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John Potokar

Researcher at University of Bristol

Publications -  73
Citations -  2439

John Potokar is an academic researcher from University of Bristol. The author has contributed to research in topics: Anxiety & Anxiety disorder. The author has an hindex of 28, co-authored 73 publications receiving 2224 citations. Previous affiliations of John Potokar include Bristol Royal Infirmary & University Hospitals Bristol NHS Foundation Trust.

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Serotonin reuptake inhibitor withdrawal

TL;DR: Reports of withdrawal symptoms in a retrospective chart review of 352 patients treated in an outpatient clinic with the nonselective serotonin reuptake inhibitor clomipramine or with one of the selective SSRIs, fluoxetine, fluvoxamine, paroxettine, or sertraline suggest a role has been suggested for serotonin in coordinating sensory and autonomic function with motor activity.
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Serotonin 5-HT1A receptor binding in people with panic disorder: positron emission tomography study

TL;DR: Panic disorder is associated with reduced 5-HT(1A) receptor availability, which is also known to have a key role in depression.
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Antidepressant-induced jitteriness/anxiety syndrome: systematic review

TL;DR: Jitteriness/anxiety syndrome remains poorly characterised and clinicians' perception of this syndrome influences prescribing and it is cited to support postulated mechanisms of drug action, but systematised evaluation of side-effects at earlier time points in antidepressant trials to further elucidate this clinically important syndrome.
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Predictive accuracy of risk scales following self-harm: Multicentre prospective cohort study

TL;DR: In this paper, a multisite prospective cohort study was conducted of adults aged 18 years and over referred to liaison psychiatry services following self-harm and evaluated the performance of risk scales (Manchester Self-Harm Rule, ReACT Self Harm Rule, SAD PERSONS scale, Modified SAD Persons scale, Barratt Impulsiveness Scale, etc.).
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A biological pathway linking inflammation and depression: activation of indoleamine 2,3-dioxygenase

TL;DR: The use of immune-activated groups at high risk of depression have been used and found novel strategies for the future development of antidepressants including inhibition of indoleamine 2,3-dioxygenase, moderating the cytokines which activate it, or addressing other targets in the kynurenine pathway.