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- Publication . Article . 2003Open AccessAuthors:Schellenberg, D; Armstrong Schellenberg, J R M; Mushi, A; Savigny de, D; Mgalula, L; Mbuya, C; Victoria, C.G.;Schellenberg, D; Armstrong Schellenberg, J R M; Mushi, A; Savigny de, D; Mgalula, L; Mbuya, C; Victoria, C.G.;Country: Tanzania (United Republic of)
Objective was to document the prevalence, age-distribution, and risk factors for anaemia in Tanzanian children less than 5 years old,thereby assisting in the development of effective strategies for controlling anaemia. Cluster sampling was used to identify 2417 households at random from four contiguous districts in south-eastern United Republic of Tanzania in mid-1999. Data on various social and medical parameters were collected and analysed. Blood haemoglobin concentrations (Hb) were available for 1979 of the 2131 (93%) children identified and ranged from 1.7 to 18.6 g/dl. Overall, 87% (1722) of children had an Hb <11 g/dl, 39% (775) had an Hb <8 g/dl and 3% (65) had an Hb <5 g/dl. The highest prevalence of anaemia of all three levels was in children aged 6–11 months, of whom 10% (22/226) had an Hb <5 g/dl. However, the prevalence of anaemia was already high in children aged 1–5 months (85% had an Hb <11 g/dl, 42% had an Hb <8 g/dl, and 6% had an Hb <5 g/dl). Anaemia was usually asymptomatic and when symptoms arose they were nonspecific and rarely identified as a serious illness by the care provider. A recent history of treatment with antimalarials and iron was rare. Compliance with vaccinations delivered through the Expanded Programme of Immunization (EPI) was 82% and was notassociated with risk of anaemia. Anaemia is extremely common in south-eastern United Republic of Tanzania, even in very young infants. Further implementation of the Integrated Management of Childhood Illness algorithm should improve the case management of anaemia. However, the asymptomatic nature of most episodes of anaemia highlights the need for preventive strategies. The EPI has good coverage of the target population and it may be an appropriate channel for delivering tools for controlling anaemia and malaria.
- Publication . Article . Other literature type . 2019Open AccessAuthors:Jürgen Dengler; Thomas J. Matthews; Manuel J. Steinbauer; Sebastian Wolfrum; Steffen Boch; Alessandro Chiarucci; Timo Conradi; Iwona Dembicz; Corrado Marcenò; Itziar García-Mijangos; +35 moreJürgen Dengler; Thomas J. Matthews; Manuel J. Steinbauer; Sebastian Wolfrum; Steffen Boch; Alessandro Chiarucci; Timo Conradi; Iwona Dembicz; Corrado Marcenò; Itziar García-Mijangos; Arkadiusz Nowak; David Storch; Werner Ulrich; Juan Antonio Campos; Laura Cancellieri; Marta Carboni; Giampiero Ciaschetti; Pieter De Frenne; Jiri Dolezal; Christian Dolnik; Franz Essl; Edy Fantinato; Goffredo Filibeck; John-Arvid Grytnes; Riccardo Guarino; Behlül Güler; Monika Janišová; Ewelina Klichowska; Łukasz Kozub; Anna Kuzemko; Michael Manthey; Anne Mimet; Alireza Naqinezhad; Christian Pedersen; Robert K. Peet; Vincent Pellissier; Remigiusz Pielech; Giovanna Potenza; Leonardo Rosati; Massimo Terzi; Orsolya Valkó; Denys Vynokurov; Hannah J. White; Manuela Winkler; Idoia Biurrun;
handle: 1854/LU-8649698 , 1956/22574 , 11104/0312153 , 10400.3/5794 , 11590/363767
Publisher: WileyCountries: Italy, Belgium, Italy, Portugal, Italy, Germany, Spain, Poland, Norway, Switzerland ...Aim Species-area relationships (SARs) are fundamental scaling laws in ecology although their shape is still disputed. At larger areas, power laws best represent SARs. Yet, it remains unclear whether SARs follow other shapes at finer spatial grains in continuous vegetation. We asked which function describes SARs best at small grains and explored how sampling methodology or the environment influence SAR shape. Location Palaearctic grasslands and other non-forested habitats. Taxa Vascular plants, bryophytes and lichens. Methods We used the GrassPlot database, containing standardized vegetation-plot data from vascular plants, bryophytes and lichens spanning a wide range of grassland types throughout the Palaearctic and including 2,057 nested-plot series with at least seven grain sizes ranging from 1 cm(2) to 1,024 m(2). Using nonlinear regression, we assessed the appropriateness of different SAR functions (power, power quadratic, power breakpoint, logarithmic, Michaelis-Menten). Based on AICc, we tested whether the ranking of functions differed among taxonomic groups, methodological settings, biomes or vegetation types. Results The power function was the most suitable function across the studied taxonomic groups. The superiority of this function increased from lichens to bryophytes to vascular plants to all three taxonomic groups together. The sampling method was highly influential as rooted presence sampling decreased the performance of the power function. By contrast, biome and vegetation type had practically no influence on the superiority of the power law. Main conclusions We conclude that SARs of sessile organisms at smaller spatial grains are best approximated by a power function. This coincides with several other comprehensive studies of SARs at different grain sizes and for different taxa, thus supporting the general appropriateness of the power function for modelling species diversity over a wide range of grain sizes. The poor performance of the Michaelis-Menten function demonstrates that richness within plant communities generally does not approach any saturation, thus calling into question the concept of minimal area. We thank all vegetation scientists who carefully collected multi‐ scale plant diversity data from Palaearctic Grasslands available in GrassPlot. The Eurasian Dry Grassland Group (EDGG) and the International Association for Vegetation Science (IAVS) sup‐ ported the EDGG Field Workshops, which generated a core part of the GrassPlot data. The Bavarian Research Alliance (grant BayIntAn_UBT_2017_58) and the Bayreuth Center of Ecology and Environmental Research (BayCEER) funded the initial GrassPlot workshop during which the database was established and the cur‐ rent paper was initiated. A.N. acknowledges support by the Center for International Scientific Studies and Collaboration (CISSC), Iran. C.M., I.B., I.G.‐M and J.A.C. were funded by the Basque Government (IT936‐16). D.V. carried out the research supported by a grant of the State Fund For Fundamental Research Ф83/53427. G.F. carried out the research in the frame of the MIUR initiative ‘Department of excellence' (Law 232/2016). I.D. was supported by the Polish National Science Centre (grant DEC‐2013/09/N/NZ8/03234). J.Do. was supported by the Czech Science Foundation (GA 17‐19376S). M.J. was supported by grant by Slovak Academy of Sciences (VEGA 02/0095/19). W.U. ac‐ knowledges support from the Polish National Science Centre (grant 2017/27/B/NZ8/00316).
