458 research outputs found
A preliminary study of the effect of closed incision management with negative pressure wound therapy over high-risk incisions
- Author
- A Colli
- A Koski
- A Li
- A Wackenfors
- A Wackenfors
- AE Guille
- BJ Stanley
- CJ Jordan
- D Herscovici Jr
- DA Mendonca
- David M. R. Sajik
- DR Holt
- DV Kipaldi
- E Krug
- EJ Harvey
- EJ Timmenga
- GI Taylor
- GK Berry
- GW Stanway
- J Bertran
- J Compston
- J Kanis
- JC Murrell
- JP Stannard
- JP Stannard
- JS Weese
- JT Thompson
- JW Fox
- Karen L. Perry
- KV Lambert
- L Holton
- LJ Owen
- Lynda Rutherford
- M Demaria
- M Pachowsky
- MF Fay
- Mieghan Bruce
- MJ Allen
- MJ Morykwas
- MJ Morywkas
- MJ Morywkas
- MW Bohling
- MW Bohling
- N Fitzpatrick
- NA Abidi
- PC Bristow
- PE Banwell
- PE Banwell
- PM Taylor
- R Ben Amotz
- R Burkhardt
- R Petzina
- RP Wilkes
- S Karlakki
- S Lindstedt
- SA Robertson
- SP Roch
- SZ Chen
- TJ Smith
- WT DeCarbo
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/2015
- Field of study
Background
Certain postoperative wounds are recognised to be associated with more complications than others and may be termed high-risk. Wound healing can be particularly challenging following high-energy trauma where wound necrosis and infection rates are high. Surgical incision for joint arthrodesis can also be considered high-risk as it requires extensive and invasive surgery and postoperative distal limb swelling and wound dehiscence are common. Recent human literature has investigated the use of negative pressure wound therapy (NPWT) over high-risk closed surgical incisions and beneficial effects have been noted including decreased drainage, decreased dehiscence and decreased infection rates. In a randomised, controlled study twenty cases undergoing distal limb high-energy fracture stabilisation or arthrodesis were randomised to NPWT or control groups. All cases had a modified Robert-Jones dressing applied for 72 h postoperatively and NPWT was applied for 24 h in the NPWT group. Morphometric assessment of limb circumference was performed at six sites preoperatively, 24 and 72 h postoperatively. Wound discharge was assessed at 24 and 72 h. Postoperative analgesia protocol was standardised and a Glasgow Composite Measure Pain Score (GCPS) carried out at 24, 48 and 72 h. Complications were noted and differences between groups were assessed.
Results
Percentage change in limb circumference between preoperative and 24 and 72 h postoperative measurements was significantly less at all sites for the NPWT group with exception of the joint proximal to the surgical site and the centre of the operated bone at 72 h. Median discharge score was lower in the NPWT group than the control group at 24 h. No significant differences in GCPS or complication rates were noted.
Conclusions
Digital swelling and wound discharge were reduced when NPWT was employed for closed incision management. Larger studies are required to evaluate whether this will result in reduced discomfort and complication rates postoperatively
Surface and Temporal Biosignatures
- Author
- A Oren
- A Segura
- AL Shields
- AM Baldridge
- C Sagan
- C Tucker
- CA Crow
- CAS Hall
- CB Pilcher
- CC Buschmann
- CD Keeling
- CE Harman
- CHL Patty
- CJ Tucker
- CM Moore
- CS Cockell
- CS Cockell
- CS Cockell
- CT Reinhard
- D Des Marais
- DJ Des Marais
- DJ Des Marais
- DJ Des Marais
- DM Gates
- DM Stam
- E Janik
- E Karkoschka
- E SanromĂĄ
- E SanromĂĄ
- EB Ford
- EB Knipling
- EW Schwieterman
- EW Schwieterman
- EW Schwieterman
- F Zhao
- G Tinetti
- G Tinetti
- GC Papageorgiou
- Giada Arney
- H Scheer
- HR Shahmohammadi
- J Bailey
- J Joiner
- J Krissansen-Totton
- J Takahashi
- JAM Nicholson
- JB Dalton
- JC Schwartz
- JM Dixon
- JM Olson
- JT OâMalley-James
- L Arnold
- L Arnold
- L Arnold
- LA Bristow
- M Archetti
- M Chen
- M Kobayashi
- M Meroni
- M. E. Zugger
- MAK Khalil
- MC Turnbull
- MF Sterzik
- N Madhusudhan
- NB Cowan
- NB Cowan
- NJ Woolf
- NY Kiang
- NY Kiang
- NY Kiang
- P Kenrick
- P Montanes-Rodriguez
- P Montanes-Rodriguez
- R Buick
- R Luger
- RA Rasmussen
- RD Wolstencroft
- RE Blankenship
- RE Blankenship
- RF Keeling
- RF Keeling
- RJ Cicerone
- RJ Cogdell
- S DasSarma
- S Hamdani
- S Hegde
- S Rugheimer
- S Seager
- S Seager
- S Seager
- SD Domagal-Goldman
- SD Miller
- SE Wood
- SHD Haddock
- SI Walker
- SV Berdyugina
- TA Livengood
- TD Brandt
- TD Robinson
- TD Robinson
- TD Robinson
- V Meadows
- Victoria S. Meadows
- Victoria S. Meadows
- VS Meadows
- WB Sparks
- WB Sparks
- Y Fujii
- Y Fujii
- Y Fujii
- Y. Sun
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/2018
- Field of study
Recent discoveries of potentially habitable exoplanets have ignited the
prospect of spectroscopic investigations of exoplanet surfaces and atmospheres
for signs of life. This chapter provides an overview of potential surface and
temporal exoplanet biosignatures, reviewing Earth analogues and proposed
applications based on observations and models. The vegetation red-edge (VRE)
remains the most well-studied surface biosignature. Extensions of the VRE,
spectral "edges" produced in part by photosynthetic or nonphotosynthetic
pigments, may likewise present potential evidence of life. Polarization
signatures have the capacity to discriminate between biotic and abiotic "edge"
features in the face of false positives from band-gap generating material.
