Zobrazeno 1 - 10 of 26 pro vyhledávání: '"Franklin Hanna"'
1
Akademický článek
Analyses of familial chylomicronemia syndrome in Pereira, Colombia 2010–2020: a cross-sectional study
Autor: Franklin Hanna Rodriguez, Jorge Mario Estrada, Henry Mauricio Arenas Quintero, Juan Patricio Nogueira, Gloria Liliana Porras-Hurtado
Publikováno v: Lipids in Health and Disease, Vol 22, Iss 1, Pp 1-9 (2023)
Abstract Background and aim Familial chylomicronemia syndrome (FCS) is a rare autosomal recessive metabolic disorder caused by mutations in genes involved in chylomicron metabolism. On the other hand, multifactorial chylomicronemia syndrome (MCS) is
Externí odkaz: https://doaj.org/article/a3f84956a19c4f3d8f59ff30ea71d23c
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2
Akademický článek
Risk Burden of Coronary Perforation in Chronic Total Occlusion Recanalization: Latin American CTO Registry Analysis
Autor: Marcelo Harada Ribeiro, Carlos M. Campos, Lucio Padilla, Antonio Carlos B. da Silva, João Eduardo T. de Paula, Marco Alcantara, Ricardo Santiago, Franklin Hanna, Franciele R. da Silva, Karlyse C. Belli, Lorenzo Azzalini, Pedro P. de Oliveira, Gustavo N. Araujo, Vincenzo Sucato, Kambis Mashayekhi, Alfredo R. Galassi, Alexandre Abizaid, Alexandre Quadros
Publikováno v: Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, Vol 11, Iss 11 (2022)
Background Coronary perforation is a life‐threatening complication of acute percutaneous coronary intervention (PCI) for chronic total occlusions (CTO), but data on midterm outcomes are limited. Methods and Results Data from LATAM (Latin American)
Externí odkaz: https://doaj.org/article/7615133d709f4e93a38966c0e554e0a1
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3
Akademický článek
Miocardiopatía de takotsubo y la arteria coronaria única: una combinación excepcional
Autor: Santiago Salazar Marín, Franklin Hanna, Néstor Ramírez, Johanna Marcela Valencia
Publikováno v: Revista Colombiana de Cardiología, Vol 23, Iss 4, Pp 303.e1-303.e6 (2016)
La miocardiopatía de takotsubo es una entidad que clínicamente simula un síndrome coronario agudo, siendo indispensable para su diagnóstico la exclusión de la enfermedad coronaria significativa. Se presenta el caso de una mujer postmenopáusica,
Externí odkaz: https://doaj.org/article/b40ed4f2781341ac9cf19ec523af2442
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4
Akademický článek
Edema pulmonar refractario secundario a estenosis valvular aórtica severa - valvuloplastia aórtica como terapia puente a cirugía: Presentación de un caso Refractory pulmonary edema secondary to severe aortic valvular stenosis - aortic valvuloplasty as bridge therapy to surgery
Autor: Santiago Salazar, Franklin Hanna, Aminta Capasso, Miguel Madero, Gustavo Cajiao
Publikováno v: Revista Colombiana de Cardiología, Vol 16, Iss 2, Pp 76-82 (2009)
La estenosis valvular aórtica es una entidad progresiva, que cuando es severa y produce síntomas, tiene un pronóstico sombrío que afecta de forma adversa la sobrevida. En estos casos el tratamiento de elección es la cirugía de cambio valvular,
Externí odkaz: https://doaj.org/article/c861dae15c384c6ba813606374f92f12
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5
Akademický článek
Analyses of familial chylomicronemia syndrome in Pereira, Colombia 2010–2020: a cross-sectional study.
Autor: Rodriguez, Franklin Hanna1 (AUTHOR) investigacionensalud@comfamiliar.com, Estrada, Jorge Mario1 (AUTHOR), Quintero, Henry Mauricio Arenas2 (AUTHOR), Nogueira, Juan Patricio3 (AUTHOR), Porras-Hurtado, Gloria Liliana1 (AUTHOR)
Publikováno v: Lipids in Health & Disease. 3/28/2023, Vol. 22 Issue 1, p1-9. 9p.
