Alejandro Porras‐Segovia, Eulalio Valmisa, Blanca Gutiérrez, Isabel Ruiz‐Pérez, Miguel Rodríguez‐Barranco, Jorge A. Cervilla,
Major depression is one of the world's leading causes of disability. Up-to-date information about the epidemiology of this disorder is key to health care planning.The aim of our study is to report prevalence and correlates of current major depressive disorder (MDD) in the province of Granada, Southern Spain.The GranadΣp is a cross-sectional study based on a community-dwelling adult population living in the province of Granada, Southern Spain. Community-dwelling adults aged 18-80 years ( n = 810) were ...
Tópico(s): Health disparities and outcomes
2018 - SAGE Publishing | International Journal of Social Psychiatry
Gerardo Gutiérrez‐Gutiérrez, Jordi Díaz‐Manera, Míriam Almendrote, Sharona Azriel, José Eulalio Bárcena, Pablo Cabezudo‐García, Ana Camacho, Carlos Casanova Rodríguez, A.-M. Cobo, Patricia Díaz Guardiola, Roberto Fernández‐Torrón, M.P. Gallano Petit, Pablo García Pavía, María Gómez Gallego, A.J. Gutiérrez Martínez, Ivonne Jericó, S. Kapetanovic García, Adolfo López de Munaín Arregui, Loreto Martorell, Germán Morís, Raúl Moreno Zabaleta, José Luis Muñoz‐Blanco, Juana Olivar Roldán, Samuel Ignacio Pascual Pascual, Rafaél Peinado, Helena Pérez, Juan José Poza Aldea, María Rabasa, Alba Ramos‐Fransí, Alfredo Rosado Bartolomé, M.Á. Rubio, Jon Andoni Urtizberea, Gustavo Zapata-Wainberg, Eduardo Gutiérrez‐Rivas,
Steinert's disease or myotonic dystrophy type 1 (MD1), (OMIM 160900), is the most prevalent myopathy in adults. It is a multisystemic disorder with dysfunction of virtually all organs and tissues and a great phenotypical variability, which implies that it has to be addressed by different specialities with experience in the disease. The knowledge of the disease and its management has changed dramatically in recent years. This guide tries to establish recommendations for the diagnosis, prognosis, follow- ...
Tópico(s): Neurological disorders and treatments
2020 - Elsevier BV | Neurología (English Edition)
Gerardo Gutiérrez‐Gutiérrez, Jordi Díaz‐Manera, Míriam Almendrote, Sharona Azriel, José Eulalio Bárcena, Pablo Cabezudo‐García, Ana Camacho, Carlos Casanova Rodríguez, Ana María Cobo, Patricia Díaz Guardiola, Roberto Fernández‐Torrón, M.P. Gallano Petit, Pablo García Pavía, María Gómez Gallego, A.J. Gutiérrez Martínez, Ivonne Jericó, S. Kapetanovic García, Adolfo López de Munaín Arregui, Loreto Martorell, Germán Morís, Raúl Moreno Zabaleta, José Luis Muñoz‐Blanco, Juana Olivar Roldán, Samuel Ignacio Pascual Pascual, Rafaél Peinado, Helena Pérez, Juan José Poza Aldea, María Rabasa, Alba Ramos‐Fransí, Alfredo Rosado Bartolomé, M.Á. Rubio, Jon Andoni Urtizberea, Gustavo Zapata-Wainberg, Eduardo Gutiérrez‐Rivas,
La enfermedad de Steinert o distrofia miotónica tipo 1 (DM1), (OMIM 160900) es la miopatía más prevalente en el adulto. Es una enfermedad multisistémica con alteración de prácticamente todos los órganos y tejidos y una variabilidad fenotípica muy amplia, lo que implica que deba ser atendida por diferentes especialistas que dominen las alteraciones más importantes. En los últimos años se ha avanzado de manera exponencial en el conocimiento de la enfermedad y en su manejo. El objetivo de la guía es ...
