Zobrazeno 1 - 10
of 57
pro vyhledávání: '"Oscar Rubio"'
Autor:
Ruth A. Benson, Maria Antonella Ruffino, Sharon Chan, Patrick Coughlin, Ayoola Awopetu, Philip Stather, Tristan Lane, Dimitrios Theodosiou, Mohamed Abozeid Ahmed, Thodur Vasudevan, Mohammed Ibrahim, Faraj Al Maadany, Mohamed Eljareh, Fatimah Saad Alkhafeefi, Raphael Coscas, Ertekin Utku Ünal, Raffaele Pulli, Sergio Zacà, Domenico Angiletta, Thomas Kotsis, Magdy Moawad, Matteo Tozzi, Nikolaos Patelis, Andreas M. Lazaris, Jason Chuen, Alexander Croo, Elpiniki Tsolaki, Gladiol Zenunaj, Dhafer Kamal, Mahmoud MH. Tolba, Martin Maresch, Vipul Khetarpaul, Joseph Mills, Gaurav Gangwani, Mohamed Elahwal, Rana Khalil, Mohammed A. Azab, Anver Mahomed, Richard Whiston, Ummul Contractor, Davide Esposito, Carlo Pratesi, Elena Giacomelli, Martín Veras Troncoso, Stephane Elkouri, Flavia Gentile Johansson, Ilias Dodos, Marie Benezit, José Vidoedo, João Rocha-Neves, António Henrique Pereira-Neves, Marina Felicidade Dias-Neto, Ana Filipa Campos Jácome, Luis Loureiro, Ivone Silva, Rodrigo Garza-Herrera, Victor Canata, Charlotte Bezard, Kathryn Bowser, Jorge Felipe Tobar, Carlos Gomez Vera, Carolina Salinas Parra, Eugenia Lopez, Yvis Gadelha Serra, Juan Varela, Vanessa Rubio, Gerardo Victoria, Adam Johnson, Leigh Ann O’Banion, Ragai Makar, Tamer Ghatwary Tantawy, Martin Storck, Vincent Jongkind, Orwa falah, Olivia McBride, Arda Isik, Athanasios Papaioannou, Paulo Eduardo Ocke Reis, Umberto Marcello Bracale, Ellie Atkins, Giovanni Tinelli, Emma Scott, Lucy Wales, Ashwin Sivaharan, Georgia Priona, Craig Nesbitt, Tabitha Grainger, Lauren Shelmerdine, Patrick Chong, Adnan Bajwa, Luke Arwynck, Nancy Hadjievangelou, Ahmed Elbasty, Oscar Rubio, Michael Ricardo, Jorge H. Ulloa, Marcos Tarazona, Manuel Pabon, Georgios Pitoulias, Kevin Corless, Orestis Ioannidis, Oliver Friedrich, Isabelle Van Herzeele, Badri Vijaynagar, Tina Cohnert, Rachel Bell, Hayley Moore, Prakash Saha, Edward Gifford, Matti Laine, Adel Barkat, Christos Karkos, Lenny Suryani Binti Safri, Gabriel Buitron, Javier Del Castillo, Paul Carrera, Nilson Salinas, Rodrigo Bruno Biagioni, Sergio Benites, César Andrés Mafla, Putera Mas Pian, Pereira Albino, Ernesto Serrano, Andres Marin, Marco González, Marsha Foreroga, Alejandro Russo, Andrés Reyes, Daniel Guglielmone, Lorena Grillo, Ronald Flumignan, Francisco Gomez Palones, Pierre Galvagni Silveira, Rosnelifaizur Bin Ramely, Sara Edeiken, Ian Chetter, Lucy Green, Abhilash Sudarsanam, Oliver Lyons, Gary Lemmon, Richard Neville, Mariano Castelli, Carlos A. Hinojosa, Rubén Rodríguez Carvajal, Aksim Rivera, Peng Wong, Laura Drudi, Jeremy Perkins, Kishore Sieunarine, Doaa Attia, Mahmoud Atef, Lostoridis Eftychios, Fred Weaver, Leong Chuo Ren, Mohannad Alomari, Reda Jamjoom, Qusai Aljarrah, Ayman Abbas, Faris Alomran, Ambrish Kumar, Abdulmajeed Altoijri, Kareem T. ElSanhoury, Ahmed Alhumaid, Tamer Fekry, Raghuram Sekhar, Panagiotis Theodoridis, Theodoridis Panagiotis, Konstantinos Roditis, Paraskevi