Temporal biosignatures -- modulations in measurable quantities such as gas
abundances (e.g., CO2), surface features, or emission of light (e.g.,
fluorescence, bioluminescence) that can be directly linked to the actions of a
biosphere -- are in general less well studied than surface or gaseous
biosignatures. However, remote observations of Earth's biosphere nonetheless
provide proofs of concept for these techniques and are reviewed here. Surface
and temporal biosignatures provide complementary information to gaseous
biosignatures, and while likely more challenging to observe, would contribute
information inaccessible from study of the time-averaged atmospheric
composition alone.Comment: 26 pages, 9 figures, review to appear in Handbook of Exoplanets.
Fixed figure conversion error
Animal Models of Dyssynchrony
- Author
- AS Barth
- BT Wyman
- BT Wyman
- C Altehoefer
- C Deursen van
- C Linde
- C Parsai
- CJ Wiggers
- D Baller
- DD Spragg
- F Bojsen-Moller
- FW Prinzen
- FW Prinzen
- FW Prinzen
- FW Prinzen
- FW Prinzen
- FW Prinzen
- FW Prinzen
- GH Roberts
- H Eppinger
- IE Geldorp van
- JG Cleland
- K Chakir
- K Russell
- K Vernooy
- K Vernooy
- Kevin Vernooy
- L Liu
- L Matzer
- Lars B. van Middendorp
- LM Rademakers
- M Mathieu
- M Strik
- Marc Strik
- MD Bogaard
- MF Oosterhout van
- MF Oosterhout van
- MF Oosterhout van
- MO Sweeney
- MR Bristow
- MR Ginks
- MR Zile
- N Derval
- NF Marrouche
- OA Breithardt
- P Zanco
- PG Masci
- RH Helm
- RW Mills
- S Ono
- S Verheule
- SA Hayat
- SD Prabhu
- SD Solomon
- T Aiba
- WT Abraham
- XA Verbeek
- XA Verbeek
- Y Hori
- Y Urabe
- Publication venue
- Springer US
- Publication date
- 01/01/2011
- Field of study
Cardiac resynchronization therapy (CRT) is an important therapy for patients with heart failure and conduction pathology, but the benefits are heterogeneous between patients and approximately a third of patients do not show signs of clinical or echocardiographic response. This calls for a better understanding of the underlying conduction disease and resynchronization. In this review, we discuss to what extent established and novel animal models can help to better understand the pathophysiology of dyssynchrony and the benefits of CRT
p53 overexpression is associated with cytoreduction and response to chemotherapy in ovarian cancer
- Author
- A De Pasqua
- A Fagotti
- A Reles
- AGJ van der Zee
- APM Heintz
- BA Werness
- D Katsaros
- D Marx
- DM Eccles
- F Buttitta
- F Maneschi
- G Della Torre
- G Ferrandina
- G Scambia
- G Scambia
- J Diebold
- J Kupryjanczyk
- J Kupryjanczyk
- J Momand
- JJO Herod
- JP Geisler
- JR Marks
- LC Hartmann
- M Bouvet
- M G Salerno
- M Mottolese
- MA Levesque
- ME Potter
- MF Kohler
- N Mantel
- P Benedetti-Panici
- P G Natali
- P Michieli
- P Perego
- P Rohlke
- PJ Klemi
- R Brown
- R Henriksen
- RA Gjerset
- RE Bristow
- S Mancuso
- SM Bodner
- Y Dong
- Publication venue
- Nature Publishing Group
- Publication date
- 01/01/1999
- Field of study
The aim of this study was to assess the association of p53 status with primary cytoreduction, response to chemotherapy and outcome in stage IIIâIV primary ovarian cancer patients. Immunohistochemical analysis of p53 was performed on formalin-fixed, paraffin-embedded specimens from 168 primary ovarian carcinomas by using the DO-7 monoclonal antibody. p53 nuclear positivity was found in 84 out of 162 (52%) malignant tumours. A higher percentage of p53 nuclear positivity was observed in patients with advanced stage of disease than in stage IâII (57% vs 23% respectively; P = 0.0022) and in poorly differentiated versus well/moderately differentiated tumours (59% vs 32% respectively; P = 0.0038). The multivariate analysis aimed to investigate the association of FIGO stage, grade and p53 status with primary cytoreduction in 136 stage IIIâIV patients showed that stage IV disease may influence the possibility to perform primary cytoreduction in ovarian cancer patients. p53-positivity also maintained a trend to be associated with poor chance of cytoreduction. In patients who underwent pathologic assessment of response, cases who did not respond to chemotherapy were much more frequently p53-positive than p53-negative (86% vs 14% respectively; P = 0.012). Moreover, patients with stage III disease and < 2-cm residual tumour were more likely to respond to treatment. In multivariate analysis, FIGO stage and p53 expression were independently correlated with pathologic response to chemotherapy. Time to progression and survival rates were shown not to be different in p53-positive versus p53-negative patients. © 1999 Cancer Research Campaig
HER2 gene amplification and EGFR expression in a large cohort of surgically staged patients with nonendometrioid (type II) endometrial cancer
- Author
- A Mariani
- AD Santin
- AR Tan
- B Thomas
- B Winterhoff
- BA Goff
- BM Slomovitz
- BM Slomovitz
- C Morrison
- C Neuper
- CE Geyer
- D Pfeiffer
- D Riehle
- DJ Hetzel
