コーパス検索結果 (１語後でソート)
通し番号をクリックするとPubMedの該当ページを表示します
1 hereditary ataxia and between CMT2 + HSP and hereditary ataxia.
2 ent clinical practice in genetic testing for hereditary ataxia.
3 rmine if any of these diseases co-occur with hereditary ataxia.
4 his and other findings for a growing list of hereditary ataxias.
5 ho were tested for molecularly characterized hereditary ataxias.
6 untington's Disease, Fragile X Syndrome, and hereditary ataxias.
7 cal characteristics, it was later focused on hereditary ataxias.
8 ia type 6 and Friedreich's ataxia are common hereditary ataxias.
10 driven bioinformatics; this in turn has made hereditary ataxias an especially well-developed model gr
11 an overlapping relationship between HSP and hereditary ataxia and between CMT2 + HSP and hereditary
12 of endogenous DNA breakage, contributing to hereditary ataxia and underlying the cytotoxicity of a w
14 let) repeats including Huntington's disease, hereditary ataxias and spinobulbar muscular atrophy.
15 m for neuronal cell dysfunction and death in hereditary ataxias and suggest that there may be a commo
16 europsychiatric symptoms (NPS) are common in hereditary ataxias as a part of the cerebellar cognitive
18 our knowledge of the genetic architecture of hereditary ataxia by leveraging functional genomic annot
19 riedreich's ataxia (FA) is a leading form of hereditary ataxia caused by autosomal recessive mutation
22 dreich ataxia (FRDA), one of the most common hereditary ataxias, depressive symptoms were previously
23 defined the pathophysiological basis of many hereditary ataxias (HAs), including loss-of-function as
24 s; so far, seven distinct autosomal dominant hereditary ataxias have been genetically mapped in the h
26 Friedreich ataxia (FRDA), the most common hereditary ataxia, is caused by mutations in the frataxi
27 ng number of ion channel genes implicated in hereditary ataxia, it remains unclear how ion channel mu
28 ipation-may be present in forms of dementia, hereditary ataxia, Parkinsonism, bipolar affective disor