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You have already added works in your ORCID record related to the merged Research product. - Publication . Article . Preprint . 2006Open Access EnglishAuthors:M. de Montigny; J. Niederle; A. G. Nikitin;M. de Montigny; J. Niederle; A. G. Nikitin;Project: NSERC
All indecomposable finite-dimensional representations of the homogeneous Galilei group which when restricted to the rotation subgroup are decomposed to spin 0, 1/2 and 1 representations are constructed and classified. These representations are also obtained via contractions of the corresponding representations of the Lorentz group. Finally the obtained representations are used to derive a general Pauli anomalous interaction term and Darwin and spin-orbit couplings of a Galilean particle interacting with an external electric field. 23 pages, 2 tables
Average popularityAverage popularity In bottom 99%Average influencePopularity: Citation-based measure reflecting the current impact.Average influence In bottom 99%Influence: Citation-based measure reflecting the total impact.add Add to ORCIDPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product. - Publication . Article . 2019Open AccessAuthors:Barbara L. Shacklett; Julià Blanco; Lisa B. Hightow-Weidman; Nyaradzo Mgodi; José Alcamí; Susan Buchbinder; Mike Chirenje; Smritee Dabee; Mamadou H. Diallo; Kostyantyn Dumchev; +18 moreBarbara L. Shacklett; Julià Blanco; Lisa B. Hightow-Weidman; Nyaradzo Mgodi; José Alcamí; Susan Buchbinder; Mike Chirenje; Smritee Dabee; Mamadou H. Diallo; Kostyantyn Dumchev; Carolina Herrera; Matthew E Levy; Enrique Martin Gayo; Nigel Aminake Makoah; Kate M. Mitchell; Kenneth K. Mugwanya; Krishnaveni Reddy; Maria Luisa Rodríguez; Marta Rodriguez-Garcia; Chelsea L. Shover; Tripti Shrivastava; Georgia D. Tomaras; Michiel T. van Diepen; Monika Walia; Mitchell Warren; Amapola Manrique; Bargavi Thyagarajan; Tamara Torri;Publisher: Mary Ann Liebert IncCountries: Spain, United States, United KingdomProject: NIH | HIV Research for Preventi... (1R13AI136762-01)
The HIV Research for Prevention (HIVR4P) conference is dedicated to advancing HIV prevention research, responding to a growing consensus that effective and durable prevention will require a combination of approaches as well as unprecedented collaboration among scientists, practitioners, and community workers from different fields and geographic areas. The conference theme in 2018, "From Research to Impact," acknowledged an increasing focus on translation of promising research findings into practical, accessible, and affordable HIV prevention options for those who need them worldwide. HIVR4P 2018 was held in Madrid, Spain, on 21-25 October, with >1,400 participants from 52 countries around the globe, representing all aspects of HIV prevention research and implementation. The program included 137 oral and 610 poster presentations. This article presents a brief summary of highlights from the conference. More detailed information, complete abstracts as well as webcasts and daily Rapporteur summaries may be found on the conference website. Supported by Gilead who provided funding. Gilead has had no input into the content of the materials used at this meeting/conference. No other pharmaceutical company has had input into the content of the materials used at this conference. HIVR4P 2018 was made possible in part by 1 R13 AI136762-01 from the National Institute of Allergy and Infectious Diseases (NIAID). The views expressed in written conference materials or publications and by speakers and moderators do not necessarily reflect the official policies of the Department of Health and Human Services; nor does mention of trade names, commercial practices, or organizations imply endorsement by the U.S. Government. Sí
Average popularityAverage popularity In bottom 99%Average influencePopularity: Citation-based measure reflecting the current impact.Average influence In bottom 99%Influence: Citation-based measure reflecting the total impact.add Add to ORCIDPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product. - Publication . Article . 2021Open Access EnglishAuthors:L. T. Ellis; C. Ah-Peng; G. Aslan; V. A. Bakalin; A. Bergamini; D. A. Callaghan; P. Campisi; F. M. Raimondo; S. S. Choi; J. Csiky; +72 moreL. T. Ellis; C. Ah-Peng; G. Aslan; V. A. Bakalin; A. Bergamini; D. A. Callaghan; P. Campisi; F. M. Raimondo; S. S. Choi; J. Csiky; É. Csikyné Radnai; B. Cykowska-Marzencka; I. V. Czernyadjeva; Yu M. Kalinina; O. M. Afonina; G. Domina; P. Drapela; V. E. Fedosov; E. Fuertes; R. Gabriel; M. Kubová; I. Soares Albergaria; G. Gospodinov; R. Natcheva; A. Graulich; T. Hedderson; E. Hernández-Rodríguez; V. Hugonnot; C. W. Hyun; M. Kırmacı; U. Çatak; S. Kubešová; J. Kučera; C. La Farge; J. Larraín; P. Martin; B. Mufeed; C. N. Manju; K. P. Rajesh; Cs. Németh; J. Nagy; N. Norhazrina; N. Syazwana; S. V. O’Leary; S. J. Park; A. P. Peña-Retes; A. Rimac; A. Alegro; V. Šegota; N. Koletić; N. Vuković; S. Rosadziński; J. A. Rosselló; M. S. Sabovljević; A. D. Sabovljević; A. Schäfer-Verwimp; C. Sérgio; A. V. Shkurko; D. Shyriaieva; V. M. Virchenko; M. Smoczyk; D. Spitale; P. Srivastava; I. Omar; A. K. Asthana; M. Staniaszek-Kik; A. Cienkowska; M.-M. Ștefănuţ; S. Ștefănuţ; G. Tamas; C.-C. Bîrsan; G.-R. Nicoară; M. C. Ion; T. Pócs; G. Kunev; E. I. Troeva; J. van Rooy; P. Wietrzyk-Pełka; M. H. Węgrzyn; G. J. Wolski; D. Bożyk; A. Cienkowska;
handle: 10400.3/6171
Publisher: HAL CCSDCountries: France, Poland, Croatia, France, PortugalProject: EC | INTERACT (262693)Pseudoamblystegium subtile (Hedw.) Vanderp. & Hedenäs. CONTRIBUTORS: R. Gabriel, M. Kubová, C. Sérgio and I. Soares Albergaria. PORTUGAL, AZORES: Terceira Island, Angra do Heroísmo, municipal garden ‘Jardim Duque da Terceira’, 38° 39′ 24.0′′N, 27°13′ 05.99′′W, 31 m a.s.l, on the base of a shrub, in acidic conditions, 7 April 2017, leg. Michaela Kubová s.n. (AZU). A new understanding of the pleurocarpous moss species Pseudoamblystegium subtile was proposed by Vanderpoorten and Hedenäs (2009). The new genus is separated from the other Amblystegiaceae primarily due to its phylogenetic consistency and is characterised by the possession of leaves with a very short nerve, and erect capsules (Vanderpoorten and Hedenäs 2009). (excerpt) info:eu-repo/semantics/publishedVersion
Average popularityAverage popularity In bottom 99%Average influencePopularity: Citation-based measure reflecting the current impact.Average influence In bottom 99%Influence: Citation-based measure reflecting the total impact.add Add to ORCIDPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product. - Publication . Article . 2013Open AccessAuthors:Shakil Ahmed; Peter Leslie Annear; Bouaphat Phonvisay; Chansaly Phommavong; Valeria de Oliveira Cruz; Asmus Hammerich; Bart Jacobs;Shakil Ahmed; Peter Leslie Annear; Bouaphat Phonvisay; Chansaly Phommavong; Valeria de Oliveira Cruz; Asmus Hammerich; Bart Jacobs;Publisher: Elsevier BV
AbstractThere is now widespread acceptance of the universal coverage approach, presented in the 2010 World Health Report. There are more and more voices for the benefit of creating a single national risk pool. Now, a body of literature is emerging on institutional design and organizational practice for universal coverage, related to management of the three health-financing functions: collection, pooling and purchasing. While all countries can move towards universal coverage, lower-income countries face particular challenges, including scarce resources and limited capacity. Recently, the Lao PDR has been preparing options for moving to a single national health insurance scheme. The aim is to combine four different social health protection schemes into a national health insurance authority (NHIA) with a single national fund- and risk-pool. This paper investigates the main institutional and organizational challenges related to the creation of the NHIA. The paper uses a qualitative approach, drawing on the World Health Organization's institutional and Organizational Assessment for Improving and Strengthening health financing (OASIS) conceptual framework for data analysis. Data were collected from a review of key health financing policy documents and from 17 semi-structured key informant interviews. Policy makers and advisors are confronting issues related to institutional arrangements, funding sources for the authority and government support for subsidies to the demand-side health financing schemes. Compulsory membership is proposed, but the means for covering the informal sector have not been resolved. While unification of existing schemes may be the basis for creating a single risk pool, challenges related to administrative capacity and cross-subsidies remain. The example of Lao PDR illustrates the need to include consideration of national context, the sequencing of reforms and the time-scale appropriate for achieving universal coverage.
