| Nr. | Year OPEN | Title | users say> | rate good | rate bad | no link | Citation |
Ataxia (spinocerebellar)Trinucleotid repeatATXN1Machado Joseph s diseaseATXN3| 1 | 2005 | Genetic and molecular aspects of spinocerebellar ataxias. | 
| + | - | nl | Neuropsychiatr Dis Treat 1(2):125-33 (2005) Honti V |
| 2 | 2009 | The spinocerebellar ataxias. | 
| + | - | nl | J Neuroophthalmol 29(3):227-37 (2009) Paulson HL |
| 3 | 1999 | Progress in pathogenesis studies of spinocerebellar ataxia type 1. | 
| + | - | nl | Philos Trans R Soc Lond B Biol Sci 354(1386):1079-81 (1999) |
| 4 | 2004 | Spinocerebellar ataxia type 17: latest member of polyglutamine disease group highlights unanswered questions. | 
| + | - | nl | Arch Neurol 61(2):183-4 (2004) Tsuji S |
| 5 | 2001 | Genetic testing in spinocerebellar ataxias: defining a clinical role. | 
| + | - | nl | Arch Neurol 58(2):191-5 (2001) |
| 6 | 2006 | Molecular pathogenesis of spinocerebellar ataxias. | 
| + | - | nl | Brain 129(Pt 6):1357-70 (2006) Duenas AM |
| 7 | 2009 | Spinocerebellar ataxias. | 
| + | - | nl | Arq Neuropsiquiatr 67(4):1133-42 (2009) |
| 8 | 2009 | Pathogenic mechanisms of a polyglutamine-mediated neurodegenerative disease, spinocerebellar ataxia type 1. | 
| + | - | nl | J Biol Chem 284(12):7425-9 (2009) |
| 9 | 2010 | Nuclear ataxias. | 
| + | - | nl | Cold Spring Harb Perspect Biol 2(5):a000786 (2010) |
| 10 | 2009 | Emerging pathogenic pathways in the spinocerebellar ataxias. | 
| + | - | nl | Curr Opin Genet Dev 19(3):247-53 (2009) |
| 11 | 2004 | Spinocerebellar ataxia type 8 in Scotland: genetic and clinical features in seven unrelated cases and a review of published reports. | 
| + | - | nl | J Neurol Neurosurg Psychiatry 75(3):459-65 (2004) |
| 12 | 2011 | Autosomal dominant cerebellar ataxia type I: a review of the phenotypic and genotypic characteristics. | 
| + | - | nl | Orphanet J Rare Dis 6(-):33 (2011) |
| 13 | 2011 | Machado-Joseph Disease: from first descriptions to new perspectives. | 
| + | - | nl | Orphanet J Rare Dis 6(-):35 (2011) |