Tópico(s): Cardiomyopathy and Myosin Studies
2019 - Elsevier BV | Neurología
Jorge A. Cervilla, Isabel Ruiz‐Pérez, Miguel Rodríguez‐Barranco, Margarita Rivera, Inmaculada Ibáñez-Casas, Esther Molina, Eulalio Valmisa, José Carmona-Calvo, Berta Moreno‐Küstner, José Eduardo Muñoz-Negro, Ana Ching-López, Blanca Gutiérrez,
El presente artículo describe la metodología general de un estudio transversal cuyo principal objetivo consiste en la detección de la prevalencia de los principales trastornos mentales en Andalucía, y el estudio de sus correlatos o posibles factores de riesgo mediante una amplia muestra representativa de adultos que vive en la comunidad. Este es un estudio transversal en el que desarrollamos un muestreo de varias fases utilizando distintos niveles de estratificación habituales y en el que teníamos ...
Tópico(s): Health disparities and outcomes
2016 - Elsevier BV | Revista de Psiquiatría y Salud Mental
Gerardo Gutiérrez‐Gutiérrez, Jordi Díaz‐Manera, Míriam Almendrote, Sharona Azriel, José Eulalio Bárcena, Pablo Cabezudo‐García, Ana Camacho, Carlos Casanova Rodríguez, Ana María Cobo, Patricia Díaz Guardiola, Roberto Fernández‐Torrón, M.P. Gallano Petit, Pablo García Pavía, María Gómez Gallego, A.J. Gutiérrez Martínez, Ivonne Jericó, S. Kapetanovic García, Adolfo López de Munaín Arregui, Loreto Martorell, Germán Morís, Raúl Moreno Zabaleta, José Luis Muñoz‐Blanco, Juana Olivar Roldán, Samuel Ignacio Pascual Pascual, Rafaél Peinado, Helena Pérez, Juan José Poza Aldea, María Rabasa, Alba Ramos‐Fransí, Alfredo Rosado Bartolomé, M.Á. Rubio, Jon Andoni Urtizberea, Gustavo Zapata-Wainberg, Eduardo Gutiérrez‐Rivas,
Steinert's disease or myotonic dystrophy type 1 (MD1), (OMIM 160900), is the most prevalent myopathy in adults. It is a multisystemic disorder with dysfunction of virtually all organs and tissues and a great phenotypical variability, which implies that it has to be addressed by different specialities with experience in the disease. The knowledge of the disease and its management has changed dramatically in recent years. This guide tries to establish recommendations for the diagnosis, prognosis, follow- ...
Tópico(s): Glycogen Storage Diseases and Myoclonus
2019 - Elsevier BV | Medicina Clínica (English Edition)
Alberto Blázquez Manzano, Sebastián Feu Molina, Eulalio Ruiz Muñoz, Juana María Gutiérrez Caballero,
This article aims to understand the aspects that influence the communicative context of the relationship of primary care health professionals (physicians and nurses) in consultation and influencing patient satisfaction and treatment adherence, among other aspects. Theoretical study was conducted through a literature review, using meta-search of the PubMed database and journals. The paper proposes strategies of persuasion and intervention guidelines to improve this relationship, focusing on nonverbal ...
Tópico(s): Patient Satisfaction in Healthcare
2012 - Carlos III University of Madrid | REVISTA ESPAÑOLA DE COMUNICACIÓN EN SALUD
Ernesto Cisneros Bernal, Eulalio Alberto Gutiérrez Rodríguez, Laura Gabriela Soto Salazar,
La enfermedad de Erdheim-Chester (ECD), es un padecimiento raro, descrito por primera vez en 1930, por Jakob Erdheim y William Chester. La presentación más común de la enfermedad consiste en dolor óseo. Su diagnóstico se realiza mediante la confirmación histopatológica junto a las manifestaciones clínicas de la enfermedad, así como con los auxiliares radiológicos. La presentación de un caso inusual nos invita a no dar por sentada ninguna manifestación clínica o paraclínica en los pacientes.
