Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Rocío Chacón Aguilar"'
Autor:
Rocío Chacón-Aguilar, Juana María Osorio-Cámara, Isabel Sanjurjo-Jimenez, Carolina González-González, Juan López-Carnero, Begoña Pérez-Moneo
Publikováno v:
Anales de Pediatría, Vol 92, Iss 6, Pp 373-374 (2020)
Externí odkaz:
https://doaj.org/article/ed9d92ae00f44d01b635534dad7ba0a2
Autor:
Rocío Chacón-Aguilar, Juana María Osorio-Cámara, Isabel Sanjurjo-Jimenez, Carolina González-González, Juan López-Carnero, B. Pérez-Moneo
Publikováno v:
Anales de Pediatría (English Edition), Vol 92, Iss 6, Pp 373-374 (2020)
Externí odkaz:
https://doaj.org/article/ee6834c4c54a40f0b5b70ba9234982cf
Autor:
Isabel, Sanjurjo-Jimenez, Cristina, Menéndez Hernando, Inmaculada, Hidalgo Montes, Rocío, Chacón Aguilar, Carolina, González González, Juan, López Carnero, Rocío, Moreno-Novillo, Begoña, Pérez-Moneo
Publikováno v:
Archivos argentinos de pediatria.
Food protein-induced enterocolitis syndrome (FPIES) is a non-IgE mediated allergic reaction with gastrointestinal symptoms, such as vomiting and diarrhea. FPIES diagnosis is based on clinical criteria and on a food challenge test. It is an unknown di
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::52f817cdf09717a03446cdbeea01ca2d
https://pubmed.ncbi.nlm.nih.gov/36194678
https://pubmed.ncbi.nlm.nih.gov/36194678
Autor:
Aida de La Huerga-López, Mercedes Fariñas-Salto, Rocío Chacón-Aguilar, Raquel Martín-Molina, Cristina Menéndez-Hernando
Publikováno v:
Revista Mexicana de Pediatría. 86:194-196
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::816da2bb2b49fe35ac46fd7ca91d2cbb
https://doi.org/10.35366/sp195f
https://doi.org/10.35366/sp195f
Autor:
Mercedes Fariñas Salto, Begoña Pérez-Moneo Agapito, Rocío Chacón Aguilar, Ma Del Rocío Pérez Crespo, Adriana Navas Carretero, Eva Sanavia Morán, Salomé Albi Rodríguez
Publikováno v:
Archivos Argentinos de Pediatria. 117
Kartagener Syndrome is an inherited autosomal recessive disorder characterized by primary ciliary dyskinesia and the triad of situs inversus viscerum, chronic sinus disease and bronchiectasis. Its prevalence varies from 1/15 000 to 1/30 000 but it is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c6726faaba0f8e32ff1b435ec1b38c82
https://doi.org/10.5546/aap.2019.e292
https://doi.org/10.5546/aap.2019.e292
Autor:
Rocío Pérez Crespo, Cristina Menéndez Hernando, Mercedes Fariñas Salto, Rocío Chacón Aguilar, María Cabrerizo Ortiz, Rocío Moreno Novillo, Raquel Martin Molina
Publikováno v:
Archivos Argentinos de Pediatria. 117
Fetomaternal transfusion (FMT) is defined by the transfer of fetal blood into the maternal circulation. The incidence of massive FMT is estimated to be approximately 0.2-0.9 % of births. Although a number of etiologies have been associated with FMT,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ad9e2270acce2d7b7eb97079b5ff0b98
https://doi.org/10.5546/aap.2019.e142
https://doi.org/10.5546/aap.2019.e142
Autor:
Ma Del Rocío, Pérez Crespo, Mercedes, Fariñas Salto, Rocío, Chacón Aguilar, Adriana, Navas Carretero, Eva, Sanavia Morán, Salomé, Albi Rodríguez, Begoña, Pérez-Moneo Agapito
Publikováno v:
Archivos argentinos de pediatria. 117(3)
Kartagener Syndrome is an inherited autosomal recessive disorder characterized by primary ciliary dyskinesia and the triad of situs inversus viscerum, chronic sinus disease and bronchiectasis. Its prevalence varies from 1/15 000 to 1/30 000 but it is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9dc1e6677f428b474f98839ec0a7acc8
https://pubmed.ncbi.nlm.nih.gov/31063320
https://pubmed.ncbi.nlm.nih.gov/31063320
Autor:
Cristina, Menéndez Hernando, Rocío, Chacón Aguilar, Mercedes, Fariñas Salto, Rocío, Pérez Crespo, Raquel, Martin Molina, Rocío, Moreno Novillo, María, Cabrerizo Ortiz
Publikováno v:
Archivos argentinos de pediatria. 117(2)
Fetomaternal transfusion (FMT) is defined by the transfer of fetal blood into the maternal circulation. The incidence of massive FMT is estimated to be approximately 0.2-0.9 % of births. Although a number of etiologies have been associated with FMT,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f16db18fcfd587de047322040864fa10
https://pubmed.ncbi.nlm.nih.gov/30869493
https://pubmed.ncbi.nlm.nih.gov/30869493