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  1. 23961
    “…VIRTUAL SLIDES: The virtual slide(s) for this article can be found here: http://www.diagnosticpathology.diagnomx.eu/vs/1348836442160205.…”
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  2. 23962
  3. 23963
    “…BACKGROUND: Combination of the inhaled long-acting muscarinic antagonist umeclidinium (UMEC; GSK573719) with the long-acting β(2)-agonist vilanterol (VI) is an approved maintenance treatment for COPD in the US and EU. We compared the efficacy and safety of UMEC/VI with placebo in patients with COPD of Asian ancestry. …”
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  4. 23964
    “…This would allow an analytical sensitivity (AS) of 0.0001 fibres per millilitre (f ml(−1)) to be achieved, which is 1000 times lower than the EU and UK workplace control limit of 0.1 f ml(−1). …”
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  5. 23965
    “…BACKGROUND: Fluticasone furoate (FF)/vilanterol (VI) is a once daily (OD) inhaled corticosteroid/long-acting β(2)-agonist combination asthma therapy approved in Japan and the EU. FF/VI efficacy and safety data from asthma studies including patients in East Asia were evaluated to assess ethnic sensitivity. …”
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  6. 23966
    “…We searched (to 2 November 2015) CENTRAL, Medline, Embase, CINAHL, PubMed, LILACS, NHSBT Transfusion Evidence Library, ClinicalTrials.gov, WHO International Clinical Trials Registry Platform, ISRCTN Register, and EU Clinical Trials Register. Authors were contacted for data whenever possible. …”
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  7. 23967
    “…METHODS: Eurolight was a cross-sectional survey sampling from the adult populations (18–65 years) of 10 EU countries. We used data from six. The questionnaire included headache-diagnostic questions based on ICHD-II, the Headache-Attributed Lost Time (HALT) questionnaire, and HADS for depression and anxiety. …”
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  8. 23968
    “…Although limited by a small sample size, our study represents a first attempt at analysing such data in six EU countries. Our findings should encourage the conduction of further studies on this topic, long-term and large sample-sized studies, ideally conducted in the general population.…”
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  9. 23969
    “…TRIAL REGISTRATION: This trial is registered at ClinicalTrials.gov (NCT01483144; November 21, 2011) and the EU Clinical Trials Register(EudraCT 2012-000427-41; May 15, 2014). …”
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  10. 23970
  11. 23971
    “…CONCLUSIONS: This study of TP300 showed good drug tolerability but it failed to demonstrate sufficient efficacy as measured by radiological response. TRIAL REGISTRATION: EU-CTR 2009-012097-12 2009-09-03…”
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  12. 23972
    “…Six agritourisms outbuilding slaughterhouses – EU-approved – were investigated. General and hygiene requirements of outbuilding slaughterhouses and animal welfare indicators of 68 piglets and 5 finishing pigs were evaluated by mean of a checklist. …”
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  13. 23973
    “…TRIAL REGISTRATION: EWO-ISO-2014/1, EudraCT 2014-001863-11; Date of registration: 29 APR 2014; Detail information web link: https://www.clinicaltrialsregister.eu/ctr-search/trial/2014-001863-11/results ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12879-016-1965-5) contains supplementary material, which is available to authorized users.…”
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  14. 23974
  15. 23975
    “…BACKGROUND AND OBJECTIVE: Once-daily oral fingolimod is approved in the EU as escalation treatment for adult patients with highly active relapsing multiple sclerosis (MS). …”
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  16. 23976
    “…CONCLUSIONS: The prevalence of LA-MRSA-positive pig farms in Poland has increased considerably since 2008, when the first MRSA EU baseline survey was conducted in Europe. On Polish pig farms CC398 of the animal clade predominates, this being also reflected in the prevalence of CC398 nasal carriage in farmers and veterinarians. …”
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  17. 23977
    “…The {Fe(4)Ln(2)}-type compounds [Fe(4)Ln(2)(O(2)CCMe(3))(6)(N(3))(4)(Htea)(4)]·2(EtOH), Ln = Dy (1a), Er (1b), Ho (1c); [Fe(4)Tb(2)(O(2)CCMe(3))(6)(N(3))(4)(Htea)(4)] (1d); [Fe(4)Ln(2)(O(2)CCMe(3))(6)(N(3))(4)(Htea)(4)]·2(CH(2)Cl(2)), Ln = Dy (2a), Er (2b); [Fe(4)Ln(2)(O(2)CCMe(3))(4)(N(3))(6)(Htea)(4)]·2(EtOH)·2(CH(2)Cl(2)), Ln = Dy (3a), Er (3b) and the {Fe(18)M(6)}-type compounds [Fe(18)M(6)(O(2)CCHMe(2))(12)(Htea)(18)(tea)(6)(N(3))(6)]·n(solvent), M = Dy (4, 4a), Gd (5), Tb (6), Ho (7), Sm (8), Eu (9), and Y (10) form in ca. 20–40% yields in direct reaction of trinuclear Fe(III) pivalate or isobutyrate clusters, lanthanide/yttrium nitrates, and bridging triethanolamine (H(3)tea) and azide ligands in different solvents: EtOH for the smaller {Fe(4)Ln(2)} wheels and MeOH/MeCN or MeOH/EtOH for the larger {Fe(18)M(6)} wheels. …”
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  18. 23978
  19. 23979
    “…METHODS: Data were collected from a questionnaire survey of nurses in a sample of English hospitals, conducted as part of the RN4CAST study, an EU 7(th) Framework funded study. The sample comprised 31 NHS acute hospital Trusts from 401 wards, in 46 acute hospital sites. …”
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  20. 23980
    “…In patients with mild to severe gastrointestinal problems, prucalopride may be effective in treating dismotility symptoms, increasing the number of complete bowel movements and improving bowel transit, reducing reflux disease and bloating. TRIAL REGISTRATION: EU Clinical Trial Registry, EudraCT2012-005348-92. …”
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