Tópico(s): Parvovirus B19 Infection Studies
2019 - National University of Colombia | Revista de la Facultad de Medicina
Eulalio Alberto Gutiérrez-Rodríguez, Manuel Ernesto Arzola-Medrano, Laura Elvira García-Labastida,
Introducción: El linfoma de Burkitt es una neoplasia causada por la proliferación clonal de células B. El objetivo de este trabajo es dar a conocer un caso de linfoma de Burkitt de localización en nasofaringe, lo cual es una presentación muy poco frecuente.Caso clínico: Paciente femenino de ocho años, con padecimiento caracterizado por ronquidos y cambios en la fonación sugestivos de sinusitis crónica.Como parte del estudio, en una tomografía se observó masa de aspecto benigno en nasofaringe.Por ...
Tópico(s): Ear and Head Tumors
2020 - | Revista Mexicana de Pediatría
Ana D. Delgado-Salgado, Laura E. García-Labastida, Eulalio A. Gutiérrez-Rodríguez, Bladimir A. Velázquez-Ramos,
Tópico(s): Management of metastatic bone disease
2021 - Elsevier BV | Gaceta Mexicana de Oncología
Gerardo Gutiérrez‐Gutiérrez, Jordi Díaz‐Manera, Míriam Almendrote, Sharona Azriel, José Eulalio Bárcena, Pablo Cabezudo‐García, Ana Camacho, Carlos Casanova Rodríguez, Ana María Cobo, Patricia Díaz Guardiola, Roberto Fernández‐Torrón, M.P. Gallano Petit, Pablo García Pavía, María Gómez Gallego, A.J. Gutiérrez Martínez, Ivonne Jericó, S. Kapetanovic García, Adolfo López de Munaín Arregui, Loreto Martorell, Germán Morís, Raúl Moreno Zabaleta, José Luis Muñoz‐Blanco, Juana Olivar Roldán, Samuel Ignacio Pascual Pascual, Rafaél Peinado, Helena Pérez, Juan José Poza Aldea, María Rabasa, Alba Ramos‐Fransí, Alfredo Rosado Bartolomé, M.Á. Rubio, Jon Andoni Urtizberea, Gustavo Zapata-Wainberg, Eduardo Gutiérrez‐Rivas,
La enfermedad de Steinert o distrofia miotónica tipo 1 (DM1), (OMIM 160900) es la miopatía más prevalente en el adulto. Es una enfermedad multisistémica con alteración de prácticamente todos los órganos y tejidos y una variabilidad fenotípica muy amplia, lo que implica que deba ser atendida por diferentes especialistas que dominen las alteraciones más importantes. En los últimos años se ha avanzado de manera exponencial en el conocimiento de la enfermedad y en su manejo. El objetivo de la guía es ...
Tópico(s): Cardiomyopathy and Myosin Studies
2019 - Elsevier BV | Medicina Clínica
Jorge A. Cervilla, Blanca Gutiérrez, Miguel Rodríguez‐Barranco, Inmaculada Ibáñez-Casas, Miguel Pérez-Garcı́a, Eulalio Valmisa, José Carmona, Esther Molina, Berta Moreno‐Küstner, Margarita Rivera, Vanessa Alcaide Lozano, José Eduardo Muñoz-Negro, Ana Ching-López, Margarita Guerrero, Alejandro Porras‐Segovia, Isabel Ruiz‐Pérez,
This is a cross-sectional study of participants from a population census living in the province of Granada (Spain). A total of 1176 persons were contacted, 367 (31%) refused and 54 (6.7%) needed substitution. A final sample of 809 participants (response rate, 69.3%) were screened for mental disorder (MD) using the MINI International Neuropsychiatric Interview, a comprehensive interview validated to generate diagnoses compatible with ICD-10/DSM-4 criteria. Current (1-month) prevalence for any MD was 11. ...
