20 research outputs found
Global Collapses and Expansions in Star-Forming Clouds
- Author
- Adams
- Adelson
- Aguti
- Arons
- Belloche
- Bernes
- Bian
- Carolan
- Di Francesco
- Evans
- Fiege
- Fiege
- Fuller
- Gao
- Hammersley
- Harvey
- Hennebelle
- Hogerheijde
- Hu
- Jørgensen
- Kenyon
- Keto
- Lada
- Larson
- Lee
- Lou
- Lou
- Lou
- Lou
- MacLow
- Mardones
- Matthews
- Matzner
- Matzner
- McKee
- Moraghan
- Moriarty-Schieven
- Myers
- Myers
- Nakano
- Ossenkopf
- Ostriker
- Park
- Park
- Park
- Rawlings
- Redman
- Redman
- Saito
- Schöier
- Shang
- Shen
- Shirley
- Shreider
- Shu
- Shu
- Shu
- Shu
- Su
- Tafalla
- Tafalla
- Tafalla
- Thompson
- Tsamis
- van der Tak
- Van Zadelhoff
- Velusamy
- Wang
- Ward-Thompson
- Wilner
- Wu
- Yang Gao
- Yu
- Yu
- Yu-Qing Lou
- Zhou
- Zhou
- Zweibel
- Publication venue
- 'Wiley'
- Publication date
- 06/09/2009
- Field of study
Spectral molecular line profile observations of star-forming molecular clouds
sometimes show distinct red asymmetric double-peaked molecular line profiles
with weaker blue peaks and stronger red peaks. For some star-forming molecular
clouds, such molecular transitions with red asymmetric line profiles and blue
asymmetric line profiles (i.e. blue asymmetric double-peaked molecular line
profiles with weaker red peaks and stronger blue peaks) may coexist in
spatially resolved spectral observations, while for others, such molecular
transitions with red asymmetric line profiles may completely dominate in
spatially resolved spectral observations. Blue asymmetric line profiles are
usually interpreted as signals of central core collapses, while red asymmetric
line profiles remain unexplained. In this paper, we advance a spherically
symmetric self-similar hydrodynamic model framework for envelope expansions
with core collapses (EECC) of a general polytropic molecular gas cloud under
self-gravity. Based on such EECC hydrodynamic cloud models, we perform tracer
molecular line profile calculations using the publicly available RATRAN code
for star-forming clouds with spectroscopic signatures of red asymmetric line
profiles. The presence of red asymmetric line profiles from molecular cloud
cores indicates that EECC processes are most likely an essential hydrodynamic
process of star formation. With spatial distributions, we explore various
profiles of molecular lines for several tracer molecules in different settings
of EECC dynamic models with and without shocks.Comment: 12 pages, 7 figures, accepted for publication in MNRA
Improved initialisation for centroidal Voronoi tessellation and optimal Delaunay triangulation
- Author
- Publication venue
- 'Elsevier BV'
- Publication date
- Field of study
Incidence, aetiology, and sequelae of viral meningitis in UK adults: a multicentre prospective observational cohort study
- Author
- Adan Guleed
- Adedeji Adekola
- Alastair Watt
- Amy Robinson
- Andrew Rosser
- Antony Cadwgan
- Beeching Nicholas J
- Bonnett Laura J
- Camelia Faris
- Christopher Murphy
- Clive Graham
- David Birkenhead
- David Chadwick
- Ed Moran
- Ennis Katherine
- Geretti Anna Maria
- Griffiths Michael J
- Gummery Alison
- Haris Rathur
- Hart Ian J
- Hassan Paraiso
- Haycox Alan
- Iain Crossingham
- Ildiko Kustos
- James Dunbar
- Jane Minton
- John Cheesbrough
- John Croall
- Jung Agam
- Karim Mahawish
- Katharine Ajdukiewicz
- Katherine Gray
- Kavya Mohandas
- Kevin Jones
- Mark Roberts
- Martin Antony P
- Martin Mostert
- Martin Wiselka
- Matthew Jones
- Mcgill Fiona
- Mckee David
- Michael Benedict D
- Miller Alastair
- Monika Pasztor
- Monty Silverdale
- Mutton Kenneth
- Mutton Kenneth J
- Neil Todd
- Nikhil Premchand
- Peter Flegg
- Philip Stanley
- Richard Cooke
- Sarah Maxwell
- Scarlett Paula
- Shirley Hammersley
- Simon Ellis
- Solomon Tom
- Stefan Schumacher
- Sulaiman Wan Aliaa Wan
- Susan Larkin
- Thomas Blanchard
- Publication venue
- 'Elsevier BV'
- Publication date