Average popularityAverage popularity In bottom 99%Average influencePopularity: Citation-based measure reflecting the current impact.Average influence In bottom 99%Influence: Citation-based measure reflecting the total impact.add Add to ORCIDPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product. - Publication . Article . 2016Restricted EnglishAuthors:Gary E. Raskob; Nick van Es; Annelise Segers; Pantep Angchaisuksiri; Doyeun Oh; Zoltán Boda; Roger M. Lyons; Karina Meijer; Ivan Gudz; Jeffrey I. Weitz; +4 moreGary E. Raskob; Nick van Es; Annelise Segers; Pantep Angchaisuksiri; Doyeun Oh; Zoltán Boda; Roger M. Lyons; Karina Meijer; Ivan Gudz; Jeffrey I. Weitz; George Zhang; Hans Lanz; Michele Mercuri; Harry R. Büller;Country: Netherlands
Venous thromboembolism occurs commonly in patients with cancer. Direct oral anticoagulants are non-inferior to conventional anticoagulants for the treatment of venous thromboembolism. We hypothesised that edoxaban, a direct oral inhibitor of activated clotting factor Xa, might be more suitable than conventional anticoagulants in the management of cancer-associated venous thromboembolism. The aim of this study was to assess the efficacy and safety of edoxaban compared with warfarin in a subgroup of patients with cancer enrolled in the Hokusai-VTE trial. We did a prespecified subgroup analysis in August, 2013, and a post-hoc analysis of non-inferiority and safety in March, 2016, of the patients with cancer enrolled in the randomised, double-blind, double-dummy, multicentre, Hokusai-VTE trial done between Jan 28, 2010, and Oct 31, 2012. In this study, patients aged at least 18 years with acute symptomatic deep-vein thrombosis or acute symptomatic pulmonary embolism (with or without deep-vein thrombosis) were assigned to receive edoxaban 60 mg once per day (or 30 mg once per day for patients with a creatinine clearance of 30-50 mL/min, bodyweight <60 kg, or who were receiving concomitant treatment with the P-glycoprotein inhibitors quinidine or verapamil) or warfarin (dose adjusted to maintain the international normalised ratio between 2·0 and 3·0) or placebos for either group for at least 3 months up to 12 months. All patients received initial therapy with open-label enoxaparin or unfractionated heparin for at least 5 days. Edoxoban (or placebo) was started after discontinuation of initial heparin; warfarin (or placebo) started concurrently with the study regimen of heparin. In our analysis we examined data for a subgroup of these patients who had a history of cancer or who had been categorised as having active cancer by the study physician at the time of enrolment. Additionally, all patients with a history of cancer were reviewed post hoc and categorised according to the presence or absence of active cancer. The primary efficacy outcome was the proportion of these patients with symptomatic recurrent venous thromboembolism during the 12-month study period, analysed in the modified intention-to-treat population, with an upper limit of the CI for the hazard ratio (HR) of 1·5. The principal safety outcome was the proportion of patients who had clinically relevant bleeding in the population of patients who received at least one dose of the study drug. This study is registered with ClinicalTrials.gov, number NCT00986154. Of 771 patients with cancer enrolled in the trial, 378 were assigned to edoxaban and 393 to warfarin. Recurrent venous thromboembolism occurred in 14 (4%) of 378 patients given edoxaban and in 28 (7%) of 393 patients given warfarin (hazard ratio [HR] 0·53, 95% CI 0·28-1·00; p=0·0007). The upper limit of this 95% CI did not exceed the non-inferiority margin of 1·5 that was prespecified for the trial. Clinically relevant bleeding (major or non-major) occurred in 47 (12%) of 378 patients who received edoxaban and in 74 (19%) of 393 patients who received warfarin; HR for clinically relevant bleeding 0·64, 95% CI 0·45-0·92; p=0·017. Major bleeding occurred in ten (3%) of 378 patients with a history of cancer who received edoxaban and in 13 (3%) of 393 who received warfarin (HR 0·80, 95% CI 0·35-1·83). Edoxaban might be as effective as warfarin for the treatment of patients with cancer with venous thromboembolism, and with less clinically relevant bleeding. Additional clinical trials of edoxaban versus low-molecular-weight heparin for the treatment of venous thromboembolism in patients with cancer are warranted. Daiichi Sankyo
Average popularityAverage popularity In bottom 99%Average influencePopularity: Citation-based measure reflecting the current impact.Average influence In bottom 99%Influence: Citation-based measure reflecting the total impact.add Add to ORCIDPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product. - Publication . Article . 2020Open AccessAuthors:Robert C. Reiner; Paulina A. Lindstedt; Brigette F. Blacker; Lucas Earl; Sandra B. Munro; Lucas Guimarães Abreu; Dilaram Acharya; Maryam Adabi; Rufus A. Adedoyin; Victor Adekanmbi; +242 moreRobert C. Reiner; Paulina A. Lindstedt; Brigette F. Blacker; Lucas Earl; Sandra B. Munro; Lucas Guimarães Abreu; Dilaram Acharya; Maryam Adabi; Rufus A. Adedoyin; Victor Adekanmbi; Beyene Meressa Adhena; Mohsen Afarideh; Keivan Ahmadi; Rushdia Ahmed; Olufemi Ajumobi; Ali S. Akanda; Turki Alanzi; Vahid Alipour; Ali Almasi; Hesham M. Al-Mekhlafi; Azmeraw T. Amare; Catalina Liliana Andrei; Masresha Tessema Anegago; Fereshteh Ansari; Carl Abelardo T. Antonio; Jalal Arabloo; Afsaneh Arzani; Alebachew Fasil Ashagre; Suleman Atique; Sachin R Atre; Getinet Ayano; Senthilkumar Balakrishnan; Maciej Banach; Aleksandra Barac; Quique Bassat; Mohsen Bayati; Masoud Behzadifar; Meysam Behzadifar; Yibeltal Alemu Bekele; Derrick A Bennett; Krittika Bhattacharyya; Suraj Bhattarai; Ali Bijani; Boris Bikbov; Somayeh Bohlouli; Sharath Burugina Nagaraja; Devasahayam J. Christopher; Vera Marisa Costa; Lalit Dandona; Rakhi Dandona; Claudio Alberto Davila; Nicole Davis Weaver; Jan-Walter De Neve; Asmamaw Bizuneh Demis; Gebre Teklemariam Demoz; Kebede Deribe; Getenet Dessie; Preeti Dhillon; Meghnath Dhimal; Christiane Dolecek; Manisha Dubey; Susanna Dunachie; Andre Rodrigues Duraes; Maha El Tantawi; Shymaa Enany; Aklilu Endalamaw; Alireza Esteghamati; Mohammad Fareed; Andrea Farioli; André Faro; Hossein Farzam; Ali Akbar Fazaeli; Eduarda Fernandes; Joel M. Francis; Joseph Frostad; Gebreamlak Gebremedhn Gebremeskel; Kebede Embaye Gezae; Paramjit Gill; Ayman Grada; Yuming