Tópico(s): Mental Health Treatment and Access
2018 - Lippincott Williams & Wilkins | The Journal of Nervous and Mental Disease
Margarita Guerrero‐Jiménez, Blanca Gutiérrez, Isabel Ruiz‐Pérez, Miguel Rodríguez‐Barranco, Inmaculada Ibáñez-Casas, Miguel Pérez-Garcı́a, Eulalio Valmisa, José Carmona, José Eduardo Muñoz-Negro, Jorge A. Cervilla,
Tópico(s): Bipolar Disorder and Treatment
2017 - Elsevier BV | The European Journal of Psychiatry
Rubén Martínez Marín, J. Sánchez, David Reyes Leiva, Angela C. Nascimento, N. Muelas, C. Dominguez, C. Paradas, M. Olivé, S. Pascual Pascual, M. Barba Romero, María Folgueras Gómez, M. Usón, R. Blanco, José Eulalio Bárcena, A. López de Munuain, A. Gutiérrez, A. Colomé, F. Pla-Junca, S. Segovia Simón, J. Díaz Manera,
Late Onset Pompe patients (LOPD) is the main phenotype on Pompe disease that start with symptoms from the age of two years to late in the adulthood. Because of the heterogeneity of the disease, it has been described the Juvenile Onset Pompe Disease (JOPD) subgroup, who become symptomatic between 2 and 18 years old. We describe the demographic and clinical features of all JOPD patients and their progression (using six-minute walking test -6MWT-, forced vital capacity -FVC- and Creatin Kinase -CK- values ...
Tópico(s): Carbohydrate Chemistry and Synthesis
2022 - Elsevier BV | Neuromuscular Disorders
Jacqueline Palace, Dean M. Wingerchuk, Kazuo Fujihara, Achim Berthele, Celia Oreja‐Guevara, Ho Jin Kim, Ichiro Nakashima, Michael Levy, Murat Terzi, N. А. Totolyan, Shanthi Viswanathan, Kaichen Wang, Amy Pace, Marcus Yountz, Larisa Miller, Róisín Armstrong, Sean J. Pittock, Daniel Muñoz, Jorge David Amor, Carolina Bocchiardo, Julieta Iourno Danielle, Alfredo Laffue, Carolina Obregon, María Fernanda Páez, Roberto Martin Perez, Viviana Ana Maria Rocchi, Loreley Deborah Teijeiro, Jesica Gómez, Andrés Villa, Florencia Aguirre, Victòria Fernández, Ramon F. Goicoechea, Luciana Melamud, A. E. Stillman, Jesica Gómez, Mariana De Virgiliis, Fátima Pagani Cassara, Marta Córdoba, M. Teresa Gutiérrez, Mariana Ingolotti, Natalia Larripa, Anahi Lupinacci, Josefina Arroyo, Alejandra Romano, Mariana Foa Torres, Carlos Ballario, Ana Elisa Chiesa, Hernán Gustavo Gómez, Hernán Gabriel Lattini, Carolina Mainella, Gisel Edith Bolner, María Soledad Eschoyez, Simon Broadley, Saman Heshmat, Arman Sabet, Andrew Swayne, Susan Freeman, Sofia Jimenez Sanchez, Neil Shuey, Linda J. Dalic, Ann French, Guru Kuma, Joshua Laing, Lai Yin Law, Jennifer MacIntyre, Andrew Neal, Christopher Plummer, Prashanth Ramachandran, Leslie Sedal, Ian Wilson, Antony Winkel, Wenwen Zhang, Tina Chen, Rani Watts, Michael Barnett, Joshua Barton, Heidi Beadnall, Justin Garber, Todd A. Hardy, Benjamin Trewin, Marinda Taha, Deleni Walters, Federico Arturo Silva Sieger, Nhora Patricia Ruiz Alfonso, Anna Maria Pinzon