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[The metabolic newborn screening as a healthcare model of the precision medicine. Perspective from the Spanish Association for the Study of Congenital Errors of Metabolism (AECOM).].
Rev Esp Salud Publica. 2021 Jan 26;95:e202101021.
Rev Esp Salud Publica. 2021.
PMID: 33496277
Free article.
Spanish.
[50 years of the Neonatal Screening Program in Catalonia.].
Marín Soria JL, López Galera RM, Argudo Ramírez A, González de Aledo JM, Pajares García S, Navarro Sastre A, Hernandez Pérez JM, Ribes Rubio A, Gort Mas L, García Villoria J, Gartner Tizano S, Rovira Amigo S, Asensio de la Cruz O, García González M, Cols Roig M, Costa Colomer J, Bádenas Orquin C, Yeste Fernández D, Campos Martorell A, Clemente León M, Mogas Viñals E, Ferrer Costa R, Giralt Arnaiz M, Campistol Plana J, García Cazorla Á, Beneitez Pastor D, Ortuño Cabrero A, Blanco Álvarez A, Tazón Vega B, Roué G, Velasco Puyo P, Murciano Carrillo T, Murillo Sanjuan L, Díaz de Heredia Rubio C, Mañú Pereira MDM, Vives Corrons JL, Arranz Amo JA, Carnicer Cáceres C, Del Toro Riera M, Ormazábal Herrero A, Artuch Iriberri R, García-Volpe C, de Los Santos MM, Sierra March C, Ruiz Hernández CJ, Meavilla Olivas SM, Martín Nalda A, Rivière JG, Parra Martínez A, Soler Palacín P, Martínez Gallo M, Colobran R, Casals Senent T, Armelles Sebastia M, Vidal Benede MJ, Jané Checa M, Fernández Bordón RM, Asso Ministral L, Prats Viedma B, Cabezas Peña C.
Marín Soria JL, et al. Among authors: gort mas l.
Rev Esp Salud Publica. 2020 Dec 16;94:e202012177.
Rev Esp Salud Publica. 2020.
PMID: 33323926
Free article.
Spanish.
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[Galactosialidosis: a new "de novo" mutation in CTSA gene in a patient with late infantile galactosialidosis].
García Hernández L, Sierra Sirvent J, Gort Mas L, Coll Roseli MJ.
García Hernández L, et al. Among authors: gort mas l.
Arch Argent Pediatr. 2018 Feb 1;116(1):e88-e92. doi: 10.5546/aap.2018.e88.
Arch Argent Pediatr. 2018.
PMID: 29333829
Free article.
Spanish.
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