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1 nt progressive external ophthalmoplegia, and oculopharyngeal muscular dystrophy.
2 s 5 multigenerational American families with oculopharyngeal muscular dystrophy.
3 some system, which is highly dysregulated in oculopharyngeal muscular dystrophy.
4 e muscle weakness in the late-onset disorder 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
11 A heat-shock response was also seen in an oculopharyngeal muscular dystrophy mouse model expressin
21 are one of the ultrastructural hallmarks of oculopharyngeal muscular dystrophy (OPMD), a disorder ca
22 ne tract in the N-terminus of PABPN1 lead to oculopharyngeal muscular dystrophy (OPMD), which is an a
26 vacuoles is described in autosomal dominant oculopharyngeal muscular dystrophy, the age of onset, th
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