Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Francisco Martínez-Castellano"'
Autor:
Carla Martín‐Grau, Carmen Orellana Alonso, Mónica Roselló Piera, Laia Pedrola Vidal, Roberto Llorens‐Salvador, Ramiro Quiroga, Purificación Marín Reina, Juan Salvador Rubio Moll, Rosa Gómez Portero, Francisco Martínez‐Castellano
Publikováno v:
Clinical Genetics.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::220327e9de635f1a0fdaa351ce3b0182
https://doi.org/10.1111/cge.14340
https://doi.org/10.1111/cge.14340
Autor:
Inmaculada Azorín, Ana Victoria Marco-Hernández, Honorio Barranco-González, Juan Jesus Vilchez Padilla, Alejandro Montoya-Filardi, Inmaculada Pitarch-Castellano, Patricia Smeyers Dura, Miguel Tomás-Vila, Francisco Martínez‐ Castellano, Sandra Monfort-Membrado
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::663ff7f5bb811d5177419b5ff77c89d0
https://doi.org/10.1111/cge.14093/v2/response1
https://doi.org/10.1111/cge.14093/v2/response1
Autor:
Juan Antonio Cerón, Ana Victoria Marco-Hernández, Yanick J. Crow, Francisco Martínez-Castellano, Jesús José Ferre-Fernández, Laia Pedrola, Miguel Tomás-Vila, Marina Martinez-Matilla, María José Aparisi
Publikováno v:
PEDIATRIC NEUROLOGY
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
instname
Martínez-Matilla, M, Ferre-Fernández, J J, Aparisi, M J, Marco-Hernández, A V, Cerón, J A, Crow, Y J, Martínez-Castellano, F, Tomas Vila, M & Pedrola, L 2020, ' Apparent radiological improvement in an infant with Labrune syndrome treated with bevacizumab ', Pediatric Neurology . https://doi.org/10.1016/j.pediatrneurol.2020.07.011
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
instname
Martínez-Matilla, M, Ferre-Fernández, J J, Aparisi, M J, Marco-Hernández, A V, Cerón, J A, Crow, Y J, Martínez-Castellano, F, Tomas Vila, M & Pedrola, L 2020, ' Apparent radiological improvement in an infant with Labrune syndrome treated with bevacizumab ', Pediatric Neurology . https://doi.org/10.1016/j.pediatrneurol.2020.07.011
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2ce50971fa4e89acc20ee7d420fea3e6
https://doi.org/10.1016/j.pediatrneurol.2020.07.011
https://doi.org/10.1016/j.pediatrneurol.2020.07.011
Autor:
Stephen R. Braddock, Francisco Galán, Petra Musilova, Doralice M. Cella, Jiri Rubes, Hidekazu Saito, Alberto Plaja, Mara Cristina de Almeida, Yingjun Xie, Kaline Ziemniczak, Paulo Augusto de Lima-Filho, Kazuki Saito, Marcelo de Bello Cioffi, Yoichi Matsubara, Xiaoman Wang, Roberto Ferreira Artoni, Kazuhiko Nakabayashi, Yoko Tanaka, Hiroshi Okada, Sonia Mayo, Min Chen, James Hejna, Weiqiang Liu, Wagner Franco Molina, Hiromichi Ishikawa, Wenyin He, Miguel del Campo, Viviane Nogaroto, Wei Jian, Yoshitomo Kobori, Viviane F. Mattos, Pruthvi Pota, Tsutomu Ogata, Mami Miyado, Luis A. Alcaraz, Marielle Cristina Schneider, Josiane B. Traldi, Maki Fukami, Marcelo Ricardo Vicari, Neus Castells, Jacqueline R. Batanian, Teresa Vendrell, Orlando Moreira-Filho, Vasiliki Grammatopoulou, Cristina Hernando, Ana Cueto, Jiri Vahala, Hana Sebestova, Nichole Owen, Vanessa Penacho, Jitka Drbalova, Luiz Antonio Carlos Bertollo, Asia D. Mitchell, Erin Torti, Xiaofang Sun, Ding Wang, Robb E. Moses, Susan B. Olson, Tina-A. Martín-Bayón, Scott Rennie, Asunción Fernández, Francisco Martínez-Castellano, Irene Manchón, Olaya Villa, Jun Wei, Karlla Danielle Jorge Amorim, Elisabet Lloveras, Svatava Kubickova, Satz Mengensatzproduktion, Momori Katsumi, Alfonso Carrasco, Navid Ziaie, Druckerei Stückle, Amy E. Hanlon Newell, Leonardo S. Carvalho
Publikováno v:
Cytogenetic and Genome Research. 144
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9be72ab69dfba30bf56eea9c9e4db99c
https://doi.org/10.1159/000381817
https://doi.org/10.1159/000381817
Autor:
Patricia Smeyers Dura, Virginia Ballesteros Cogollos, Francisco Martínez‐ Castellano, Miguel Tomás Vila, Ruben Gómez Fornell
Publikováno v:
European Journal of Paediatric Neurology. 21:e56
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::14382d0ebb430813ca3789f6ccc6cfdc
https://doi.org/10.1016/j.ejpn.2017.04.909
https://doi.org/10.1016/j.ejpn.2017.04.909
Autor:
Alfonso Carrasco, Francisco Galán, Irene Manchón, Vanessa Penacho, Sonia Mayo, Francisco Martínez-Castellano, Luis A. Alcaraz, Tina-A. Martín-Bayón
Publikováno v:
Cytogenetic and genome research. 144(4)
Ring chromosomes are circular structures formed as a result of breaks in the chromosome arms and the fusion of the proximal broken ends with a loss of distal material, or by fusion of dysfunctional telomeres without any loss. The mechanism underlying
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0a1324c2cbe526095b0d3958a1855173
https://pubmed.ncbi.nlm.nih.gov/25722017
https://pubmed.ncbi.nlm.nih.gov/25722017
Publikováno v:
Revista de Neurología. 42:S077
Introduccion. El retraso mental inespecifico se define por la ausencia de rasgos somaticos, neurologicos, bioquimicos o conductuales que caractericen una variante clinica concreta, y supone una elevada fraccion del retraso mental ligado al X (RMLX).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0a22764eb2a09b114adb80b752e9d8d0
https://doi.org/10.33588/rn.42s01.2005711
https://doi.org/10.33588/rn.42s01.2005711