Camacho, Alexander Pabón Moreno, Jorge Armando Castellanos Prad, Adriana Paola Duarte Rueda, Tatiana Castillo, K. Gonzalez, Martha Yolanda Moreno Pico, Judith Castill, Mario Habek, Ivan Adamec, Barbara Barun, Luka Crnošija, Tereza Gabelić, Petra Nytrová, Eva Krasulová, Jana Pavlíčková, Michaela Týblová, J. V. Zubkova, Thor Petersen, G Dale, Peter Vestergaard Rasmussen, Morten Stilund, Kristina Bacher Svendsen, Vivi Brandt, Nicolas Collongues, Marie‐Céline Fleury, Laurent Kremer, Sandrine Bendele, Valérie Neff, Ricarda Diem, Michael Platten, Anne Berberich, J Jansen, Hannah Jaschoneck, Brigitte Wildemann, Ursula Aures, Tanja Brandenburger, Tanja Haut, Maria-Lourdes Treceno Fernández, Lilian Aly, K. P. Brinkhoff, Dorothea Buck, Daniel Golkowski, Mirjam Hermisson, Muna‐Miriam Hoshi, Miriam Kaminski, Markus C. Kowarik, Helena Kronsbein, Klaus Lehmann‐Horn, Viola Pongratz, Andreas Schweiker, L Leddy, Silvia Melitta Mueller, Kim Obergfell, Marion Wanka, Uwe K. Zettl, Jan Klinke, Micha Loebermann, Stefanie Meister, Florian Rimmele, Alexander Winkelmann, Ina Schroeder, Alexander Yuk Lun Lau, Lisa Wing-Chi Au, Florence Sin-Ying Fan, Vincent Hing‐Lung Ip, K. Kayan, Sze Ho, Vincent Mok, Cheryl Au, Pauline Kwan, Francesco Patti, Andrea Caramma, Clara Grazia Chisari, Salvatore Lo Fermo, Silvia Messina, Maria Projetto, Cinzia Caserta, Alessandro Filla, Teresa Costabile, Chiara Pane, Francesco Saccà, Angela Marsili, Giorgia Puorro, Roberto Bergamaschi, Eliana Berra, Giulia Mallucci, Cinzia Fattore, Claudio Gasperini, Simonetta Galgani, Shalom Haggiag, Serena Ruggieri, Claudio Vento, Esmeralda Quartuccio, Carlo Pozzilli, Valeria Barletta, Giovanna Borriello, Laura De Giglio, F. Marinelli, Miriam Tasillo, Alessandra Amadori, Mariano Fischetti, Flavia Gurreri, Masahiro Mori, Hiroki Masuda, Ryohei Ohtani, Yukari Sekiguchi, Tomohiko Uchida, Akiyuki Uzawa, Hiromi Ito, Emi Kabasawa, Yoko Kaneko, Takuya Matsushita, Dai Matsuse, Hiroyuki Murai, Shintaro Hayashi, Katsuhisa Masak, Hidenori Ogata, Koji Shinoda, Taira Uehara, Mitsuru Watanabe, Hiroo Yamaguchi, Ryo Yamasaki, Tomomi Yonekawa, Maki Jingu, M Nagano, Yumiko Nakamura, Yoshiko Sano, M. Araki, Youwei Lin, Madoka Mori, Yohei Mukai, Terunori Sano, Wakiro Sato, Naoya Gogun, Yuriko Maeda, A Nishimoto, Sachiko Tsukamoto, Ritsuko Yanagi, Takahiko Saida, Shinichi Nakamura, Tetsuya Nasu, Kyoko Saida, Yuko Shikata, Yoshimi Kodani, Megumi Saeki, Yukako Sawada, Hiroo Yoshikawa, Takashi Kimura, Masamitsu Nishi, Shun Sakamoto, Shinichiro Ukon, Shohei Watanabe, Saori Ebisuya, Nami Kimura, M Matsuura, Yukie Morisaki, Yoshiko Muroi, Kuniko Onishi, Ikuko Oshima, Yuki Washino, Tomomi Yamashita, Tatsuro Misu, Kimihiko Kaneko, Masaaki Kato, Hiroshi Kuroda, Kazuhiro Kurosawa, Shuhei Nishiyama, Hirohiko Ono, Yoshiki Takai, Keiko Abe, Hitomi Hoshi, Mari Jinushi, Azusa Oyama, M. Sakuma, Yuko