2026-04-29T01:50:34Zhttps://repisalud.isciii.es/rest/oai/request

oai:repisalud.isciii.es:20.500.12105/226842025-05-08T11:11:06Zcom_20.500.12105_15322com_20.500.12105_2051col_20.500.12105_16967col_20.500.12105_16988

00925njm 22002777a 4500 dc Gartner, Silvia author Mondejar-Lopez, Pedro author Asensio de la Cruz, Oscar author Alonso, Maria Jose author Alvarez, Marina author Andres Martin, Anselmo author Barrio Gomez de Aguero, Maria Isabel author Cabero Perez, Maria Jesus author Caro Aguilera, Pilar author Cols Roig, Maria author Cortell Aznar-Perez, Isidoro author Costa Colomer, Jordi author Delgado-Pecellin, Isabel author Escribano Montaner, Amparo author Figuerola Mulet, Joan author Garcia Hernandez, Gloria author Guayarte, Pilar author Gil Ortega, David author Gomez Pastrana, David author Lamas Ferreiro, Adelaida author Marin Soria, Jose Luis author Martin de Vicente, Carlos author Navarro Merino, Martin author Oliva Hernandez, Concepcion author Perez-Frias, Javier author Perez Ruiz, Estela author Rovira Amigo, Sandra author Salcedo Posadas, Antonio author Sánchez-Solís, Manuel author Sirvent Gomez, Josep author Vazquez Cordero, Carlos author Villa Asensi, Jose Ramon author Soc Espanola Neumologia Pediat author 2019-04 Newborn screening (NBS) for cystic fibrosis (CF) is well-established in many countries and provides the opportunity for an early diagnosis and treatment before the development of irreversible structural lung damage. In 1999, Catalonia, Castilla-Leon, and the Balearic Islands started the NBS programme for CF. In the last 10 years its implementation rapidly spread and all the autonomies offer the NBS programme for CF since 2015. There are many different strategies across Spain. It is believed that it is very opportune to have an updated and consensual guide for the diagnosis, follow-up, and treatment of patients diagnosed by neonatal screening. (c) 2019 Asociacion Espanola de Pediatria. Published by Elsevier Espana, S.L.U. Gartner S, Mondejar-Lopez P, Asensio De La Cruz O, Alonso MJ, Alvarez M, Andres Martin A, et al. Follow-up protocol of patients with cystic fibrosis diagnosed by newborn screening. An Pediatr. 2019 Apr;90(4):251.e1. Epub 2018 Dec 28. 1695-4033 http://hdl.handle.net/20.500.13003/17443 https://hdl.handle.net/20.500.12105/22684 30598406 10.1016/j.anpedi.2018.11.009 1696-4608 Anales de Pediatria 2-s2.0-85058706003 462858100012 L2001417385 Cystic fibrosis Newborn screening Guidelines for diagnosis and treatment Follow-up protocol of patients with cystic fibrosis diagnosed by newborn screening