- EH Romond
- G E Konecny
- G L Keeney
- G Scambia
- GE Konecny
- GL Maxwell
- H Niikura
- H-J Wang
- J Baselga
- J Baselga
- JJ Reinartz
- JK Chan
- JL Hecht
- K C Podratz
- K Ejskjaer
- KC Podratz
- L Muderspach
- L Ramondetta
- L Santos
- M F Press
- M Hatmal
- M Jones
- MA Khalifa
- MF Press
- PJ Hoskins
- RE Bristow
- S Acharya
- S Dowdy
- SF Lax
- TA Grushko
- VM Abeler
- Publication venue
- Nature Publishing Group
- Publication date
- 01/01/2009
- Field of study
Type II endometrial cancers (uterine serous papillary and clear cell histologies) represent rare but highly aggressive variants of endometrial cancer (EC). HER2 and EGFR may be differentially expressed in type II EC. Here, we evaluate the clinical role of HER2 and EGFR in a large cohort of surgically staged patients with type II (nonendometrioid) EC and compare the findings with those seen in a representative cohort of type I (endometrioid) EC. In this study HER2 gene amplification was studied by fluorescence in situ hybridisation (FISH) and EGFR expression by immunohistochemistry. Tissue microarrays were constructed from 279 patients with EC (145 patients with type I and 134 patients with type II EC). All patients were completely surgically staged and long-term clinical follow up was available for 258 patients. The rate of HER2 gene amplification was significantly higher in type II EC compared with type I EC (17 vs 1%, P<0.001). HER2 gene amplification was detected in 17 and 16% of the cases with uterine serous papillary and clear cell type histology, respectively. In contrast, EGFR expression was significantly lower in type II compared with type I EC (34 vs 46%, P=0.041). EGFR expression but not HER2 gene amplification was significantly associated with poor overall survival in patients with type II EC, (EGFR, median survival 20 vs 33 months, P=0.028; HER2, median survival 18 vs 29 months, P=0.113) and EGFR expression retained prognostic independence when adjusting for histology, stage, grade, and age (EGFR, P=0.0197; HER2, P=0.7855). We conclude that assessment of HER2 gene amplification and/or EGFR expression may help to select type II EC patients who could benefit from therapeutic strategies targeting both HER2 and EGFR
Usefulness of NT-pro BNP monitoring to identify echocardiographic responders following cardiac resynchronization therapy
- Author
- A Da Costa
- B Tuccillo
- C Linde
- C Valzania
- C Ypenburg
- C Ypenburg
- CM Yu
- DR Murdoch
- FM Fruhwald
- François Philippon
- Gilles O'Hara
- H Bader
- H Kanzaki
- J Madaric
- JA White
- Jean Champagne
- Jean G Dumesnil
- JG Cleland
- Julien Magne
- JW Fung
- M Kubanek
- M Moonen
- Mario Sénéchal
- MF Piepoli
- Michelle Dubois
- MM Henneman
- MR Bristow
- MV Pitzalis
- N Lellouche
- P de Groote
- P Flevari
- P Lancellotti
- P Lancellotti
- P Lim
- P Sogaard
- Philippe Pibarot
- Q Ciampi
- RW Troughton
- S Chalil
- TP Cappola
- WA Zoghbi
- WL Miller
- WT Abraham
- Publication venue
- BioMed Central
- Publication date
- 01/01/2009
- Field of study
<p>Abstract</p> <p>Background</p> <p>Cardiac resynchronization therapy (CRT) improves left ventricular (LV) volumes, mitral regurgitation (MR) severity and symptoms of patients with heart failure (HF). However, â„ 30% of patients have no significant clinical or echocardiographic improvement following CRT. Reverse remodeling after CRT correlates with improved clinical outcomes. We hypothesized that in NT-pro BNP monitoring is accurate to identify responders following CRT.</p> <p>Methods</p> <p>42 consecutive patients (mean age 66 ± 12 years, male 68%) with HF undergoing CRT were prospectively enrolled. Responders at follow-up were defined by echocardiography (decrease in LV end systolic volume â„ 15%). Echocardiography and NT-pro BNP measurement were performed at baseline and repeated 3 to 6 month after CRT.</p> <p>Results</p> <p>There was no significant difference between responders (n = 29, 69%) and non-responders (n = 13, 31%) regarding baseline NT-pro BNP level. Responders had significantly higher decrease in NT-pro BNP levels during follow-up than non-responders (absolute: -1428 ± 1333 pg.ml<sup>-1 </sup>vs. -61 ± 959 pg.ml<sup>-1</sup>, p = 0.002; relative: -45 ± 28% vs. 2 ± 28%, p < 0.0001). A decrease of â„ 15% in NT-pro BNP 3â6 months after CRT identifies echocardiographic responders with a sensitivity of 90% and a specificity of 77%.</p> <p>Conclusion</p> <p>NT-pro BNP monitoring can accurately identify echocardiographic responders after CRT.</p
Search for direct pair production of the top squark in all-hadronic final states in proton-proton collisions at sâ=8 TeV with the ATLAS detector
- Author
- Aad G
- Abbott B
- Abdallah J
- Abdinov O
- Aben R
- Abi B
- Abolins M
- AbouZeid OS
- Abramowicz H
- Abreu H
- Abreu R
- Abulaiti Y
- Acharya BS
- Adamczyk L
- Adams DL
- Adelman J
- Adomeit S
- Adye T
- Agatonovic-Jovin T
- Aguilar-Saavedra JA
- Agustoni M
- Ahlen SP
- Ahmadov F
- Aielli G