Sawada, Satoru Ishibashi, Takanori Yokota, Yoichiro Nishida, Kokoro Ozaki, Nobuo Sanjo, Nozomu Sato, Fuki Denno, Haruko Hiraki, Yumi Matsubara, Takashi Kanda, Masaaki Abe, Masaya Honda, Motoharu Kawai, Michiaki Koga, Toshihiko Maeda, Jun‐ichi Ogasawara, Masatoshi Omoto, Yasuteru Sano, Ryota Sato, Fumitaka Shimizu, Hideki Arima, Sachie Fukui, Yoshiko Ishikawa, Tomoko Koyama, Shigemi Shimose, Hirokazu Shinozaki, Masanori Watanabe, Sachi Yasuda, Chieko Yoshiwaka, Suffian Adenan, Mohd Azman M Aris, Ahmad Shahir Mawardi, Muhammad Al Hafiz Adnan, Nanthini Munusamy, Siti Nur Omaira Razali, P Somasundram,
Antibodies to the aquaporin-4 (AQP4) water channel in neuromyelitis optica spectrum disorder (NMOSD) are reported to trigger the complement cascade, which is implicated in astrocyte damage and subsequent neuronal injury. The PREVENT study demonstrated that the terminal complement inhibitor eculizumab reduces adjudicated relapse risk in patients with anti-AQP4 immunoglobulin G-positive (AQP4+) NMOSD. The objective of this analysis was to evaluate the efficacy of eculizumab in reducing relapse risk and ...
Elsevier BV
Jorge A. Cervilla, Isabel Ruiz‐Pérez, Miguel Rodríguez‐Barranco, Margarita Rivera, Inmaculada Ibáñez-Casas, Esther Molina, Eulalio Valmisa, José Carmona-Calvo, Berta Moreno‐Küstner, José Eduardo Muñoz-Negro, Ana Ching-López, Blanca Gutiérrez,
Tópico(s): Mental Health and Psychiatry
2016 - Elsevier BV | Revista de Psiquiatría y Salud Mental (English Edition)
Huai Zhang, Giovanni Targher, Christopher D. Byrne, Seung Up Kim, Vincent Wai-Sun Wong, Luca Valenti, Myer Glickman, Jaime Ponce, Christos S. Mantzoros, Javier Crespo, Henning Grønbæk, Wah Yang, Mohammed Eslam, Robert J. Wong, Mariana Verdelho Machado, Ming‐Lung Yu, Omar M. Ghanem, Takeshi Okanoue, Junfeng Liu, Yong‐ho Lee, Xiao-Yuan Xu, Qiuwei Pan, Meili Sui, Amedeo Lonardo, Yusuf Yılmaz, Liyong Zhu, Christophe Moreno, Luca Miele, Monica Lupșor‐Platon, Lei Zhao, Teresa LaMasters, Robert G. Gish, Huijie Zhang, Marius Nedelcu, Wah‐Kheong Chan, Mingfeng Xia, Fernando Bril, Junping Shi, Christian Datz, Stefano Romeo, Jian Sun, Dan Liu, Silvia Sookoian, Yimin Mao, Nahúm Méndez‐Sánchez, Xiaoyan Wang, Nikolaos Pyrsopoulos, Jian‐Gao Fan, Yasser Fouad, Dan‐Qin Sun, Cosimo Giannini, J. W. Chai, Ze-Feng Xia, Dae Won Jun, Guojing Li, Sombat Treeprasertsuk, Yingxu Li, Tan To Cheung, Faming Zhang, George Boon‐Bee Goh, Masato Furuhashi, Wai‐Kay Seto, Hui Huang, Anna Di Sessa, Qinghong Li, Εvangelos Cholongitas, Le Zhang, Themis Reverbel da Silveira, Giada Sebastiani, Leon A. Adams, Wei Chen, Xiaolong Qi, Ivan Ranković, Victor de Lédinghen, Wenjie Lv, Masahide Hamaguchi, Radwan Kassir, Dirk Müller‐Wieland, Manuel Romero‐Gómez, Ying Xu, Yicong Xu, Shiyao Chen, Mohammad Kermansaravi, Mohammad Shafi Kuchay, Sander Lefere, Chetan Parmar, Gregory