- 01/01/2018
- Field of study
© 2018 The Author(s). Published by Elsevier Ltd. This is an Open Access article under the CC BY 4.0 license Background: Viral meningitis is increasingly recognised, but little is known about the frequency with which it occurs, or the causes and outcomes in the UK. We aimed to determine the incidence, causes, and sequelae in UK adults to improve the management of patients and assist in health service planning. Methods: We did a multicentre prospective observational cohort study of adults with suspected meningitis at 42 hospitals across England. Nested within this study, in the National Health Service (NHS) northwest region (now part of NHS England North), was an epidemiological study. Patients were eligible if they were aged 16 years or older, had clinically suspected meningitis, and either underwent a lumbar puncture or, if lumbar puncture was contraindicated, had clinically suspected meningitis and an appropriate pathogen identified either in blood culture or on blood PCR. Individuals with ventricular devices were excluded. We calculated the incidence of viral meningitis using data from patients from the northwest region only and used these data to estimate the population-standardised number of cases in the UK. Patients self-reported quality-of-life and neuropsychological outcomes, using the EuroQol EQ-5D-3L, the 36-Item Short Form Health Survey (SF-36), and the Aldenkamp and Baker neuropsychological assessment schedule, for 1 year after admission. Findings: 1126 patients were enrolled between Sept 30, 2011, and Sept 30, 2014. 638 (57%) patients had meningitis: 231 (36%) cases were viral, 99 (16%) were bacterial, and 267 (42%) had an unknown cause. 41 (6%) cases had other causes. The estimated annual incidence of viral meningitis was 2·73 per 100 000 and that of bacterial meningitis was 1·24 per 100 000. The median length of hospital stay for patients with viral meningitis was 4 days (IQR 3–7), increasing to 9 days (6–12) in those treated with antivirals. Earlier lumbar puncture resulted in more patients having a specific cause identified than did those who had a delayed lumbar puncture. Compared with the age-matched UK population, patients with viral meningitis had a mean loss of 0·2 quality-adjusted life-years (SD 0·04) in that first year. Interpretation: Viruses are the most commonly identified cause of meningitis in UK adults, and lead to substantial long-term morbidity. Delays in getting a lumbar puncture and unnecessary treatment with antivirals were associated with longer hospital stays. Rapid diagnostics and rationalising treatments might reduce the burden of meningitis on health services. Funding: Meningitis Research Foundation and UK National Institute for Health Research
Antropologia, etnografia e narrativa: caminhos que se cruzam na compreensão do processo saúde-doença
- Author
- ACKERKNECHT Edwin
- ALVES Paulo César
- ALVES Paulo César
- BECKER Sandra Greice
- BOSI Alfredo
- BRUNER Jerome
- CANESQUI Ana Maria
- CAPRARA Andrea
- CARDOSO DE OLIVEIRA Roberto
- CHAUÍ Marilena
- CLIFFORD James
- COELHO Maria Thereza Ávila Dantas
- CORTAZZI Martin
- COSTA Maria Cristina Silva
- Dulce M.R. Gualda
- ECKERT Cornelia
- FONSECA Claúdia
- Gabriela M.C. Costa
- GADAMER Hans George
- GEANELLOS Rene
- GEERTZ Clifford
- GOOD Byron
- GOOD Byron
- GUALDA Dulce Maria Rosa
- GUALDA Dulce Maria Rosa
- GUALDA Dulce Maria Rosa
- GUALDA Dulce Maria Rosa
- HAMMERSLEY Martyn
- HELMAN Cecil G.
- KLEINMAN Arthur
- KLEINMAN Arthur
- KLEINMAN Arthur
- LANGDON Esther Jean
- LAPLANTINE François
- LIEBLICH Amia
- MALINOWSKI Bronislaw
- MATTINGLY Cheryl
- MELLO Luiz Gonzaga
- MINAYO Maria Cecília
- MINAYO Maria Cecília
- MORSE Janice M.
- OLIVEIRA Francisco Arsego
- PRICE Richard
- RABELO Miriam Cristina
- RAYNAUT Claude
- RICOUER Paul
- ROSALDO Renato
- SHIRLEY Robert Weaver
- UCHÔA Elizabeth
- VICTORA Ceres Gomes
- VIDICH Arthur J.
