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Institution

University of Turin

EducationTurin, Piemonte, Italy
About: University of Turin is a education organization based out in Turin, Piemonte, Italy. It is known for research contribution in the topics: Population & Cancer. The organization has 29607 authors who have published 77952 publications receiving 2480900 citations. The organization is also known as: Universita degli Studi di Torino & Università degli Studi di Torino.


Papers
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Journal ArticleDOI
TL;DR: In this paper, a self-consistent empirical model for several plasma parameters of a polar coronal hole near solar minimum, derived from observations with the Solar and Heliospheric Observatory Ultraviolet Coronagraph Spectrometer, is presented.
Abstract: We present a self-consistent empirical model for several plasma parameters of a polar coronal hole near solar minimum, derived from observations with the Solar and Heliospheric Observatory Ultraviolet Coronagraph Spectrometer. The model describes the radial distribution of density for electrons, H0, and O5 + and the outflow velocity and unresolved most probable velocities for H0 and O5 + during the period between 1996 November and 1997 April. In this Letter, we compare observations of H I Lyα and O VI λλ1032, 1037 emission lines with spatial models of the plasma parameters, and we iterate for optimal consistency between measured and synthesized observable quantities. The unexpectedly large line widths of H0 atoms and O5 + ions at most radii are the result of anisotropic velocity distributions, which are not consistent with purely thermal motions or the expected motions from a combination of thermal and transverse wave velocities. Above 2 R, the observed transverse, most probable speeds for O5 + are significantly larger than the corresponding motions for H0, and the outflow velocities of O5 + are also significantly larger than the corresponding velocities of H0. We discuss the constraints and implications on various theoretical models of coronal heating and acceleration.

432 citations

Journal ArticleDOI
TL;DR: Surgery is recommended for masses with suspicious radiological aspects and masses causing overt catecholamine or steroid excess and adrenalectomy may be considered when an adequate medical therapy does not reach the treatment goals of associated diseases potentially linked to hypercortisolism.
Abstract: Objective: To assess currently available evidence on adrenal incidentaloma and provide recommendations for clinical practice. Design: A panel of experts (appointed by the Italian Association of Clinical Endocrinologists (AME)) appraised the methodological quality of the relevant studies, summarized their results, and discussed the evidence reports to find consensus. Radiological assessment: Unenhanced computed tomography (CT) is recommended as the initial test with the use of an attenuation value of %10 Hounsfield units (HU) to differentiate between adenomas and non-adenomas. For tumors with a higher baseline attenuation value, we suggest considering delayed contrast-enhanced CT studies. Positron emission tomography (PET) or PET/CT should be considered when CT is inconclusive, whereas fine needle aspiration biopsy may be used only in selected cases suspicious of metastases (after biochemical exclusion of pheochromocytoma). Hormonal assessment: Pheochromocytoma and excessive overt cortisol should be ruled out in all patients, whereas primary aldosteronism has to be considered in hypertensive and/or hypokalemic patients. The 1 mg overnight dexamethasone suppression test is the test recommended for screening of subclinical Cushing’s syndrome (SCS) with a threshold at 138 nmol/l for considering this condition. A value of 50 nmol/l virtually excludes SCS with an area of uncertainty between 50 and 138 nmol/l. Management: Surgery is recommended for masses with suspicious radiological aspects and masses causing overt catecholamine or steroid excess. Data are insufficient to make firm recommendations for or against surgery in patients with SCS. However, adrenalectomy may be considered when an adequate medical therapy does not reach the treatment goals of associated diseases potentially linked to hypercortisolism.

