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Institution

Hebron University

EducationHebron, Palestinian Territory
About: Hebron University is a education organization based out in Hebron, Palestinian Territory. It is known for research contribution in the topics: Population & Cancer. The organization has 2714 authors who have published 4180 publications receiving 163736 citations.


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Journal ArticleDOI
TL;DR: In this population of patients treated with entecvir after CHB‐related LT, entecavir was well tolerated and effective in maintaining viral suppression, even in individuals who experienced a reappearance of HBsAg.

45 citations

Journal ArticleDOI
TL;DR: Although the authors' patients had more severe disease than those in the pivotal study, a similar reduction in ARR was observed, in line with previous observational studies, the effect was independent of baseline EDSS.
Abstract: Natalizumab has been shown to be effective in pivotal clinical trials in multiple sclerosis; however, the patients in whom treatment is indicated in clinical practice have a different clinical profile from those included in the clinical trials. The aim of this study is therefore to collect data on natalizumab use in everyday clinical practice in Spain. The 86 participating centers throughout Spain submitted data on disease characteristics at baseline and after treatment. Valid data were available for 1,364 patients (69.3% women, 86.9% with relapsing–remitting disease). Ninety-three percent had received prior therapy for multiple sclerosis. For the 825 patients on treatment for at least a year, the annualized relapse rate (ARR) decreased from median 2.0 [mean 2.01, 95% confidence interval (CI) 1.92–2.11] in the year prior to natalizumab to 0.0 (mean 0.25, 95% CI 0.21–0.29) at 1 year (p < 0.001). The Expanded Disability Status Scale (EDSS) score decreased from median 3.5 at baseline (mean 3.71, 95% CI 3.60–3.82) to 3.0 (mean 3.37, 95% CI 3.25–3.49) (p < 0.0001). The discontinuation rate was 14%. One patient discontinued natalizumab due to progressive multifocal leukoencephalopathy (PML) and another due to probable PML (subsequently confirmed). Although our patients had more severe disease than those in the pivotal study, a similar reduction in ARR was observed. This finding is in line with previous observational studies. The effect was independent of baseline EDSS.

45 citations

Journal ArticleDOI
TL;DR: This study, which is the largest conducted to date in a South American population, provides a comprehensive analysis on the type and distribution of BRCA1/2 mutations and allelic variants.
Abstract: The distribution of BRCA1/2 germline mutations in breast/ovarian cancer (BC/OC) families varies among different populations. In the Chilean population, there are only two reports of mutation analysis of BRCA1/2, and these included a low number of BC and/or OC patients. Moreover, the prevalence of BRCA1/2 genomic rearrangements in Chilean and in other South American populations is unknown. In this article, we present the mutation-detection data corresponding to a set of 326 high-risk families analyzed by conformation-sensitive gel electrophoresis and heteroduplex analysis. To determine the contribution of BRCA1/2 LGRs in Chilean BC patients, we analyzed 56 high-risk subjects with no pathogenic BRCA1/2 point mutations. Germline BRCA1/2 point mutations were found in 23 (7.1%) of the 326 Chilean families. Families which had at least three BC and/or OC cases showed the highest frequency of mutations (15.9%). We identified 14 point pathogenic mutations. Three recurrent mutations in BRCA1 (c.187_188delAG, c.2605_2606delTT, and c.3450_3453delCAAG) and three in BRCA2 (c.4969_4970insTG, c.5374_5377delTATG, and c.6503_6504delTT) contributed to 63.6 and 66.7% of all the deleterious mutations of each gene, which may reflect the presence of region-specific founder effects. Taken together BRCA1/2 recurrent point mutations account for 65.2% (15/23) of the BRCA1/2 (+) families. No large deletions or duplications involving BRCA1/2 were identified in a subgroup of 56 index cases negative for BRCA1/2 point mutations. Our study, which is the largest conducted to date in a South American population, provides a comprehensive analysis on the type and distribution of BRCA1/2 mutations and allelic variants.