- Akerstedt H
- Akesson TPA
- Akimoto G
- Akimov AV
- Alberghi GL
- Albert J
- Albrand S
- Alconada Verzini MJ
- Aleksa M
- Aleksandrov IN
- Alexa C
- Alexander G
- Alexandre G
- Alexopoulos T
- Alhroob M
- Alimonti G
- Alio L
- Alison J
- Allbrooke BMM
- Allison LJ
- Allport PP
- Almond J
- Aloisio A
- Alonso A
- Alonso F
- Alpigiani C
- Altheimer A
- Alviggi MG
- Amako K
- Amaral Coutinho Y
- Amelung C
- Amidei D
- Amor Dos Santos SP
- Amorim A
- Amoroso S
- Amram N
- Amundsen G
- Anastopoulos C
- Ancu LS
- Andari N
- Andeen T
- Anders CF
- Anders G
- Anderson KJ
- Andreazza A
- Andrei V
- Anduaga XS
- Angelidakis S
- Angelozzi I
- Anger P
- Angerami A
- Anghinolfi F
- Anh TV
- Anisenkov AV
- Anjos N
- Annovi A
- Antonaki A
- Antonelli M
- Antonov A
- Antos J
- Anulli F
- Aoki M
- Apolle R
- Arabidze G
- Aracena I
- Arai Y
- Araque JP
- Arce ATH
- Arguin J-F
- Argyropoulos S
- Arik M
- Armbruster AJ
- Arnaez O
- Arnal V
- Arnold H
- Arratia M
- Arslan O
- Artamonov A
- Artoni G
- Asai S
- Asbah N
- Ashkenazi A
- Asman B
- Asquith L
- Assamagan K
- Astalos R
- Atkinson M
- Atlay NB
- Auerbach B
- Augsten K
- Aurousseau M
- Avolio G
- Azuelos G
- Azuma Y
- Baak MA
- Baas A
- Bacci C
- Bachacou H
- Bachas K
- Backes M
- Backhaus M
- Badescu E
- Bagiacchi P
- Bagnaia P
- Bai Y
- Bain T
- Baines JT
- Baker OK
- Balek P
- Balli F
- Banas E
- Banerjee S
- Bannoura AAE
- Bansal V
- Bansil HS
- Barajas CAC
- Barak L
- Baranov SP
- Barberio EL
- Barberis D
- Barbero M
- Barillari T
- Barisonzi M
- Barklow T
- Barlow N
- Barnett BM
- Barnett RM
- Barnovska Z
- Baroncelli A
- Barone G
- Barr AJ
- Barreiro F
- Barrera CO
- Bartoldus R
- Barton AE
- Bartos P
- Bartsch V
- Bassalat A
- Basye A
- Bates RL
- Batkova L
- Batley JR
- Battaglia M
- Battistin M
- Bauer F
- Bawa HS
- Beau T
- Beauchemin PH
- Beccherle R
- Bechtle P
- Beck HP
- Becker K
- Becker S
- Beckingham M
- Becot C
- Beddall A
- Beddall AJ
- Bedikian S
- Bednyakov VA
- Bee CP
- Beemster LJ
- Beermann TA
- Begel M
- Behr K
- Belanger-Champagne C
- Belenguer MJ
- Bell PJ
- Bell WH
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- Bella LA
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- Bellerive A
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- Belotskiy K
- Beltramello O
- Benary O
- Benchekroun D
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- Benhammou Y
- Benjamin DP
- Bensinger JR
- Benslama K
- Bentvelsen S
- Berge D
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- Bernard C
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- Bernlochner FU
- Berry T
- Berta P
- Bertella C
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- Bertolucci F
- Bertsche D
- Besana MI
- Besjes GJ
- Bessidskaia O
- Bessner MF
- Besson N
- Betancourt C
- Bethke S
- Bhimji W
- Bianchi RM
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- Biebel O
- Bieniek SP
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- Biglietti M
- Bilokon H
- Bindi M
- Binet S
- Bingul A
- Bini C
- Black CW
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- Blocker C
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- Castanheira MTD
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- Castillo IS
- Castillo LRF
- Castro NF
- Catastini P
- Catinaccio A
- Catmore JR
- Cattai A
- Cattani G
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- Cavaliere V
- Cavalli D
- Cavalli-Sforza M
- Cavasinni V
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- Cervelli A
- Cetin SA
- Chafaq A
- Chakraborty D
- Chalupkova I
- Chang P
- Chapleau B
- Chapman JD
- Charfeddine D
- Charlton DG
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- Chekulaev SV
- Chelkov GA
- Chelstowska MA
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- Chen H
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- Cheplakov A
- Cherkaoui El Moursli R
- Chernyatin V
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- Chiarella V
- Chiefari G
- Childers JT
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- Chiodini G
- Chisholm AS
- Chislett RT
- Chitan A
- Chizhov MV
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- Chow BKB
- Chromek-Burckhart D
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- Citron ZH
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- Clemens JC
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- Collaboration ATLAS
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- Coniavitis E
- Conidi MC
- Connell SH
- Connelly IA
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- Cooper BD
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- Youssef S
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- Yusuff I
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- Zaidan R
- Zaitsev AM
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- Zambito S
- Zanello L
- Zanzi D
- Zeitnitz C
- Zeman M
- Zemla A
- Zengel K
- Zenin O
- Zenis T
- Zerwas D
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- Zhemchugov A
