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268 results

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Page 1
[Cost-effectiveness methods of newborn screening assessment.].
Valcárcel Nazco C, García Pérez L, Linertová R, Castilla I, Vallejo Torres L, Ramos Goñi JM, Labrador Cañadas V, Couce ML, Espada Sáenz-Torres M, Dulín Íñiguez E, Posada M, Imaz Iglesia I, Serrano Aguilar P. Valcárcel Nazco C, et al. Among authors: couce ml. Rev Esp Salud Publica. 2021 Jan 26;95:e202101009. Rev Esp Salud Publica. 2021. PMID: 33496278 Free article. Spanish.
Cost-Effectiveness Methods and Newborn Screening Assessment.
Castilla-Rodríguez I, Vallejo-Torres L, Couce ML, Valcárcel-Nazco C, Mar J, Serrano-Aguilar P. Castilla-Rodríguez I, et al. Among authors: couce ml. Adv Exp Med Biol. 2017;1031:267-281. doi: 10.1007/978-3-319-67144-4_16. Adv Exp Med Biol. 2017. PMID: 29214578 Review.
[Clinical and genetic findings in patients with biotinidase deficiency detected through newborn screening or selective screening for hearing loss or inherited metabolic disease].
Couce ML, Pérez-Cerdá C, García Silva MT, García Cazorla A, Martín-Hernández E, Castiñeiras D, Pineda M, Navarrete R, Campistol J, Fraga JM, Pérez B, Ugarte M. Couce ML, et al. Med Clin (Barc). 2011 Oct 22;137(11):500-3. doi: 10.1016/j.medcli.2011.01.018. Epub 2011 Jul 12. Med Clin (Barc). 2011. PMID: 21752405 Spanish.
Newborn screening for homocystinurias: Recent recommendations versus current practice.
Keller R, Chrastina P, Pavlíková M, Gouveia S, Ribes A, Kölker S, Blom HJ, Baumgartner MR, Bártl J, Dionisi-Vici C, Gleich F, Morris AA, Kožich V, Huemer M; individual contributors of the European Network and Registry for Homocystinurias and Methylation Defects (E-HOD); Barić I, Ben-Omran T, Blasco-Alonso J, Bueno Delgado MA, Carducci C, Cassanello M, Cerone R, Couce ML, Crushell E, Delgado Pecellin C, Dulin E, Espada M, Ferino G, Fingerhut R, Garcia Jimenez I, Gonzalez Gallego I, González-Irazabal Y, Gramer G, Juan Fita MJ, Karg E, Klein J, Konstantopoulou V, la Marca G, Leão Teles E, Leuzzi V, Lilliu F, Lopez RM, Lund AM, Mayne P, Meavilla S, Moat SJ, Okun JG, Pasquini E, Pedron-Giner CC, Racz GZ, Ruiz Gomez MA, Vilarinho L, Yahyaoui R, Zerjav Tansek M, Zetterström RH, Zeyda M. Keller R, et al. Among authors: couce ml. J Inherit Metab Dis. 2019 Jan;42(1):128-139. doi: 10.1002/jimd.12034. J Inherit Metab Dis. 2019. PMID: 30740731 Free article.
[Home births in Spain].
Sánchez Redondo MD, Cernadas M, Couce ML. Sánchez Redondo MD, et al. Among authors: couce ml. An Pediatr (Engl Ed). 2021 May;94(5):346. doi: 10.1016/j.anpedi.2020.11.014. Epub 2020 Dec 25. An Pediatr (Engl Ed). 2021. PMID: 33358529 Free article. Spanish. No abstract available.
Evolution of tyrosinemia type 1 disease in patients treated with nitisinone in Spain.
Couce ML, Sánchez-Pintos P, Aldámiz-Echevarría L, Vitoria I, Navas V, Martín-Hernández E, García-Volpe C, Pintos G, Peña-Quintana L, Hernández T, Gil D, Sánchez-Valverde F, Bueno M, Roca I, López-Ruzafa E, Díaz-Fernández C. Couce ML, et al. Medicine (Baltimore). 2019 Sep;98(39):e17303. doi: 10.1097/MD.0000000000017303. Medicine (Baltimore). 2019. PMID: 31574857 Free PMC article.
268 results