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6
Emergent Endovascular Repair of a Ruptured Ascending Aorta Pseudoaneurysm With Thoracic Aortic Stent Graft
Autor: Santiago Salazar, Carlos Augusto Homem de Magalhães Campos, Marcelo Harada Ribeiro, Andrés Marín, Jhon Castrillon, James Nieto, Franklin Hanna Quesada, Franklin Hanna Rodríguez, Francesco Moroni, Lorenzo Azzalini, Luis Augusto Palma Dallan, Diego Mejía
Publikováno v: Cardiovascular Revascularization Medicine. 40:167-169
Pseudoaneurysm of the ascending aorta is a rare complication of cardiac surgery due to tissue degeneration at the site of graft anastomosis , aortotomy, or extracorporeal circulation cannulation . We describe the case of a patient who developed an as
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::b07127f2ca2f7ecf5ca882436459f3f8
https://doi.org/10.1016/j.carrev.2021.07.016
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7
Analyses of Familial Chylomicronemia Syndrome And Multifactorial Chylomicronemia In Colombia 2010-2020: A Cross-Sectional Study
Autor: Franklin Hanna Rodriguez, Jorge Mario Estrada Alvarez, Henry Mauricio Arenas Quintero, Juan Patricio Nogueira, Gloria Liliana Porras Hurtado
Background and aim Familial chylomicronemia syndrome (FCS) is a rare autosomal recessive metabolic disorder caused by mutations in genes involved in chylomicron metabolism. On the other hand, multifactorial chylomicronemia syndrome (MCS) is a polygen
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::58f1113e3c1eb65f2462e62afdf4e105
https://doi.org/10.21203/rs.3.rs-2154973/v1
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9
Global Chronic Total Occlusion Crossing Algorithm
Autor: Kambis Mashayekhi, Ashish Pershad, Alexandre Avran, Nidal Abi Rafeh, Jaikirshan Khatri, R. Leung, Lei Ge, Michael Behnes, Wissam Jaber, William Lombardi, Alexandre Schaan de Quadros, Hung M. Ngo, Göran K. Olivecrona, William J. Nicholson, Colm G. Hanratty, Kevin Croce, José P.S. Henriques, Roberto Garbo, Franklin Hanna Quesada, Anthony Spaedy, Nenad Z. Bozinovic, Gregg W. Stone, Gerald S. Werner, James C. Spratt, Ravinay Bhindi, Angela Hoye, Minh Vo, Tony De Martini, Javier Escaned, Jennifer A. Tremmel, Arun Kalyanasundaram, Khaldoon Alaswad, Jason R Wollmuth, Christopher E. Buller, Anbukarasi Maran, Ji Yan Chen, Avtandil M. Babunashvili, Qi Zhang, Vu Hoang Vu, Raja Hatem, Emmanouil S. Brilakis, Baktash Bayani, Vithala Surya Prakasa Rao, Farouc A. Jaffer, Andrea Gagnor, Achim Buttner, Yu Li, Khalid Tammam, Félix Damas de los Santos, Basem Elbarouni, Aurel Toma, Jie Qian, David Hildick-Smith, Paul Knaapen, Sergey Furkalo, Nicolaus Reifart, Marouane Boukhris, Omer Goktekin, Alexander Bufe, Joseph Dens, Eugene B. Wu, Artis Kalnins, Mohaned Egred, Carlo Di Mario, Margaret McEntegart, Seung-Whan Lee, Risto Jussila, Oleg Krestyaninov, Scott A. Harding, Mauro Carlino, Dimitri Karmpaliotis, Muhammad Munawar, Bo Xu, Alfredo R. Galassi, David E. Kandzari, Jarosław Wójcik, Yue Li, Imre Ungi, M. Nicholas Burke, Yangsoo Jang, Thierry Lefèvre, Luiz F. Ybarra, Robert F. Riley, Julian Strange, Mario Araya, Lucio Padilla, Hsien-Li Kao, Stéphane Rinfret, Craig Thompson, Simon J Walsh, Pravin K. Goel, Sidney Lo, Allison B. Hall, Robert W. Yeh, Andres Navarro, Marin Postu, Gabriele Gasparini, Ran Kornowski, Masahisa Yamane, A. V.Ganesh Kumar, Anja Øksnes, Hussien Heshmat Kassem, Stefan Harb, Soo Teik Lim, Kefei Dou, Nieves Gonzalo, George Sianos, Truls Råmunddal, Lorenzo Azzalini, Pablo Lamelas, Mitul Patel, Nicolas Boudou, Antonio Colombo, Evald Hoej Christiansen, Jeffrey W. Moses, Luca Grancini, Jonathan Hill, Ahmed ElGuindy, Etsuo Tsuchikane, Elliot J. Smith, Ricardo Santiago Trinidad, Leszek Bryniarski, Pedro Cardoso, Meruzhan Saghatelyan, Junbo Ge
Publikováno v: Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
© 2021 The Authors. Published by Elsevier on behalf of the American College of Cardiology Foundation. This is an open access article under the CC By-NC-ND License (http://creativecommons.org/licenses/by-nc-nd/4)
The authors developed a global c
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2fe0e47618c1cf806254bd4ac61afe02
https://hdl.handle.net/10400.26/37429
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