Guo; Rahul Gupta; Nima Hafezi-Nejad; Arvin Haj-Mirzaian; Arya Haj-Mirzaian; Brian J. Hall; Demelash Woldeyohannes Handiso; Hamidreza Haririan; Ninuk Hariyani; Ahmed I. Hasaballah; Amir Hasanzadeh; Hadi Hassankhani; Claudiu Herteliu; Chi Linh Hoang; Naznin Hossain; Mowafa Househ; Ayesha Humayun; Syed Ather Hussain; Leeberk Raja Inbaraj; Seyed Sina Naghibi Irvani; Chinwe Juliana Iwu; Nader Jafari Balalami; Ravi Prakash Jha; Vivekanand Jha; John S. Ji; Peng Jia; Jost B. Jonas; Zubair Kabir; Behzad Karami Matin; André Karch; Surendra Karki; Amir Kasaeian; Gebremicheal Gebreslassie Kasahun; Yousef Khader; Morteza Abdullatif Khafaie; Nauman Khalid; Ali Talha Khalil; Khaled Khatab; Aliasghar Ahmad Kiadaliri; Yun Jin Kim; Adnan Kisa; Niranjan Kissoon; Margaret Kosek; Kewal Krishan; G Anil Kumar; Pushpendra Kumar; Dian Kusuma; Van C. Lansingh; Savita Lasrado; Tsegaye Lolaso Lenjebo; Shanshan Li; Shai Linn; Platon D. Lopukhov; Deborah Carvalho Malta; Farzad Manafi; Navid Manafi; Ana Laura Manda; Francisco Rogerlandio Martins-Melo; Manu Raj Mathur; Colm McAlinden; Gebrekiros Gebremichael Meles; Ritesh G. Menezes; Bartosz Miazgowski; Kebadnew Mulatu Mihretie; Edward J Mills; Parvaneh Mirabi; Erkin M. Mirrakhimov; Amjad Mohamadi-Bolbanabad; Dara K. Mohammad; Aso Mohammad Darwesh; Jemal Abdu Mohammed; Shafiu Mohammed; Farnam Mohebi; Lorenzo Monasta; Yoshan Moodley; Masoud Moradi; Maziar Moradi-Lakeh; Seyyed Meysam Mousavi; Miliva Mozaffor; Gudlavalleti Vs Murthy; Vinay Nangia; Javad Nazari; Duduzile Ndwandwe; Quynh Anh P. Nguyen; Dabere Nigatu; Dina Nur Anggraini Ningrum; Marzieh Nojomi; Andrew T Olagunju; Ahmed Omar Bali; Jagadish Rao Padubidri; Adrian Pana; Tahereh Pashaei; Sanghamitra Pati; Veincent Christian Filipino Pepito; Alexandre C. Pereira; Norberto Perico; Konrad Pesudovs; David M. Pigott; Mohammad Rabiee; Navid Rabiee; Fakher Rahim; Vafa Rahimi-Movaghar; Muhammad Aziz Rahman; Fatemeh Rajati; Chhabi Lal Ranabhat; Davide Rasella; Salman Rawaf; Andre M. N. Renzaho; Melese Abate Reta; Ana Isabel Ribeiro; Carlos Miguel Rios González; Maria Jesus Rios-Blancas; Luca Ronfani; Ali Rostami; Enrico Rubagotti; Rajesh Sagar; Nasir Salam; Farkhonde Salehi; Saleh Salehi Zahabi; Yahya Salimi; Hamideh Salimzadeh; Itamar S. Santos; Alyssa N. Sbarra; Lauren E. Schaeffer; Hosein Shabaninejad; Amira Shaheen; Masood Ali Shaikh; Ali S. Shalash; Seifadin Ahmed Shallo; Mehran Shams-Beyranvand; MohammadBagher Shamsi; Muki Shey; Jae Il Shin; Rahman Shiri; Reza Shirkoohi; Si Si; Narinder Pal Singh; Malede Mequanent Sisay; Eirini Skiadaresi; Anton Sokhan; Moslem Soofi; Muluken Bekele Sorrie; Ireneous N. Soyiri; Hafiz Ansar Rasul Suleria; Koku Sisay Tamirat; Nuno Taveira; Bineyam Taye; Mohamad-Hani Temsah; Berhe Etsay Tesfay; Fisaha Haile Tesfay; Kavumpurathu Raman Thankappan; Sathish Thirunavukkarasu; Nihal Thomas; Irfan Ullah; Sahel Valadan Tahbaz; Santosh Varughese; Sebastian Vollmer; Fiseha Wadilo Wada; Yasir Waheed; Taweewat Wiangkham; Tissa Wijeratne; Ali Yadollahpour; Seyed Hossein Yahyazadeh Jabbari; Tomohide Yamada; Mehdi Yaseri; Alex Yeshaneh; Ebrahim M Yimer; Engida Yisma; Mohammad Zamani; Hamed Zandian; Dongyu Zhang; Yunquan Zhang; Sanjay Zodpey;Publisher: Elsevier BV
Reiner RC Jr, Hay SI. Mapping geographical inequalities in childhood diarrhoeal morbidity and mortality in low-income and middle-income countries, 2000–17: analysis for the Global Burden of Disease Study 2017. Lancet 2020; 395: 1779–801—In this Article, the author byline has been amended to Local Burden of Disease Diarrhoea Collaborators. This correction has been made to the online version as of June 4, 2020, and the printed version is correct. © 2020 Elsevier Ltd
add Add to ORCIDPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product. - Publication . Article . 2020Open Access EnglishAuthors:Mykola Beshley; Natalia Kryvinska; Marian Seliuchenko; Halyna Beshley; Elhadi M. Shakshuki; Ansar-Ul-Haque Yasar;Mykola Beshley; Natalia Kryvinska; Marian Seliuchenko; Halyna Beshley; Elhadi M. Shakshuki; Ansar-Ul-Haque Yasar;Publisher: MDPI AGCountries: Belgium, Austria
This paper proposes a modified architecture of the Long-Term Evolution (LTE) mobile network to provide services for the Internet of Things (IoT). This is achieved by allocating a narrow bandwidth and transferring the scheduling functions from the eNodeB base station to an NB-IoT controller. A method for allocating uplink and downlink resources of the LTE/NB-IoT hybrid technology is applied to ensure the Quality of Service (QoS) from end-to-end. This method considers scheduling traffic/resources on the NB-IoT controller, which allows eNodeB planning to remain unchanged. This paper also proposes a prioritization approach within the IoT traffic to provide End-to-End (E2E) QoS in the integrated LTE/NB-IoT network. Further, we develop &ldquo management algorithms for the IoT traffic prioritization. To demonstrate the feasibility of our approach, we performed a number of experiments using simulations. We concluded that our proposed approach ensures high end-to-end QoS of the real-time traffic by reducing the average end-to-end transmission delay. smart queue&rdquo
Average popularityAverage popularity In bottom 99%Average influencePopularity: Citation-based measure reflecting the current impact.Average influence In bottom 99%Influence: Citation-based measure reflecting the total impact.add Add to ORCIDPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product. - Publication . Article . Preprint . 2018 . Embargo End Date: 01 Jan 2018Open AccessAuthors:Anne MacKay; Alexander Melnikov; Yuliya Mishura;Anne MacKay; Alexander Melnikov; Yuliya Mishura;Publisher: arXivProject: NSERC
In this paper, we investigate two-sided bounds for the small ball probability of a mixed fractional Brownian motion with a general deterministic trend function, in terms of respective small ball probability of a mixed fractional Brownian motion without trend. To maximize the lower bound, we consider various ways to split the trend function between the components of the mixed fractional Brownian motion for the application of Girsanov theorem, and we show that the optimal split is the solution of a Fredholm integral equation. We find that the upper bound for the probability is also a function of this optimal split. The asymptotic behaviour of the probability as the ball becomes small is analyzed for zero trend function and for the particular choice of the upper limiting function.