45 citations

Journal ArticleDOI
Petra Seibold1, A. Webb2, Miguel E. Aguado-Barrera3, David Azria4, Céline Bourgier4, Muriel Brengues5, Erik Briers, Renée Bultijnck6, Patricia Calvo-Crespo, Ana Carballo, Ananya Choudhury7, Alessandro Cicchetti, Johannes Claßen, Elena Delmastro, Alison M. Dunning8, Rebecca Elliott7, Laura Fachal8, Marie-Pierre Farcy-Jacquet, Pietro Gabriele, Elisabetta Garibaldi, Antonio Gómez-Caamaño, Sara Gutiérrez-Enríquez, Daniel S. Higginson9, Kerstie Johnson2, Ramón Lobato-Busto, M. Molla10, Anusha Müller1, Debbie Payne11, Paula Peleteiro, Giselle Post6, Tiziana Rancati, Tim Rattay2, V. Reyes10, Barry S. Rosenstein12, Dirk De Ruysscher13, Dirk De Ruysscher14, Maria De Santis, Jörg Schäfer, Thomas Schnabel, Elena Sperk15, R. Paul Symonds2, Hilary Stobart, Begoña Taboada-Valladares, Christopher J. Talbot2, Riccardo Valdagni16, Ana Vega3, Liv Veldeman17, Liv Veldeman6, Timothy H Ward18, Christian Weißenberger, Catharine M L West7, Jenny Chang-Claude19, Jenny Chang-Claude1, Yolande Lievens6, Yolande Lievens17, Marc van Eijkeren17, Marc van Eijkeren6, Katrien Vandecasteele6, Katrien Vandecasteele17, Elhaseen Elhamin6, Elhaseen Elhamin17, Piet Ost6, Piet Ost17, Valérie Fonteyne17, Valérie Fonteyne6, Martijn Swimberghe6, Martijn Swimberghe17, Pieter Deseyne17, Pieter Deseyne6, Wilfried De Neve6, Wilfried De Neve17, F. Duprez17, F. Duprez6, Marcus Mareel17, Marcus Mareel6, Christel Monten17, Christel Monten6, Annick Van Greveling17, Tom Vercauteren6, Tom Vercauteren17, Leen Paelinck17, Gilles Defraene13, R Aerts13, Soumia Arredouani13, Maarten Lambrecht13, Ben G. L. Vanneste14, Roxana Draghici4, Frank A. Giordano15, Carsten Herskind15, Marlon R. Veldwijk15, Irmgard Helmbold1, Ulrich Giesche, Petra Stegmaier, Christian Weiß, Thomas Blaschke, Burkhard Neu, Laura Lozza, Barbara Avuzzi, S. Morlino, Claudia Sangalli, Marzia Franceschini, Belina Rodriguez-Lage, Juan Fernández-Tajes, Olivia Fuentes-Rios, Isabel Dominguez-Rios, Irene Fajardo-Paneque, Paloma Sosa-Fajardo, Laura Torrado-Moya, Mónica Ramos-Albiac10, A. Giraldo10, Manolo Altabas10, Bibiana Piqué-Leiva10, David García-Relancio10, Alejandro Seoane-Ramallo10, Samuel Lavers2, Simon Wright20, Hannah Dobbelaere2, Donna Appleton21, Donna Appleton20, Monika Kaushik20, Frances Kenny20, Hazem Khout20, Hazem Khout22, Jaroslaw Krupa20, Kelly Lambert20, Simon Pilgrim20, Sheila Shokuhi20, Kalliope Valassiadou20, Luis Aznar-Garcia22, Luis Aznar-Garcia20, Ion Boiangui23, Ion Boiangui20, Kiran Kancherla20, Christopher Kent20, Kufre Sampson20, Ahmed Osman20, Thiagarajan Sridhar20, Subramaniam Vasanthan20, Corinne Faivre-Finn11, Victoria Harrop24, Manjusha Keni25, Karen Foweraker22, Abigail Pascoe22, Claire P. Esler22, Richard G. Stock12, Sheryl Green12, Ava Golchin12, William Li26 
TL;DR: The comprehensive centralised database and linked biobank is a valuable resource for the radiotherapy community for validating predictive models and biomarkers and will also enable a better understanding of how many people suffer with radiotherapy toxicity.

