Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Adriana Navas Carretero"'
Autor:
Cristina Calvo, Alfredo Tagarro, Enrique Otheo, Cristina Epalza, Francisco José Sanz Santaufemia, Marta Llorente Romano, Cinta Moraleda, M. Luz García García, María Dolores Rodríguez Mesa, Elvira Cobo Vázquez, Sara Pérez Muñoz, María Penin, Mar Santos, Arantxa Berzosa, Adriana Navas Carretero, Paula Vidal Lana, María José Hernández Rodríguez, Pilar Galán del Río, Lucía Figueroa Ospina, Sara Guillen Martín, Ana Belén Jimenez, Amanda Bermejo Gomez, M. José Cilleruelo, Mariann Tóvizi
Publikováno v:
Anales de Pediatría, Vol 92, Iss 4, Pp 239-240 (2020)
Externí odkaz:
https://doaj.org/article/debd3a08ad2c402cbb6b68f198c16cdc
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:
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