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Barry Jones

Researcher at Eli Lilly and Company

Publications -  49
Citations -  3671

Barry Jones is an academic researcher from Eli Lilly and Company. The author has contributed to research in topics: Olanzapine & Risperidone. The author has an hindex of 28, co-authored 49 publications receiving 3600 citations. Previous affiliations of Barry Jones include University of Ottawa & McMaster University.

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A Canadian multicenter placebo-controlled study of fixed doses of risperidone and haloperidol in the treatment of chronic schizophrenic patients.

TL;DR: It is suggested that risperidone, at the optimal therapeutic dose of 6 mg/day, produced significant improvement in both positive and negative symptoms without an increase in drug-induced parkinsonian symptoms and with a significant beneficial effect on tardive dyskinesia.
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Neuropsychological Change in Early Phase Schizophrenia During 12 Months of Treatment With Olanzapine, Risperidone, or Haloperidol

TL;DR: Olanzapine has some superior cognitive benefits relative to haloperidol and risperidone, and a larger sample replication study is necessary to confirm and generalize the observations of this study.
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Neuroleptic-induced supersensitivity psychosis: clinical and pharmacologic characteristics.

TL;DR: An implication of neuroleptic-induced mesolimbic supersensitivity is that the tenaency toward psychotic relapse in such patients is determined by more than just the normal course of the illness.
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Neuroleptic-Induced Supersensitivity Psychosis

TL;DR: The anticholinergic effects of chlorpromazine, amitriptyline, scopolamine (Sominex) (0), and tropicamide were probably additive and although her disorientation cleared rapidly, Ms. A maintained that her hallucinations persisted during her 2-week hospitalization.
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Comparison of rapidly acting intramuscular olanzapine, lorazepam, and placebo: a double-blind, randomized study in acutely agitated patients with dementia.

TL;DR: Intramuscular injection of olanzapine may provide substantial benefit in rapidly treating inpatients with acute dementia-related agitation and no significant differences among treatment groups were seen in vital signs, including orthostasis.