Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Leopoldo, Martínez Martínez"'
Autor:
The International EA-QOL Group, Michaela Dellenmark Blom, Stefanie Witt, Benjamin Zendejas, Ivana Sabolić, Juan Domingo Porras-Hernandez, Natalie Durkin, Simon Eaton, Kjersti Birketvedt, Alba Sánchez Galán, Katalin Eszter Müller, Anna Rozensztrauch, Tutku Soyer, Siqi Li, Anastasia Fourtaka, Corne de Vos, Graham Slater, Ana Špoljarić, John Bennett, Ragnhild Emblem, Zita Andrásdi, Robert Smigiel, Dariusz Patkowski, Çiğdem Ulukaya Durakbaşa, Marina Stilinović, Frederic Gottrand, Dora Škrljak Šoša, Tomislav Luetić, Sylwester Gerus, Shen Yang, Yong Zhao, Yichao Gu, Shuangshuang Li, Diego Rodriguez-Alvirde, Orsolya Kadenczki, Miram Pasini, Vuokko Wallace, Anke Widenmann, Feliciana Milagres Sikwete, Jinshi Huang, Leopoldo Martínez Martínez, Kate Abrahamsson, Shawn Izadi, Benno M Ure, Daniel Sidler, Julia H Quitmann, Jens Dingemann
Publikováno v:
Frontiers in Pediatrics, Vol 11 (2023)
BackgroundEsophageal atresia (EA) is a rare congenital anomaly characterized by a discontinuity of the esophagus. Following surgical repair, survival rates have improved dramatically the past decenniums and today exceed 90%, but the children commonly
Externí odkaz:
https://doaj.org/article/4829ecacbcbb4ffebab6b964fbec1314
Autor:
Julio Guerrero-Fernández, Cristina Azcona San Julián, Jesús Barreiro Conde, José Antonio Bermúdez de la Vega, Atilano Carcavilla Urquí, Luis Antonio Castaño González, José María Martos Tello, Amaya Rodríguez Estévez, Diego Yeste Fernández, Leopoldo Martínez Martínez, María José Martínez-Urrutia, Cristina Mora Palma, Laura Audí Parera
Publikováno v:
Anales de Pediatría, Vol 89, Iss 5, Pp 315.e1-315.e19 (2018)
Resumen: Las anomalías de la diferenciación sexual (ADS) engloban un amplio espectro de discordancias entre los criterios cromosómico, gonadal y fenotípico (genital) que definen la diferenciación sexual; actualmente, se aboga por la denominació
Externí odkaz:
https://doaj.org/article/2346869bef1446dd802fbb7b0a7021d7
Autor:
Julio Guerrero-Fernández, Cristina Azcona San Julián, Jesús Barreiro Conde, José Antonio Bermúdez de la Vega, Atilano Carcavilla Urquí, Luis Antonio Castaño González, José María Martos Tello, Amaya Rodríguez Estévez, Diego Yeste Fernández, Leopoldo Martínez Martínez, María José Martínez-Urrutia, Cristina Mora Palma, Laura Audí Parera
Publikováno v:
Anales de Pediatría (English Edition), Vol 89, Iss 5, Pp 315.e1-315.e19 (2018)
Disorders of sex development (DSD) include a wide range of anomalies among the chromosomal, gonadal, and phenotypic (genital) characteristics that define sexual differentiation. At present, a definition as Different sexual development (DSD) is curren
Externí odkaz:
https://doaj.org/article/f368ac114b2641eab1d3904ad89d68ec
Autor:
Muñoz-Serrano AJ, Estefanía-Fernández K, Oterino C, Ramírez Amoros C, Navarro G, Ana Sastre Urgelles, Antonio Pérez-Martínez, Barrena S, Hernández Oliveros F, Leopoldo Martínez-Martínez
Aim: Sarcopenia is associated with poor prognosis in adult oncologic patients, with little evidence of this association in pediatric population, including hepatoblastoma. Methods: Retrospective study in patients with hepatoblastoma, divided into thos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::98b712876f16c0fe466735b160ab7e68
https://doi.org/10.22541/au.167567947.73263102/v1
https://doi.org/10.22541/au.167567947.73263102/v1
Autor:
Elena Fernández Dueñas, Pascual Sanabria Carretero, Francisco Reinoso-Barbero, Ana Fernández Dueñas, Leopoldo Martínez Martínez
Publikováno v:
Open Journal of Anesthesiology. 12:322-337
Autor:
Mariela Dore, Paloma Triana Junco, Carlos De La Torre, Alejandra Vilanova-Sánchez, Monserrat Bret, Gaspar Gonzalez, Vanesa Nuñez Cerezo, Javier Jimenez Gomez, Jose Luis Encinas, Francisco Hernandez, Leopoldo Martínez Martínez, Manuel Lopez Santamaria
Publikováno v:
European Journal of Pediatric Surgery Reports, Vol 06, Iss 01, Pp e18-e22 (2018)
Abstract Introduction Minimally invasive repair for pectus excavatum (MIRPE) is controversial in extremely severe cases of pectus excavatum (PE) and an open repair is usually favored. Our aim is to describe a case of a patient with an extremely sev
Externí odkaz:
https://doaj.org/article/b2636712f0ed47cfb9673b7e5d188ccc
Autor:
Carlos Sánchez-Montenegro, Alejandra Vilanova-Sánchez, Saturnino Barrena-Delfa, Jair Tenorio, Fernando Santos-Simarro, Sixto García-Miñaur, Pablo Lapunzina, Leopoldo Martínez-Martínez
Publikováno v:
Case Reports in Genetics, Vol 2017 (2017)
Costello syndrome is caused by heterozygous de novo missense mutations in the protooncogene HRAS with tumor predisposition, especially rhabdomyosarcoma. We here report two pediatric patients with Costello syndrome and umbilical ligament rhabdomyosarc
Externí odkaz:
https://doaj.org/article/df0439c942704519a6be6279ebf7314f
Autor:
Julio, Guerrero-Fernández, Cristina, Azcona San Julián, Jesús, Barreiro Conde, José Antonio, Bermúdez de la Vega, Atilano, Carcavilla Urquí, Luis Antonio, Castaño González, José María, Martos Tello, Amaya, Rodríguez Estévez, Diego, Yeste Fernández, Leopoldo, Martínez Martínez, María José, Martínez-Urrutia, Cristina, Mora Palma, Laura, Audí Parera
Publikováno v:
Anales de pediatria. 89(5)
Disorders of Sex Development (DSD) include a wide range of anomalies among the chromosomal, gonadal, and phenotypic (genital) characteristics that define sexual differentiation. At present, a definition as Different Sexual Development (DSD) is curren
Autor:
Alejandra Vilanova-Sanchez, Sixto García-Miñaur, Jair Tenorio, Pablo Lapunzina, Saturnino Barrena-Delfa, Leopoldo Martínez-Martínez, Carlos Sánchez-Montenegro, Fernando Santos-Simarro
Publikováno v:
Case Reports in Genetics
Case Reports in Genetics, Vol 2017 (2017)
Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid
Consejería de Sanidad de la Comunidad de Madrid
Case Reports in Genetics, Vol 2017 (2017)
Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid
Consejería de Sanidad de la Comunidad de Madrid
Costello syndrome is caused by heterozygous de novo missense mutations in the protooncogene HRAS with tumor predisposition, especially rhabdomyosarcoma. We here report two pediatric patients with Costello syndrome and umbilical ligament rhabdomyosarc