45 citations

Journal ArticleDOI
Julien Cohen-Adad1, Julien Cohen-Adad2, Eva Alonso-Ortiz1, Mihael Abramovic, Carina Arneitz, Nicole Atcheson3, Laura Barlow4, Robert L. Barry5, Robert L. Barry6, Markus Barth3, Marco Battiston7, Christian Büchel8, Matthew D. Budde9, Virginie Callot10, Anna J.E. Combes11, Benjamin De Leener1, Benjamin De Leener2, Maxime Descoteaux12, Paulo Loureiro de Sousa13, Marek Dostál14, Julien Doyon15, Adam V. Dvorak4, Falk Eippert16, Karla R. Epperson17, Kevin S. Epperson17, Patrick Freund18, Jürgen Finsterbusch8, Alexandru Foias1, Michela Fratini, Issei Fukunaga19, Claudia A. M. Wheeler-Kingshott20, Claudia A. M. Wheeler-Kingshott21, Giancarlo Germani, Guillaume Gilbert22, Federico Giove, Charley Gros1, Charley Gros3, Francesco Grussu21, Akifumi Hagiwara19, Pierre-Gilles Henry23, Tomáš Horák24, Masaaki Hori25, James M. Joers23, Kouhei Kamiya26, Haleh Karbasforoushan27, Haleh Karbasforoushan17, Miloš Keřkovský14, Ali Khatibi28, Ali Khatibi15, Joo Won Kim29, Nawal Kinany30, Nawal Kinany31, Hagen H. Kitzler32, Shannon H. Kolind4, Yazhuo Kong33, Yazhuo Kong34, Petr Kudlička24, Paul Kuntke32, Nyoman D. Kurniawan3, Slawomir Kusmia35, Slawomir Kusmia21, Slawomir Kusmia36, René Labounek23, Maria Marcella Laganà, Cornelia Laule4, Christine S. Law17, Christophe Lenglet23, Tobias Leutritz16, Yaou Liu37, Sara Llufriu38, Sean Mackey17, Eloy Martinez-Heras38, Loan Mattera, Igor Nestrasil23, Kristin P. O’Grady11, Nico Papinutto39, Daniel Papp1, Daniel Papp34, Deborah Pareto40, Todd B. Parrish27, Anna Pichiecchio20, Ferran Prados21, Ferran Prados41, Alex Rovira40, Marc J. Ruitenberg3, Rebecca S. Samson7, Giovanni Savini, Maryam Seif16, Maryam Seif18, Alan C. Seifert29, Alex K. Smith34, Seth A. Smith11, Zachary A. Smith42, Elisabeth Solana38, Yuichi Suzuki26, George Tackley36, Alexandra Tinnermann8, Jan Valošek, Dimitri Van De Ville30, Dimitri Van De Ville31, Marios C. Yiannakas7, Kenneth A. Weber17, Nikolaus Weiskopf16, Nikolaus Weiskopf43, Richard G. Wise36, Richard G. Wise44, P Wyss, Junqian Xu29 
TL;DR: The spine generic protocol as mentioned in this paper provides guidance for assessing SC macrostructural and microstructural integrity: T1-weighted and T2-weighting imaging for SC crosssectional area computation, multi-echo gradient echo for gray matter cross-sectional area, and magnetization transfer and diffusion weighted imaging for assessing white matter microstructure.
Abstract: Quantitative spinal cord (SC) magnetic resonance imaging (MRI) presents many challenges, including a lack of standardized imaging protocols. Here we present a prospectively harmonized quantitative MRI protocol, which we refer to as the spine generic protocol, for users of 3T MRI systems from the three main manufacturers: GE, Philips and Siemens. The protocol provides guidance for assessing SC macrostructural and microstructural integrity: T1-weighted and T2-weighted imaging for SC cross-sectional area computation, multi-echo gradient echo for gray matter cross-sectional area, and magnetization transfer and diffusion weighted imaging for assessing white matter microstructure. In a companion paper from the same authors, the spine generic protocol was used to acquire data across 42 centers in 260 healthy subjects. The key details of the spine generic protocol are also available in an open-access document that can be found at https://github.com/spine-generic/protocols . The protocol will serve as a starting point for researchers and clinicians implementing new SC imaging initiatives so that, in the future, inclusion of the SC in neuroimaging protocols will be more common. The protocol could be implemented by any trained MR technician or by a researcher/clinician familiar with MRI acquisition.

45 citations


Authors

Showing all 2723 results

NameH-indexPapersCitations
José Baselga156707122498
M. I. Martínez134125179885
Josep Tabernero11180368982
Jordi Rello10369435994
Xavier Montalban9576252842
James M. Downey9138129506
Enriqueta Felip8362253364
Joaquim Bellmunt8266041472
Joan Montaner8048922413
Marc Miravitlles7665125671
David H. Salat7524136779
Eduard Gratacós7553120178
Alex Rovira7435619586
Ramon Bataller7228319316
Maria Buti7149326596
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
20232
202212
2021568
2020545
2019483
2018385