- Publication venue
- 'FapUNIFESP (SciELO)'
- Publication date
- Field of study
Dimethyl fumarate in patients admitted to hospital with COVID-19 (RECOVERY): a randomised, controlled, open-label, platform trial
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- Abernethy K.
- Aboelela H.
- Abouzaid M.
- Abraham M.
- Abraham T.
- Abrams J.
- Abu H.
- Abu-Arafeh A.
- Acton C.
- Adam F.
- Adam M.
- Adams C.
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- Adams D.
- Adams L.
- Addo A.
- Adedeji O.
- Adegoke K.
- Adewunmi E.
- Adeyemo T.
- Agbeko R.
- Aggarwal S.
- Ahmad S.
- Ahmed A.
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- Ainsworth M.
- Ajmi A.
- Akili S.
- Al Aaraj A.
- Al Balushi A.
- Al-Asadi A.
- Al-Khalil M.
- Al-Ramadhani B.
- Al-Saadi Z.
- Al-Shahi Salman R.
- Al-Sheklly B.
- Albert P.
- Alegria A.
- Alexander A.
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- Publication venue
- Springer Science and Business Media LLC
- Publication date
- 31/01/2024
- Field of study
Dimethyl fumarate (DMF) inhibits inflammasome-mediated inflammation and has been proposed as a treatment for patients hospitalised with COVID-19. This randomised, controlled, open-label platform trial (Randomised Evaluation of COVID-19 Therapy [RECOVERY]), is assessing multiple treatments in patients hospitalised for COVID-19 (NCT04381936, ISRCTN50189673). In this assessment of DMF performed at 27 UK hospitals, adults were randomly allocated (1:1) to either usual standard of care alone or usual standard of care plus DMF. The primary outcome was clinical status on day 5 measured on a seven-point ordinal scale. Secondary outcomes were time to sustained improvement in clinical status, time to discharge, day 5 peripheral blood oxygenation, day 5 C-reactive protein, and improvement in day 10 clinical status. Between 2 March 2021 and 18 November 2021, 713 patients were enroled in the DMF evaluation, of whom 356 were randomly allocated to receive usual care plus DMF, and 357 to usual care alone. 95% of patients received corticosteroids as part of routine care. There was no evidence of a beneficial effect of DMF on clinical status at day 5 (common odds ratio of unfavourable outcome 1.12; 95% CI 0.86-1.47; p = 0.40). There was no significant effect of DMF on any secondary outcome
Dimethyl fumarate in patients admitted to hospital with COVID-19 (RECOVERY): a randomised, controlled, open-label, platform trial
- Author
- Abbas M.
- Abdul Rasheed A.
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Dimethyl fumarate (DMF) inhibits inflammasome-mediated inflammation and has been proposed as a treatment for patients hospitalised with COVID-19. This randomised, controlled, open-label platform trial (Randomised Evaluation of COVID-19 Therapy [RECOVERY]), is assessing multiple treatments in patients hospitalised for COVID-19 (NCT04381936, ISRCTN50189673). In this assessment of DMF performed at 27 UK hospitals, adults were randomly allocated (1:1) to either usual standard of care alone or usual standard of care plus DMF. The primary outcome was clinical status on day 5 measured on a seven-point ordinal scale. Secondary outcomes were time to sustained improvement in clinical status, time to discharge, day 5 peripheral blood oxygenation, day 5 C-reactive protein, and improvement in day 10 clinical status. Between 2 March 2021 and 18 November 2021, 713 patients were enroled in the DMF evaluation, of whom 356 were randomly allocated to receive usual care plus DMF, and 357 to usual care alone. 95% of patients received corticosteroids as part of routine care. There was no evidence of a beneficial effect of DMF on clinical status at day 5 (common odds ratio of unfavourable outcome 1.12; 95% CI 0.86-1.47; p = 0.40). There was no significant effect of DMF on any secondary outcome
The choice between analysis of variance and analysis of covariance with special reference to the analysis of organ weights in toxicology studies
- Publication venue
- 'Wiley'
- Publication date
- Field of study
Progressive Multi-Jittered Sample Sequences
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- Publication venue
- 'Wiley'
- Publication date
- Field of study
Bidirectional Estimators for Light Transport
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- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/1995
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Thigh-length compression stockings and DVT after stroke