Tsiantoula, Afroditi Antoniou, Raphael Soler, Natasha Hasemaki, Efstratia Baili, Eustratia Mpaili, Bella Huasen, Tom Wallace, Andrew Duncan, Matthew Metcalfe, Kristyn Mannoia, Carlos F. Bechara, Nikolaos Tsilimparis, Nathan Aranson, David Riding, Mariano Palena, Ciarán McDonnell, Nicolas J. Mouawad, Shonda Banegas, Peter Rossi, Taohid Oshodi, Rodney Diaz, Rana Afifi, Shiva Dindyal, Ankur Thapar, Ali Kordzadeh, Gonzalo Pullas, Stephanie Lin, Chris Davies, Katy Darvall, Akio Kodama, Thushan Gooneratne, Nalaka Gunawansa, Alberto Munoz, Ng Jun Jie, Nicholas Bradley, Wissam Al-Jundi, Felicity Meyer, Cheong Lee, Martin Malina, Sophie Renton, Dennis Lui, Andrew Batchelder, Grzegorz Oszkinis, Antonio Freyrie, Jacopo Giordano, Nikolaos Saratzis, Konstantinos Tigkiropoulos, Stavridis Kyriakos, Guriy Popov, Muhammad Usman Cheema, Pierfrancesco Lapolla, Yih Chun Ling Patricia, Raed Ennab, Brant W. Ullery, Ketino Pasenidou, Jacky Tam, Gabriel Sidel, Vivek Vardhan Jayaprakash, Lisa Bennett, Simon Hardy, Emma Davies, Sara Baker, Lasantha Wijesinghe, Adam Tam, Ken McCune, Manik Chana, Chris Lowe, Aaron Goh, Katarzyna Powezka, Ioanna Kyrou, Nishath Altaf, Denis Harkin, Hannah Travers, James Cragg, Atif sharif, Tasleem Akhtar, José Antonio Chávez, Claudia Ordonez, Martin Mazzurco, Edward Choke, Imran Asghar, Virginia Summerour, Paul Dunlop, Rachel Morley, Thomas Hardy, Paul Bevis, Robert Cuff, Konstantinos Stavroulakis, Efthymios Beropoulis, Angeliki Argyriou, Ian Loftus, Bilal Azhar, Sharvil Sheth, Marco Virgilio Usai, Asad Choudhry, Kira Nicole, Emily Boyle, Doireann Joyce, Mohammed Hassan Abdelaty Hassan, Alberto Saltiel, Gert Frahm-Jensen, George Antoniou, Muhammed Elhadi, Ali Kimyaghalam, Rafael Malgor, Leigh Ann O'Banion, Diego Telve, Andrej Isaak, Jürg Schmidli, Kevin McKevitt, Tam Siddiqui, Giuseppe Asciutto, Nikolaos Floros, George Papadopoulos, Alexandros Kafetzakis, Stylianos G. Koutsias, Petroula Nana, Athanasios Giannoukas, Stavros Kakkos, Konstantinos G. Moulakakis, Natasha Shafique, Arkadiusz Jawien, Matthew Popplewell, Chris Imray, Kumar Abayasekara, Timothy Rowlands, Ganesh Kuhan, Sriram Rajagopalan, Anthony Jaipersad, Uzma Sadia, Isaac Kobe, Devender Mittapalli, Ibrahim Enemosah, Christian-Alexander Behrendt, Adam Beck, Muayyad Almudhafer, Stefano Ancetti, Donald Jacobs, Priya Jayakumar, Fatemeh Malekpour, Sherene Shalhub, Boboyor Keldiyorov, Meryl Simon, Manar Khashram, Nicole Rich, Amanda Shepherd, Lewis Meecham, Daniel Doherty
Publikováno v:
EJVES Vascular Forum, Vol 57, Iss , Pp 28-34 (2022)
Objective: To document the recovery of vascular services in Europe following the first COVID-19 pandemic peak. Methods: An online structured vascular service survey with repeated data entry between 23 March and 9 August 2020 was carried out. Unit lev
Externí odkaz:
https://doaj.org/article/aa7eee6418ae4275b81fd8ce2d75a291
Autor:
Luis Carlos Domínguez, Nelson Niño, Oscar Rubio, Eduardo Valdivieso, Saúl Rugeles, Álvaro Sanabria
Publikováno v:
