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The NeuroStar TMS Device: Conducting the FDA Approved Protocol for Treatment of Depression
Published on: November 12, 2010
The 2004 FDA warning on antidepressant suicidality risk changed outpatient treatment patterns for young people with
Jeffrey A Bridge1, Kelly J Kelleher
1The Research Institute at Nationwide Children's Hospital, The Ohio State University, Columbus, Ohio, USA.
Evidence-Based Mental Health
|April 20, 2011
Abstract
No abstract available in PubMed .
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