11 research outputs found

    Isokinetic Evaluation of the Elbow Joint at 45° and 80° of Shoulder Abduction

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    Since Hislop and Thistle published the first reports on isokinetic exercise, a lot of progress has been made towards the use of isokinetic exercise and isokinetic evaluation of muscle and joint performance in sports and orthopedic physical therapy. Cybex II+ with the Cybex Data Reduction Computer is one of the most widely used isokinetic systems for research and rehabilitation purposes. There are more than 500 published works describing the use of Cybex in various applications, Many investigations have used the Cybex isokinetic system to develop normative data on torque and work measurements of various muscle groups. Normative data are valuable to clinicians in the evaluation of the severity of an injury in terms of muscle performance deficits. In addition, such data provide physical therapists with objective data in setting rehabilitation goals, and enabling sports medicine experts to identify functional deficiencies during screening of athletes. There is a limited number of published works that have developed normative data for elbow flexor and extensor muscle groups. While there is some information about peak torque and agonist-antagonist ratios, minimal information is available about torque acceleration energy, work endurance ratios, average power and flexion-extension total work ratios. The purpose of this study was to examine the effects of 450 and 800 of shoulder abduction on torque and work measurements of the elbow joint. In addition, normative data for elbow flexion and extension at both arm positions (testing positions suggested by Cybex) were developed

    Effects of increased paternal age on sperm quality, reproductive outcome and associated epigenetic risks to offspring

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    Endoscopic Treatment of Posterior Ankle Impingement Secondary to Os Trigonum in Recreational Athletes

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    Background: The os trigonum (OT)—the most common accessory bone of the foot—although usually asymptomatic, may cause posterior ankle impingement syndrome (PAIS), which may be a severely debilitating problem for recreational or competitive athletes. The aim of the present study was to evaluate effectiveness of posterior ankle arthroscopy and to assess the outcome in the treatment of PAIS secondary to OT impingement or OT fractures within a group of young athletes and their return to previous sports level. Methods: From 2011 to 2018, a retrospective review of 81 recreational athletes of mean age 27.8 years was performed. All patients were diagnosed with PAIS due to OT pathology and were operated on endoscopically with resection of the OT. Pre- and postoperative clinical evaluation were performed at 3 months, 1 year, and 2 years based on visual analog scale (VAS), ankle range of motion (ROM), American Orthopaedic Foot & Ankle Society (AOFAS) hindfoot score, and the Foot & Ankle Disability Index (FADI) scores, in a follow-up of at least 2 years. Results: VAS score was significantly improved from an average of 7.5 (5-9) preoperatively to 1.9 (1-3) at 3 months postoperatively and to 0.6 (0-2) and 0.3 (0 -1) at 1 and 2 years postoperatively. Ankle ROM was significantly improved from an average of 24.8 (10-35) preoperatively to 58.0 (50-65) at 3 months postoperatively and to 64.0 (50-65) at 1 year and 64.7 (60-65) at 2 years postoperatively. AOFAS and FADI scores were significantly improved from 39.4 (18-55) and 49.7 (42.3-62.5) preoperatively to 85.2 (74-89) and 87.3 (81.7-88.5) postoperatively at 3 months to 97.7 (85-100) and 97.9 (93.3-100) postoperatively at 1 year, respectively (P <.001). Only 5 patients dropped to a lower activity level. There were 5 complications (4 transient). Conclusion: Endoscopic treatment of PAIS due to OT pathology demonstrated excellent results. Posterior ankle arthroscopy was an effective treatment and allowed for a prompt return to a high activity level of their athletic performance. Level of Evidence: Level IV, therapeutic study / retrospective case series. © The Author(s) 2020

    Response of Plasma-Polymerized Hexamethyldisiloxane Films to Aqueous Environments

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    Thin plasma polymer films were deposited in hexamethyldisiloxane (HMDSO) and HMDSO/O2 low-pressure discharges and their chemical structures analyzed using infrared (IR) spectroscopy and neutron reflectometry (NR). The (plasma-polymerized) ppHMDSO film exhibits hydrophobic, poly(dimethylsiloxane)-like properties, while the retention of carbon groups is reduced by O2 addition, yielding a more inorganic, hydrophilic ppSiOx film. Both films show a minor (vertical) density gradient perpendicular to the substrate, where the exposed film surface seems to be more oxidized, indicating oxidative aging reactions upon contact with air. The hydration and water uptake abilities of the films in aqueous environments were investigated in humid environments using ellipsometry, NR in D2O, and multiple transmission-reflection IR measurements after equilibration of the films in water.ISSN:0743-7463ISSN:1520-582

    Essential role of the Cdk2 activator RingoA in meiotic telomere tethering to the nuclear envelope

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    Cyclin-dependent kinases (CDKs) play key roles in cell cycle regulation. Genetic analysis in mice has revealed an essential role for Cdk2 in meiosis, which renders Cdk2 knockout (KO) mice sterile. Here we show that mice deficient in RingoA, an atypical activator of Cdk1 and Cdk2 that has no amino acid sequence homology to cyclins, are sterile and display meiotic defects virtually identical to those observed in Cdk2 KO mice including non-homologous chromosome pairing, unrepaired double-strand breaks, undetectable sex-body and pachytene arrest. Interestingly, RingoA is required for Cdk2 targeting to telomeres and RingoA KO spermatocytes display severely affected telomere tethering as well as impaired distribution of Sun1, a protein essential for the attachment of telomeres to the nuclear envelope. Our results identify RingoA as an important activator of Cdk2 at meiotic telomeres, and provide genetic evidence for a physiological function of mammalian Cdk2 that is not dependent on cyclins
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