Medicina, Vol 33, Iss 3, Pp 160-175 (2011)
RESUMENIntroducción: La predicción de coledocolitiasis en pacientes con colelitiasis continúa siendo debatible. El objetivo de este estudio es diseñar un instrumento para la evaluación preoperatoria de pacientes con colelitiasis en riesgo de col
Externí odkaz:
https://doaj.org/article/ebd77a4fb70a4820b6627ffee3c338e2
Autor:
Carmen-María García-Herrero, Oscar Rubio-Cabezas, Sharona Azriel, Angel Gutierrez-Nogués, Angel Aragonés, Olivier Vincent, Angel Campos-Barros, Jesús Argente, María-Angeles Navas
Publikováno v:
PLoS ONE, Vol 7, Iss 1, p e30518 (2012)
Glucokinase (GK) acts as a glucose sensor in the pancreatic beta-cell and regulates insulin secretion. Heterozygous mutations in the human GK-encoding GCK gene that reduce the activity index increase the glucose-stimulated insulin secretion threshold
Externí odkaz:
https://doaj.org/article/922a1fa58b42429c864ff12388c797d1
Autor:
Intza Garin, Guiomar Perez de Nanclares, Elena Gastaldo, Lorna W Harries, Oscar Rubio-Cabezas, Luis Castaño
Publikováno v:
PLoS ONE, Vol 7, Iss 1, p e29205 (2012)
The aim of this study was to characterize the genetic etiology in a patient who presented with permanent neonatal diabetes at 2 months of age.Regulatory elements and coding exons 2 and 3 of the INS gene were amplified and sequenced from genomic and c
Externí odkaz:
https://doaj.org/article/a0360a5e7d2d43d1b669e1dc94f432e9
Publikováno v:
Revista Argentina de Cirugía; Jun2022, Vol. 114 Issue 2, p107-110, 4p
Autor:
Pål R. Njølstad, Luis Castaño, Wojciech Młynarski, Sian Ellard, Andrew T. Hattersley, Siri Atma W. Greeley, Maria E. Craig, Dung V. Chi, Klemens Raile, Annelie Carlsson, Oscar Rubio-Cabezas, Michel Polak
Publikováno v:
Pediatric Diabetes. 19:47-63
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5372673225e932634020748b2e546346
https://doi.org/10.1111/pedi.12772
https://doi.org/10.1111/pedi.12772
Autor:
Luis González-Gutiérrez-Solana, Michaela Prochazkova, Saturnino Santos Santos, Verónica Cantarín Extremera, Anna Duat Rodríguez, Oscar Rubio Cabezas
Publikováno v:
Pediatric Neurology. 71:60-64
Background CAPOS syndrome (cerebellar ataxia, areflexia, pes cavus, optic atrophy, and sensorineural hearing loss) is a rare disease that has been reported in 22 patients so far. In all cases, the mutation c.2452G>A (p.Glu818Lys) in the ATP1A3 gene w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b2460c6f7e7a1c6e10e3480d34b0095a
https://doi.org/10.1016/j.pediatrneurol.2017.01.009
https://doi.org/10.1016/j.pediatrneurol.2017.01.009
Publikováno v:
Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid
Consejería de Sanidad de la Comunidad de Madrid
The Journal of Clinical Endocrinology and Metabolism
Consejería de Sanidad de la Comunidad de Madrid
The Journal of Clinical Endocrinology and Metabolism
Context: Biallelic mutations in NEUROG3 are known to cause early-onset malabsorptive diarrhea due to congenital anendocrinosis and diabetes mellitus at a variable age. No other endocrine disorders have been described so far. We report four patients w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e4bb35ad8e957f345727956ef492bcb2
