Jerry Avorn. Show Affiliations »
Abstract
Mesh: See more » Device ApprovalElectric Stimulation Therapy/instrumentationEpilepsy/therapyEquipment SafetyEuropeHumansProduct Surveillance, PostmarketingUnited StatesUnited States Food and Drug Administration
Year: 2010 PMID: 21045051 DOI: 10.1136/bmj.c5730
Source DB: PubMed Journal: BMJ ISSN: 0959-8138