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- Zhukov K
- Zibell A
- Zieminska D
- Zimine NI
- Zimmermann C
- Zimmermann R
- Zimmermann S
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- Zinonos Z
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- Zobernig G
- Zoccoli A
- zur Nedden M
- Zurzolo G
- Zutshi V
- Zwalinski L
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/2014
- Field of study
The results of a search for direct pair production of the scalar partner to the top quark using an integrated luminosity of 20.1fbâ1 of protonâproton collision data at âs = 8 TeV recorded with the ATLAS detector at the LHC are reported. The top squark is assumed to decay via tËâtÏË01 or tËâ bÏ˱1 âbW(â)ÏË01 , where ÏË01 (Ï˱1 ) denotes the lightest neutralino (chargino) in supersymmetric models. The search targets a fully-hadronic final state in events with four or more jets and large missing transverse momentum. No significant excess over the Standard Model background prediction is observed, and exclusion limits are reported in terms of the top squark and neutralino masses and as a function of the branching fraction of tË â tÏË01 . For a branching fraction of 100%, top squark masses in the range 270â645 GeV are excluded for ÏË01 masses below 30 GeV. For a branching fraction of 50% to either tË â tÏË01 or tË â bÏ˱1 , and assuming the Ï˱1 mass to be twice the ÏË01 mass, top squark masses in the range 250â550 GeV are excluded for ÏË01 masses below 60 GeV
Measurement of the cross-section of high transverse momentum vector bosons reconstructed as single jets and studies of jet substructure in pp collisions at âs = 7 TeV with the ATLAS detector
- Author
- Aad G
- Abajyan T
- Abbott B
- Abdallah J
- Abdinov O
- Aben R
- Abi B
- Abolins M
- AbouZeid OS
- Abramowicz H
- Abreu H
- Abulaitia Y
- Acharya BS
- Adamczyk L
- Adams DL
- Addy TN
- Adelman J
- Adomeit S
- Adye T
- Agatonovic-Jovin T
- Aguilar-Saavedra JA
- Agustoni M
- Ahlen SP
- Ahmadov F
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- Bagiacchi P
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- Bailey DC
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- Benary O
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- Bessidskaia O
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- Blazeka T
- Bloch I
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- Buchholz P
- Buckingham RM
- Buckley AG
- Buda SI
- Budagov IA
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- Buescher V
- Bugge L
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- Bulekov O
- Bundock AC
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- Burghgrave B
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- Burmeister I
- Busato E
- Bussey P
- Bustos ACF
- Buszello CP
- Butler B
- Butler JM
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- Buttar CM
- Butterworth JM
- Buttinger W
- Buzatu A
- Byszewski M
- Cabrera Urban S
- Caforio D
- Cakir IT
- Cakir O
- Calafiura P
- Calderini G
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- Calkins R
- Caloba LP
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- Calvet S
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- Camillocci ES
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- Caminal Armadans R
- Campana S
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- Carter JR
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- Castanheira MTD
- Castelli A
- Castillo Gimenez V
- Castillo IS
- Castillo LRF
- Castillo LRF
- Castro NF
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- Catinaccio A
- Catmore JR
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- Chalupkova I
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- Chekulaev SV
- Chelkov GA
- Chelstowska MA
- Chen C
- Chen H
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- Chen S
- Chen X
- Chen Y
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- Cheng Y
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- Chernyatin V
- Cheu E
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- Chiarella V
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- Childers JT
- Chilingarov A
- Chiodini G
- Chisholm AS
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- Chouridou S
- Chow BKB
- Christidi IA
- Chromek-Burckhart D
- Chu ML
- Chudoba J
- Ciapetti G
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- Cindro V
- Ciocio A
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- Coniavitis E
- Conidi MC
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- Consorti V
- Constantinescu S
- Conta C
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- Correia AMH
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- Cortes-Gonzalez A
- Cortiana G
- Costa G
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- Da Costa JGPF
- Da Costa JGPF
- Da Cunha Sargedas De Sousa MJ
- Da Via C
- Dabrowski W
- Dafinca A
- Dai T
- Dale O
