Showing 21 - 40 results of 79 for search '"USA Track ', query time: 0.06s Refine Results
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    Efficacy and Safety of Cataract Surgery Combined with Ab Interno Canaloplasty and Micro-Trabecular Bypass Stent Surgery in Open-Angle Glaucoma by Porter MS, Flowers A, Wood BP, Gallardo MJ

    Published 2025-02-01
    “…Matthew S Porter,1 Addie Flowers,1 Brandon P Wood,1 Mark J Gallardo2 1Texas Tech University Health Sciences Center School of Medicine, Lubbock, TX, USA; 2El Paso Eye Surgeons, El Paso, TX, USACorrespondence: Matthew S Porter, Department of Ophthalmology and Visual Sciences, Texas Tech University Health Sciences School of Medicine, 3601 4th St, Lubbock, TX, 79430, USA, Tel +1-806-742-2011, Email matt.porter@ttuhsc.eduPurpose: To evaluate the effectiveness of canaloplasty via an ab-interno technique using the iTrack (Nova Eye Medical, Fremont, USA) combined with microtrabecular bypass stent surgery with the Hydrus microstent (Ivantis, Inc, Irvine, CA) following cataract surgery (CE) in patients with primary open-angle glaucoma (POAG).Methods: A retrospective, two-center, case series of 51 POAG eyes that underwent phacoemulsification followed by canaloplasty combined with microtrabecular bypass stent surgery. …”
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    Improving 1-year liver allograft survival hazard ratios by Resham­ Ramkissoon, Ashley Rosier, Savitha Iyengar, Timucin Taner, William Sanchez

    Published 2025-01-01
    “…Background The Scientific Registry for Transplant Recipients (SRTR) publishes outcomes of all transplant centres in the USA two times a year. The outcomes are publicly available and used by insurance payers and patients to assess the performance of a programme. …”
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    Association of expedited review programmes with postmarketing safety events of new drugs approved by the US food and drug administration between 2007 and 2017 by Bao Liu, Xingyue Zhu

    Published 2022-07-01
    “…Objective To explore the associations between the risks of postmarketing safety events of new drugs and the four expedited programmes of priority review, accelerated approval, fast track and breakthrough therapy established by the US Food and Drug Administration (FDA); and to investigate whether multiple uses of expedited programmes, and the combinations of expedited programmes with orphan designation, were relevant to different safety profiles.Design Cohort study.Setting USA.Participants All new drugs approved by the FDA between 1 January 2007 and 31 December 2017, followed up until 10 April 2021.Outcome measures Safety events included safety-related withdrawal, new boxed warning, drug safety communication, postapproval risk evaluation mitigation strategy and safety-related labelling changes. …”
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    Experimental gillnet study to inform future large fish monitoring in the San Francisco Estuary by Dylan Keating Stompe, James A. Hobbs

    Published 2024-12-01
    “…As a result, the adult life stage of many SFE fish species is not completely sampled, representing a shortcoming in our ability to track changes in age-structured regional fish assemblages. …”
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