戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

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 Emery-Dreifuss; distal; facioscapulohumeral; oculopharyngeal; and limb-girdle which is the most heter
2 ogressive muscular dystrophy, reminiscent of oculopharyngeal muscular dystrophy (OPMD) but of much ea
3                                              Oculopharyngeal muscular dystrophy (OPMD) is a genetic d
4                                              Oculopharyngeal muscular dystrophy (OPMD) is a late onse
5                                              Oculopharyngeal muscular dystrophy (OPMD) is a late-onse
6                                              Oculopharyngeal muscular dystrophy (OPMD) is a late-onse
7                                              Oculopharyngeal muscular dystrophy (OPMD) is a late-onse
8                                              Oculopharyngeal muscular dystrophy (OPMD) is a rare auto
9                                              Oculopharyngeal muscular dystrophy (OPMD) is a rare late
10                                              Oculopharyngeal muscular dystrophy (OPMD) is a rare myop
11                                              Oculopharyngeal muscular dystrophy (OPMD) is an adult-on
12                                              Oculopharyngeal muscular dystrophy (OPMD) is an autosoma
13                                              Oculopharyngeal muscular dystrophy (OPMD) is an autosoma
14                                              Oculopharyngeal muscular dystrophy (OPMD) is an autosoma
15                                              Oculopharyngeal muscular dystrophy (OPMD) is an autosoma
16  are one of the ultrastructural hallmarks of oculopharyngeal muscular dystrophy (OPMD), a disorder ca
17                                           In oculopharyngeal muscular dystrophy (OPMD), dysphagia is
18 ne tract in the N-terminus of PABPN1 lead to oculopharyngeal muscular dystrophy (OPMD), which is an a
19 tion of pathogenic aggregates, a hallmark of Oculopharyngeal Muscular Dystrophy (OPMD).
20 a specific form of muscular dystrophy termed oculopharyngeal muscular dystrophy (OPMD).
21 nal group is altered in the transcriptome of oculopharyngeal muscular dystrophy (OPMD).
22 ng protein nuclear-1 (PABPN1) protein causes oculopharyngeal muscular dystrophy (OPMD).
23 ed a different chromosomal haplotype for the oculopharyngeal muscular dystrophy alleles than did the
24 expansion in PABPN1 that is thought to cause oculopharyngeal muscular dystrophy cannot completely res
25                                              Oculopharyngeal muscular dystrophy is a late-onset disea
26                                              Oculopharyngeal muscular dystrophy is a late-onset, auto
27    A heat-shock response was also seen in an oculopharyngeal muscular dystrophy mouse model expressin
28                                   Linkage of oculopharyngeal muscular dystrophy to 14q11.2-q13 has be
29 gton's disease (HD), Parkinson's disease and oculopharyngeal muscular dystrophy, are associated with
30 osis type 1, congenital myasthenic syndrome, oculopharyngeal muscular dystrophy, chronic progressive
31  vacuoles is described in autosomal dominant oculopharyngeal muscular dystrophy, the age of onset, th
32 some system, which is highly dysregulated in oculopharyngeal muscular dystrophy.
33 e muscle weakness in the late-onset disorder oculopharyngeal muscular dystrophy.
34 nt progressive external ophthalmoplegia, and oculopharyngeal muscular dystrophy.
35 s 5 multigenerational American families with oculopharyngeal muscular dystrophy.
36 me, neuronal intranuclear inclusion disease, oculopharyngeal myopathy with leukodystrophy, and oculop
37 siblings who developed a rapidly progressive oculopharyngeal somatic syndrome, at the ages of 11 and
38 ly is an example of a GCG expansion-negative oculopharyngeal syndrome requiring further genetic inves