These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

127 related articles for article (PubMed ID: 31984352)

  • 41. Lasers and energy-based devices marketed for vaginal rejuvenation: A cross-sectional analysis of the MAUDE database.
    Ahluwalia J; Avram MM; Ortiz AE
    Lasers Surg Med; 2019 Oct; 51(8):671-677. PubMed ID: 30924953
    [TBL] [Abstract][Full Text] [Related]  

  • 42. The First 4 Years of Postmarketing Safety Surveillance Related to the MitraClip Device: A United States Food and Drug Administration MAUDE Experience.
    Mahabir CA; DeFilippis EM; Aggarwal S; Bath A; Qamar A; Patel NK; Goldsweig AM; Vaduganathan M
    J Invasive Cardiol; 2020 May; 32(5):E130-E132. PubMed ID: 32269176
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Adverse Events Associated with the Use of Guide Extension Catheters during Percutaneous Coronary Intervention: Reports from the Manufacturer and User Facility Device Experience (MAUDE) database.
    Chen Y; Shah AA; Shlofmitz E; Khalid N; Musallam A; Khan JM; Iantorno M; Gajanana D; Rogers T; Hashim H; Bernardo NL; Waksman R
    Cardiovasc Revasc Med; 2019 May; 20(5):409-412. PubMed ID: 31079818
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Complications associated with PEAK PlasmaBlade from 2010 to 2020 from MAUDE.
    Lee E; Elzomor A; Boulos S; Silva O; Pasick LJ; Benito DA; Tong J; Zapanta P; Joshi AS; Goodman JF; Thakkar PG
    Proc (Bayl Univ Med Cent); 2022; 35(5):615-620. PubMed ID: 35991750
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Adverse Events in Hypoglossal Nerve Stimulator Implantation: 5-Year Analysis of the FDA MAUDE Database.
    Bellamkonda N; Shiba T; Mendelsohn AH
    Otolaryngol Head Neck Surg; 2021 Feb; 164(2):443-447. PubMed ID: 32957866
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Techniques to Optimize the Use of Optical Coherence Tomography: Insights from the Manufacturer and User Facility Device Experience (MAUDE) Database.
    Shlofmitz E; Garcia-Garcia HM; Rogers T; Khalid N; Chen Y; Kajita AH; Khan JM; Iantorno M; Gallino RA; Bernardo NL; Hashim H; Torguson R; Waksman R
    Cardiovasc Revasc Med; 2019 Jun; 20(6):507-512. PubMed ID: 30962083
    [TBL] [Abstract][Full Text] [Related]  

  • 47. The nature, magnitude, and reporting compliance of device-related events for intravenous patient-controlled analgesia in the FDA Manufacturer and User Facility Device Experience (MAUDE) database.
    Lawal OD; Mohanty M; Elder H; Skeer M; Erpelding N; Lanier R; Katz N
    Expert Opin Drug Saf; 2018 Apr; 17(4):347-357. PubMed ID: 29463158
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Perceptual Gaps Between Clinicians and Technologists on Health Information Technology-Related Errors in Hospitals: Observational Study.
    Ndabu T; Mulgund P; Sharman R; Singh R
    JMIR Hum Factors; 2021 Feb; 8(1):e21884. PubMed ID: 33544089
    [TBL] [Abstract][Full Text] [Related]  

  • 49. A prototype of knowledge-based patient safety event reporting and learning system.
    Kang H; Zhou S; Yao B; Gong Y
    BMC Med Inform Decis Mak; 2018 Dec; 18(Suppl 5):110. PubMed ID: 30526567
    [TBL] [Abstract][Full Text] [Related]  

  • 50. A cross-sectional analysis of 284 complications for lumbar disc replacements from medical device reports maintained by the United States Food and Drug Administration.
    Koutsogiannis P; Khan S; Phillips F; Qureshi S; Dowling TJ; Song J; Virk S
    Spine J; 2022 Feb; 22(2):278-285. PubMed ID: 34478867
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Adverse events and modes of failure related to the FilterWire EZ Embolic Protection System: Lessons learned from an analytic review of the FDA MAUDE database.
    Khalid N; Javed H; Rogers T; Hashim H; Shlofmitz E; Chen Y; Khan JM; Musallam A; Torguson R; Bernardo NL; Waksman R
    Catheter Cardiovasc Interv; 2019 Jul; 94(1):157-164. PubMed ID: 30985082
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Surgical stapler-associated fatalities and adverse events reported to the Food and Drug Administration.
    Brown SL; Woo EK
    J Am Coll Surg; 2004 Sep; 199(3):374-81. PubMed ID: 15325606
    [TBL] [Abstract][Full Text] [Related]  

  • 53. A Review of Reported Adverse Events in MRI-Safe and MRI-Conditional Cochlear Implants.
    Bestourous DE; Davidson L; Reilly BK
    Otol Neurotol; 2022 Jan; 43(1):42-47. PubMed ID: 34510115
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Timely recognition of total elbow and radial head arthroplasty adverse events: an analysis of reports to the US Food and Drug Administration.
    Somerson JS; Matsen FA
    J Shoulder Elbow Surg; 2019 Mar; 28(3):510-519. PubMed ID: 30466818
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Using Active Learning to Identify Health Information Technology Related Patient Safety Events.
    Fong A; Howe JL; Adams KT; Ratwani RM
    Appl Clin Inform; 2017 Jan; 8(1):35-46. PubMed ID: 28097287
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Vaginal laser treatment of genitourinary syndrome of menopause: does the evidence support the FDA safety communication?
    Guo JZ; Souders C; McClelland L; Anger JT; Scott VCS; Eilber KS; Ackerman AL
    Menopause; 2020 Oct; 27(10):1177-1184. PubMed ID: 32796292
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Safety profiles of percutaneous left atrial appendage closure devices: An analysis of the Food and Drug Administration Manufacturer and User Facility Device Experience (MAUDE) database from 2009 to 2016.
    Jazayeri MA; Vuddanda V; Turagam MK; Parikh V; Lavu M; Atkins D; Earnest M; Di Biase L; Natale A; Wilber D; Reddy YM; Lakkireddy DR
    J Cardiovasc Electrophysiol; 2018 Jan; 29(1):5-13. PubMed ID: 28988455
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Classification of Health Information Technology Safety Events in a Pediatric Tertiary Care Hospital.
    Khan A; Karavite DJ; Muthu N; Shelov E; Nawab U; Desai B; Luo B
    J Patient Saf; 2023 Jun; 19(4):251-257. PubMed ID: 37094555
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Adverse events involving hallux metatarsophalangeal joint implants: Analysis of the United States Food and Drug Administration data from 2010 to 2018.
    Akoh CC; Chen J; Kadakia R; Park YU; Kim H; Adams SB
    Foot Ankle Surg; 2021 Jun; 27(4):381-388. PubMed ID: 32505511
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Thoracic Endovascular Aortic Repair Adverse Events Reported In The Food And Drug Administration Manufacturer And User Facility Device Experience Database.
    Mansukhani NA; Haleem MS; Eskandari MK
    Med Devices (Auckl); 2019; 12():461-467. PubMed ID: 31814779
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.