Average popularityAverage popularity In bottom 99%Average influencePopularity: Citation-based measure reflecting the current impact.Average influence In bottom 99%Influence: Citation-based measure reflecting the total impact.add Add to ORCIDPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
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- Publication . Article . 2003Open AccessAuthors:Schellenberg, D; Armstrong Schellenberg, J R M; Mushi, A; Savigny de, D; Mgalula, L; Mbuya, C; Victoria, C.G.;Schellenberg, D; Armstrong Schellenberg, J R M; Mushi, A; Savigny de, D; Mgalula, L; Mbuya, C; Victoria, C.G.;Country: Tanzania (United Republic of)
Objective was to document the prevalence, age-distribution, and risk factors for anaemia in Tanzanian children less than 5 years old,thereby assisting in the development of effective strategies for controlling anaemia. Cluster sampling was used to identify 2417 households at random from four contiguous districts in south-eastern United Republic of Tanzania in mid-1999. Data on various social and medical parameters were collected and analysed. Blood haemoglobin concentrations (Hb) were available for 1979 of the 2131 (93%) children identified and ranged from 1.7 to 18.6 g/dl. Overall, 87% (1722) of children had an Hb <11 g/dl, 39% (775) had an Hb <8 g/dl and 3% (65) had an Hb <5 g/dl. The highest prevalence of anaemia of all three levels was in children aged 6–11 months, of whom 10% (22/226) had an Hb <5 g/dl. However, the prevalence of anaemia was already high in children aged 1–5 months (85% had an Hb <11 g/dl, 42% had an Hb <8 g/dl, and 6% had an Hb <5 g/dl). Anaemia was usually asymptomatic and when symptoms arose they were nonspecific and rarely identified as a serious illness by the care provider. A recent history of treatment with antimalarials and iron was rare. Compliance with vaccinations delivered through the Expanded Programme of Immunization (EPI) was 82% and was notassociated with risk of anaemia. Anaemia is extremely common in south-eastern United Republic of Tanzania, even in very young infants. Further implementation of the Integrated Management of Childhood Illness algorithm should improve the case management of anaemia. However, the asymptomatic nature of most episodes of anaemia highlights the need for preventive strategies. The EPI has good coverage of the target population and it may be an appropriate channel for delivering tools for controlling anaemia and malaria.
- Publication . Article . Other literature type . 2019Open AccessAuthors:Jürgen Dengler; Thomas J. Matthews; Manuel J. Steinbauer; Sebastian Wolfrum; Steffen Boch; Alessandro Chiarucci; Timo Conradi; Iwona Dembicz; Corrado Marcenò; Itziar García-Mijangos; +35 moreJürgen Dengler; Thomas J. Matthews; Manuel J. Steinbauer; Sebastian Wolfrum; Steffen Boch; Alessandro Chiarucci; Timo Conradi; Iwona Dembicz; Corrado Marcenò; Itziar García-Mijangos; Arkadiusz Nowak; David Storch; Werner Ulrich; Juan Antonio Campos; Laura Cancellieri; Marta Carboni; Giampiero Ciaschetti; Pieter De Frenne; Jiri Dolezal; Christian Dolnik; Franz Essl; Edy Fantinato; Goffredo Filibeck; John-Arvid Grytnes; Riccardo Guarino; Behlül Güler; Monika Janišová; Ewelina Klichowska; Łukasz Kozub; Anna Kuzemko; Michael Manthey; Anne Mimet; Alireza Naqinezhad; Christian Pedersen; Robert K. Peet; Vincent Pellissier; Remigiusz Pielech; Giovanna Potenza; Leonardo Rosati; Massimo Terzi; Orsolya Valkó; Denys Vynokurov; Hannah J. White; Manuela Winkler; Idoia Biurrun;
handle: 1854/LU-8649698 , 1956/22574 , 11104/0312153 , 10400.3/5794 , 11590/363767
Publisher: WileyCountries: Italy, Belgium, Italy, Portugal, Italy, Germany, Spain, Poland, Norway, Switzerland ...Aim Species-area relationships (SARs) are fundamental scaling laws in ecology although their shape is still disputed. At larger areas, power laws best represent SARs. Yet, it remains unclear whether SARs follow other shapes at finer spatial grains in continuous vegetation. We asked which function describes SARs best at small grains and explored how sampling methodology or the environment influence SAR shape. Location Palaearctic grasslands and other non-forested habitats. Taxa Vascular plants, bryophytes and lichens. Methods We used the GrassPlot database, containing standardized vegetation-plot data from vascular plants, bryophytes and lichens spanning a wide range of grassland types throughout the Palaearctic and including 2,057 nested-plot series with at least seven grain sizes ranging from 1 cm(2) to 1,024 m(2). Using nonlinear regression, we assessed the appropriateness of different SAR functions (power, power quadratic, power breakpoint, logarithmic, Michaelis-Menten). Based on AICc, we tested whether the ranking of functions differed among taxonomic groups, methodological settings, biomes or vegetation types. Results The power function was the most suitable function across the studied taxonomic groups. The superiority of this function increased from lichens to bryophytes to vascular plants to all three taxonomic groups together. The sampling method was highly influential as rooted presence sampling decreased the performance of the power function. By contrast, biome and vegetation type had practically no influence on the superiority of the power law. Main conclusions We conclude that SARs of sessile organisms at smaller spatial grains are best approximated by a power function. This coincides with several other comprehensive studies of SARs at different grain sizes and for different taxa, thus supporting the general appropriateness of the power function for modelling species diversity over a wide range of grain sizes. The poor performance of the Michaelis-Menten function demonstrates that richness within plant communities generally does not approach any saturation, thus calling into question the concept of minimal area. We thank all vegetation scientists who carefully collected multi‐ scale plant diversity data from Palaearctic Grasslands available in GrassPlot. The Eurasian Dry Grassland Group (EDGG) and the International Association for Vegetation Science (IAVS) sup‐ ported the EDGG Field Workshops, which generated a core part of the GrassPlot data. The Bavarian Research Alliance (grant BayIntAn_UBT_2017_58) and the Bayreuth Center of Ecology and Environmental Research (BayCEER) funded the initial GrassPlot workshop during which the database was established and the cur‐ rent paper was initiated. A.N. acknowledges support by the Center for International Scientific Studies and Collaboration (CISSC), Iran. C.M., I.B., I.G.‐M and J.A.C. were funded by the Basque Government (IT936‐16). D.V. carried out the research supported by a grant of the State Fund For Fundamental Research Ф83/53427. G.F. carried out the research in the frame of the MIUR initiative ‘Department of excellence' (Law 232/2016). I.D. was supported by the Polish National Science Centre (grant DEC‐2013/09/N/NZ8/03234). J.Do. was supported by the Czech Science Foundation (GA 17‐19376S). M.J. was supported by grant by Slovak Academy of Sciences (VEGA 02/0095/19). W.U. ac‐ knowledges support from the Polish National Science Centre (grant 2017/27/B/NZ8/00316).
