1 rmine if any of these diseases co-occur with hereditary ataxia.

2 cal characteristics, it was later focused on hereditary ataxias.

3 ho were tested for molecularly characterized hereditary ataxias.

4 ia type 6 and Friedreich's ataxia are common hereditary ataxias.

5 his and other findings for a growing list of hereditary ataxias.

6 driven bioinformatics; this in turn has made hereditary ataxias an especially well-developed model gr

7  of endogenous DNA breakage, contributing to hereditary ataxia and underlying the cytotoxicity of a w

8  a hitherto unrecognized association between hereditary ataxias and gluten sensitivity.

9 let) repeats including Huntington's disease, hereditary ataxias and spinobulbar muscular atrophy.

10 m for neuronal cell dysfunction and death in hereditary ataxias and suggest that there may be a commo

11                                    Among the hereditary ataxias, autosomal recessive spinocerebellar

12                                              Hereditary ataxias comprise a group of genetically heter

13 s; so far, seven distinct autosomal dominant hereditary ataxias have been genetically mapped in the h

14                                Patients with hereditary ataxia (including asymptomatic patients with

15    Friedreich ataxia (FRDA), the most common hereditary ataxia, is caused by mutations in the frataxi

16 ipation-may be present in forms of dementia, hereditary ataxia, Parkinsonism, bipolar affective disor

17                                          The hereditary ataxias represent a clinically and geneticall