- Dallaire F
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- De Bruin PHS
- De Castro S
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- de Graat J
- De Groot N
- de Jong P
- De la Taille C
- De la Torre H
- de Lima DEF
- de Lima DEF
- De Lorenzi F
- De Mendizabal JB
- De Nooij L
- De Pedis D
- De Regie JBDV
- de Renstrom PAB
- De Salvo A
- De Sanctis U
- De Santo A
- De Zorzi G
- De K
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- Debbe R
- Debenedetti C
- Dechenaux B
- Dedovich DV
- Degenhardt J
- Deigaard I
- Del Peso J
- Del Prete T
- Delemontex T
- Deliot F
- Deliyergiyev M
- Dell'Acqua A
- Dell'Asta L
- Della Pietra M
- della Porta GZ
- della Volpe D
- Delmastro M
- Delsart PA
- Deluca C
- Demers S
- Demichev M
- Demilly A
- Demirkoz B
- Denisov SP
- Derendarz D
- Derkaoui JE
- Derue F
- Dervan P
- Desch K
- Deviveiros PO
- Dewhurst A
- Dhaliwal S
- Di Ciaccio A
- Di Ciaccio L
- Di Domenico A
- Di Donato C
- Di Girolamo A
- Di Girolamo B
- Di Mattia A
- Di Micco B
- Di Nardo R
- Di Simone A
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- Dimitrievska A
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- Dionisi C
- Dita P
- Dita S
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- Djama F
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- do Vale MAB
- Doan TKO
- Dobos D
- Dobson E
- Doglioni C
- Doherty T
- Dohmae T
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- Dolezal Z
- Dolgoshein BA
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- Dos Santos DR
- Dotti A
- Dova MT
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- Dris M
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- Dubreuil E
- Duchovni E
- Duckeck G
- Ducu OA
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- Dudarev A
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- Dueren M
- Duflot L
- Duguid L
- Dunford M
- Dwuznik M
- Ebke J
- Edson W
- Edwards NC
- Ehrenfeld W
- Eifert T
- Eigen G
- Einsweiler K
- Ekelof T
- El Kacimi M
- El Moursli A
- El Moursli RC
- Ellert M
- Elles S
- Ellinghaus F
- Ellinghaus F
- Ellis N
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- Elmsheuser J
- Elmsheuser J
- Elsing M
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- Emeliyanov D
- Emeliyanov D
- Enari Y
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- Endner OC
- Endner OC
- Endo M
- Endo M
- Engelmann R
- Engelmann R
- Erdmann J
- Erdmann J
- Ereditato A
- Ereditato A
- Eriksson D
- Eriksson D
- Ernis G
- Ernis G
- Ernst J
- Ernst J
- Ernst M
- Ernst M
- Ernwein J
- Ernwein J
- Errede D
- Errede D
- Errede S
- Errede S
- Ertel E
- Ertel E
- Escalier M
- Escalier M
- Esch H
- Esch H
- Escobar C
- Escobar C
- Espinal Curull X
- Espinal Curull X
- Esposito B
- Esposito B
- Etienne F
- Etienne F
- Etienvre AI
- Etienvre AI
- Etzion E
- Etzion E
- Evans H
- Evans H
- Fabbri L
- Fabbri L
- Facini G
- Facini G
- Fajardo LSG
- Fajardo LSG
- Fakhrutdinov RM
- Fakhrutdinov RM
- Falciano S
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- Faltova J
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- Fang Y
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- Fanti M
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- Farbin A
- Farbin A
- Farilla A
- Farilla A
- Farooque T
- Farooque T
- Farrell S
- Farrell S
- Farrington SM
- Farrington SM
- Farthouat P
- Farthouat P
- Fassi F
- Fassi F
- Fassnacht P
- Fassnacht P
- Fassouliotis D
- Fassouliotis D
- Favareto A
- Favareto A
- Fayard L
- Fayard L
- Federic P
- Federic P
- Fedin OL
- Fedin OL
- Fedorko W
- Fedorko W
- Fehling-Kaschek M
- Fehling-Kaschek M
- Feigl S
- Feigl S
- Feligioni L
- Feligioni L
- Feng C
- Feng C
- Feng EJ
- Feng EJ
- Feng H
- Feng H
- Fenyuk AB
- Fenyuk AB
- Fernando W
- Fernando W
- Ferrag S
- Ferrag S
- Ferrando BMS
- Ferrando J
- Ferrando J
- Ferrara V
- Ferrara V
- Ferrari A
- Ferrari A
- Ferrari P
- Ferrari P
- Ferrari R
- Ferrari R
- Ferrer A
- Ferrer A
- Ferrere D
- Ferrere D
- Ferretti C
- Ferretti C
- Fiascaris M
- Fiascaris M
- Fiedler F
- Fiedler F
- Filipcic A
- Filipcic A
- Filipuzzi M
- Filipuzzi M
- Filthaut F
- Filthaut F
- Fincke-Keeler M
- Fincke-Keeler M
- Finelli KD
- Finelli KD
- Fiolhais MCN
- Fiolhais MCN
- Fiorini L
- Fiorini L
- Firan A
- Firan A
- Fischer J
- Fischer J
- Fisher MJ
- Fisher MJ
- Fitzgerald EA
- Fitzgerald EA
- Flechl M
- Flechl M
- Fleck I
- Fleck I
- Fleischmann P
- Fleischmann P
- Fleischmann S
- Fleischmann S
- Fletcher G
- Fletcher G
- Fletcher GT
- Fletcher GT
- Flick T
- Flick T
- Floderus A
- Floderus A
- Florez Bustos AC
- Flowerdew MJ
- Flowerdew MJ
- Formica A
- Formica A
- Forti A
- Forti A
- Fortin D
- Fortin D
- Fournier D
- Fournier D
- Fox H
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- Francavilla P
- Francavilla P
- Franchini M
- Franchini M
- Franchino S
- Franchino S
- Francis D
- Francis D
- Franklin M
- Franklin M
- Franz S
- Franz S
- Fraternali M
- Fraternali M
- Fratin S