https://doi.org/10.1210/jc.2016-2319
https://doi.org/10.1210/jc.2016-2319
Publikováno v:
Graphic Imprints ISBN: 9783319937489
Architects work with graphic narratives frequently dedicated to the elaboration of images that either inspire or surprise; typically for architectural competitions. These images, unlike architectural drawings, have clear communicative objectives aime
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d545e8c51a0c3147a9a2e1363ce7dd71
https://doi.org/10.1007/978-3-319-93749-6_70
https://doi.org/10.1007/978-3-319-93749-6_70
Autor:
Michael N. Weedon, Jill T. Norman, Monika Mozere, Michael Koettgen, Andrew Parrish, Anne Kesselheim, Naomi Issler, R. Drynda, André W. Brändli, Sofia A. Rahman, Anna Marie Bussell, Mehmet Tekman, Jesús Pozo, Horia Stanescu, Elizabeth Crowne, Elena García-Martínez, Patricia D. Wilson, Detlef Bockenhauer, Craig Jefferies, Oscar Rubio Cabezas, José María Martos, Vaksha Patel, Enriko Klootwijk, Richard Caswell, Montserrat Antón-Gamero, Daniela Iancu, Chris Cheshire, Simona Dumitriu, Hana Lango-Allen, Matthew B. Johnson, Peter B. Jones, Neil J. Sebire, Jesús Argente, Khalid Hussain, Sarah E. Flanagan, Julian P Hamilton-Shield, Celia Pérez-Cerdá, Peter D. Turnpenny, William van’t Hoff, Wesley Hayes, Daan H H M Viering, Lisa M. Guay-Woodford, Wendy Lewis, Alexis Hofherr, Robert Kleta, Sian Ellard
Publikováno v:
Cabezas, O R, Flanagan, S E, Stanescu, H, García-Martínez, E, Caswell, R, Lango-Allen, H, Antón-Gamero, M, Argente, J, Bussell, A M, Brandli, A, Cheshire, C, Crowne, E, Dumitriu, S, Drynda, R, Hamilton-Shield, J P, Hayes, W, Hofherr, A, Iancu, D, Issler, N, Jefferies, C, Jones, P, Johnson, M, Kesselheim, A, Klootwijk, E, Koettgen, M, Lewis, W, Martos, J M, Mozere, M, Norman, J, Patel, V, Parrish, A, Pérez-Cerdá, C, Pozo, J, Rahman, S A, Sebire, N, Tekman, M, Turnpenny, P D, Van'T Hoff, W, Viering, D H H M, Weedon, M N, Wilson, P, Guay-Woodford, L, Kleta, R, Hussain, K, Ellard, S & Bockenhauer, D 2017, ' Polycystic Kidney Disease with Hyperinsulinemic Hypoglycemia Caused by a Promoter Mutation in Phosphomannomutase 2 ', Journal of the American Society of Nephrology, vol. 28, no. 8, pp. 2529-2539 . https://doi.org/10.1681/ASN.2016121312
Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid
Consejería de Sanidad de la Comunidad de Madrid
Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid
Consejería de Sanidad de la Comunidad de Madrid
Hyperinsulinemic hypoglycemia (HI) and congenital polycystic kidney disease (PKD) are rare, genetically heterogeneous disorders. The co-occurrence of these disorders (HIPKD) in 17 children from 11 unrelated families suggested an unrecognized genetic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5950ac964fcee8818a8545a3098a42c6
https://europepmc.org/articles/PMC5533241/
https://europepmc.org/articles/PMC5533241/