PMC:2940021 / 31384-31844 JSONTXT

{"project":"0_colil","denotations":[{"id":"20422195-10711989-60982","span":{"begin":262,"end":264},"obj":"10711989"},{"id":"20422195-19078757-60983","span":{"begin":456,"end":458},"obj":"19078757"}],"text":"Oculopharyngeal muscular dystrophy\nOculopharyngeal muscular dystrophy (OPMD) is a late-onset autosomal dominant dystrophy, and is clinically characterised by slowly progressive ptosis, dysphagia and dysphonia. Proximal limb weakness often develops subsequently [59]. There are few reports on muscle imaging in OPMD. Abnormal fatty infiltration of the tongue, masseter, neck, shoulder girdle, lumbar paraspinous and the gluteus muscles have been described [60]."}

{"project":"2_test","denotations":[{"id":"20422195-10711989-29368066","span":{"begin":262,"end":264},"obj":"10711989"},{"id":"20422195-19078757-29368067","span":{"begin":456,"end":458},"obj":"19078757"}],"text":"Oculopharyngeal muscular dystrophy\nOculopharyngeal muscular dystrophy (OPMD) is a late-onset autosomal dominant dystrophy, and is clinically characterised by slowly progressive ptosis, dysphagia and dysphonia. Proximal limb weakness often develops subsequently [59]. There are few reports on muscle imaging in OPMD. Abnormal fatty infiltration of the tongue, masseter, neck, shoulder girdle, lumbar paraspinous and the gluteus muscles have been described [60]."}

{"project":"TEST0","denotations":[{"id":"20422195-52-58-60982","span":{"begin":262,"end":264},"obj":"[\"10711989\"]"},{"id":"20422195-140-146-60983","span":{"begin":456,"end":458},"obj":"[\"19078757\"]"}],"text":"Oculopharyngeal muscular dystrophy\nOculopharyngeal muscular dystrophy (OPMD) is a late-onset autosomal dominant dystrophy, and is clinically characterised by slowly progressive ptosis, dysphagia and dysphonia. Proximal limb weakness often develops subsequently [59]. There are few reports on muscle imaging in OPMD. Abnormal fatty infiltration of the tongue, masseter, neck, shoulder girdle, lumbar paraspinous and the gluteus muscles have been described [60]."}

{"project":"MyTest","denotations":[{"id":"20422195-10711989-29368066","span":{"begin":262,"end":264},"obj":"10711989"},{"id":"20422195-19078757-29368067","span":{"begin":456,"end":458},"obj":"19078757"}],"namespaces":[{"prefix":"_base","uri":"https://www.uniprot.org/uniprot/testbase"},{"prefix":"UniProtKB","uri":"https://www.uniprot.org/uniprot/"},{"prefix":"uniprot","uri":"https://www.uniprot.org/uniprotkb/"}],"text":"Oculopharyngeal muscular dystrophy\nOculopharyngeal muscular dystrophy (OPMD) is a late-onset autosomal dominant dystrophy, and is clinically characterised by slowly progressive ptosis, dysphagia and dysphonia. Proximal limb weakness often develops subsequently [59]. There are few reports on muscle imaging in OPMD. Abnormal fatty infiltration of the tongue, masseter, neck, shoulder girdle, lumbar paraspinous and the gluteus muscles have been described [60]."}