- Fratina S
- French ST
- French ST
- Friedrich C
- Friedrich C
- Friedrich F
- Friedrich F
- Froidevaux D
- Froidevaux D
- Frost JA
- Frost JA
- Fukunaga C
- Fukunaga C
- Fulsom BG
- Fulsom BG
- Fuster J
- Fuster J
- Gabaldon C
- Gabaldon C
- Gabizon O
- Gabizon O
- Gabrielli A
- Gabrielli A
- Gabrielli A
- Gabrielli A
- Gadatsch S
- Gadatsch S
- Gadomski S
- Gadomski S
- Gagliardi G
- Gagliardi G
- Gagnon P
- Gagnon P
- Galea C
- Galea C
- Galhardo B
- Galhardo B
- Gallas EJ
- Gallas EJ
- Gallo V
- Gallo V
- Gallop BJ
- Gallop BJ
- Gallus P
- Gallus P
- Galster G
- Galster G
- Gan KK
- Gan KK
- Gandrajula RP
- Gandrajula RP
- Gao J
- Gao YS
- Gao YS
- Gaob J
- Garberson F
- Garberson F
- Garcia Navarro JE
- Garcia Navarro JE
- Garcia BRM
- Garcia C
- Garcia C
- Garcia JAB
- Garcia-Sciveres M
- Garcia-Sciveres M
- Gardner RW
- Gardner RW
- Garelli N
- Garelli N
- Garonne V
- Garonne V
- Garrido MDMC
- Gatti C
- Gatti C
- Gaudio G
- Gaudio G
- Gaur B
- Gaur B
- Gauthier L
- Gauthier L
- Gauzzi P
- Gauzzi P
- Gavrilenko IL
- Gavrilenko IL
- Gay C
- Gay C
- Gaycken G
- Gaycken G
- Gazis EN
- Gazis EN
- Ge P
- Ge P
- Gecse Z
- Gecse Z
- Gee CNP
- Gee CNP
- Geerts DAA
- Geerts DAA
- Geich-Gimbel C
- Geich-Gimbel C
- Gellerstedt K
- Gellerstedt K
- Gemme C
- Gemme C
- Gemmell A
- Gemmell A
- Genest MH
- Genest MH
- Gentile S
- Gentile S
- George M
- George M
- George S
- George S
- Gerbaudo D
- Gerbaudo D
- Gershon A
- Gershon A
- Ghazlane H
- Ghazlane H
- Ghodbane N
- Ghodbane N
- Giacobbe B
- Giacobbe B
- Giagu S
- Giagu S
- Giangiobbe V
- Giangiobbe V
- Giannetti P
- Giannetti P
- Gianotti F
- Gianotti F
- Gibbard B
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- Gibson SM
- Gibson SM
- Gilchriese M
- Gilchriese M
- Gillam TPS
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- Gillberg D
- Gillberg D
- Gillman AR
- Gillman AR
- Gingrich DM
- Gingrich M
- Giokaris N
- Giokaris N
- Giordani MP
- Giordani MP
- Giordano R
- Giordano R
- Giorgi FM
- Giorgi FM
- Giraud PF
- Giraud PF
- Giugni D
- Giugni D
- Giuliani C
- Giuliani C
- Giunta M
- Giunta M
- Gjelsten BK
- Gjelsten BK
- Gkialas I
- Gkialas I
- Gladilin LK
- Gladilin LK
- Glasman C
- Glasman C
- Glatzer J
- Glatzer J
- Glazov A
- Glazov A
- Glonti GL
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- Goblirsch-Kolb M
- Goblirsch-Kolb M
- Goddard JR
- Goddard JR
- Godfrey J
- Godfrey J
- Godlewski J
- Godlewski J
- Goeringer C
- Goeringer C
- Goessling C
- Goessling C
- Goldfarb S
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- Golling T
- Golling T
- Golubkov D
- Golubkov D
- Gomes A
- Gomes A
- Gonalo R
- Goncalo R
- Gonella L
- Gonella L
- Gonzalez de la Hoz S
- Gonzalez de la Hoz S
- Gonzalez Parra G
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- Gonzalez BA
- Gonzalez-Sevilla S
- Gonzalez-Sevilla S
- Goossens L
- Goossens L
- Gorbounov PA
- Gorbounov PA
- Gordon HA
- Gordon HA
- Gorelov I
- Gorelov I
- Gorini B
- Gorini B
- Gorini E
- Gorini E
- Gorisek A
- Gorisek A
- Gornicki E
- Gornicki E
- Goshaw AT
- Goshaw AT
- Gostkin MI
- Gostkin MI
- Gouighri M
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- Goujdami D
- Goujdami D
- Goulette MP
- Goulette MP
- Goussiou AG
- Goussiou AG
- Goy C
- Goy C
- Gozpinar S
- Gozpinar S
- Grabas HMX
- Grabas HMX
- Graber L
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- Grabowska-Bold I
- Grabowska-Bold I
- Grafstroem P
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- Gramling J
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- Grancagnolo F
- Grancagnolo S
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- Grancagnoloa F
- Grassi V
- Grassi V
- Gratchev V
- Gratchev V
- Gray HM
- Gray HM
- Graziani E
- Graziani E
- Grebenyuk OG
- Grebenyuk OG
- Greenwood ZD
- Greenwood ZD
- Gregersen K
- Gregersen K
- Gregor IM
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- Griffiths J
- Griffiths J
- Grillo AA
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- Grimm K
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- Grinstein S
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- Gris P
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- Grishkevich YV
- Grishkevich YV
- Griso SP
- Grivaz J-F
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- Grohs JP
- Grohs JP
- Grohsjean A
- Gross AGE
- Gross E
- Grosse-Knetter J
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- Grossi GC
- Grossi GC
- Groth-Jensen J
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- Guescini F
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- Guest D
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- Gueta O
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- Guicheney C
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- Guido E
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- Guindon S
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- Publication venue
- 'IOP Publishing'
- Publication date
