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