CrossRef Text and Data Mining
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Adverse Events Associated With Synthetic Male Slings: An Analysis of the Food and Drug Administration Manufacturer and User Facility Device Experience Database
Hanson Zhao, Colby P. Souders, Paige K. Kuhlmann, Kai Dallas, Karyn Eilber, Jennifer T. Anger
Int Neurourol J. 2021;25(2):172-176.   Published online 2021 May 5
DOI: https://doi.org/10.5213/inj.2040294.147

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Adverse Events Associated With Synthetic Male Slings: An Analysis of the Food and Drug Administration Manufacturer and User Facility Device Experience Database
International Neurourology Journal. 2021;25(2):172-176   Crossref logo
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Thoracic Endovascular Aortic Repair Adverse Events Reported In The Food And Drug Administration Manufacturer And User Facility Device Experience Database

Medical Devices: Evidence and Research. 2019;Volume 12:461-467   Crossref logo
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Deaths associated with implantable cardioverter defibrillator failure and deactivation reported in the United States Food and Drug Administration Manufacturer and User Facility Device Experience Database
Heart Rhythm. 2004;1(4):399-405   Crossref logo
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Analysis of adverse events with uterine artery embolization reported to the manufacturer and user facility device experience database
Fertility and Sterility. 2017;108(3):e205   Crossref logo
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Analysis of the US Food and Drug Administration Manufacturer and User Facility Device Experience database for adverse events involving Amplatzer septal occluder devices and comparison with the Society of Thoracic Surgery congenital cardiac surgery database
The Journal of Thoracic and Cardiovascular Surgery. 2009;137(6):1334-1341   Crossref logo
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Analysis of the Food and Drug Administration Manufacturer and User Facility Device Experience Database for Patient- and Circuit-Related Adverse Events Involving Extracorporeal Membrane Oxygenation
Cardiovascular Revascularization Medicine. 2020;21(2):230-234   Crossref logo
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Recombinant human bone morphogenetic protein-2: adverse events reported to the Manufacturer and User Facility Device Experience database
The Spine Journal. 2012;12(10):894-899   Crossref logo
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Response to: “Adverse Events and Complications Associated With Intrathecal Drug Delivery Systems: Insights From the Manufacturer and User Facility Device Experience ( MAUDE ) Database”
Neuromodulation: Technology at the Neural Interface. 2021;24(4):796-797   Crossref logo
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Adverse Events and Complications Associated With Intrathecal Drug Delivery Systems: Insights From the Manufacturer and User Facility Device Experience (MAUDE) Database
Neuromodulation: Technology at the Neural Interface. 2020;   Crossref logo
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Response to Letter to the Editor Regarding: “Adverse Events and Complications Associated With Intrathecal Drug Delivery Systems: Insights From the Manufacturer and User Facility Device Experience ( MAUDE ) Database”
Neuromodulation: Technology at the Neural Interface. 2021;24(4):798-798   Crossref logo
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