Average popularityAverage popularity In bottom 99%Average influencePopularity: Citation-based measure reflecting the current impact.Average influence In bottom 99%Influence: Citation-based measure reflecting the total impact.add Add to ORCIDPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product. - Publication . Article . Preprint . 2006Open Access EnglishAuthors:M. de Montigny; J. Niederle; A. G. Nikitin;M. de Montigny; J. Niederle; A. G. Nikitin;Project: NSERC
All indecomposable finite-dimensional representations of the homogeneous Galilei group which when restricted to the rotation subgroup are decomposed to spin 0, 1/2 and 1 representations are constructed and classified. These representations are also obtained via contractions of the corresponding representations of the Lorentz group. Finally the obtained representations are used to derive a general Pauli anomalous interaction term and Darwin and spin-orbit couplings of a Galilean particle interacting with an external electric field. 23 pages, 2 tables
Average popularityAverage popularity In bottom 99%Average influencePopularity: Citation-based measure reflecting the current impact.Average influence In bottom 99%Influence: Citation-based measure reflecting the total impact.add Add to ORCIDPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product. - Publication . Article . 2019Open AccessAuthors:Barbara L. Shacklett; Julià Blanco; Lisa B. Hightow-Weidman; Nyaradzo Mgodi; José Alcamí; Susan Buchbinder; Mike Chirenje; Smritee Dabee; Mamadou H. Diallo; Kostyantyn Dumchev; +18 moreBarbara L. Shacklett; Julià Blanco; Lisa B. Hightow-Weidman; Nyaradzo Mgodi; José Alcamí; Susan Buchbinder; Mike Chirenje; Smritee Dabee; Mamadou H. Diallo; Kostyantyn Dumchev; Carolina Herrera; Matthew E Levy; Enrique Martin Gayo; Nigel Aminake Makoah; Kate M. Mitchell; Kenneth K. Mugwanya; Krishnaveni Reddy; Maria Luisa Rodríguez; Marta Rodriguez-Garcia; Chelsea L. Shover; Tripti Shrivastava; Georgia D. Tomaras; Michiel T. van Diepen; Monika Walia; Mitchell Warren; Amapola Manrique; Bargavi Thyagarajan; Tamara Torri;Publisher: Mary Ann Liebert IncCountries: Spain, United States, United KingdomProject: NIH | HIV Research for Preventi... (1R13AI136762-01)
The HIV Research for Prevention (HIVR4P) conference is dedicated to advancing HIV prevention research, responding to a growing consensus that effective and durable prevention will require a combination of approaches as well as unprecedented collaboration among scientists, practitioners, and community workers from different fields and geographic areas. The conference theme in 2018, "From Research to Impact," acknowledged an increasing focus on translation of promising research findings into practical, accessible, and affordable HIV prevention options for those who need them worldwide. HIVR4P 2018 was held in Madrid, Spain, on 21-25 October, with >1,400 participants from 52 countries around the globe, representing all aspects of HIV prevention research and implementation. The program included 137 oral and 610 poster presentations. This article presents a brief summary of highlights from the conference. More detailed information, complete abstracts as well as webcasts and daily Rapporteur summaries may be found on the conference website. Supported by Gilead who provided funding. Gilead has had no input into the content of the materials used at this meeting/conference. No other pharmaceutical company has had input into the content of the materials used at this conference. HIVR4P 2018 was made possible in part by 1 R13 AI136762-01 from the National Institute of Allergy and Infectious Diseases (NIAID). The views expressed in written conference materials or publications and by speakers and moderators do not necessarily reflect the official policies of the Department of Health and Human Services; nor does mention of trade names, commercial practices, or organizations imply endorsement by the U.S. Government. Sí
Average popularityAverage popularity In bottom 99%Average influencePopularity: Citation-based measure reflecting the current impact.Average influence In bottom 99%Influence: Citation-based measure reflecting the total impact.add Add to ORCIDPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product. - Publication . Article . 2021Open Access EnglishAuthors:L. T. Ellis; C. Ah-Peng; G. Aslan; V. A. Bakalin; A. Bergamini; D. A. Callaghan; P. Campisi; F. M. Raimondo; S. S. Choi; J. Csiky; +72 moreL. T. Ellis; C. Ah-Peng; G. Aslan; V. A. Bakalin; A. Bergamini; D. A. Callaghan; P. Campisi; F. M. Raimondo; S. S. Choi; J. Csiky; É. Csikyné Radnai; B. Cykowska-Marzencka; I. V. Czernyadjeva; Yu M. Kalinina; O. M. Afonina; G. Domina; P. Drapela; V. E. Fedosov; E. Fuertes; R. Gabriel; M. Kubová; I. Soares Albergaria; G. Gospodinov; R. Natcheva; A. Graulich; T. Hedderson; E. Hernández-Rodríguez; V. Hugonnot; C. W. Hyun; M. Kırmacı; U. Çatak; S. Kubešová; J. Kučera; C. La Farge; J. Larraín; P. Martin; B. Mufeed; C. N. Manju; K. P. Rajesh; Cs. Németh; J. Nagy; N. Norhazrina; N. Syazwana; S. V. O’Leary; S. J. Park; A. P. Peña-Retes; A. Rimac; A. Alegro; V. Šegota; N. Koletić; N. Vuković; S. Rosadziński; J. A. Rosselló; M. S. Sabovljević; A. D. Sabovljević; A. Schäfer-Verwimp; C. Sérgio; A. V. Shkurko; D. Shyriaieva; V. M. Virchenko; M. Smoczyk; D. Spitale; P. Srivastava; I. Omar; A. K. Asthana; M. Staniaszek-Kik; A. Cienkowska; M.-M. Ștefănuţ; S. Ștefănuţ; G. Tamas; C.-C. Bîrsan; G.-R. Nicoară; M. C. Ion; T. Pócs; G. Kunev; E. I. Troeva; J. van Rooy; P. Wietrzyk-Pełka; M. H. Węgrzyn; G. J. Wolski; D. Bożyk; A. Cienkowska;
handle: 10400.3/6171
Publisher: HAL CCSDCountries: France, Poland, Croatia, France, PortugalProject: EC | INTERACT (262693)Pseudoamblystegium subtile (Hedw.) Vanderp. & Hedenäs. CONTRIBUTORS: R. Gabriel, M. Kubová, C. Sérgio and I. Soares Albergaria. PORTUGAL, AZORES: Terceira Island, Angra do Heroísmo, municipal garden ‘Jardim Duque da Terceira’, 38° 39′ 24.0′′N, 27°13′ 05.99′′W, 31 m a.s.l, on the base of a shrub, in acidic conditions, 7 April 2017, leg. Michaela Kubová s.n. (AZU). A new understanding of the pleurocarpous moss species Pseudoamblystegium subtile was proposed by Vanderpoorten and Hedenäs (2009). The new genus is separated from the other Amblystegiaceae primarily due to its phylogenetic consistency and is characterised by the possession of leaves with a very short nerve, and erect capsules (Vanderpoorten and Hedenäs 2009). (excerpt) info:eu-repo/semantics/publishedVersion
Average popularityAverage popularity In bottom 99%Average influencePopularity: Citation-based measure reflecting the current impact.Average influence In bottom 99%Influence: Citation-based measure reflecting the total impact.add Add to ORCIDPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product. - Publication . Article . 2013Open AccessAuthors:Shakil Ahmed; Peter Leslie Annear; Bouaphat Phonvisay; Chansaly Phommavong; Valeria de Oliveira Cruz; Asmus Hammerich; Bart Jacobs;Shakil Ahmed; Peter Leslie Annear; Bouaphat Phonvisay; Chansaly Phommavong; Valeria de Oliveira Cruz; Asmus Hammerich; Bart Jacobs;Publisher: Elsevier BV
AbstractThere is now widespread acceptance of the universal coverage approach, presented in the 2010 World Health Report. There are more and more voices for the benefit of creating a single national risk pool. Now, a body of literature is emerging on institutional design and organizational practice for universal coverage, related to management of the three health-financing functions: collection, pooling and purchasing. While all countries can move towards universal coverage, lower-income countries face particular challenges, including scarce resources and limited capacity. Recently, the Lao PDR has been preparing options for moving to a single national health insurance scheme. The aim is to combine four different social health protection schemes into a national health insurance authority (NHIA) with a single national fund- and risk-pool. This paper investigates the main institutional and organizational challenges related to the creation of the NHIA. The paper uses a qualitative approach, drawing on the World Health Organization's institutional and Organizational Assessment for Improving and Strengthening health financing (OASIS) conceptual framework for data analysis. Data were collected from a review of key health financing policy documents and from 17 semi-structured key informant interviews. Policy makers and advisors are confronting issues related to institutional arrangements, funding sources for the authority and government support for subsidies to the demand-side health financing schemes. Compulsory membership is proposed, but the means for covering the informal sector have not been resolved. While unification of existing schemes may be the basis for creating a single risk pool, challenges related to administrative capacity and cross-subsidies remain. The example of Lao PDR illustrates the need to include consideration of national context, the sequencing of reforms and the time-scale appropriate for achieving universal coverage.