Y.H. Lip, Chun‐Jen Liu, Fredrik Åberg, George Lau, Jacob George, Shiv Kumar Sarin, Jingya Zhou, Ming‐Hua Zheng, Huai Zhang, Giovanni Targher, Christopher D. Byrne, Seung Up Kim, Vincent Wai-Sun Wong, Luca Valenti, Myer Glickman, Jaime Ponce, Christos S. Mantzoros, Javier Crespo, Henning Grønbæk, Wah Yang, Mohammed Eslam, Robert J. Wong, Mariana Verdelho Machado, Ming‐Lung Yu, Omar M. Ghanem, Takeshi Okanoue, Junfeng Liu, Yong‐ho Lee, Xiao-Yuan Xu, Qiuwei Pan, Meili Sui, Amedeo Lonardo, Yusuf Yılmaz, Liyong Zhu, Christophe Moreno, Luca Miele, Monica Lupșor‐Platon, Lei Zhao, Teresa LaMasters, Robert G. Gish, Huijie Zhang, Marius Nedelcu, Wah‐Kheong Chan, Mingfeng Xia, Fernando Bril, Junping Shi, Christian Datz, Stefano Romeo, Jian Sun, Dan Liu, Silvia Sookoian, Yimin Mao, Nahúm Méndez‐Sánchez, Xiaoyan Wang, Nikolaos Pyrsopoulos, Jian‐Gao Fan, Yasser Fouad, Dan‐Qin Sun, Cosimo Giannini, J. W. Chai, Ze-Feng Xia, Dae Won Jun, Guojing Li, Sombat Treeprasertsuk, Yingxu Li, Tan To Cheung, Faming Zhang, George Boon‐Bee Goh, Masato Furuhashi, Wai‐Kay Seto, Hui Huang, Anna Di Sessa, Qinghong Li, Εvangelos Cholongitas, Le Zhang, Themis Reverbel da Silveira, Giada Sebastiani, Leon A. Adams, Wei Chen, Xiaolong Qi, Ivan Ranković, Victor de Lédinghen, Wenjie Lv, Masahide Hamaguchi, Radwan Kassir, Dirk Müller‐Wieland, Manuel Romero‐Gómez, Ying Xu, Yicong Xu, Shiyao Chen, Mohammad Kermansaravi, Mohammad Shafi Kuchay, Sander Lefere, Chetan Parmar, Gregory Y.H. Lip, Chun‐Jen Liu, Fredrik Åberg, George Lau, Jacob George, Shiv Kumar Sarin, Jingya Zhou, Ming‐Hua Zheng, Zaigham Abbas, Sherief Abd‐Elsalam, Ludovico Abenavoli, Adel Abou‐Mrad, Adam Abu-Abeid, Débora Acín-Gándara, Sandeep Aggarwal, Golo Ahlenstiel, Fardah Akil, Shahinul Alam, Mohamed Alboraie, Nawal M. Alkhalidi, Maytham Hameed Al-Qanbar, Laith Alrubaiy, Mário Reis Álvares‐da‐Silva, Antônio Alves, Bassem Amr, Prooksa Ananchuensook, Nikolaos-Andreas Anastasopoulos, Vladimir Andreevski, Marco Anselmino, Shadike Apaer, M. Arias, Juan Armendáriz‐Borunda, Anil Arora, Ambika P. Ashraf, Rabah Asreah, Rahmatullah Athar, Dina Attia, Selmy Awad, Oidov Baatarkhuu, Flora Bacopoulou, Honglian Bai, F Bai, Sandra Maria Barbalho, Ilaria Barchetta, Jaideep Behari, Estuardo Behrens, Francesco Bellanti, Francesco Bellinato, Muhammad Begawan Bestari, Saptarshi Bhattacharya, Hua Bian, Quentin Binet, Ruth Blackham, Joost Boeckmans, Ivo Boškoski, Carlos Brotons, Guillermo Cabrera-Álvarez, Cristina Cadenas‐Sánchez, Dachuan Cai, Giuliano Peixoto Campelo, Zhujun Cao, Haixia Cao, Yu-Rui Cao, J.M. Carrascosa, Francesca Carubbi, Thomas Carus, Alfredo Caturano, X.D. Cha, C. Anwar A. Chahal, Daniel L. Chan, Lawrence Chan, Man Pan Chan, Siew Pheng Chan, Yun-Peng Chang, Yoosoo Chang, Phunchai Charatcharoenwitthaya, Norberto C. Chávez‐Tapia, Mark Chang Chuen Cheah, Yu Chen, Huiting Chen, Jing