432 citations

Journal ArticleDOI
William D. Travis1, Hisao Asamura2, Alexander A. Bankier3, Mary Beth Beasley4, Frank C. Detterbeck5, Douglas B. Flieder6, Jin Mo Goo7, Heber MacMahon8, David P. Naidich9, Andrew G. Nicholson10, Charles A. Powell, Mathias Prokop11, Ramón Rami-Porta12, Valerie W. Rusch1, Paul Van Schil, Yasushi Yatabe, Peter Goldstraw10, David Ball13, David G. Beer14, Ricardo Beyruti15, Vanessa Bolejack16, Kari Chansky16, John Crowley16, Wilfried Eberhardt17, John G. Edwards18, Françoise Galateau-Salle19, Dorothy Giroux16, Fergus V. Gleeson20, Patti A. Groome21, James Huang1, Catherine Kennedy22, Jhingook Kim23, Young Tae Kim24, Laura Kingsbury16, Haruhiko Kondo25, Mark Krasnik26, Kaoru Kubota27, Antoon Lerut28, Gustavo Lyons29, Mirella Marino, Edith M. Marom30, Jan P. van Meerbeeck31, Alan Mitchell16, Takashi Nakano32, Anna K. Nowak33, Michael D Peake34, Thomas W. Rice35, Kenneth E. Rosenzweig36, Enrico Ruffini37, Nagahiro Saijo, Jean-Paul Sculier38, Lynn Shemanski16, Kelly G. Stratton16, Kenji Suzuki39, Yuji Tachimori40, Charles F. Thomas41, William D. Travis1, Ming-Sound Tsao42, Andrew T. Turrisi43, Johan Vansteenkiste28, Hirokazu Watanabe, Yi-Long Wu, Paul Baas44, Jeremy J. Erasmus30, Seiki Hasegawa32, Kouki Inai45, Kemp H. Kernstine46, Hedy L. Kindler8, Lee M. Krug1, Kristiaan Nackaerts28, Harvey I. Pass9, David C. Rice30, Conrad Falkson21, Pier Luigi Filosso37, Giuseppe Giaccone47, Kazuya Kondo48, Marco Lucchi49, Meinoshin Okumura50, Eugene H. Blackstone35 
TL;DR: Codes for the primary tumor categories of AIS and minimally invasive adenocarcinoma (MIA) and a uniform way to measure tumor size in part‐solid tumors for the eighth edition of the tumor, node, and metastasis classification of lung cancer are proposed.

431 citations

Journal ArticleDOI
TL;DR: The study was terminated after the interim analysis concluded that the study was highly unlikely to meet its primary end point, and no clinical benefit was observed from adding sorafenib to CP chemotherapy as first-line treatment for NSCLC.
Abstract: Purpose This phase III, multicenter, randomized, placebo-controlled trial assessed the efficacy and safety of sorafenib, an oral multikinase inhibitor, in combination with carboplatin and paclitaxel in chemotherapy-naive patients with unresectable stage IIIB or IV non–small-cell lung cancer (NSCLC). Patients and Methods Nine hundred twenty-six patients were randomly assigned to receive up to six 21-day cycles of carboplatin area under the curve 6 and paclitaxel 200 mg/m2 (CP) on day 1, followed by either sorafenib 400 mg twice a day (n = 464, arm A) or placebo (n = 462, arm B) on days 2 to 19. The maintenance phase after CP consisted of sorafenib 400 mg or placebo twice a day. The primary end point was overall survival (OS); secondary end points included progression-free survival and tumor response. Results Overall demographics were balanced between arms; 223 patients (24%) had squamous cell histology. On the basis of a planned interim analysis, median OS was 10.7 months in arm A and 10.6 months in arm B ...

431 citations

Journal ArticleDOI
11 Jul 2008-Cell
TL;DR: It is demonstrated that a Rab5-to-Rac circuitry controls the morphology of motile mammalian tumor cells and primordial germinal cells during zebrafish development, suggesting that this circuitry is relevant for the regulation of migratory programs in various cells, in both in vitro settings and whole organisms.

430 citations


Authors

Showing all 30045 results

NameH-indexPapersCitations
Michael Grätzel2481423303599
Lewis C. Cantley196748169037
Kenneth C. Anderson1781138126072
Elio Riboli1581136110499
Giacomo Bruno1581687124368
Silvia Franceschi1551340112504
Thomas E. Starzl150162591704
Paolo Boffetta148145593876
Marco Costa1461458105096
Pier Paolo Pandolfi14652988334
Andrew Ivanov142181297390
Chiara Mariotti141142698157
Tomas Ganz14148073316
Jean-Pierre Changeux13867276462
Dong-Chul Son138137098686
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
2023202
2022623
20215,733
20205,428
20194,544
20184,233