Average popularityAverage popularity In bottom 99%Average influencePopularity: Citation-based measure reflecting the current impact.Average influence In bottom 99%Influence: Citation-based measure reflecting the total impact.add Add to ORCIDPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product. - Publication . Article . 2016Restricted EnglishAuthors:Gary E. Raskob; Nick van Es; Annelise Segers; Pantep Angchaisuksiri; Doyeun Oh; Zoltán Boda; Roger M. Lyons; Karina Meijer; Ivan Gudz; Jeffrey I. Weitz; +4 moreGary E. Raskob; Nick van Es; Annelise Segers; Pantep Angchaisuksiri; Doyeun Oh; Zoltán Boda; Roger M. Lyons; Karina Meijer; Ivan Gudz; Jeffrey I. Weitz; George Zhang; Hans Lanz; Michele Mercuri; Harry R. Büller;Country: Netherlands
Venous thromboembolism occurs commonly in patients with cancer. Direct oral anticoagulants are non-inferior to conventional anticoagulants for the treatment of venous thromboembolism. We hypothesised that edoxaban, a direct oral inhibitor of activated clotting factor Xa, might be more suitable than conventional anticoagulants in the management of cancer-associated venous thromboembolism. The aim of this study was to assess the efficacy and safety of edoxaban compared with warfarin in a subgroup of patients with cancer enrolled in the Hokusai-VTE trial. We did a prespecified subgroup analysis in August, 2013, and a post-hoc analysis of non-inferiority and safety in March, 2016, of the patients with cancer enrolled in the randomised, double-blind, double-dummy, multicentre, Hokusai-VTE trial done between Jan 28, 2010, and Oct 31, 2012. In this study, patients aged at least 18 years with acute symptomatic deep-vein thrombosis or acute symptomatic pulmonary embolism (with or without deep-vein thrombosis) were assigned to receive edoxaban 60 mg once per day (or 30 mg once per day for patients with a creatinine clearance of 30-50 mL/min, bodyweight <60 kg, or who were receiving concomitant treatment with the P-glycoprotein inhibitors quinidine or verapamil) or warfarin (dose adjusted to maintain the international normalised ratio between 2·0 and 3·0) or placebos for either group for at least 3 months up to 12 months. All patients received initial therapy with open-label enoxaparin or unfractionated heparin for at least 5 days. Edoxoban (or placebo) was started after discontinuation of initial heparin; warfarin (or placebo) started concurrently with the study regimen of heparin. In our analysis we examined data for a subgroup of these patients who had a history of cancer or who had been categorised as having active cancer by the study physician at the time of enrolment. Additionally, all patients with a history of cancer were reviewed post hoc and categorised according to the presence or absence of active cancer. The primary efficacy outcome was the proportion of these patients with symptomatic recurrent venous thromboembolism during the 12-month study period, analysed in the modified intention-to-treat population, with an upper limit of the CI for the hazard ratio (HR) of 1·5. The principal safety outcome was the proportion of patients who had clinically relevant bleeding in the population of patients who received at least one dose of the study drug. This study is registered with ClinicalTrials.gov, number NCT00986154. Of 771 patients with cancer enrolled in the trial, 378 were assigned to edoxaban and 393 to warfarin. Recurrent venous thromboembolism occurred in 14 (4%) of 378 patients given edoxaban and in 28 (7%) of 393 patients given warfarin (hazard ratio [HR] 0·53, 95% CI 0·28-1·00; p=0·0007). The upper limit of this 95% CI did not exceed the non-inferiority margin of 1·5 that was prespecified for the trial. Clinically relevant bleeding (major or non-major) occurred in 47 (12%) of 378 patients who received edoxaban and in 74 (19%) of 393 patients who received warfarin; HR for clinically relevant bleeding 0·64, 95% CI 0·45-0·92; p=0·017. Major bleeding occurred in ten (3%) of 378 patients with a history of cancer who received edoxaban and in 13 (3%) of 393 who received warfarin (HR 0·80, 95% CI 0·35-1·83). Edoxaban might be as effective as warfarin for the treatment of patients with cancer with venous thromboembolism, and with less clinically relevant bleeding. Additional clinical trials of edoxaban versus low-molecular-weight heparin for the treatment of venous thromboembolism in patients with cancer are warranted. Daiichi Sankyo
Average popularityAverage popularity In bottom 99%Average influencePopularity: Citation-based measure reflecting the current impact.Average influence In bottom 99%Influence: Citation-based measure reflecting the total impact.add Add to ORCIDPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product. - Publication . Article . 2020Open AccessAuthors:Robert C. Reiner; Paulina A. Lindstedt; Brigette F. Blacker; Lucas Earl; Sandra B. Munro; Lucas Guimarães Abreu; Dilaram Acharya; Maryam Adabi; Rufus A. Adedoyin; Victor Adekanmbi; +242 moreRobert C. Reiner; Paulina A. Lindstedt; Brigette F. Blacker; Lucas Earl; Sandra B. Munro; Lucas Guimarães Abreu; Dilaram Acharya; Maryam Adabi; Rufus A. Adedoyin; Victor Adekanmbi; Beyene Meressa Adhena; Mohsen Afarideh; Keivan Ahmadi; Rushdia Ahmed; Olufemi Ajumobi; Ali S. Akanda; Turki Alanzi; Vahid Alipour; Ali Almasi; Hesham M. Al-Mekhlafi; Azmeraw T. Amare; Catalina Liliana Andrei; Masresha Tessema Anegago; Fereshteh Ansari; Carl Abelardo T. Antonio; Jalal Arabloo; Afsaneh Arzani; Alebachew Fasil Ashagre; Suleman Atique; Sachin R Atre; Getinet Ayano; Senthilkumar Balakrishnan; Maciej Banach; Aleksandra Barac; Quique Bassat; Mohsen Bayati; Masoud Behzadifar; Meysam Behzadifar; Yibeltal Alemu Bekele; Derrick A Bennett; Krittika Bhattacharyya; Suraj Bhattarai; Ali Bijani; Boris Bikbov; Somayeh Bohlouli; Sharath Burugina Nagaraja; Devasahayam J. Christopher; Vera Marisa Costa; Lalit Dandona; Rakhi Dandona; Claudio Alberto Davila; Nicole Davis Weaver; Jan-Walter De Neve; Asmamaw Bizuneh Demis; Gebre Teklemariam Demoz; Kebede Deribe; Getenet Dessie; Preeti Dhillon; Meghnath Dhimal; Christiane Dolecek; Manisha Dubey; Susanna Dunachie; Andre Rodrigues Duraes; Maha El Tantawi; Shymaa Enany; Aklilu Endalamaw; Alireza Esteghamati; Mohammad Fareed; Andrea Farioli; André Faro; Hossein Farzam; Ali Akbar Fazaeli; Eduarda Fernandes; Joel M. Francis; Joseph Frostad; Gebreamlak Gebremedhn Gebremeskel; Kebede Embaye Gezae; Paramjit Gill; Ayman Grada; Yuming Guo; Rahul Gupta; Nima Hafezi-Nejad; Arvin Haj-Mirzaian; Arya Haj-Mirzaian; Brian J. Hall; Demelash Woldeyohannes Handiso; Hamidreza Haririan; Ninuk Hariyani; Ahmed I. Hasaballah; Amir