- 01/01/2014
- Field of study
This paper presents a measurement of the cross-section for high transverse momentum W and Z bosons produced in pp collisions and decaying to all-hadronic final states. The data used in the analysis were recorded by the ATLAS detector at the CERN Large Hadron Collider at a centre-of-mass energy of âs = 7 TeV;{\rm Te}{\rm V}andcorrespondtoanintegratedluminosityof4.6\;{\rm f}{{{\rm b}}^{-1}}.ThemeasurementisperformedbyreconstructingtheboostedWorZbosonsinsinglejets.ThereconstructedjetmassisusedtoidentifytheWandZbosons,andajetsubstructuremethodbasedonenergyclusterinformationinthejetcentreâofâmassframeisusedtosuppressthelargemultiâjetbackground.ThecrossâsectionforeventswithahadronicallydecayingWorZboson,withtransversemomentum{{p}_{{\rm T}}}\gt 320\;{\rm Ge}{\rm V}andpseudorapidity|\eta |\lt 1.9,ismeasuredtobe{{\sigma }_{W+Z}}=8.5\pm 1.7$ pb and is compared to next-to-leading-order calculations. The selected events are further used to study jet grooming techniques
Search for pair-produced long-lived neutral particles decaying to jets in the ATLAS hadronic calorimeter in ppcollisions at âs=8TeV
- Author
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- Youssef S
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- Zaidan R
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- Zanzi D
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- Zhao Z
- Zhemchugov A
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- Zhuang X
- Zhukov K
- Zibell A
- Zieminska D
- Zimine NI
- Zimmermann C
- Zimmermann R
- Zimmermann S
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- Zinonos Z
- Ziolkowski M
- Zobernig G
- Zoccoli A
- zur Nedden M
- Zurzolo G
- Zutshi V
- Zwalinski L
- Publication venue
- 'Elsevier BV'
- Publication date
- 01/01/2014
- Field of study
The ATLAS detector at the Large Hadron Collider at CERN is used to search for the decay of a scalar boson to a pair of long-lived particles, neutral under the Standard Model gauge group, in 20.3fbâ1of data collected in protonâproton collisions at âs=8TeV. This search is sensitive to long-lived particles that decay to Standard Model particles producing jets at the outer edge of the ATLAS electromagnetic calorimeter or inside the hadronic calorimeter. No significant excess of events is observed. Limits are reported on the product of the scalar boson production cross section times branching ratio into long-lived neutral particles as a function of the proper lifetime of the particles. Limits are reported for boson masses from 100 GeVto 900 GeV, and a long-lived neutral particle mass from 10 GeVto 150 GeV
Observation of associated near-side and away-side long-range correlations in âsNN=5.02ââTeV proton-lead collisions with the ATLAS detector
- Author
- Aad G
- Abajyan T
- Abbott B
- Abdallah J
- Abdel Khalek S
- Abdelalim AA
- Abdinov O
- Aben R
- Abi B
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- Yamanaka T
- Yamauchi K
- Yamazaki T
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- Yen AL
- Yilmaz M
- Yoosoofmiya R
- Yorita K
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- Youssef S
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- Yurkewicz A
- Zabinski B
- Zaidan R
- Zaitsev AM
- Zambito S
- Zanello L
- Zanzi D
- Zaytsev A
- Zeitnitz C
- Zeman M
- Zemla A
- Zenin O
- ZeniĆĄ T
- Zerwas D
- Zevi Della Porta G
- Zhang D
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- Zhao Z
- Zhemchugov A
- Zhong J
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- Zhuang X
- Zhuravlov V
- Zibell A
- Zieminska D
- Zimin NI
- Zimmermann R
- Zimmermann S
- Zimmermann S
- Zinonos Z
- Ziolkowski M
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- Zmouchko VV
- Zobernig G
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- Zur Nedden M
- Zutshi V
- Zwalinski L
- Publication venue
- American Physical Society
- Publication date
- 01/01/2012
- Field of study
Two-particle correlations in relative azimuthal angle (ÎÏ) and pseudorapidity (Îη) are measured in âsNN=5.02ââTeV p+Pb collisions using the ATLAS detector at the LHC. The measurements are performed using approximately 1ââÎŒb-1 of data as a function of transverse momentum (pT) and the transverse energy (ÎŁETPb) summed over 3.1<η<4.9 in the direction of the Pb beam. The correlation function, constructed from charged particles, exhibits a long-range (2<|Îη|<5) ânear-sideâ (ÎÏâŒ0) correlation that grows rapidly with increasing ÎŁETPb. A long-range âaway-sideâ (ÎÏâŒÏ) correlation, obtained by subtracting the expected contributions from recoiling dijets and other sources estimated using events with small ÎŁETPb, is found to match the near-side correlation in magnitude, shape (in Îη and ÎÏ) and ÎŁETPb dependence. The resultant ÎÏ correlation is approximately symmetric about Ï/2, and is consistent with a dominant cosâĄ2ÎÏ modulation for all ÎŁETPb ranges and particle pT
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