Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Josep Sirvent-Gómez"'
Autor:
Silvia Gartner, Pedro Mondéjar-López, Óscar Asensio de la Cruz, María José Alonso, Marina Álvarez, Anselmo Andrés Martín, María Isabel Barrio Gómez de Agüero, María Jesús Cabero Pérez, Pilar Caro Aguilera, María Cols Roig, Isidoro Cortell Aznar-Pérez, Jordi Costa Colomer, Isabel Delgado Pecellín, Amparo Escribano Montaner, Joan Figuerola Mulet, Gloria García Hernández, Pilar Guayarte, David Gil Ortega, David Gómez Pastrana, Adelaida Lamas Ferreiro, José Luis Marín Soria, Carlos Martín de Vicente, Martín Navarro Merino, Concepción Oliva Hernández, Javier Pérez Frías, Estela Pérez Ruiz, Sandra Rovira Amigo, Antonio Salcedo Posadas, Manuel Sánchez-Solís, Josep Sirvent Gómez, Carlos Vázquez Cordero, José Ramón Villa Asensi
Publikováno v:
Anales de Pediatría (English Edition), Vol 90, Iss 4, Pp 251.e1-251.e10 (2019)
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-León,
Externí odkaz:
https://doaj.org/article/8dd249170a644c38af89ff7e0f733184
Autor:
Vanesa González-Bellido, Verónica Veláz-Baza, Noelia Rama-Suárez, Carmen Jimeno-Esteo, Josep Sirvent-Gomez, Juan Nicolás Cuenca-Zaldívar, Sari Mayorales-lises, Márcio Vinícius Fagundes Donadio, Samuel Fernández-Carnero
Publikováno v:
Hong Kong Physiotherapy Journal, Vol 43, Iss 02, Pp 105-115 (2023)
Background: The International Study of Wheezing in Infants defines recurrent wheezing as the presence of three or more medically documented episodes of wheezing within one year. To date, there is no evidence on the use of hypertonic saline (HS) combi
Externí odkaz:
https://doaj.org/article/66fdd1f75d364019bc458a06fd96e65c
Autor:
Francisco Barros-Angueira, Alfonso Solar-Boga, María L. Couce, Ana Moreno-Álvarez, Cristóbal Colon-Mejeras, Ana Estefanía Fernández-Lorenzo, Rosaura Leis, Josep Sirvent-Gómez
Publikováno v:
Minerva. Repositorio Institucional de la Universidad de Santiago de Compostela
instname
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The frequency of some Cystic Fibrosis (CF) Transmembrane Conductance Regulator gene (CFTR) mutations varies between populations. Genetic testing during newborn screening (NBS) for CF can identify less common mutations with low clinical expression in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eb9249f0b82e5fb3dbf616a430f040e4
https://doi.org/10.1097/md.0000000000011397
https://doi.org/10.1097/md.0000000000011397