Chen, Lili Chen, Tao Chen, Lanlan Chen, Jin Chen, Yuanwen Chen, Yu Chen, Li Chen, Haitao Chen, En‐Qiang Chen, Jing-She Chen, Liangmiao Chen, Shun‐Ping Chen, Yong-Ping Chen, Gang Chen, Yunzhi Chen, Qin‐Fen Chen, Kangjie Chen, Xu Chen, Qiang Chen, Yuan Cheng, N. Wah Cheung, Ramsey Cheung, Xiaoling Chi, Sonja Chiappetta, Bogdan Augustin Chiş, Kee Huat Chuah, Stefano Ciardullo, Nicholas Cocomello, Li Cong, Adryana Cordeiro, Omero Pereira Costa Filho, Harry Crane, Ian Homer Yee, Kai Dai, Zhijuan Dai,
Springer Science+Business Media
LUIS MARIO ALTAMIRANO GUTIÉRREZ, Ulises Loreto Nava, Rubén Torres González, IVÁN RAMSÉS ÁGUILA LEDESMA, ERIKA VANESSA TAPIA FLORES, RENÉ MORALES DE LOS SANTOS, José Manuel Pérez Atanasio, Eulalio Elizalde Martínez,
ABSTRACT Objective: To identify the incidence and type of postoperative hospital complications in patients with cervical spondylotic myelopathy (CSM) treated by anterior approach, and to describe comorbidities present in patients who had complications. Methods: Retrospective, observational, descriptive cohort study of secondary sources (medical records), over a period of 3 years. We included 180 cases treated by anterior approach, excluding revision surgeries. Results: There was an incidence of complications ...
Tópico(s): Spine and Intervertebral Disc Pathology
2017 - Sociedade Brasileira de Coluna (SBC) | Coluna/Columna
Rafael Jenaro Martinez-Marin, David Reyes‐Leiva, A. Nascimento, Nuria Muelas, Cristina Domínguez‐González, Carmen Paradas, Montse Olivé, Mar García-Romero, Samuel Ignacio Pascual Pascual, Josep M. Grau, Miguel Ángel Barba-Romero, María Teresa Gómez‐Caravaca, Javier de las Heras, Pilar Casquero, María Dolores Mendoza, Juan Carlos de León, Antonio Gutiérrez, Germán Morís, Raquel Blanco-Lago, Alba Ramos‐Fransí, Guillem Pintos‐Morell, Maria José García-Antelo, María Rabasa, Yolanda Blanco Morgado, Mercedes Usón, Francisco Javier Miralles, José Eulalio Bárcena, Ana Gómez-Belda, María Isabel Pedraza-Hueso, Miryam Hortelano, Antoni Colomé, Guillermina García Martín, Adolfo López de Munaín, Ivonne Jericó, Lucía Galán-Dávila, Julio Pardo, Giorgina Salgueiro-Origlia, Jorge Alonso‐Pérez, Francesc Pla‐Juncà, Marianela Schiava, Sonia Segovia‐Simón, Jordi Díaz‐Manera,
Pompe disease is a rare genetic disorder with an estimated prevalence of 1:60.000. The two main phenotypes are Infantile Onset Pompe Disease (IOPD) and Late Onset Pompe Disease (LOPD). There is no published data from Spain regarding the existing number of cases, regional distribution, clinical features or, access and response to the treatment. We created a registry to collect all these data from patients with Pompe in Spain. Here, we report the data of the 122 patients registered including nine IOPD ...
Tópico(s): Carbohydrate Chemistry and Synthesis
2023 - Elsevier BV | Neuromuscular Disorders