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• W2094268539 endingPage "362" @default.
• W2094268539 startingPage "362" @default.
• W2094268539 abstract "UNTIL 1950 the syndrome of progressive ptosis and ophthalmoplegia was generally considered to be neurogenic in origin as indicated by the designation progressive nuclear ophthalmoplegia. This concept was based upon two cases^1,2in which there were neuronal abnormalities in postmortem study of the oculomotor nuclei. In 1951, however, Kiloh and Nevin³concluded that the ocular signs were due to myopathy because of histological abnormalities in the medial rectus muscle in one case; they considered the neural changes of earlier cases to be insignificant, and they introduced the terms ocular myopathy or ocular dystrophy. Their view dominated the subsequent literature, and six later autopsy cases^4-9also supported the concept of myopathy. In our own experience, however, the same syndrome has sometimes been associated with a variety of neurological abnormalities. There have also been several reports^10-31of similar cases associated with neural disease. These combined disorders raise" @default.
• W2094268539 created "2016-06-24" @default.
• W2094268539 creator A5076356260 @default.
• W2094268539 date "1968-10-01" @default.
• W2094268539 modified "2023-09-25" @default.
• W2094268539 title "Progressive Ophthalmoplegia" @default.
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• W2094268539 doi "https://doi.org/10.1001/archneur.1968.00480040028002" @default.
• W2094268539 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/4175668" @default.
• W2094268539 hasPublicationYear "1968" @default.
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