Hasanzadeh; Hadi Hassankhani; Claudiu Herteliu; Chi Linh Hoang; Naznin Hossain; Mowafa Househ; Ayesha Humayun; Syed Ather Hussain; Leeberk Raja Inbaraj; Seyed Sina Naghibi Irvani; Chinwe Juliana Iwu; Nader Jafari Balalami; Ravi Prakash Jha; Vivekanand Jha; John S. Ji; Peng Jia; Jost B. Jonas; Zubair Kabir; Behzad Karami Matin; André Karch; Surendra Karki; Amir Kasaeian; Gebremicheal Gebreslassie Kasahun; Yousef Khader; Morteza Abdullatif Khafaie; Nauman Khalid; Ali Talha Khalil; Khaled Khatab; Aliasghar Ahmad Kiadaliri; Yun Jin Kim; Adnan Kisa; Niranjan Kissoon; Margaret Kosek; Kewal Krishan; G Anil Kumar; Pushpendra Kumar; Dian Kusuma; Van C. Lansingh; Savita Lasrado; Tsegaye Lolaso Lenjebo; Shanshan Li; Shai Linn; Platon D. Lopukhov; Deborah Carvalho Malta; Farzad Manafi; Navid Manafi; Ana Laura Manda; Francisco Rogerlandio Martins-Melo; Manu Raj Mathur; Colm McAlinden; Gebrekiros Gebremichael Meles; Ritesh G. Menezes; Bartosz Miazgowski; Kebadnew Mulatu Mihretie; Edward J Mills; Parvaneh Mirabi; Erkin M. Mirrakhimov; Amjad Mohamadi-Bolbanabad; Dara K. Mohammad; Aso Mohammad Darwesh; Jemal Abdu Mohammed; Shafiu Mohammed; Farnam Mohebi; Lorenzo Monasta; Yoshan Moodley; Masoud Moradi; Maziar Moradi-Lakeh; Seyyed Meysam Mousavi; Miliva Mozaffor; Gudlavalleti Vs Murthy; Vinay Nangia; Javad Nazari; Duduzile Ndwandwe; Quynh Anh P. Nguyen; Dabere Nigatu; Dina Nur Anggraini Ningrum; Marzieh Nojomi; Andrew T Olagunju; Ahmed Omar Bali; Jagadish Rao Padubidri; Adrian Pana; Tahereh Pashaei; Sanghamitra Pati; Veincent Christian Filipino Pepito; Alexandre C. Pereira; Norberto Perico; Konrad Pesudovs; David M. Pigott; Mohammad Rabiee; Navid Rabiee; Fakher Rahim; Vafa Rahimi-Movaghar; Muhammad Aziz Rahman; Fatemeh Rajati; Chhabi Lal Ranabhat; Davide Rasella; Salman Rawaf; Andre M. N. Renzaho; Melese Abate Reta; Ana Isabel Ribeiro; Carlos Miguel Rios González; Maria Jesus Rios-Blancas; Luca Ronfani; Ali Rostami; Enrico Rubagotti; Rajesh Sagar; Nasir Salam; Farkhonde Salehi; Saleh Salehi Zahabi; Yahya Salimi; Hamideh Salimzadeh; Itamar S. Santos; Alyssa N. Sbarra; Lauren E. Schaeffer; Hosein Shabaninejad; Amira Shaheen; Masood Ali Shaikh; Ali S. Shalash; Seifadin Ahmed Shallo; Mehran Shams-Beyranvand; MohammadBagher Shamsi; Muki Shey; Jae Il Shin; Rahman Shiri; Reza Shirkoohi; Si Si; Narinder Pal Singh; Malede Mequanent Sisay; Eirini Skiadaresi; Anton Sokhan; Moslem Soofi; Muluken Bekele Sorrie; Ireneous N. Soyiri; Hafiz Ansar Rasul Suleria; Koku Sisay Tamirat; Nuno Taveira; Bineyam Taye; Mohamad-Hani Temsah; Berhe Etsay Tesfay; Fisaha Haile Tesfay; Kavumpurathu Raman Thankappan; Sathish Thirunavukkarasu; Nihal Thomas; Irfan Ullah; Sahel Valadan Tahbaz; Santosh Varughese; Sebastian Vollmer; Fiseha Wadilo Wada; Yasir Waheed; Taweewat Wiangkham; Tissa Wijeratne; Ali Yadollahpour; Seyed Hossein Yahyazadeh Jabbari; Tomohide Yamada; Mehdi Yaseri; Alex Yeshaneh; Ebrahim M Yimer; Engida Yisma; Mohammad Zamani; Hamed Zandian; Dongyu Zhang; Yunquan Zhang; Sanjay Zodpey;Publisher: Elsevier BV
Reiner RC Jr, Hay SI. Mapping geographical inequalities in childhood diarrhoeal morbidity and mortality in low-income and middle-income countries, 2000–17: analysis for the Global Burden of Disease Study 2017. Lancet 2020; 395: 1779–801—In this Article, the author byline has been amended to Local Burden of Disease Diarrhoea Collaborators. This correction has been made to the online version as of June 4, 2020, and the printed version is correct. © 2020 Elsevier Ltd
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You have already added works in your ORCID record related to the merged Research product. - Publication . Article . 2020Open Access EnglishAuthors:Mykola Beshley; Natalia Kryvinska; Marian Seliuchenko; Halyna Beshley; Elhadi M. Shakshuki; Ansar-Ul-Haque Yasar;Mykola Beshley; Natalia Kryvinska; Marian Seliuchenko; Halyna Beshley; Elhadi M. Shakshuki; Ansar-Ul-Haque Yasar;Publisher: MDPI AGCountries: Belgium, Austria
This paper proposes a modified architecture of the Long-Term Evolution (LTE) mobile network to provide services for the Internet of Things (IoT). This is achieved by allocating a narrow bandwidth and transferring the scheduling functions from the eNodeB base station to an NB-IoT controller. A method for allocating uplink and downlink resources of the LTE/NB-IoT hybrid technology is applied to ensure the Quality of Service (QoS) from end-to-end. This method considers scheduling traffic/resources on the NB-IoT controller, which allows eNodeB planning to remain unchanged. This paper also proposes a prioritization approach within the IoT traffic to provide End-to-End (E2E) QoS in the integrated LTE/NB-IoT network. Further, we develop &ldquo management algorithms for the IoT traffic prioritization. To demonstrate the feasibility of our approach, we performed a number of experiments using simulations. We concluded that our proposed approach ensures high end-to-end QoS of the real-time traffic by reducing the average end-to-end transmission delay. smart queue&rdquo
Average popularityAverage popularity In bottom 99%Average influencePopularity: Citation-based measure reflecting the current impact.Average influence In bottom 99%Influence: Citation-based measure reflecting the total impact.add Add to ORCIDPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product. - Publication . Article . Preprint . 2018 . Embargo End Date: 01 Jan 2018Open AccessAuthors:Anne MacKay; Alexander Melnikov; Yuliya Mishura;Anne MacKay; Alexander Melnikov; Yuliya Mishura;Publisher: arXivProject: NSERC
In this paper, we investigate two-sided bounds for the small ball probability of a mixed fractional Brownian motion with a general deterministic trend function, in terms of respective small ball probability of a mixed fractional Brownian motion without trend. To maximize the lower bound, we consider various ways to split the trend function between the components of the mixed fractional Brownian motion for the application of Girsanov theorem, and we show that the optimal split is the solution of a Fredholm integral equation. We find that the upper bound for the probability is also a function of this optimal split. The asymptotic behaviour of the probability as the ball becomes small is analyzed for zero trend function and for the particular choice of the upper limiting function.
Average popularityAverage popularity In bottom 99%Average influencePopularity: Citation-based measure reflecting the current impact.Average influence In bottom 99%Influence: Citation-based measure reflecting the total impact.add Add to ORCIDPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.