553 research outputs found

    Determining Your Stocking Rate

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    Calculating Available Forage

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    Drill Calibration

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    Useful Conversion Factors in Rangeland Management

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    Head and Neck Manifestations of Eosinophilic Granulomatosis with Polyangiitis: A Systematic Review.

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    OBJECTIVE: To conduct the first and only systematic review of the existing literature on head and neck manifestations of eosinophilic granulomatosis with polyangiitis to guide clinical decision making for the otolaryngologist. DATA SOURCES: PubMed, Cochrane Library, Scopus, and LILACS. REVIEW METHODS: A systematic review of the aforementioned sources was conducted per the PRISMA guidelines. RESULTS: From an initial 574 studies, 28 trials and reports were included, accounting for a total of 1175 patients with eosinophilic granulomatosis with polyangiitis. Among clinical and cohort studies, 48.0% to 96.0% of all included patients presented with head and neck manifestations. In a distinct group of patients detailed in case reports describing patients presenting with head and neck manifestations, patients on average fulfilled 4.6 diagnostic criteria per the American College of Rheumatology. Furthermore, 95.8% of reported cases were responsive to steroids, and 60% required additional therapy. CONCLUSION: Otolaryngologists are in a unique position for the early diagnosis and prevention of late complications of eosinophilic granulomatosis with polyangiitis. The American College of Rheumatology criteria should be relied on in the diagnostic workup. Close surveillance of these patients in a multidisciplinary fashion and with baseline complete blood counts, chest radiographs, and autoimmune laboratory tests is often necessary. Such patients with head and neck manifestations of the disease are nearly always responsive to steroids and often require additional immunosuppressive therapy or surgical intervention in cases of cranial neuropathies, temporal bone involvement, and refractory symptoms

    Seedbed Preparation

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    Biphenotypic Sinonasal Sarcoma-Case Report and Review of Clinicopathological Features and Diagnostic Modalities.

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    Background Biphenotypic sinonasal sarcoma is a recently described malignancy showing dual differentiation with both myogenic and neural elements. Due to its histologic similarities to other sinonasal malignancies, it is a diagnostic challenge. Objective The main purpose of this article is to report a case of biphenotypic sinonasal sarcoma and to consolidate data and provide a comprehensive review regarding pathological differences between biphenotypic sarcoma and other sinonasal malignancies and diagnostic modalities used for biphenotypic sarcoma. Material and Methods A systematic review of all cases of biphenotypic sinonasal sarcoma was performed using electronic databases (PubMed and Medline). Data collected included age, gender, symptoms, sub-site of origin, immunophenotyping, metastasis, recurrence, treatment, duration of follow-up, and survival outcomes. Results Ninety-five cases of biphenotypic sarcoma were found with mean age at diagnosis of 52.36 years (range, 24-87 years). Female to male ratio was 2.27:1. Extra-sinonasal extension was present in 28%. Immunophenotyping revealed that S-100 and SMA (smooth muscle actin) were consistently positive, while SOX-10 was consistently negative. PAX3-MAML3 fusion [t (2; 4) (q35; q31.1)] was the most common genetic rearrangement. Surgical excision with or without adjuvant radiotherapy was the most frequent treatment modality used. Recurrence was observed in 32% of cases with follow-up. None of the cases reported metastasis. Three patients had died at the time of publication that included one case with intracranial extension. Conclusion Biphenotypic sarcoma is distinct sinonasal malignancy with unique clinicopathological features. Testing involving a battery of myogenic and neural immunomarkers is essential for diagnostic confirmation and is a clinically useful endeavor when clinical suspicion is high. © 2019 Georg Thieme Verlag KG Stuttgart. New York

    South Puget Sound dissolved oxygen study: water quality model calibration and scenarios

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    Portions of South and Central Puget Sound are on the Clean Water Act Section 303(d) list of impaired waters because observed dissolved oxygen measurements do not meet the Washington State water quality standards. Human sources of nutrients can increase algae growth, which can decrease oxygen as the additional organic matter decays. Low oxygen can impair fish and other marine life. Computer modeling tools are needed to isolate the impacts of human contributions. The purpose of this study is to identify how much human contributions are contributing to low dissolved oxygen (DO) in South Puget Sound. Previous reports summarize data collection, nutrient load estimates for marine point sources and watershed inflows that include point and nonpoint sources, and the circulation model. This report summarizes the calibration and application of the water quality model to isolate the impacts from groups of sources. The model predicts the regional and seasonal patterns of chlorophyll, DO, and nitrogen throughout South and Central Puget Sound. The model predicts that internal (inside the model domain) current human nutrient loads from marine point sources and watersheds as well as external (north of model domain) current anthropogenic loads are causing DO to decline by as much as 0.4 mg/L in portions of Totten, Eld, Budd, Carr, and Case inlets, and East Passage, which violates the standards. There are not violations across the entire South or Central Puget Sound. While keeping the external anthropogenic load constant, internal marine point sources exert a greater impact than human sources within watershed inflows. Reducing the internal human nutrient load would decrease the magnitude and extent of DO depletion. Additional scenarios are needed to isolate the effects of individual sources

    Range Judging In Utah

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