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- Umaipalan A
- Umeojiako W
- Unsworth A
- Uppal V Singh
- Urruela S
- Usher M
- Usher R
- Ustianowski A
- Ustianowski A
- Vaccari L Cheyenne
- Valeria B
- Vamplew L
- van de Venne M
- van der Meer A
- van der Stelt N
- van Someren C
- Vankayalapati P
- Vara S
- Varghese A
- Varghese M
- Varnier G
- Vasadi V
- Vasu V
- Vasudevan V
- Vathenen R
- Vatish M
- Vattekkat R Renu
- Vayalaman H
- Vaz C
- Veale N
- Velan B
- Velauthar L
- Vella N
- Venables I
- Venditti M
- Venkataramakrishnan R
- Veres M
- Vergnano S
- Verma A
- Vertue M
- Vethanayagam N
- Vilimiene N
- Vinay S
- Vincent R
- Vincent R
- Visentin E
- Vithian K
- Vyras E
- Wadd S
- Waddington N
- Wadsworth K
- Wafa SEI
- Wagstaff D
- Wagstaff L
- Wahbi Z
- Wake R
- Wakefield E
- Wakefield H
- Wakeford W
- Wakinshaw F
- Walden A
- Walker C
- Walker I
- Walker K
- Walker L
- Walker L
- Walker M
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- Wall E
- Wallendszus K
- Waller R
- Wallis G
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- Walsh D
- Walshaw L
- Walter D
- Walters H
- Walters J
- Walton E
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- Walton M
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- Wan M
- Wan T
- Wands M
- Wane R
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- Warburton S
- Ward E
- Ward K
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- Warden S Andrew
- Wardle S
- Wardy H
- Warmington J
- Warner B
- Warner C
- Warren Y
- Watchorn HJ
- Waterfall H
- Waters A
- Waterstone M
- Watkins L
- Watson AJR
- Watson E
- Watson E
- Watson R
- Watters M
- Watterson D
- Watts M
- Waugh V
- Wayman E
- Weatherly N
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- Webster T
- Weerasinghe T
- Weeratunga J
- Weetman M
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- Weller S
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- Welters I
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- Wessex D Porter
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- Whileman A
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- Whitehead C
- Whitehouse A
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- Whittaker E
- Whittam L
- Whittington A
- Wiafe E
- Wibli L
- Widdrington J
- Wiesender C
- Wiffen L
- Wight A
- Wilcock D
- Wilcock E
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- Wild S
- Wilde M
- Wildsmith T
- Wiles J
- Wiles K
- Wiliams T
- Wilkinson I
- Wilkinson S
- Wilkinson S
- Willetts S
- Williams A
- Williams C
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- Williams G
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- Williams J
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- Williams JR
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- Williams K Barker
- Williams M
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- Williams T
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- Williamson D
- Williamson J
- Willis E
- Willis H
- Willis H
- Willis J
- Willis J
- Wilson A
- Wilson A
- Wilson A
- Wilson D
- Wilson J
- Wilson J
- Wilson K
- Wilson L
- Wilson T
- Win M
- Winder L
- Winder P
- Winn S
- Winstanley M
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- Wiselka M
- Wittes J
- Wolodimeroff E
- Wong N
- Wood C
- Wood F
- Wood J
- Wood L
- Wood T
- Woodford J
- Woodhead L
- Woodland P
- Woodward Z
- Wooldridge G
- Woollen L
- Woosey D
- Wootton D
- Worton S
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- Wu P
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- Wynter I
- Xavier B
- Xia Z
- Yan M
- Yanney M
- Yasmin S
- Yates B
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- Yates D
- Yates H
- Yein K
- Yelnoorkar F
- Yip K
- Ynter I
- Yorke J
- Youssouf S
- Yousuf A
- Yung B
- Zafar A-M
- Zaher S
- Zalewska K
- Zaman M
- Zaman S
- Zammit L
- Zammit-Mangion M
- Zdanaviciene A
- Zehnde D
- Zhixin J
- Zhu D
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- Zin E Thant
- Zinyemba V
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- Zulaikha R
- Zullo C
- Publication venue
- 'Elsevier BV'
- Publication date
- 01/07/1994
- Field of study
Controversy exists as to whether neoadjuvant chemotherapy improves survival in patients with invasive bladder cancer, despite randomised controlled trials of more than 3000 patients. We undertook a systematic review and meta-analysis to assess the effect of such treatment on survival in patients with this disease