W
W. King Engel
Researcher at University of Southern California
Publications - 212
Citations - 10138
W. King Engel is an academic researcher from University of Southern California. The author has contributed to research in topics: Inclusion body myositis & Skeletal muscle. The author has an hindex of 57, co-authored 212 publications receiving 9934 citations. Previous affiliations of W. King Engel include National Institutes of Health.
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Ocular motor abnormalities in hereditary cerebellar ataxia
TL;DR: The results support the suggestion that the cerebellum specifically helps maintain eccentric gaze; produces smooth pursuit eye movements; and modulates the amplitude of saccadic eye movements.
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Slow saccades in spinocerebellar degeneration.
TL;DR: A neural network was hypothesized that made saccades by driving the eyes to an orbital position rather than preprogramming a distance for movement, and computer simulation of this model produced both realistically appearing normal saccade and, when appropriately "lesioned" to simulate a loss of saccadic "burst" neurons in the pontine reticular formation, slow saccading that could be modified in flight.
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Oculocraniosomatic Neuromuscular Disease With Ragged-Red Fibers: Histochemical and Ultrastructural Changes in Limb Muscles of a Group of Patients With Idiopathic Progressive External Ophthalmoplegia
TL;DR: The described morphologic abnormalities, in combination with idiopathic progressive ophthalmoplegia, may represent a distinct clinicopathologic syndrome, "oculocraniosomatic neuromuscular disease with ragged-red fibers," which usually includes elevated cerebrospinal fluid protein levels and sometimes cardiac conduction abnormalities.
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Muscle-specific mutations accumulate with aging in critical human mtDNA control sites for replication
Yan Wang,Yuichi Michikawa,Con Mallidis,Yan Bai,Linda J. Woodhouse,Kevin E. Yarasheski,Carol A. Miller,Valerie Askanas,W. King Engel,Shalender Bhasin,Giuseppe Attardi +10 more
TL;DR: The striking tissue specificity of the muscle mtDNA mutations detected here and their mapping at critical sites for mtDNA replication strongly point to the involvement of a specific mutagenic machinery and to the functional relevance of these mutations.
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Selective and nonselective susceptibility of muscle fiber types. A new approach to human neuromuscular diseases.
TL;DR: This report summarizes the current analytical techniques and conceptualizations, illustrated by examples from the present and previous investigations, and investigates whether there is selective or nonselective involvement of muscle fiber types in each human and animal condition studied.