal communities of Groote Eylandt and Yirrkala.
Martins S; Soong BW; Wong VC; Giunti P; Stevanin G; Ranum LP; Sasaki H; Riess O; Tsuji S; Coutinho P; Amorim A; Sequeiros J; Nicholson GA
Arch Neurol; 2012 Jun; 69(6):746-51. PubMed ID: 22351852
[TBL] [Abstract][Full Text] [Related]
40. Genetic Variation in ATXN3 (Ataxin-3) 3'UTR: Insights into the Downstream Regulatory Elements of the Causative Gene of Machado-Joseph Disease/Spinocerebellar Ataxia Type 3.
Melo ARV; Raposo M; Ventura M; Martins S; Pavão S; Alonso I; Bettencourt C; Lima M
Cerebellum; 2023 Feb; 22(1):37-45. PubMed ID: 35034258
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
